Memory consolidation during sleep relies on the precisely timed interaction of rhythmic neural events. Here, we investigate differences in slow oscillations (SO; 0.5–1 Hz), sleep spindles (SP), and their coupling across the adult human lifespan and ask whether observed alterations relate to the ability to retain associative memories across sleep. We demonstrate that older adults do not show the fine-tuned coupling of fast SPs (12.5–16 Hz) to the SO peak present in younger adults but, instead, are characterized most by a slow SP power increase (9–12.5 Hz) at the end of the SO up-state. This slow SP power increase, typical for older adults, coincides with worse memory consolidation in young age already, whereas the tight precision of SO–fast SP coupling promotes memory consolidation across younger and older adults. Crucially, brain integrity in source regions of SO and SP generation, including the medial prefrontal cortex, thalamus, hippocampus and entorhinal cortex, reinforces this beneficial SO–SP coupling in old age. Our results reveal that cognitive functioning is not only determined by maintaining structural brain integrity across the adult lifespan, but also by the preservation of precisely timed neural interactions during sleep that enable the consolidation of declarative memories.
Research in animals and younger adults yields converging evidence that newly acquired information is reprocessed during deep non-rapid eye movement (NREM) sleep. According to the framework of system consolidation1,2 declarative memories are initially processed by a fast learning system in the hippocampus that binds information into a transient representation3. Only repeated reactivation of memories in the hippocampus then eventually allows transfer to a long-term store in the neocortex4,5,6. But how does the brain ensure precise communication between cortical modules that allows for the reorganization of memory traces during sleep?
During sleep, effective communication is enabled by the fine-tuned hierarchical succession of several brain rhythms governed by large-amplitude, low-frequency oscillations, so-called slow oscillations (SO; 0.5–1 Hz) that mainly emerge from prefrontal brain areas7,8,9,10. Via cortico–thalamic projections, neurons in the thalamic reticular nucleus are activated during the depolarized up-states of SOs resulting in the initiation of fast sleep spindles (SP; 12.5–16 Hz)11,12,13,14. These fast SPs, in turn, synchronize cortical activity in a precise spatiotemporal manner thereby establishing a correlated activation between the hippocampus and frontal brain regions15,16,17,18. As the excited neurons exhibit a massive influx of Ca2+, synaptic changes become facilitated and memory consolidation is enabled19,20. Further nesting of hippocampal high-frequency bursts, known as sharp-wave ripples, within the excitable troughs of fast SPs16,21,22 optimizes the hippocampo–neocortical dialogue. A second SP type, so-called slow SPs (9–12.5 Hz), occurs during a time window in which neural depolarization (i.e., the SO up-state) transitions into hyperpolarized down-states12,23,24. A specific role of slow SPs in the consolidation of memories is not yet established2,23,25.
Typically, SOs and SPs are studied with regard to their independent contribution to consolidation mechanisms. However, as system consolidation is assumed to rely on a tight coupling of SOs, SPs, and sharp-wave ripples4,26, recent studies have started to focus on the exact timing of brain rhythms11,23,24,27,28 and its functional significance for sleep-dependent memory consolidation23,28,29,30,31. Recent experiments in rats demonstrated that reinforcing the coordinated pattern of SOs, SPs, and sharp-wave ripples boosts memory consolidation of object locations29, whereas suppression of these patterns has disruptive effects on sleep-dependent memory consolidation30. In humans, SO–SP coupling is enhanced by prior learning23,28 and is triggered by replaying previously learned material during sleep32. Although first studies have highlighted the involvement of SO–SP coupling in memory consolidation, particularly in humans, evidence for this link is still sparse. Further, it remains to be established under which circumstances the coordination of SOs and SPs is most beneficial in supporting the sleep-dependent reorganization and stabilization of memory contents.
SO–SP coupling, for instance, can be critically impaired in disrupted sleep. This is particularly common in elderly adults who often lack the deepest NREM sleep stage, so-called slow-wave sleep33,34,35. In old age, SOs and SPs themselves appear less often and with reduced amplitudes36,37,38. Age-related changes in brain structure possibly contribute to the observed sleep alterations by impairing SO and SP generation and propagation37,39,40,41,42. This may also impact SO–SP coupling itself, thereby resulting in impaired memory stabilization during sleep43. In fact, several studies report age-related loss in overnight memory retention44,45,46, which can be linked to reduced slow-wave sleep39,40 and a decline in SP occurrence47. In light of the growing interest in the interaction of SOs and SPs, very recent evidence highlights that SO–SP coupling is indeed dispersed in elderly adults, resulting in impaired overnight memory consolidation43. As this disturbed nesting of SOs and SPs may constitute a possible target for clinical interventions48, the preconditions and the functional significance of SO–SP coupling across the entire adult lifespan require investigation.
Following this rationale, it was our aim to examine age-related changes in the coupling of SOs and both slow and fast SPs. We asked whether observed alterations can be explained by structural brain atrophy in source regions of SO and SP generation and whether the resulting SO–SP dispersion negatively impacts the ability to retain associative memories across sleep. In the present study, younger and older adults completed an associative memory paradigm, consisting of a learning session of scene–word pairs on the first day and a delayed cued-recall task on the following day (Fig. 1). During the nights before and after learning, sleep was monitored using ambulatory polysomnography (PSG). Structural brain integrity was assessed by voxel-based morphometry (VBM) of structural magnetic resonance images (MRI). By comparing the PSG recordings of younger and older adults, we identify age-related differences in the coordination of SOs and SPs. Using estimates of gray matter volume we further establish the role of structural brain integrity in the coordination of SOs and SPs. Finally, we relate the pattern of SO–SP coupling to the behavioral measure of overnight memory retention and show that the observed ‘aged’ SO–SP coordination indeed explains deficient memory consolidation in old age.
Rhythmic neural events during NREM sleep are affected by aging
Sleep architecture changes drastically across the adult lifespan34. To capture these changes, we recorded electrical neuronal activity during sleep before and after learning scene–word pairs using ambulatory PSG devices at participants’ homes (Materials and Methods). In the following, we focus on sleep after learning only. In comparison to younger adults, we found a lower proportion of slow-wave sleep in older adults, accompanied by a higher proportion of lighter NREM sleep stages 1 and 2 (Table 1). As almost one third of our older sample (n = 9) failed to meet the amplitude criteria of slow-wave sleep when visually scoring the PSG data49, we combined NREM sleep stage 2 and slow-wave sleep for further analyses.
Within NREM sleep we were particularly interested in the occurrence of SOs, as well as slow and fast SPs (slow SP: 9–12.5 Hz, fast SP: 12.5–16 Hz, cf. Materials and Methods). In line with the previously reported topography of slow and fast SPs24, we focused our analyses on frontal slow SPs and central fast SPs. Here, we observed the expected reduction in the occurrence of frontal SOs and slow SPs (SO number: z = 3.14, p = 0.002, MdYA = 1162.5, MdOA = 970.50; SO density: z = 2.09, p = 0.037, MdYA = 3.83 events/min, MdOA = 3.56 events/min; slow SP number: z = 3.41, p < 0.001, MdYA = 275.75, MdOA = 141.50; slow SP density: z = 3.16, p = 0.002, MdYA = 0.83 events/min, MdOA = 0.48 events/min) as well as central fast SPs (fast SP number: z = 5.89, p < 0.001, MdYA = 511, MdOA = 162; fast SP density: z = 5.32, p < 0.001, MdYA = 1.70 events/min, MdOA = 0.58 events/min) (see also Supplementary Table S1 and Supplementary Fig. S1).
Slow and fast SPs sustain their dependency on SOs in older adults
To determine whether SP events indeed coincide with the detected SOs, we calculated the amount of SPs whose center occurred in an interval of ± 1.2 s around the trough of the identified SOs (Fig. 2a). The time window was chosen to cover one whole SO cycle (0.5–1 Hz, i.e., 1–2 s). To cross-check, we also calculated the proportion of SOs with SPs whose center occurred within ±1.2 s around the respective trough of the oscillation (Fig. 2b). In both age groups we identified a comparable percentage of slow SPs coupled to SOs (t(48) = −0.67, p = 0.508, MYA = 57.13%, MOA = 59.60%, Fig. 2a) and, vice versa, a similar amount of SOs co-occurring with slow SPs (t(50) = 1.61, p = 0.115, MYA = 14.36.75%, MOA = 11.18%, Fig. 2b). Although we found a reduced proportion of SOs occurring in coordination with fast SPs in older adults (t(48) = 4.06, p < 0.001, MYA = 14.43%, MOA = 7.34%), the occurring fast SPs were as likely to coincide with SOs in older as in younger adults (t(52) = −2.08, p = 0.043, not significant after applying Bonferroni correction for multiple comparisons, MYA = 31.92%, MOA = 37.92%). This suggests a generally constant pattern of SP–SO coupling across adulthood, with potentially the same mechanisms underlying SP generation. SOs might partly forfeit their ability to initiate fast SP generation in old age. However, those SPs that do occur in older adults are still bound to the occurrence of SOs.
Having established the general presence of SO–SP coordination in old age, we focused on the precise temporal association between SOs and SPs in the next step. We thus calculated peri-event time histograms (PETHs) of SOs co-occurring with fast and slow SP events (Fig. 3, Supplementary Figs S3 and S4, cf. Materials and Methods). In short, these PETHs summarize the probability of fast and slow SP events occurring at a specific time point within ±1.2 s around the SO trough. Stability of these estimates was tested by contrasting the PETHs with their randomly shuffled surrogates (cf. Materials and Methods). In younger adults, we demonstrate the expected preferential occurrence of fast SPs during the positive peaks preceding and following the SO trough (both clusters: p ≤ 0.012), whereas slow SPs were reliably enhanced during the up- to down-state transitions (both clusters: p ≤ 0.008, Fig. 3a,c). Whereas in older adults neither fast nor slow SPs increased before the SO trough, SP increases following the trough resembled those of younger adults: slow SPs peaked during the up- to down-state transition (cluster p = 0.002) and fast SPs during the up-state (cluster p = 0.002, Fig. 3b,d). While the fast SP increase in younger adults co-occurred with the positive SO peak (SO peak at 480 ms, significant positive cluster from 200 to 700 ms), fast SPs peaked before the SO peak in older adults (SO peak at 618 ms, significant positive cluster from 200 to 400 ms) and their temporal specificity was overall less pronounced.
SO–SP coupling differentially changes for fast and slow SPs in younger and older adults
Having established the overall maintenance of a time-specific SO–SP coordination in older adults, we further probed this pattern by comparing the oscillatory power in the SP frequency range for time segments with and without SOs (cf. Materials and Methods). During SO trials (centered on the trough of the respective SO ± 1.2 s), power in the SP frequency range indeed differed significantly from randomly selected intervals without SOs (for all clusters: p < 0.001, Figs 4b and S2). This effect was present in both age groups and suggests a coupling of SPs to specific phases of the underlying SO. Nevertheless, each age group displayed a distinct modulation of the effect (Figs 4b and S2).
In younger adults, we observed increases in fast SP power (12.5–16 Hz) during the SO up-state but not during the down-state (Fig. 4b). Fast SP power increased most strongly during and shortly after the SO peak following the down-state (400 to 700 ms, SO peak at 480 ms). Although this effect was visible across all chosen derivations (Supplementary Figs S2 and S3), it was more pronounced over centroparietal sites. Frontal and central slow SP activity (9–12.5 Hz) was increased during the whole SO interval, but peaked during the up- to down-state transition (−500 to 200 ms; Supplementary Figs S2 and S4).
In older adults, as expected, SOs themselves were expressed differently than in younger adults, with a decreased amplitude and frequency (SO amplitude: z = 5.69, p < 0.001, MdYA = 123.54 μV, MdOA = 74.82 μV; SO frequency: z = 2.68, p = 0.007, MdYA = 0.79 Hz, MdOA = 0.78 Hz, Fig. 4a). But SO-modulated EEG activity also differed from younger adults (Fig. 4b–d). To identify age-specific characteristics of this global pattern we directly compared the time–frequency patterns (i.e., the SO–baseline power differences) of both age groups (Fig. 4c). Further, the temporal evolution of frontal slow SP (9–12.5 Hz) and central fast SP power modulation (12.5–16 Hz; averaged t-values of the SO–baseline contrast within the respective frequency band) was extracted for both age groups and compared by means of a cluster-based permutation test (Fig. 4d). Finally, as studies so far have indicated that SP activity during the SO up-state is critical for memory consolidation28,32, we precisely determined in which frequencies SP activity was modulated most strongly during the SO up-state (cf. Materials and Methods). We thus compared the probability of frequency peaks between 9 and 16 Hz (maximal t-values of the SO–baseline contrast) during the SO up-state (0.2–1.2 s after the SO trough) between younger and older adults (line subplot to the right of Fig. 4c).
Over all derivations, power in higher frequencies (16–20 Hz) was globally reduced during SOs in older compared to younger adults whereas fast SP power differences (12.5–16 Hz) were reduced during the SO up-states only (all significant positive clusters: p ≤ 0.015, Figs 4c and S2). In older adults, the power peak over central sites during the up-state was more stretched in time and shifted to lower frequencies (9–13 Hz, i.e., the slow SP frequency band, Fig. 4b). Moreover, SO-specific fast SP activity was reduced during and following the positive SO peak (SO peak at 618 ms; significant cluster: 459 ms–927 ms; cluster p = 0.013, Fig. 4d). In contrast, older adults revealed a strong increase in slow SP activity during the SO up-state (Figs 3D and 4B). Both the age comparison of the global time–frequency pattern (Fig. 4d) but also the age comparison of slow SP activity modulated during SOs (Fig. 4d, lower panel) indicated a similar SO-specific slow SP power increase in both younger and older adults (all clusters: p ≥ 0.073). Nevertheless, while younger adults showed an almost equal modulation of slow and fast SP power during the SO up-state, older adults displayed a stronger emphasis on lower frequencies: compared to younger adults, fast SP activity was significantly less and slow SP activity significantly more increased during the SO up-state (all clusters: p ≤ 0.007, line subplot to the right of Fig. 4c).
To summarize, we found a characteristic SO–SP coupling pattern in younger adults that was marked by a strong increase in fast SPs coupled to the SO peak as well as an increase in slow SPs during the up- to down-state transition. This pattern changed significantly across the adult lifespan. Within this ‘aged’ SO–SP coupling, three characteristics were striking: First, fast SP modulation was reduced overall in the elderly. Second, a reliable fast SP increase comparable to that of younger adults was limited to the time period before the SO peak. Together with an overall reduced frequency of SOs, fast SPs were thus no longer precisely tied to the SO peak. Finally, slow SPs were similarly modulated in younger and older adults. Together, these changes result in the typical appearance of an ‘aged’ SO-SP coupling pattern with higher coupling in the slow SP frequency range at the end of the SO up-state.
Reduced memory retention is associated with dispersed SO–SP coordination in younger adults
After establishing age-related changes in SO–SP coordination during the SO up-state, we asked how these alterations relate to the ability to retain memories across sleep. As central fast SP activity tied to the SO up-state is critically involved in memory consolidation28,32, we focused our analyses on SP frequencies during the SO up-state (9–16 Hz, 0.2–1.2 s) and on electrode Cz, where we observed a lack of SO–fast SP coupling in older adults (Figs 3 and 4; for frontal channels and Pz, see Supplementary Fig. S5). As a control, we ran the same analysis for a second time window (−500 to 200 ms) during the SO up- to down-state transition that reflects SO-modulated slow SP activity. Here, no significant associations with memory retention were observed after controlling for multiple comparisons (cluster p = 0.169, Supplementary Fig. S6). To minimize biases in SP activity arising from potentially preceding SOs23, all reported analyses were restricted to the up-state following the SO trough.
To quantify memory retention, we measured each participant’s ability to recall scene–word associations that had been successfully encoded the day before. We calculated the percentage of correctly recalled items during delayed recall relative to all items that were correctly retrieved during immediate recall before sleep. Whereas younger and older adults did not differ with regard to their learning performance on Day 1 (t(59) = 1.62, p = 0.11; MYA = 53.83%, SDYA = 20.80%; MOA = 45.80%, SDOA = 19.02%), memory consolidation was significantly reduced in older adults. On Day 2, younger adults retained on average 90.21% of the previously learned pairs (SDYA = 7.42%). However, older adults showed significantly worse memory retention across sleep (MOA = 71.13%, SDOA = 13.33%, t(56) = 7.33, p < 0.001; Fig. 5a).
Correlational analyses between SO–baseline power differences (expressed in t-values) and memory retention were performed separately for each time–frequency point. Significant associations were identified by testing against a bootstrapped reference distribution of the EEG–memory correlations. In this way, we could identify significant correlation clusters that represent the association between memory retention and a specific pattern of EEG activity modulated during the SO up-state (cf. Materials and Methods, Fig. 5b for a schematic depiction of the performed correlation technique). Across both age groups, we identified a significant positive correlation cluster (cluster p = 0.024, mean r = 0.36, Fig. 5c): more fast SP activity during the SO up-state, which is in general more typical for SO–SP coupling in younger adults, was associated with better memory retention.
To further probe the association between memory retention and SO-modulated EEG activity, we then proceeded to conduct the very same analysis within each age group separately. Here, we found a significant negative correlation cluster in younger adults (cluster p = 0.028, mean r = −0.52, Fig. 5d): Younger adults showing a SO-specific power modulation with less emphasis on fast SP activity during the SO peak but rather on lower frequencies (9–13 Hz) during and following the SO peak showed worse overnight retention of memories. As depicted in the right panel of Fig. 5d, the cluster extracted in younger adults overlapped with the typical SO-related activity pattern of older adults that is marked by a shift to lower SP frequencies and a more stretched power peak sustained until the end of the SO up-state. Younger adults displaying a coupling pattern typical for older adults tended to be worse at retaining previously learned information overnight (cf. Supplementary Fig. S7). Although no significant correlation cluster was extracted in older adults, the average correlation within the cluster identified in younger adults did not differ significantly between age groups (rOA = −0.11, z = −1.64, p = 0.10, Fig. 5d). This suggests that the same functional association between SO-modulated SP activity and memory retention exists in both younger and older adults.
To conclude, we found evidence for an association between the coordination of SOs and SPs and memory retention. In general, high levels of fast SP power during and following the positive SO peak were related to better memory retention. Moreover, our results suggest that inter-individual differences in SO–SP coupling as maximized between age groups also drive differences in memory retention within age groups. Dispersed SO–SP coupling, which was characteristic of older adults, already predicted worse memory retention among younger adults.
Structural brain integrity in old age promotes ‘youth-like’ SO–SP coupling
In line with previous reports on the influence of age-related brain atrophy on the generation of sleep oscillations39,40, we finally asked whether the identified age-specific modulation of SP activity during the SO up-state is associated with measures of brain volume in specific regions of interest (ROI). As ROIs we primarily included brain regions that are considered source regions for the generation of SOs and SPs9,11 and proposed to be involved in memory processing during sleep5 (Fig. 6a). To exclude any age-related confounds, measures of brain volume were derived by using voxel-based morphometry (VBM) and correcting the extracted ROI-specific measures for total intracranial volume (TIV)50. Again, we focused our analysis on frequencies between 9 and 16 Hz and a time window between 0.2 and 1.2 s after the SO trough. Whereas the cluster-corrected correlation analysis (cf. Fig. 5b, Materials and Methods) did not indicate any significant association between brain volume and EEG power in younger adults (all clusters: p ≥ 0.073; Supplementary Fig. S8), we observed a very specific pattern in older adults.
In older adults, larger medial prefrontal cortex (mPFC) volume was associated with higher power in the fast SP range during the SO peak (mean rmPFC = 0.43, cluster pmPFC = 0.018). Thalamus volume showed a similar positive relation with SP activity during the SO peak. This effect, though, was less precise with regard to the frequency range (mean rthalamus = 0.45, cluster pthalamus = 0.013, see Fig. 6). For hippocampus, entorhinal, and occipital cortex even broader effects were observed. Greater volume in these regions was not only associated with higher fast SP power during the SO peak, but generally with more global neuronal activation during the SO up-state. In particular, the observed effect extended to slow SP frequencies at the end of the SO up-state (mean rhippocampus = 0.47, cluster phippocampus = 0.004; both mean rentorhinal cortex = 0.46, cluster pentorhinal cortex = 0.013 and 0.031; mean roccipital lobe = 0.42 and 0.43, cluster p occipital lobe = 0.027 and 0.035).
To summarize, older adults with less age-related decline in mPFC and thalamus volume showed a more precise coupling between fast SPs and SOs time-locked to the SO peak – precisely the pattern observed in younger adults. Less age-related decline in medial temporal lobe areas was moreover associated with overall enhanced neuronal activity during the SO up-state. We thus conclude that structural brain integrity in old age promotes ‘youth-like’ SO–SP coupling.
This study investigated whether the coupling of SOs and SPs during sleep changes across the adult lifespan and how these alterations relate to the ability to retain associative memories across sleep. We demonstrate that older adults do not display the central fast SP power increase time-locked to the SO peak that we observed in younger adults. Instead, they exhibit overall reduced fast SP power modulations and a fast SP peak that is shifted before the SO peak. Overall, the ‘aged’ SO–SP coupling pattern is most characterized by increases in slow SP power at the end of the SO up-state. We find evidence that this increase in slow SP power, typical for older adults, coincides with worse memory consolidation, whereas a ‘youth-like’ precision of fast SPs coupled to the SO peak promotes memory consolidation across the entire adult lifespan. Moreover, greater structural integrity in brain regions involved in the generation of SOs and SPs relates to an intact ‘youth-like’ SO–SP coupling in old age. Overall, our results resonate well with a recent report by Helfrich and colleagues on age-related differences in SO–SP phase–amplitude couplings and their functional significance for memory retention43. We extend these findings by applying analysis methods that are sensitive to age-related shifts in both the time and frequency domain and explicitly base our analyses on the differentiation between slow and fast SPs. Together with Helfrich and co-authors43, we are the first to demonstrate that an age-related dispersion of SO–SP coupling, as caused by structural brain atrophy, relates to impaired memory consolidation in old age.
Age-related dispersion of SO–SP coupling
Effective neural communication during NREM sleep is governed by SOs that, during their up-states, initiate the generation of thalamic fast SPs11. Here, we found that a generally constant pattern of SP–SO co-occurrence exists across adulthood, although SO and SPs did not co-occur in a one-to-one fashion (Fig. 2). Our results imply that: (1) Although it appears that thalamic SP generation is triggered by frontal SOs11,12, at least one other mechanism initiating SPs exists. (2) SO-induced SP initiation is not a necessity, but rather a rare occurrence. Nevertheless, if SOs and SPs co-occur, they do so in a precisely timed manner, as discussed next.
Consistent with a wide range of studies, we identified a precisely timed hierarchical structure of SOs and SPs in younger adults with fast SPs appearing during the highly depolarized SO peak and slow SPs occurring at the up- to down-state transition21,23,24,27. SOs themselves change their appearance in old age and exhibit reduced amplitudes and slower frequencies in older adults (Fig. 4a)35,37. Flatter SOs have previously been associated with less synchronous neuronal switches between phases of depolarization and hyperpolarization38. As these phases precisely time the generation of SP events themselves, SO–SP coordination should, as a consequence, disperse in old age.
Indeed, consistent with recent reports43,48, in older adults EEG activity during SOs was differentially modulated than in younger adults. (1) In line with previously reported reductions in central fast SPs in old age36,51, fast SP increases during the SO up-state proved less pronounced in older adults. (2) If fast SPs appeared, they were no longer precisely tied to the SO peak as observed in younger adults. Rather, they occurred before the up-state reached its maximum. (3) Over central sites modulation of EEG activity during the SO up-state dispersed, the power peak was stretched in time and shifted to lower frequencies (9–13 Hz). All things considered, we argue that even in older adults a very specific pattern of SO–SP coupling exists, although its appearance changes compared to younger adults, with more emphasis on lower frequencies occurring later during the SO up-state. Possible causes and mechanisms of this ‘aged’ pattern will be discussed next.
Structural correlates of SO–SP coupling
The process of SO–SP coupling involves intact communication between different brain regions11. SOs, generated mainly in prefrontal areas, propagate throughout the brain9 and potentially trigger the initiation of fast SPs in the thalamus11. Here, we indicate that in old age structural integrity in the mPFC accounts for a ‘youth-like’ SO–SP coupling (Fig. 6). This is in line with Helfrich and colleagues (2018) who recently demonstrated that greater mPFC volume relates to a more precise coupling of fast SPs to the SO peak43. Expanding on that observation, we show that additional brain regions are associated with inter-individual differences in SO–SP coupling. Greater thalamus volume, the main source region of fast SP generation13, related to more SP activity during the SO peak. The specificity of these effects strongly suggests that structural integrity in both mPFC and thalamus is crucial for pacing a ‘youth-like’ SO–SP succession. In contrast, hippocampus and entorhinal cortex volumes were linked to both fast SP activity coupled to the SO peak and slow SP activity occurring at the up- to down-state transition. Both hippocampus and entorhinal cortex are key players in the overnight consolidation of memories2. In particular, sharp-wave ripples are generated within the hippocampus and thereby complete SO–SP coupling21 as the basis for successful memory reprocessing during sleep29,30. Thus, we speculate that the association between structural integrity of the medial temporal lobe and a successful coordination of oscillatory processes during sleep is indicative for sharp-wave ripple activity.
In our analyses, significant associations between SO–SP coupling and VBM measures were only found within the older sample. Importantly, this does not imply that those brain areas do not contribute to an effective hierarchical nesting of neuronal oscillations during sleep in younger adults. We rather suggest that brain integrity in mPFC, thalamus and medial temporal lobe areas forms the basis for an effective ‘youth-like’ SO–SP coupling independent of age. Under conditions of impaired structural integrity in these regions, as is the case in aging50, the precise timing of SOs and SPs vanishes. This reasoning is in line with Nyberg and colleagues (2012) who argue that the individuals who experience fewer age-related structural brain changes are more likely to show neural activity patterns that resemble those of younger adults and that are associated with better performance52.
Functional significance of precise SO–SP coupling
Current theory holds that hippocampal–neocortical communication during sleep is only enabled by the precise hierarchical coordination of SOs, SPs, and hippocampal sharp-wave ripples53,54. This is achieved by locking fast SPs to the SO peak and further nesting sharp-wave ripples within the troughs of fast SPs21. Thus, memories initially dependent on a temporary store in the hippocampus become more reliant on neocortical areas, where they are permanently stored4,26,55.
Here, we show that, across younger and older adults, ‘youth-like’ SO–SP coupling, that is marked by a tight precision fast SPs to the SO peak, coincided with better memory retention (Fig. 5c). In contrast, a SO–SP coupling pattern most characterized by an increase in slow SP power at the end of the SO up-state, as typically displayed by older adults, was associated with worse memory retention in younger adults already (Fig. 5d). Our results support previous evidence showing that the precisely timed interaction of neural rhythms indeed supports sleep-dependent memory consolidation29,30,31,32,43,48. Brain activity is globally synchronized during the SO up-state and maximized during the SO peak14. This constitutes a moment of effective interregional brain communication. Fast SPs occurring at this very moment induce a massive influx of Ca2+ into excited neurons. This enables synaptic plasticity and promotes the stabilization and integration of memory representations56. As most recently demonstrated, fast SPs are misaligned in older adults, resulting in worse memory retention43. But what is it that makes the ‘aged’ SO–SP coupling detrimental?
First, the temporal dispersion of ‘aged’ SO–SP coordination in older adults is striking. In older adults, the fast SP power increase during the SO up-state reaches its maximum before the SO peak (Figs 3 and 4). This may be explained in two ways: (1) During flatter SOs, as observed in older adults, the switch between up- and down-states is more variable35,37,38 and as a result SP initiation is also less precise. (2) The mechanism initiating SPs might be similarly timed in younger and older adults, but as SOs are slower in older adults, fast SPs appear too early during the SO up-state. Here, global brain synchrony has not reached its maximum yet and interregional brain communication might not be optimal for reorganization of memories on a brain system level.
The second characteristic of ‘aged’ SO–SP coupling is a power shift to lower frequencies in the slow SP band at the end of the SO up-state (Fig. 3). At young age already, this shift related to worse memory retention (Figs 5 and S7). Recent evidence suggests that fast and slow SPs are generated via distinct mechanisms57,58 and have different functional significances. While the occurrence of fast SPs probably reflects thalamo–cortical information processing necessary for memory transfer, slow SPs may mirror cortico–cortical communication59. Slow SPs per se may not be sufficient to enable effective memory consolidation during sleep2,23,25,32. When focusing our analysis on the up- to down-state transition, where slow SPs preferentially occur23,24, no association with memory retention was detected (Supplementary Fig. S6). To conclude, our results replicate the finding that a precise ‘youth-like’ SO-fast SP coupling is beneficial for memory consolidation43,48. Vice versa,’aged’ coupling coincides with worse memory consolidation already in young adulthood. This lines up with the concept of “brain maintenance”52 stating that cognitive functioning is not only determined by maintained structural integrity across the adult lifespan, but also by the preservation of functionally specific processes and networks52,60,61. Maintenance of ‘youth-like’ processing during both encoding60 and memory retrieval61 has previously shown to relate to better long-term memory in older adults. Here we complement this view by demonstrating that consolidation processes also benefit from maintained brain mechanisms during sleep.
Materials and Methods
Participants and procedure
Thirty-four healthy younger adults (19–28 years) and 41 healthy older adults (63–74 years) participated in the experiment. Due to technical failures, data collection from 4 younger and 4 older adults could not be completed. One older adult had to be excluded due to an incidental MR finding. Accordingly, the final sample for our behavioral analysis consisted of 30 younger (Mage = 23.7 years, SDage = 2.6; 17 females) and 37 older adults (Mage = 68.92 years, SDage = 3.04; 16 females). For some participants, parts of the neural data (PSG or MRI) were missing or of bad quality. Final PSG analyses were hence conducted with 24 younger (Mage = 23.61 years, SDage = 2.55; 13 females) and 31 older adults (Mage = 68.63 years, SDage = 3.10; 15 females), VBM analyses with 24 younger (Mage = 23.61 years, SDage = 2.55; 13 females) and 29 older adults (Mage = 68.64 years, SDage = 3.10; 14 females). The different samples did not differ with regard to any behavioral measure.
All participants were right-handed native German speakers with no reported history of psychiatric or neurological disease, or any use of psychoactive medication. To screen for cognitive impairments in the sample of the elderly, all older adults completed the Mini-Mental State Examination (MMSE; M = 29.24, SD = 1.12, Range: 26–30)62 and passed a brief memory screening beforehand. General subjective sleep quality was controlled by assessing the Pittsburgh Sleep Quality Index (PSQI)63 and did not show differences between the two age groups. The study was approved by the Ethics Committee of the Deutsche Gesellschaft für Psychologie (DGPs) and, in accordance with their guidelines, conducted at the Max Planck Institute for Human Development in Berlin. After being informed about the complete study procedure, all participants gave written consent to their participation in the experiment.
The present data were derived from a series of studies investigating age-related differences in the encoding, consolidation, and retrieval of associative memories (see Fandakova et al., 2018, for the effects of age and memory quality on false memory retrieval64). Core of the experimental design was a paired-associative scene–word memory paradigm, consisting of a learning session on the first day (Day 1) as well as a delayed cued-recall task approximately 24 hours later (Day 2) (see Fig. 1, for illustration of the study procedure). During the nights before and after learning (experimental nights PRE and POST) sleep was monitored at participants’ home using ambulatory PSG. Prior to the first experimental night an adaptation night familiarized the participants with the PSG procedure. Structural MRI data were collected on Day 2. Furthermore, EEG was recorded during learning on Day 1. Additionally, functional MRI data were collected during delayed recall on Day 2. Neither the EEG nor the fMRI data are included in the present report. Participants completed a short cognitive screening prior to participation in the main study, but did not engage in any other behavioral task during the course of the experimental procedure described above.
Day 1 – Encoding and immediate cued-recall
During initial study, scene–word pairs were presented on a black background for 4000 ms. Scene–word pairs were randomized combinations of indoor and outdoor scenes and concrete nouns. Participants were instructed to remember the scene–word pair using a previously trained imagery strategy and to indicate how well they were able to form an integrated image of the scene–word pair. Cued-recall blocks followed immediately after the initial learning phase. Scenes served as cues for participants to verbally recall the associated word. Recall time was not constrained. Independent of recall accuracy, the correct scene–word pair was presented again for 3 seconds and participants were instructed to use this opportunity to remember the word–scene pair by forming an integrated image of the two. Finally, participants completed a final cued-recall test without feedback at the end of Day 1. This phase served as a measure of learning performance. Importantly, task difficulty was adjusted between the age groups to achieve comparable recall success of approximately 50% in each age group. This was done in two ways. First, younger adults learned 440 pairs, whereas older adults learned 280 pairs on Day 1. Second, younger adults completed one cued-recall block with feedback, whereas older adults completed two cued-recall blocks with feedback. Further details about the encoding task and the stimulus set are described by Fandakova et al.64.
Day 2 – Delayed cued-recall
Delayed cued-recall of the scene–word pairs consisted of four blocks of 70 experimental trials each and was conducted inside a 3T MRI scanner. For the older age group, all of the 280 studied pairs were presented. For younger adults items were chosen with regard to their learning history. This resulted in a selection of pairs, half of which had been recalled in the criterion cued-recall the day before. The 280 pictures were displayed for 3500 ms. Meanwhile participants had to decide via keypress if they still remembered the corresponding word (“remembered” vs. “forgotten”). Afterwards, four letters were presented for 3500 ms. One of these was the second letter of the correct word and had to be selected by pressing the corresponding key. If the according word had been forgotten or none of the letters fitted their remembered answer word, participants were told to choose one of the letters at random. Answers during delayed recall were only classified as correct if participants both responded that they remembered the word and selected the right letter afterwards.
Sleep EEG data acquisition and analyses
During the two experimental nights before (PRE) and after learning (POST), sleep was recorded using an ambulatory PSG device (SOMNOscreen plus; SOMNOmedics, Germany). Eight scalp electrodes were attached according to the international 10–20 system for electrode positioning (Fz, F3, F4, C3, C4, Cz, Pz, Oz)65,66 along with two electrodes on the mastoids A1 and A2 that later served as the offline reference. All impedances were kept below 6 kΩ. Data were recorded using Cz as the online reference for all EEG derivations and AFz as ground. Additionally, a bilateral electrooculogram (EOG) was assessed. Two submental electromyogram channels (EMG) were positioned left and right inferior of the labial angle and referenced against one chin electrode. Electrical activity of the heart was recorded using two electrocardiogram channels (ECG). All electrodes were attached to a small recorder fixed with two straps either to the front or back of the torso depending on the participant’s sleep habits. EEG channels were recorded between 0.2–75 Hz with a sampling rate of 128 Hz.
Data was preprocessed using BrainVision Analyzer 2.1 (Brain Products, Germany). Here, all EEG channels were re-referenced against the average of A1 and A2. Afterwards, sleep stages 1 and 2, slow-wave sleep, REM sleep, awakenings, and body movements were visually scored in 30-second epochs according to the standard criteria suggested by the American Academy for Sleep Medicine (AASM)49. Participants provided markers for switching the light off and on again, narrowing the time period to be analyzed. Visual determination of sleep onset and offset took place when participants did not remember to set the markers (n = 5). Total sleep time (TST) was calculated as time spent in stage 1, 2, SWS, and REM sleep. Wake after sleep onset (WASO) was defined as the time participants were awake between sleep onset and final morning awakening.
Further analyses of the sleep EEG data were conducted using Matlab R2014b (Mathworks Inc., Sherbom, MA) and the open-source toolbox Fieldtrip67. Bad EEG channels were visually rejected. For the remaining channels, artefact detection was implemented on 1-second long segments. Segments that were visually identified as body movement or exhibited amplitude differences of more than 500 μV were marked as bad. To further exclude segments that strongly deviated from the observed overall amplitude distribution, mean amplitude differences for each segment were z-standardized within each channel. Segments with a z-score of more than 5 in any of the channels were excluded.
SPs were detected using an established automated algorithm23,24,68. For all NREM epochs (i.e., stage 2, and slow-wave sleep), EEG data were band-pass filtered using a 6th-order Butterworth filter (in forward and backward direction to prevent phase distortions) between 9 and 12.5 Hz for the detection of slow SPs, respectively 12.5 and 16 Hz for fast SPs69,70. The root-mean-square (RMS) representation of the signal was calculated at every sample point using a sliding window of 200 ms. Afterwards, the RMS signal was smoothed by applying a moving average of 200 ms. To increase sensitivity and specificity of our algorithm71, we accounted for individual differences in EEG amplitude by anchoring the SP identification on individually determined amplitude thresholds. A potential SP was tagged if the amplitude of the smoothed RMS signal exceeded its mean by 1.5 SD of the filtered signal for 0.5 to 3 seconds. SPs with boundaries closer than 0.25 seconds were eventually merged in the following way: in each processing run, starting with the smallest boundary difference, two SPs were merged if the resulting SP event remained within the time limit of 3 seconds. As soon as a SP was combined with another one, it could not be merged with another SP in the very same run anymore. Only if all boundary differences were revised and no further merging of putative SPs was possible, the new resulting SP events were processed in a next run. Starting again with the smallest boundary difference, two putative SPs could be merged if the merged event remained within the required time limit. These runs were repeated until no further merging was possible. Finally, only SPs not overlapping with previously marked artefact segments were considered SPs.
Slow oscillation detection
Detection of SOs at frontal electrodes was based on Mölle et al.27 and Ngo et al.72. For all NREM epochs, EEG data was band-pass filtered between 0.2 and 4 Hz using a 6th-order Butterworth filter (in forward and backward direction). The whole signal was then divided into negative and positive half-waves that were separated by zero-crossings of the filtered signal. The combination of a negative half wave with the succeeding positive half wave was considered a putative SO when its frequency was between 0.5 and 1 Hz. The amplitude of each potential slow wave was calculated as the distance between the SO trough and positive peak, defined as its maximal negative and positive potential, respectively. As in the SP detection, adaptive amplitude thresholds were defined separately for each participant: Putative SOs exceeding a trough of 1.25 times the mean trough of all putative SOs as well as an amplitude of 1.25 times the average amplitude of all potential SOs, were marked. Only artefact-free SOs were considered in further analyses.
Statistical analyses were conducted using Matlab R2014b (Mathworks Inc., Sherbom, MA) and the open-source toolbox Fieldtrip67 as well as RStudio 1.0.53 (RStudio, Inc., Boston, MA). Not all sleep variables used in our analysis followed a normal distribution. To identify age differences in the sleep architecture and the expressed sleep oscillations between younger and older adults, non-parametric Mann-Whitney U Tests for independent samples were calculated and median and quartile values of the variables were reported.
Temporal relation between detected SO and SP events: The coordination of SOs and SPs was evaluated for NREM sleep as a combination of stage 2 and slow-wave sleep as SO–SP coupling has been demonstrated to be stable across stage 2 and slow-wave sleep73. The general temporal relation between SO and SP events was calculated by determining the proportion of SPs whose center occurred in an interval of ±1.2 s around the trough of the identified SOs, and the amount of SOs with SPs whose center occurred within ±1.2 s around the respective trough of the oscillation. The time window of ±1.2 s was chosen to cover one whole SO cycle (0.5–1 Hz, i.e., 1–2 s). The exact timing of SO and SP events was visualized by peri-event time histograms (PETHs) of fast and slow SP centers (seed events) occurring within a time interval of ±1.2 s around each SO trough (target event). Probabilities of seed event occurrence were summed within bins of 100 ms and normalized to add up to 100%. Following the same pipeline, PETHs were also calculated for intervals of ±5 s to demonstrate the general specificity of SP appearance to the actual presence of SOs (Supplementary Figs S3 and S4). To test for the temporal stability of the PETHs, we implemented a randomization procedure by randomly shuffling the temporal order of the PETH bins 1000 times. The resulting surrogates were averaged for each individual and tested against the original PETHs using dependent sample t-tests. Control for multiple comparisons was achieved by applying a cluster-based permutation test with 5000 permutations74.
Time–frequency analyses: To describe the temporal association between SPs and SOs, we selected 6-second long artefact-free trials from the EEG data, centered on the trough of the SOs ± 3 s. The longer time segments were selected to prevent filter artefacts during later analysis steps (e.g., due to wavelet filtering). All analyses described in the following were first conducted separately for SOs detected at the two frontal derivations F3 and F4, and then averaged. Time–frequency analyses were performed at frontal electrodes as well as at electrodes Cz and Pz. To achieve an appropriate baseline contrast allowing for the interpretation of SO specific power decreases and increases, we matched every detected SO with a randomly chosen artefact-free time segment of 6 seconds during the same sleep stage as the respective SO. To obtain time–frequency representations of trials with and without SOs, we applied a Morlet-wavelet transformation (12 cycles) to the unfiltered EEG data of SO and baseline trials between 5 Hz and 20 Hz in steps of 1 Hz and 2 ms. Trials with and without SOs were then contrasted for each subject using independent-sample t-tests. The resulting t-maps reflect the increase/decrease in both the fast and slow SP frequency range for trials with SOs, compared to trials without. Due to the high prevalence of SOs during slow-wave sleep, the number of identified baseline trials sometimes differed from the number of SO trials during this sleep stage. Thus, to calculate the within-subject contrasts, we drew 100 random sets of baseline and SO trials while maintaining the ratio of stage 2 to slow-wave sleep trials (average trial number: 599 ± 225). t-maps for all these random trial sets were averaged for each subject. These t-maps were further averaged across F3 and F4 SOs for each participant before subjecting the results to group-level analyses. Separately for each age group, t-maps were tested against zero using a cluster-based permutation test with 5000 permutations in a time window of –1.2 to 1.2 s74.
Age comparison of SO–SP coupling: Age differences in SO-modulated SP activity were quantified in three ways: (1) The time–frequency t-maps (SO vs. baseline trials) of both age groups were compared using a cluster-based permutation test with 5000 permutations. (2) The time course of frontal slow SP (9–12.5 Hz) and central fast SP power modulation (12.5–16 Hz) was extracted by averaging the t-values of the SO–baseline contrast within the respective frequency band. SO-specific SP power modulation was extracted at each time point during the SO (SO trough ± 1.2 s) for both age groups and compared by means of a cluster-based permutation test with 5000 permutations. (3) Finally, we determined the frequencies with strongest power modulation during the SO up-state. We focused on a time–frequency window covering the whole SP range (9–16 Hz) and the entire SO up-state (0.2–1.2 s). For each frequency, we determined the peak power modulation (i.e., the maximal t-values of the SO–baseline contrast) during the SO up-state. For each subject, the maximum t-values across frequencies were scaled between 0 (lowest t-value) and 1 (peak modulation). The resulting distribution reflects the probability of observing the maximum power differences between SO and baseline trials at a given frequency during the SO up-state. Age differences in the peak probability distribution were calculated using a cluster-based permutation test with 5000 permutations.
EEG–behavior correlation: As we aimed to identify the functional significance of the detected SO–SP association during the SO up-state, we then correlated each participant’s individual time–frequency t-maps for the comparison with/without SOs with the participant’s ability to retain previously learned information overnight (cf. Fig. 5b for a schematic depiction of the correlation analysis). For each time–frequency point (9–16 Hz, 0.2–1.2 s) a Pearson’s correlation with the behavioral outcome variable was computed. Control for multiple comparisons was achieved using a cluster-corrected correlation approach with 5000 bootstrap samples to create the reference distribution. Correlation analyses were performed across all subjects and within each age group separately.
MRI data acquisition and structural MRI analyses
Whole-brain MRI data was acquired with a Siemens Magnetom 3 T TimTrio machine. For each participant a high-resolution T1-weighted MPRAGE sequence (TR = 2500 ms, TE = 4.77 ms, FOV = 256 mm, voxel size = 1 × 1 × 1 mm3) was collected. To get estimates of brain volume in regions of interest (ROI) we conducted voxel-based morphometry (VBM) using statistical parametric mapping software (SPM12, http://www.fil.ion.ucl.ac.uk/spm) and the Computational Anatomy Toolbox (CAT 12, http://www.neuro.uni-jena.de/cat). Images were normalized to Montreal Neurological Institute (MNI) space and segmented into gray matter, white matter, and cerebrospinal fluid. Data were then modulated, i.e., corrected by the volume changes due to spatial normalization. For this, each voxel value was multiplied with the Jacobian determinant derived from the spatial normalization step. Afterwards images were smoothed with a 8 mm full width at half maximum (FWHM) kernel. Total intracranial volume (TIV) was estimated by summing volume of gray matter, white matter, and cerebrospinal fluid. Due to their involvement in sleep-dependent memory processes and especially in the generation of SPs and SOs5,9,11, we selected bilateral medial prefrontal cortex (mPFC), thalamus, entorhinal cortex, hippocampus, and the medial occipital lobe (Fig. 6A). The mPFC mask was kindly provided by Bryce A. Mander39. All other ROIs were defined using the WFU PickAtlas toolbox (http://fmri.wfubmc.edu/software/pickatlas). Measures of gray matter volume in all ROIs were extracted using the REX toolbox (http://web.mit.edu/swg/rex/rex.pdf) and adjusted for differences in TIV based on the formula provided by Raz et al. (2005) (adjusted volume = raw volume −b × (TIV − mean TIV), where b is the slope of the regression of ROI volume on TIV)50.
EEG–brain structure correlation
The association between structural brain integrity and SP activity coupled to the SO up-state was similar to the cluster-corrected correlation analysis described above (cf. Fig. 5b). Each participant’s individual time–frequency t-map was related to gray matter volumes in the different ROIs and referenced to a bootstrapped reference distribution (5000 bootstrap samples).
A previous version of the article was deposited on the preprint repository bioRxiv in February 201875.
The custom code and data necessary to reproduce all statistical results, Figures and Supplementary Material of this article is available on the Open Science Framework repository (https://osf.io/3ycre/). Raw data along with all preprocessing scripts and first level analyses are available from the corresponding authors upon reasonable request.
Diekelmann, S. & Born, J. The memory function of sleep. Neuroscience 11, 114–126 (2010).
Rasch, B. & Born, J. About sleep’s role in memory. Physiol. Rev. 93, 681–766 (2013).
Simons, J. S. & Spiers, H. J. Prefrontal and medial temporal lobe interactions in long-term memory. Nat. Rev. Neurosci. 4, 637–48 (2003).
Born, J. & Wilhelm, I. System consolidation of memory during sleep. Psychol. Res. 76, 192–203 (2012).
Gais, S. & Born, J. Declarative memory consolidation: Mechanisms acting during human sleep. Learn. Mem. 11, 679–685 (2004).
Walker, M. P. The role of slow wave sleep in memory processing. J. Clin. Sleep Med. 5, S20–S26 (2009).
Achermann, P. & Borbély, A. A. Low-frequency (<1H z) oscillations in the human sleep electroencephalogram. Neuroscience 81, 213–222 (1997).
Murphy, M. et al. Source modeling sleep slow waves. Proc. Natl. Acad. Sci. USA 106, 1608–1613 (2009).
Nir, Y. et al. Regional slow waves and spindles in human sleep. Neuron 70, 153–169 (2011).
Cox, R., van Driel, J., de Boer, M. & Talamini, L. M. Slow oscillations during sleep coordinate interregional communication in cortical networks. J. Neurosci. 34, 16890–16901 (2014).
Steriade, M. Grouping of brain rhythms in corticothalamic systems. Neuroscience 137, 1087–1106 (2006).
Gennaro, L. D. & Ferrara, M. Sleep spindles: An overview. Sleep Med. Rev. 7, 423–440 (2003).
Steriade, M., Domich, L., Oakson, G. & Deschenes, M. The deafferented reticular thalamic nucleus generates spindle rhythmicity. J. Neurophysiol. 57, 260–273 (1987).
Amzica, F. & Steriade, M. Electrophysiological correlates of sleep delta waves. Electroencephalogr. Clin. Neurophysiol. 107, 69–83 (1998).
Muller, L. et al. Rotating waves during human sleep spindles organize global patterns of activity that repeat precisely through the night. Elife 5, 1–16 (2016).
Siapas, A. G. & Wilson, M. A. Coordinated interactions between hippocampal ripples and cortical spindles during slow-wave sleep. Neuron 21, 1123–1128 (1998).
Schabus, M. et al. Hemodynamic cerebral correlates of sleep spindles during human non-rapid eye movement sleep. Proc. Natl. Acad. Sci. USA 104, 13164–13169 (2007).
Andrade, K. C. et al. Sleep spindles and hippocampal functional connectivity in human NREM sleep. J. Neurosci. 31, 10331–10339 (2011).
Lüthi, A. Sleep spindles: Where they come from, what they do. Neurosci. 20, 243–256 (2014).
Schabus, M. et al. Sleep spindles and their significance for declarative memory consolidation. Sleep 27, 1479–1485 (2004).
Staresina, B. P. et al. Hierarchical nesting of slow oscillations, spindles and ripples in the human hippocampus during sleep. Nat. Neurosci. 18, 1679–1686 (2015).
Clemens, Z. et al. Temporal coupling of parahippocampal ripples, sleep spindles and slow oscillations in humans. Brain 130, 2868–2878 (2007).
Mölle, M., Bergmann, T. O., Marshall, L. & Born, J. Fast and slow spindles during the sleep slow oscillation: Disparate coalescence and engagement in memory processing. Sleep 34, 1411–1421 (2011).
Klinzing, J. G. et al. Spindle activity phase-locked to sleep slow oscillations. Neuroimage 134, 607–616 (2016).
Barakat, M. et al. Fast and slow spindle involvement in the consolidation of a new motor sequence. Behav. Brain Res. 217, 117–121 (2011).
Marshall, L. & Born, J. The contribution of sleep to hippocampus-dependent memory consolidation. Trends Cogn. Sci. 11, 442–450 (2007).
Mölle, M., Marshall, L., Gais, S. & Born, J. Grouping of spindle activity during slow oscillations in human non-rapid eye movement sleep. J. Neurosci. 22, 10941–10947 (2002).
Mölle, M., Eschenko, O., Gais, S., Sara, S. J. & Born, J. The influence of learning on sleep slow oscillations and associated spindles and ripples in humans and rats. Eur. J. Neurosci. 29, 1071–1081 (2009).
Maingret, N., Girardeau, G., Todorova, R., Goutierre, M. & Zugaro, M. Hippocampo-cortical coupling mediates memory consolidation during sleep. Nat. Neurosci. 19, 959–964 (2016).
Latchoumane, C.-F. V., Ngo, H. V. & Born, J. Thalamic spindles promote memory formation during sleep through triple phase-locking of cortical, thalamic, and hippocampal rhythms. Neuron 95, 424–435.e6 (2017).
Niknazar, M., Krishnan, G. P., Bazhenov, M. & Mednick, S. C. Coupling of thalamocortical sleep oscillations are important for memory consolidation in humans. PLoS One 10, e0144720 (2015).
Cairney, S. A., Marj, N. El. & Staresina, B. P. Memory consolidation is linked to spindle-mediated information processing during sleep. Curr. Biol. 28, 948–954 (2018).
Mander, B. A., Winer, J. R. & Walker, M. P. Sleep and human aging. Neuron 94, 19–36 (2017).
Ohayon, M. M., Carskadon, M. A., Guilleminault, C. & Vitiello, M. V. Meta-analysis of quantitative sleep parameters from childhood to old age in healthy individuals: Developing normative sleep values across the human lifespan. Sleep 27, 1255–1273 (2004).
Carrier, J. et al. Sleep slow wave changes during the middle years of life. Eur. J. Neurosci. 33, 758–766 (2011).
Crowley, K., Trinder, J., Kim, Y., Carrington, M. & Colrain, I. M. The effects of normal aging on sleep spindle and K-complex production. Clin. Neurophysiol. 113, 1615–1622 (2002).
Dubé, J. et al. Cortical thinning explains changes in sleep slow waves during adulthood. J. Neurosci. 35, 7795–7807 (2015).
Fogel, S. et al. NREM sleep oscillations and brain plasticity in aging. Front. Neurol. 3 (2012).
Mander, B. A. et al. Prefrontal atrophy, disrupted NREM slow waves and impaired hippocampal-dependent memory in aging. Nat. Neurosci. 16, 357–364 (2013).
Varga, A. W. et al. Effects of aging on slow wave sleep dynamics and human spatial navigational memory consolidation. Neurobiol. Aging 42, 142–149 (2016).
Landolt, H.-P. & Borbély, A. A. Age-dependent changes in sleep EEG topography. Clin. Neurophysiol. 112, 369–377 (2001).
Fogel, S. et al. Sleep spindles: A physiological marker of age-related changes in grey matter in brain regions. Neurobiol. Aging 49, 154–164 (2017).
Helfrich, R. F., Mander, B. A., Jagust, W. J., Knight, R. T. & Walker, M. P. Old brains come uncoupled in sleep: Slow wave-spindle synchrony, brain atrophy, and forgetting. Neuron 97, 221–230.e7 (2018).
Backhaus, J. et al. Midlife decline in declarative memory consolidation is correlated with a decline in slow wave sleep. Learn. Mem. 14, 336–341 (2007).
Cherdieu, M., Reynaud, E., Uhlrich, J., Versace, R. & Mazza, S. Does age worsen sleep-dependent memory consolidation? J. Sleep Res. 23, 53–60 (2014).
Baran, B., Mantua, J. & Spencer, R. M. C. Age-related changes in the sleep-dependent reorganization of declarative memories. J. Cogn. Neurosci. 28, 792–802 (2016).
Seeck-Hirschner, M. et al. Declarative memory performance is associated with the number of sleep spindles in elderly women. Am. J. Geriatr. Psychiatry 20, 782–788 (2012).
Ladenbauer, J. et al. Promoting sleep oscillations and their functional coupling by transcranial stimulation enhances memory consolidation in mild cognitive impairment. J. Neurosci. 37, 7111–7124 (2017).
Iber, C., Ancoli-Israel, S., Chesson, A. L. & Quan, S. F. The AASM manual for the scoring of sleep and associted events: Rules, terminology and technical specifications. (American Academy of Sleep Medicine, 2007).
Raz, N. et al. Regional brain changes in aging healthy adults: General trends, individual differences and modifiers. Cereb. Cortex 15, 1676–1689 (2005).
Martin, N. et al. Topography of age-related changes in sleep spindles. Neurobiol. Aging 34, 468–476 (2013).
Nyberg, L., Lövdén, M., Riklund, K., Lindenberger, U. & Bäckman, L. Memory aging and brain maintenance. Trends Cogn. Sci. 16, 292–305 (2012).
Buzsáki, G. Memory consolidation during sleep: A neurophysiological perspective. J. Sleep Res. 7, 17–23 (1998).
Logothetis, N. K. et al. Hippocampal-cortical interaction during periods of subcortical silence. Nature 491, 547–553 (2013).
Kitamura, T. et al. Engrams and circuits crucial for systems consolidation of a memory. Science 356, 73–78 (2017).
Bergmann, T. O. & Born, J. Phase-amplitude coupling: A general mechanism for memory processing and synaptic plasticity? Neuron 97, 10–13 (2018).
Ayoub, A. et al. Differential effects on fast and slow spindle activity, and the sleep slow oscillation in humans with carbamazepine and flunarizine to antagonize voltage-dependent Na+ and Ca2+ channel activity. Sleep 36, 905–911 (2013).
Timofeev, I. & Chauvette, S. The spindles: Are they still thalamic? Sleep 36, 825–826 (2013).
Doran, S. M. The dynamic topography of individual sleep spindles. Sleep Res. Online 5, 133–139 (2003).
Düzel, E., Schütze, H., Yonelinas, A. P. & Heinze, H.-J. Functional phenotyping of successful aging in long-term memory: Preserved performance in the absence of neural compensation. Hippocampus 21, 803–814 (2010).
Fandakova, Y., Lindenberger, U. & Shing, Y. L. Maintenance of youth-like processing protects against false memory in later adulthood. Neurobiol. Aging 36, 933–941 (2015).
Folstein, M. F., Folstein, S. E. & McHugh, P. R. ‘Mini-Mental State’: A practical method for grading the cognitive state of patients for the clinician. J. Psychiatr. Res. 12, 189–198 (1975).
Buysse, D. J., Reynolds, III. C. F., Monk, T. H., Berman, S. R. & Kupfer, D. J. The Pittsburg Sleep Quality Index: A new instrument for psychiatric pratcice and research. Psychiatry Res. 28, 193–213 (1989).
Fandakova, Y. et al. Age differences in false memory: The importance of retrieval monitoring processes and their modulation by memory quality. Psychol. Aging 33, 119–135 (2018).
Jasper, H. H. The ten-twenty electrode system of the International Federation. Electroencephalogr. Clin. Neurophysiol. 10, 371–375 (1958).
Oostenveld, R. & Praamstra, P. The five percent electrode system for high-resolution EEG and ERP measurement. Clin. Neurophysiol. 112, 713–719 (2001).
Oostenveld, R., Fries, P., Maris, E. & Schoffelen, J. M. FieldTrip: Open source software for advanced analysis of MEG, EEG, and invasive electrophysiological data. Comput. Intell. Neurosci. 2011 (2011).
Klinzing, J. G. et al. Odor cueing during slow-wave sleep benefits memory independently of low cholinergic tone. Psychopharmacology (Berl). 235, 291–299 (2018).
Cox, R., Schapiro, A. C., Manoach, D. S. & Stickgold, R. Individual differences in frequency and topography of slow and fast sleep spindles. Front. Hum. Neurosci. 11, 433 (2017).
Ujma, P. P. et al. A comparison of two sleep spindle detection methods based on all night averages: individually adjusted vs. fixed frequencies. Front. Hum. Neurosci. 9, 52 (2015).
Coppieters’t Wallant, D., Maquet, P. & Phillips, C. Sleep spindles as an electrographic element: Description and automatic detection methods. Neural Plast. 2016, 6783812 (2016).
Ngo, H.-V. V., Martinetz, T., Born, J. & Mölle, M. Auditory closed-loop stimulation of the sleep slow oscillation enhances memory. Neuron 78, 545–553 (2013).
Cox, R., Mylonas, D. S., Manoach, D. S. & Stickgold, R. Large-scale structure and individual fingerprints of locally coupled sleep oscillations. Sleep (2018).
Maris, E. & Oostenveld, R. Nonparametric statistical testing of EEG- and MEG-data. J. Neurosci. Methods 164, 177–190 (2007).
Muehlroth, B. E. et al. Precise slow oscillation–spindle coupling promotes memory consolidation in younger and older adults. bioRxiv, https://doi.org/10.1101/268474 (2018).
This study was conducted within the ‘Cognitive and Neuronal Dynamics of Memory across the Lifespan (ConMem)’ project at the Center for Lifespan Psychology, Max Planck Institute for Human Development. The research was partially financed by the Max Planck Society. Beate E. Muehlroth was supported by the Max Planck International Research Network on Aging. Markus Werkle-Bergner’s work was supported by a grant from the German Research Foundation (DFG, WE 4269/3-1, Yee Lee Shing as Co-PI) as well as an Early Career Research Fellowship 2017–2019 awarded by the Jacobs Foundation. Yee Lee Shing and Myriam C. Sander were each supported via Minerva Research Groups awarded by the Max Planck Society. We thank Maren J. Cordi for helping us to set up the technical equipment, Xenia Grande for organizing data collection, Kristina Günther for help in participant recruitment, Julia Delius for editorial assistance, and all student assistants of the ConMem project collecting the data. We are grateful to all members of the ConMem project for helpful feedback on the analysis. Finally, we thank all study participants for their time.
The authors declare no competing interests.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
About this article
Cite this article
Muehlroth, B.E., Sander, M.C., Fandakova, Y. et al. Precise Slow Oscillation–Spindle Coupling Promotes Memory Consolidation in Younger and Older Adults. Sci Rep 9, 1940 (2019). https://doi.org/10.1038/s41598-018-36557-z
This article is cited by
How coupled slow oscillations, spindles and ripples coordinate neuronal processing and communication during human sleep
Nature Neuroscience (2023)
Cellular and Molecular Neurobiology (2023)
Association of spermidine blood levels with microstructure of sleep—implications from a population-based study
Monatsschrift Kinderheilkunde (2023)
npj Microgravity (2021)