Recurrent major depressive disorder (rMDD) is a relapsing-remitting disease with high morbidity and a 5-year risk of recurrence of up to 80%. This was a prospective pilot study to examine the potential diagnostic and prognostic value of targeted plasma metabolomics in the care of patients with rMDD in remission. We used an established LC-MS/MS platform to measure 399 metabolites in 68 subjects with rMDD (n = 45 females and 23 males) in antidepressant-free remission and 59 age- and sex-matched controls (n = 40 females and 19 males). Patients were then followed prospectively for 2.5 years. Metabolomics explained up to 43% of the phenotypic variance. The strongest biomarkers were gender specific. 80% of the metabolic predictors of recurrence in both males and females belonged to 6 pathways: (1) phospholipids, (2) sphingomyelins, (3) glycosphingolipids, (4) eicosanoids, (5) microbiome, and (6) purines. These changes traced to altered mitochondrial regulation of cellular redox, signaling, energy, and lipid metabolism. Metabolomics identified a chemical endophenotype that could be used to stratify rrMDD patients at greatest risk for recurrence with an accuracy over 0.90 (95%CI = 0.69–1.0). Power calculations suggest that a validation study of at least 198 females and 198 males (99 cases and 99 controls each) will be needed to confirm these results. Although a small study, these results are the first to show the potential utility of metabolomics in assisting with the important clinical challenge of prospectively identifying the patients at greatest risk of recurrence of a depressive episode and those who are at lower risk.
Major depressive disorder (MDD) affects 16.1 million US adults and costs $210 billion annually1. MDD’s worldwide point prevalence is 6%2. Recurrence risk after a first MDD-episode is 3–6 times the background population risk3, with most patients having a recurring-remitting course with five lifetime episodes on average. This lifelong recurrence risk accounts substantially to the overall burden of MDD4 and to the risk of suicide5. If we could better understand molecular bases of recurrent major depressive disorder (rMDD), we might develop prospective risk markers and novel targets for prevention.
Standard clinical variables moderately predict recurrence risk4 but more robust biomarkers are needed. Evidence for psychological theories of MDD-recurrence is limited and has not yet resulted in risk prediction tools that have been included in clinical guidelines6. Several biological pathways have been related to MDD in general, but only a limited number of studies specifically investigated rMDD. A recent meta-analysis comprehensively reviewed all evidence on biological factors predicting recurrence, including neuroimaging, immunological, and hormonal biomarkers7. It showed that only increased cortisol had a small predictive effect on recurrence, but even this effect disappeared when baseline clinical diagnoses, publication bias, or study quality were considered.
More recently, increasing focus has been on metabolic alterations in MDD8. Metabolomic and lipidomic studies showed more widespread alterations in MDD9,10,11, that have been hypothesized to constitute a trait associated with recurrence12. Recently, a targeted metabolomic study focusing on neurotransmitters and their metabolites in plasma, found a biochemical signature that could diagnose MDD-patients with up to 95% accuracy13,14. Moreover, metabolomics may predict MDD-recovery15, and response to therapy16,17. However, similar studies of biochemical signatures of remitted rMDD (rrMDD), with prospective follow-up to identify subjects at increased risk of future recurrence have not yet been conducted. The emerging recognition that the brain controls metabolism through neuroendocrine, autonomic, immune, and microbiome circuits18, implies that peripheral blood metabolomics can provide a uniquely accessible set of biomarkers that are diagnostic of real-time changes in brain-body function. This has now been shown in studies of myalgic encephalomyelitis/chronic fatigue syndrome19, schizophrenia20, Gulf War Illness21, response to treatment in autism spectrum disorder22, and treatment-refractory MDD with suicidal ideation23.
Aims of the study
In this discovery phase pilot study, we tested the utility of metabolomic analysis for two purposes: (1) as a diagnostic tool to distinguish patients with rrMDD from controls, and (2) as a prognostic tool to assess the future risk of recurrence in patients with rMDD in drug-free remission at the time of sample collection.
Patients and methods
A cross-sectional patient-control design was used to compare medication-free rrMDD patients with age- and sex-matched, never-depressed controls to identify a metabolic profile of rrMDD patients4. In addition, rrMDD patients were followed prospectively every 4 months for 2.5 years by measuring depressive symptoms. Occurrence and time to recurrence of a new major depressive episode were documented.
Approvals, inclusion and exclusion criteria
We included subjects who experienced ≥2 previous MDD-episodes according to the structured clinical interview for Diagnostic and Statistical Manual of Mental Disorders, fourth edition (DSM-IV) diagnoses (SCID), but were in stable remission (≥8 weeks 17-item Hamilton Depression Rating Scale (HAM-D) ≤ 7 (the lowest qualifying score for remission24), and not currently in an MDD-episode (SCID). Participants were 35–65 years, to include a homogeneous age group and minimize the risk of later conversion to bipolar disorder. Second, we included never-depressed controls without personal psychiatric history by SCID-analysis, or first-degree familial psychiatric history, matched to the rrMDD subjects for age, sex, educational level, working class and ethnicity. Both groups were recruited using identical advertisements in freely available sources and from previous studies4. This study was approved by the accredited Academic Medical Centre (AMC) Medical Ethical Committee (METC), and conformed to the Declaration of Helsinki25. Eleven of 40 healthy control females and 7 out of 19 healthy control males were recruited at the University of California, San Diego (UCSD) under IRB-approved protocol #140072 with signed informed consent. We excluded subjects with current diagnoses of alcohol and/or drug dependence, psychotic or bipolar symptoms, predominant anxiety or severe personality disorder. Other exclusion criteria included standard MRI-exclusion criteria, history of severe head trauma or neurological disease, or severe general physical illness. All participants had to be without psychoactive medication for ≥4 weeks.
At baseline we administered the SCID and HAM-D to check inclusion criteria and residual depressive symptoms. Subsequently, we followed-up rrMDD subjects using the SCID for 2.5 years to prospectively assess time to recurrence with ≥5 depressive symptoms lasting at least 2 weeks according to the DSM-IV criteria. HAM-D evaluations were conducted upon enrollment of 41 of the 59 healthy controls. Healthy controls were not followed prospectively.
Targeted, broad-spectrum, metabolomic analysis of 612 intracellular and plasma metabolites was performed by LC-MS/MS as described26 with minor modifications. A total of 399 of the 612 targeted metabolites were measurable in plasma of both males and females. This platform broadly interrogates 63 biochemical pathways and permits analysis of many of the metabolites known to be core features of the cell danger and integrated stress response (CDR and ISR)27,28,29.
See Supplementary Methods for additional methods
Sixty-eight drug-free rrMDD patients were enrolled and followed for 2.5 years (Flow diagram: Fig. 1). Fifty-nine age- and sex-matched controls were also enrolled.
The rrMDD patients had a long history of illness (25 ± 2.4 years for males, and 27 ± 1.9 years for females), with a high total number of MDD-episodes (mean = 9.7 ± 2.5 for males; 8.1 ± 1.9 for females) (Table 1). Mean HAM-D score for the rrMDD subjects was 2 and 3 for males and females, respectively. A major epidemiologic difference between males and females with rrMDD was the median time to recurrence after enrollment (males: 5.5 months IQR = 1.9–7.6; females: 10.1 IQR = 4.9–17.2; Table 1). During follow-up three participants restarted antidepressants when experiencing a recurrence and two participants restarted antidepressants while in remission during follow-up. This occurred after blood sample collection for metabolomics at enrollment and did not affect the drug-free analysis.
Drug-free rrMDD subjects had a metabolic profile that could be distinguished from healthy controls. Multivariate analysis showed a clear separation between the 2 groups in both males and females (Fig. 2A, B). Top discriminating metabolites are shown in Fig. 2C, D. Relative metabolic impact and significance of these differences are shown in Fig. 2E, F. Tables S1 and S2 report the raw data and Tables S3 and S4 list the rank order of biochemical pathways that were disturbed in rrMDD female and male subjects, respectively, when compared to healthy age- and sex-matched controls. Figure 2G summarizes shared and gender-specific metabolic differences. Principal components analysis (PCA) showed that metabolomics explained up to 39.1% of the phenotypic variance between patients with rrMDD and healthy controls in both males and females (Fig. S1AC). Metabolomics explained up to 43.7% of the phenotypic variance between females who experienced recurrence of depressive symptoms and those with non-recurrence over the 2.5 years of prospective observation (Fig. S1B), and up to 50.6% in males (Fig. S1D).
Overall, alterations in lipid metabolism dominated the rrMDD metabolic signature. Lipid abnormalities constituted 80% of the top 10 pathway alterations in females (Table S3 and Fig. S1). In males, lipid abnormalities constituted 70% of the top 10 pathways (Table S4 and Fig. S2). The 8 lipid pathways most affected were phospholipids, fatty acids and acyl-carnitines, cardiolipins, two classes of sphingolipids (ceramides and sphingomyelins), eicosanoids, bile acids, sterols, and non-gonadal steroids.
The top non-lipid pathway alteration was purine metabolism (Tables S3 and S4 and Fig. S2). Pyrimidines, microbiome metabolites, GABA-glutamate-pyrroline-5-carboxylate-proline, folate-1-carbon, inositol, and tryptophan-serotonin metabolism were also altered in rrMDD subjects (Fig. 2 and S2). Gender-specific differences are discussed in Supplementary Results.
Metabolic alterations shared by males and females
When analyzed at the pathway level,16 pathways were shared by both males and females with rrMDD (Fig. 2E, F and Tables S3 and S4). All 8 lipid pathways found to be abnormal were shared by both males and females. The other 8 shared pathways involved diverse non-lipid pathways.
Acyl-carnitines, cardiolipins, and vitamin B2
One of the most consistent lipid abnormalities found in both males and females was an increase in acyl-carnitines (Tables S3 and S4), which are a marker of decreased mitochondrial fatty acid oxidation30. In females, this was confined to increases in medium chain (C6–C10) acyl-carnitines, while in males, the long-chain (C12–C18), and very long-chain (≥C20) acyl-carnitines were increased (Tables S5 and S6). Cardiolipins, markers for inner mitochondrial membrane complexity and biomass, were also decreased. Phosphatidic acids (PA-lipids), precursors for cardiolipin synthesis, were increased in both males and females (Fig. 2G). Vitamin B2-metabolism needed for mitochondrial fatty acid oxidation was decreased in both males and females. In males this was reflected in a decrease of plasma riboflavin. In females, this was associated with a decrease in plasma flavin adenine dinucleotide (FAD; Fig. 2G, Tables S5 and S6).
Sphingolipids (ceramides, sphingomyelins, and glycosphingolipids) are major structural and signaling lipids that facilitate the exchange of materials between lysosomes and the plasma membrane to regulate cell growth and inflammation31,32, form membrane lipid rafts33, exosomes released from cells34, and are involved in synapses35,36,37. rrMDD males and females shared a specific abnormality in sphingolipid metabolism: a decrease in 2′-hydroxy sphingomyelin SM(d18:1/26:0 OH) (Fig. 2G). The 2′-hydroxylation (2′-OH) of the fatty acid precursor of the amide acyl chain of sphingolipids is catalyzed by the peroxisomal enzyme fatty acid 2′-hydroxylase (FA2H)38. 2′-hydroxy sphingomyelins are precursors for the 2′-OH glycosphingolipids needed for cell differentiation, neuronal connectivity, myelin stability, and have antitumor properties39.
Eicosanoids and oxylipins
Both males and females had alterations in eicosanoid (20-carbon, polyunsaturated) lipids made from arachidonic acid40, but the specific metabolites and the direction of change differed. Females also showed a decrease in an 18-carbon oxylipin made from linoleic acid41 called 13(S)-hydroxyoctadecadienoic acid (13-HODE), which was unchanged in males. 15(S)-hydroxyeicosatetraenoic acid (15(S)-HETE) was decreased in females, but not in males (Fig. 2C and Tables S5 and S6). 13-HODE and 15-HETE are anti-inflammatory and pro-resolving oxylipins that also have antitumor effects42. In contrast, rrMMD-males had increases in 3 eicosanoids: 11-HETE, 9-HETE, and 5-HETE, which are pro-inflammatory mediators made by neutrophils, eosinophils, and mast cells43,44. Males also had an increase in the vasodilatory and anti-inflammatory epoxyeicosatrienoic acids 8,9-EET, and 11,12-EET (Fig. 2G). The large number of alterations in eicosanoid metabolism made this the most statistically significant pathway alteration in males (Fig. 2F).
Sterols are needed for the synthesis of cholesterol, glucocorticoid, and steroid hormones and bile acids. Sterol synthesis requires coordinated enzyme activity in the endoplasmic reticulum (ER) and mitochondria. Sterols were decreased in both male and female rrMDD subjects (Fig. 2G, Tables S3 and S4). In females, both 24,25-epoxycholesterol and cholesteryl-sulfate were decreased. In males, cholesterol precursors 24,25-dihydrolanosterol and lathosterol were decreased (Tables S5 and S6).
Bile acid metabolism requires coordinated activities of enzymes located in mitochondria, peroxisomes, ER, and the gut microbiome45. Bile acids are signaling molecules that bind to several classes of nuclear receptors (FXR, PXR, and CAR), and permit real-time coordination between food intake, the microbiome, liver, and systemic detoxification systems46. Bile acids are made from cholesterol and represent the major disposal route for excess cholesterol. Both males and females had decreased plasma levels of bile acids. rrMDD-females had decreased levels of four glycine- and taurine-conjugated secondary bile acids including glycocholic and taurocholic acids (Tables S3–S6 and Fig. 2). Bile acid abnormalities were the most statistically significant single pathway alteration in females (Fig. 2E). rrMDD males had decreased levels of the secondary bile acid, deoxycholic acid, which is formed by dehydroxylation of cholic acid by normal gut bacteria.
Purine nucleosides adenosine, guanosine, and inosine were decreased and xanthine was increased in both males and females with rrMDD (Fig. 2G and Tables S3 and S4). Plasma purine nucleosides are derived by dephosphorylation of purine nucleotides like ATP, ADP, AMP, GMP, and IMP. Xanthine is a purine nucleobase that has been shown to connect purine metabolism with the immune system, memory, and anxiety47. De novo synthesis, salvage, and metabolism of purine nucleotides depends on cooperative activities of extracellular, cell membrane-associated, cytosolic, and mitochondrial enzymes.
Metabolomics as a diagnostic tool
Area under the receiver operator curve (AUROC)-analysis was used to test the accuracy of metabolites to distinguish between rrMDD subjects and healthy controls (Fig. S3). The classifier for females used 12 metabolites, resulting in an AUC of 0.83 (95%Cl = 0.68–0.96; sensitivity = 80%, 95%Cl = 0.66–0.89; specificity = 87%, 95%Cl = 0.74–0.95). For males, seven metabolites were used as classifier, resulting in an AUC of 0.83 (95%Cl = 0.64–1.0; sensitivity = 74%, 95%Cl = 0.53–0.87; specificity = 79%, 95%Cl = 0.57–0.91).
Metabolomics as a prognostic tool
Predictors shared by males and females
Median time to recurrence during the 2.5 years follow-up for all rrMDD subjects was 588 days for females and 291 days for males (Kaplan–Meier analyses; Fig. 3A, B). Multivariate analysis permitted the metabolomic signature of subjects who experienced recurrence to be distinguished from those who did not (Fig. 3C, D and Tables S7 and S8). The top discriminating metabolites are shown in Fig. 3E, F. Overall, most predictive metabolite classes for both genders were sphingomyelins and phospholipids (Fig. 3G, H). AUROC-analysis was used to test the prognostic accuracy of a female-specific classifier using 7 metabolites and a male-specific classifier that used 3 metabolites (Fig. 3I, J). The predictive accuracy for recurrence in females was 0.90 (95%CI = 0.69–1.0; sensitivity = 0.88; specificity = 0.89; Fig. 3I, K). Although different from female rrMDD subjects, the predictive accuracy for recurrence of depression in males was 0.99 (95% CI = 0.9–1.0; sensitivity = 0.91; specificity = 1.0; Fig. 3J, L).
Three metabolite classes predicted recurrence risk in both males and females by Cox proportional hazard analysis (Fig. 4 and Tables S7–S10). These were a decrease in 2′-hydroxy sphingomyelins (2′-OH SM), trihexosylceramides (THC), and phosphatidylcholine (PC) lipids. In both males and females, nearly 80% of the predictive metabolites identified had a negative correlation with recurrence risk (Tables S9 and S10). This means that when the blood level was low compared to the other rrMDD subjects, recurrence risk was higher, and conversely.
Female-specific predictors of recurrence
All of the strongest predictors of recurrence were gender specific. In females the strongest predictor was low methylcysteine (Fig. 3K, M and Table S9). Female rrMDD subjects in the bottom half of plasma methylcysteine were found to have a median time to recurrence of 1.1 years (403 ± 63 days, mean ± SEM). Women in the top 50th methylcysteine percentile were much slower to experience recurrence (median = 2.3 years; 848 ± 58 days; Cox beta coefficient = −1.8; p < 0.00006; Table S9 and Fig. 3M). Monohexosylceramide (MHC(d18:1/20:0)) was another example of a metabolite that protected against future recurrence (Fig. 3O and Table S9). Two metabolites that increased recurrence risk were lysophosphatidylcholine 16:0 (LysoPC(16:0)) and arachidonic acid (20:4). These two lipids can be produced from the same parental phosphatidylcholine lipid, PC(16:0/20:4) through the action of lipoprotein associated phospholipase A2 (LP-PLA2) and other PLA2-types under conditions of stress48. Metabolites found to increase and decrease recurrence risk are listed in Table S9. Of the 399 measured metabolites, 33 were significant predictors of recurrence risk in females, and in 82% of these metabolites (27/33) higher levels decreased recurrence risk (Table S7 and S9). Correcting for number of previous episodes and residual symptoms did not change hazard-ratios of these metabolites.
Male-specific predictors of recurrence
Of the 399 measured metabolites, 17 were significant predictors of recurrence risk in males (Table S8 and S10). The eicosanoid lipid, 15-hydroxyeicosatetraenoic acid (15-HETE) was the top predictor of recurrence in males. When males were stratified into top and bottom 50th percentiles, rrMDD subjects in the bottom half for this plasma 15-HETE were found to have a median time to recurrence of 0.7 years (245 ± 85 days). Males in the top 50th percentile for this anti-inflammatory eicosanoid were much slower to experience recurrence (median = 1.7 years; 614 ± 108 days; Fig. 3N; Cox beta coefficient = −1.5; p < 0.0006; Table S10). Beta carotene was also protective. Males in the lowest 50th percentile for plasma beta-carotene had a median time to recurrence of 0.5 years (175 ± 103 days), while the upper 50th percentile had a median time to recurrence of 1.9 years (677 ± 104 days; Fig. 3N and P; Table S8 and S10). Increased alanine and allantoin were associated with an increased risk of recurrence in males. Increased alanine is produced as a transamination product of pyruvate and is a marker of mitochondrial dysfunction49. Allantoin is produced non-enzymatically from uric acid by exposure to reactive oxygen species (ROS) and is a marker of oxidative shielding50 and stress51. Increased levels of 14 of 18 (78%) predictors in males decreased recurrence risk. Figures S4 and S5 illustrate the Kaplan–Meier style recurrence profiles of the top predictive metabolites determined by Cox proportional hazard analysis in females and males, respectively. Correcting for number of previous episodes and residual symptoms did not change the hazard-ratios of these metabolites, except for beta-carotene, SM(d18:1/20:2 OH), PS(18:0/18:1), PE(34:1), or SM(d18:1/20:1), where correction for especially previous lifetime episodes of depression increased the hazard-ratios.
Sample size calculation for validation studies
Three methods were used to estimate the sample size needed in future studies to validate the results of this pilot study (see Supplemental Methods). The median Pearson r for the metabolites in females having VIP scores ≥1.5 was r = 0.2. The median Z-score difference was 0.39 (Tables S5, S11–S14). Using correlation analysis and a requirement for a Pearson r ≥ 0.2, the total number of subjects of a single sex (cases plus controls) was 194. Using multiple regression analysis and a threshold of at least 35 significant metabolites and a Cohen’s f2 = 0.15, the study size was 201. Using a Z-score threshold of ≥0.4 (significant metabolites in cases must differ from controls by at least 0.4 standard deviations), the study size was 198. The mean estimate was 198 ± 3.5 (mean ± sd). These results showed that a validation-scale study of at least 198 females and 198 males (99 cases and 99 controls each) will be needed to confirm the results.
See Supplementary Results for additional results.
Metabolomic analysis revealed an underlying biochemical signature in remitted recurrent major depressive disorder (rrMDD) that distinguished patients from healthy controls. This difference was psychometrically inapparent as patients were studied during antidepressant-free remission. Patterns of metabolic abnormalities that we found reflected alterations in chemical communication across lipid membranes and between organelles, cells, organ systems, and the microbiome. Lipid abnormalities constituted 60–70% of the total metabolic impact. Even more striking was the finding that metabolomic analysis was able to unmask a latent signature of future risk of recurrence with 90–99% accuracy. If replicated, this finding could have a significant impact on clinical practice by permitting patients with major depressive disorder to be stratified according to future risk, and new preventive treatments to be tested systematically in clinical trials. To the best of our knowledge, this is the first report to show that broad-spectrum targeted metabolomics can predict future recurrence risk.
Interestingly, the top metabolites that distinguished rrMDD cross-sectionally from controls were not the same biomarkers that predicted future recurrence risk. Reciprocally, the top predictors of future risk were not the same biomarkers that distinguished patients with recurrent MDD in drug-free remission cross-sectionally from healthy controls. A similar pattern of metabolites being used differently in health than in disease has been observed previously for other biological markers. For example, a study showed that cortisol52 was increased in rrMDD subjects compared to controls, while decreased cortisol predicted recurrence in the same study. In this example, higher levels of cortisol actually protected against future recurrence in patients at risk. Altogether, these differences between diagnostic and prognostic biomarkers makes it unlikely that these observations merely represent epiphenomena or consequences of earlier MDD episodes.
Measuring latent risk
These data suggest that once a new disease state such as MDD has been entered, asymptomatic remission comes with a latent (hidden) future risk that can be objectively measured, permitting patients to be stratified. In this new state of latent risk, biochemical and endocrine pathways are used differently to prevent disease progression and recurrence than in healthy control subjects. These results suggest that natural recovery from disease is not the simple reversal of the sequence of pathogenic events that led to disease. Metabolomic analysis unmasked new interaction patterns between metabolites that changed the future risk in patients in a disease state, but that had either no utility, or even an opposite effect, in predicting the future risk of developing that disease state in healthy controls53. Rephrasing this, the clinical context of the patient in health or disease determines the meaning of the data, and the pathophysiologic sequence of events that produced the original disease is different than the path that is used to minimize future complications, or to recover and heal from that disease18.
Membrane properties are determined by lipids and transporters that conduct material across those membranes. Changes in membrane-dependent cell-to-cell and interorganellar communication provide a rationale for why over half of all the prognostic metabolites for recurrence risk in rrMDD were lipids, and why those that were not lipids, like purines, are potent regulators of membrane and transporter properties. We found that several nucleosides of purines such as inosine and guanosine were decreased while certain nucleobases like xanthine were increased. This has been reported in independent studies of MDD54 and confirms an important role of purines and purinergic signaling in regulating affective and several other neuropsychiatric and neurodegenerative disorders55,56. Metabolic abnormalities found in rrMDD support the notion that interorganellar and intercellular exchange and the transformation of metabolites across membranes—the connectivity and communication between organelles, cells, and organ systems—is altered. Impaired communication across membranes, as measured by plasma metabolomics, permits the pathogenesis of major depressive disorder to be reframed as a neurometabolic disorder8,57,58. When reframed under this new paradigm as a neurometabolic disorder, novel approaches to treatment become apparent that may never have been considered under the old paradigm of MDD as an isolated disorder of brain function independent of whole-body changes in metabolism.
The mitochondrial nexus
Mitochondria have been shown to coordinate many of the metabolic features of stress that can play a causal role in mental health disorders27,59,60. Mitochondria are the hub of the wheel of cellular metabolism. This nexus point is a crossroads for many neurodevelopmental and psychiatric disorders61. Mitochondria naturally respond to chemical and physical environmental changes, making their membrane structures of fundamental interest62. Although typically thought of as an energy factory, mitochondria catalyze over 700 biochemical reactions63 needed to produce building blocks for cell growth, repair, and signaling. Mitochondria can also shift dynamically between three major modes of function, or functional types designated M1-, M0-, and M2-organelles, according to cellular needs18. Cells in which M1- and M0-mitochondria predominate are pro-inflammatory and dependent on glycolytic metabolism for energy. M1- and M0-cells release more lactic acid in order to maintain intracellular redox. Lactic acid elevation was found in females with a history of rMDD in this study (Fig. 2G), and is a known feature of symptomatic depression that decreases with treatment64,65. Moreover, both males and females had several other markers of decreased mitochondrial function and/or biomass. These included decreased purines like adenosine, inosine, and guanosine, and decreases in the pyrimidine precursor orotic acid, and decreased cardiolipins, which are markers of inner mitochondrial membrane surface area and biomass. Mitochondria specialized for oxidative phosphorylation are designated M2-organelles, needed for burning fatty acids for energy to make ATP. When M2-mitochondrial function is impaired, several fatty acyl-carnitines increase in the blood30. Acyl-carnitines were increased in both males and females with antidepressant-free rrMDD, and the major vitamins needed for fatty acid oxidation (riboflavin and FAD) were decreased. Disturbances in mitochondrial function leading to acyl-carnitine abnormalities have been observed in several other independent studies of MDD66. These findings support the hypothesis that even in remitted rMDD a shift in mitochondrial function exists and persists. This change is functionally dynamic, shifting mitochondria away from the M2-polarized oxidative phosphorylation phenotype, to the M1 and M0 phenotypes associated with inflammation and proliferation, respectively18,63.
A limitation of this study was the relatively smaller number of rrMDD subjects enrolled. This was a greater problem for males than for females. The smaller sample size for males captured a smaller proportion of the natural phenotypic variation, making the results vulnerable to overfitting. The small sample size influenced the calculated false discovery rates (FDRs). FDRs for the significant metabolites in females ranged from 0.6 to 0.96. FDRs for the 54 discriminating metabolites in males ranged from 0.82 to 0.91. As expected for a small-scale pilot study, these FDRs were higher than would be desired for a validation study. To further test the statistical validity of these results we used repeated double cross validation (rdCV) analysis. rdCV analysis showed modest values of 0.74–0.76 for males and females in remission, while a similar analysis of the prognostic classifiers for high and low risk of future recurrence of MDD symptoms reached rdCV values of 0.91 and 0.80 for males and females, respectively. Despite these high values for the in-sample validation statistics, the generalizability of these findings is not currently known, and will require independent testing in future cohorts. Larger studies will be needed for validation, and verification of the sensitivity and specificity of our results. Moreover, we did not include first-episode MDD-patients. Although this allowed focus on recurrent patients with a high recurrence risk, it precluded comparative analyses with patients with a relatively low risk. Future studies applying comprehensive metabolomics in untreated first-episode MDD may further elucidate the role of different metabolites in the prognosis of MDD.
See Supplementary Discussion for additional discussion
Targeted broad-spectrum LC-MS/MS-metabolomics of 399 plasma metabolites was used to study recurrent major depressive disorder in remission (rrMDD), and the time to recurrence, in 126 cases and controls. Lipid abnormalities dominated rrMDD’s metabolic signature. The most powerful statistical inferences came from the 2.5-year prospective study of subjects at risk for recurrence. Stratification of rrMDD subjects using metabolomics was able to predict recurrence risk with >90% accuracy in both males and females. Nearly 80% of the metabolites with greatest predictive accuracy for recurrence risk belonged to just six pathways: phospholipids, sphingomyelins, glycosphingolipids, eicosanoids, microbiome, and purines. Abnormalities in these pathways support the emerging conceptual framework that mitochondria act as a metabolic nexus61—as sensors and regulators of cell function that respond to environmental threat, stress, or injury18,27,62. After correcting for residual symptoms and lifetime MDD-episodes, metabolomic analysis was found to add new information that was not statistically correlated with any other neuropsychiatric parameter measured during remission and was highly significant in prospectively identifying the rrMDD patients at greatest risk of recurrence. New clinical trials designed to restore normal lipid metabolism67, mitochondrial health68, metabokine signaling18,22, and microbiome health69,70 through dietary, supplement, psychological stress reduction, and medical interventions will be required to confirm these results.
Greenberg, P. E., Fournier, A. A., Sisitsky, T., Pike, C. T. & Kessler, R. C. The economic burden of adults with major depressive disorder in the United States (2005 and 2010). J. Clin. Psychiatry 76, 155–162 (2015).
Malhi, G. S. & Mann, J. J. Depression. Lancet 392, 2299–2312 (2018).
Hoertel, N. et al. A comprehensive model of predictors of persistence and recurrence in adults with major depression: results from a national 3-year prospective study. J. Psychiatr. Res. 95, 19–27 (2017).
Mocking, R. J. et al. Vulnerability for new episodes in recurrent major depressive disorder: protocol for the longitudinal DELTA-neuroimaging cohort study. BMJ Open 6, e009510 (2016).
Isometsa, E. Suicidal behaviour in mood disorders–who, when, and why? Can. J. Psychiatry 59, 120–130 (2014).
Brouwer, M. E. et al. Psychological theories of depressive relapse and recurrence: A systematic review and meta-analysis of prospective studies. Clin. Psychol. Rev. 74, 101773 (2019).
Kennis, M. et al. Prospective biomarkers of major depressive disorder: a systematic review and meta-analysis. Mol. Psychiatry 25, 321–338 (2020).
Mocking, R. J. T., Assies, J., Ruhe, H. G. & Schene, A. H. Focus on fatty acids in the neurometabolic pathophysiology of psychiatric disorders. J. Inherit. Metab. Dis. 41, 597–611 (2018).
Walther, A. et al. Lipidomics in major depressive disorder. Front. Psychiatry 9, 459 (2018).
Bot, M. et al. Metabolomics profile in depression: a pooled analysis of 230 metabolic markers in 5283 cases with depression and 10,145 controls. Biol. Psychiatry 87, 409–418 (2020).
Kaddurah-Daouk, R. et al. Cerebrospinal fluid metabolome in mood disorders-remission state has a unique metabolic profile. Sci. Rep. 2, 667 (2012).
Thesing, C. S. et al. Fatty acids and recurrence of major depressive disorder: combined analysis of two Dutch clinical cohorts. Acta Psychiatr. Scandin. 14, 362–373 (2020).
Pan, J. X. et al. Diagnosis of major depressive disorder based on changes in multiple plasma neurotransmitters: a targeted metabolomics study. Transl. Psychiatry 8, 130 (2018).
Zhou, X. et al. Polyunsaturated fatty acids metabolism, purine metabolism and inosine as potential independent diagnostic biomarkers for major depressive disorder in children and adolescents. Mol. Psychiatry 24, 1478–1488 (2019).
Czysz, A. H. et al. Can targeted metabolomics predict depression recovery? Results from the CO-MED trial. Transl. Psychiatry 9, 11 (2019).
Bhattacharyya, S. et al. Pilot study of metabolomic clusters as state markers of major depression and outcomes to CBT treatment. Front. Neurosci. 13, 926 (2019).
Bhattacharyya, S. et al. Metabolomic signature of exposure and response to citalopram/escitalopram in depressed outpatients. Transl. Psychiatry 9, 173 (2019).
Naviaux, R. K. Metabolic features and regulation of the healing cycle-A new model for chronic disease pathogenesis and treatment. Mitochondrion 46, 278–297 (2019).
Naviaux, R. K. et al. Metabolic features of chronic fatigue syndrome. Proc. Natl Acad. Sci. USA 113, E5472–E5480 (2016).
Wang, D. et al. Metabolic profiling identifies phospholipids as potential serum biomarkers for schizophrenia. Psychiatry Res. 272, 18–29 (2019).
Naviaux, R. K. et al. Metabolic features of Gulf War illness. PLoS ONE 14, e0219531 (2019).
Naviaux, R. K. et al. Low-dose suramin in autism spectrum disorder: a small, phase I/II, randomized clinical trial. Ann. Clin. Transl. Neurol. 4, 491–505 (2017).
Pan, L. A., et al. Neurometabolic disorders: potentially treatable abnormalities in patients with treatment-refractory depression and suicidal behavior. Am. J. Psychiatry https://doi.org/10.1176/appi.ajp.2016.15111500 (2016).
Zimmerman, M., Martinez, J. H., Young, D., Chelminski, I. & Dalrymple, K. Severity classification on the Hamilton Depression Rating Scale. J. Affect. Disord. 150, 384–388 (2013).
World Medical Association. World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects. JAMA 310, 2191–2194 (2013).
Li, K., Naviaux, J. C., Bright, A. T., Wang, L. & Naviaux, R. K. A robust, single-injection method for targeted, broad-spectrum plasma metabolomics. Metabolomics 13, 122 (2017).
Naviaux, R. K. Metabolic features of the cell danger response. Mitochondrion 16, 7–17 (2014).
Buzkova, J. et al. Metabolomes of mitochondrial diseases and inclusion body myositis patients: treatment targets and biomarkers. EMBO Mol. Med. 10, e9091 (2018).
Pakos-Zebrucka, K. et al. The integrated stress response. EMBO Rep. 17, 1374–1395 (2016).
Olsen, R. K. et al. ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency. Brain 130, 2045–2054 (2007).
Samarani, M. et al. A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest. FASEB J. 32, 5685–5702 (2018).
Chiricozzi, E. et al. Sphingolipids role in the regulation of inflammatory response: From leukocyte biology to bacterial infection. J. Leukoc. Biol. 103, 445–456 (2018).
Ma, Y., Hinde, E. & Gaus, K. Nanodomains in biological membranes. Essays Biochem. 57, 93–107 (2015).
Grey, M. et al. Acceleration of alpha-synuclein aggregation by exosomes. J. Biol. Chem. 290, 2969–2982 (2015).
Area-Gomez, E. et al. A key role for MAM in mediating mitochondrial dysfunction in Alzheimer disease. Cell Death Dis. 9, 335 (2018).
Wu, W., Shi, X. & Xu, C. Regulation of T cell signalling by membrane lipids. Nat. Rev. Immunol. 16, 690–701 (2016).
Olsen, A. S. B. & Faergeman, N. J. Sphingolipids: membrane microdomains in brain development, function and neurological diseases. Open Biol. 7, 170069 (2017).
Kota, V. & Hama, H. 2’-Hydroxy ceramide in membrane homeostasis and cell signaling. Adv. Biol. Regul. 54, 223–230 (2014).
Yao, Y. et al. Fatty acid 2-hydroxylation inhibits tumor growth and increases sensitivity to cisplatin in gastric cancer. EBioMedicine 41, 256–267 (2019).
Buczynski, M. W., Dumlao, D. S. & Dennis, E. A. Thematic review series: proteomics. An integrated omics analysis of eicosanoid biology. J. Lipid Res. 50, 1015–1038 (2009).
Vangaveti, V. N., Jansen, H., Kennedy, R. L. & Malabu, U. H. Hydroxyoctadecadienoic acids: Oxidised derivatives of linoleic acid and their role in inflammation associated with metabolic syndrome and cancer. Eur. J. Pharmacol. 785, 70–76 (2016).
Li, M. Y. et al. Antineoplastic effects of 15(S)-hydroxyeicosatetraenoic acid and 13-S-hydroxyoctadecadienoic acid in non-small cell lung cancer. Cancer 121, 3130–3145 (2015).
Powell, W. S., Gravelle, F. & Gravel, S. Metabolism of 5(S)-hydroxy-6,8,11,14-eicosatetraenoic acid and other 5(S)-hydroxyeicosanoids by a specific dehydrogenase in human polymorphonuclear leukocytes. J. Biol. Chem. 267, 19233–19241 (1992).
Goetzl, E. J., Weller, P. F. & Sun, F. F. The regulation of human eosinophil function by endogenous mono-hydroxy-eicosatetraenoic acids (HETEs). J. Immunol. 124, 926–933 (1980).
Vaz, F. M. & Ferdinandusse, S. Bile acid analysis in human disorders of bile acid biosynthesis. Mol. Asp. Med. 56, 10–24 (2017).
Garcia, M. et al. Nuclear receptor metabolism of bile acids and xenobiotics: a coordinated detoxification system with impact on health and diseases. Int. J. Mol. Sci. 19, 3630 (2018).
Fan, K. Q. et al. Stress-induced metabolic disorder in peripheral CD4(+) T cells leads to anxiety-like behavior. Cell 179, 864–879. e819 (2019).
Vasquez, A. M., Mouchlis, V. D. & Dennis, E. A. Review of four major distinct types of human phospholipase A2. Adv. Biol. Regul. 67, 212–218 (2018).
Shaham, O. et al. A plasma signature of human mitochondrial disease revealed through metabolic profiling of spent media from cultured muscle cells. Proc. Natl Acad. Sci. USA 107, 1571–1575 (2010).
Naviaux, R. K. Oxidative shielding or oxidative stress? J. Pharmacol. Exp. Ther. 342, 608–618 (2012).
De Becker, B. et al. Severe hypouricemia impairs endothelium-dependent vasodilatation and reduces blood pressure in healthy young men: a randomized, placebo-controlled, and crossover study. J. Am. Heart Assoc. 8, e013130 (2019).
Lok, A. et al. Longitudinal hypothalamic-pituitary-adrenal axis trait and state effects in recurrent depression. Psychoneuroendocrinology 37, 892–902 (2012).
Assies, J. et al. Effects of oxidative stress on fatty acid- and one-carbon-metabolism in psychiatric and cardiovascular disease comorbidity. Acta Psychiatr. Scand. 130, 163–180 (2014).
Ali-Sisto, T. et al. Purine metabolism is dysregulated in patients with major depressive disorder. Psychoneuroendocrinology 70, 25–32 (2016).
Kaddurah-Daouk, R. et al. Alterations in metabolic pathways and networks in Alzheimer’s disease. Transl. Psychiatry 3, e244 (2013).
Yao, J. K. et al. Associations between purine metabolites and monoamine neurotransmitters in first-episode psychosis. Front. Cell. Neurosci. 7, 90 (2013).
Lamers, F., Milaneschi, Y., de Jonge, P., Giltay, E. J. & Penninx, B. Metabolic and inflammatory markers: associations with individual depressive symptoms. Psychol. Med. 48, 1102–1110 (2018).
Milaneschi, Y. et al. Genetic association of major depression with atypical features and obesity-related immunometabolic dysregulations. JAMA Psychiatry 74, 1214–1225 (2017).
Daniels, T. E., Olsen, E. M. & Tyrka, A. R. Stress and psychiatric disorders: the role of mitochondria. Annu. Rev. Clin. Psychol. 16, 165–186 (2020).
Hoffmann, A. & Spengler, D. The mitochondrion as potential interface in early-life stress brain programming. Front. Behav. Neurosci. 12, 306 (2018).
Picard, M., Juster, R. P., Sloan, R. P. & McEwen, B. S. Mitochondrial nexus to allostatic load biomarkers. Psychosom. Med. 79, 114–117 (2017).
Naviaux, R. K. Perspective: cell danger response Biology-The new science that connects environmental health with mitochondria and the rising tide of chronic illness. Mitochondrion 51, 40–45 (2020).
Naviaux, R. K. Incomplete healing as a cause of aging: the role of mitochondria and the cell danger response. Biology 8, 27 (2019).
Kaddurah-Daouk, R. et al. Pharmacometabolomic mapping of early biochemical changes induced by sertraline and placebo. Transl. Psychiatry 3, e223 (2013).
Machado-Vieira, R. et al. Increased brain lactate during depressive episodes and reversal effects by lithium monotherapy in drug-naive bipolar disorder: a 3-T 1H-MRS study. J. Clin. Psychopharmacol. 37, 40–45 (2017).
Ahmed, A. T. et al. Acylcarnitine metabolomic profiles inform clinically-defined major depressive phenotypes. J. Affect. Disord. 264, 90–97 (2020).
Li, K. J., Borresen, E. C., Jenkins-Puccetti, N., Luckasen, G. & Ryan, E. P. Navy bean and rice bran intake alters the plasma metabolome of children at risk for cardiovascular disease. Front. Nutr. 4, 71 (2017).
Parikh, S. et al. Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society. Genet. Med. 19, 1–18 (2017).
Chambers, E. S. et al. Dietary supplementation with inulin-propionate ester or inulin improves insulin sensitivity in adults with overweight and obesity with distinct effects on the gut microbiota, plasma metabolome and systemic inflammatory responses: a randomised cross-over trial. Gut 68, 1430–1438 (2019).
Borresen, E. C. et al. A randomized controlled trial to increase navy bean or rice bran consumption in colorectal cancer survivors. Nutr. Cancer 68, 1269–1280 (2016).
We thank the participants and families who donated their time and effort in helping to make this study possible. We also thank Wes Thompson, Tuo Lin, and Joe Ix for help with the Cox proportional hazard analysis. This work was supported in part by the UCSD Christini Fund, The Wright Family Foundation, The Lennox Foundation, and the UCSD Mitochondrial Disease Research Fund. Funding for the mass spectrometers used in this study was provided by a gift from the Jane Botsford-Johnson Foundation. J.A. also thanks all the individuals and the foundations who helped make this project possible with their support. The DELTA-neuroimaging study was supported by unrestricted personal grants from the Amsterdam UMC to RJTM (AMC PhD Scholarship) and CAF (AMC MD-PhD Scholarship), and a dedicated grant from the Dutch Brain Foundation (Hersenstichting Nederland: 2009(2)-72). H.G.R. was supported by an NWO/ZonMW VENI-Grant #016.126.059.
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Mocking, R.J.T., Naviaux, J.C., Li, K. et al. Metabolic features of recurrent major depressive disorder in remission, and the risk of future recurrence. Transl Psychiatry 11, 37 (2021). https://doi.org/10.1038/s41398-020-01182-w