Brain-derived neurotrophic factor (BDNF) is implicated in the survival of striatal neurons. BDNF function is reduced in Huntington’s disease (HD), possibly because mutant huntingtin impairs its cortico-striatal transport, contributing to striatal neurodegeneration. The BDNF trophic pathway is a therapeutic target, and blood BDNF has been suggested as a potential biomarker for HD, but BDNF has not been quantified in cerebrospinal fluid (CSF) in HD. We quantified BDNF in CSF and plasma in the HD-CSF cohort (20 pre-manifest and 40 manifest HD mutation carriers and 20 age and gender-matched controls) using conventional ELISAs and an ultra-sensitive immunoassay. BDNF concentration was below the limit of detection of the conventional ELISAs, raising doubt about previous CSF reports in neurodegeneration. Using the ultra-sensitive method, BDNF concentration was quantifiable in all samples but did not differ between controls and HD mutation carriers in CSF or plasma, was not associated with clinical scores or MRI brain volumetric measures, and had poor ability to discriminate controls from HD mutation carriers, and premanifest from manifest HD. We conclude that BDNF in CSF and plasma is unlikely to be a biomarker of HD progression and urge caution in interpreting studies where conventional ELISA was used to quantify CSF BDNF.
Huntington’s disease (HD) is a fatal neurodegenerative disorder caused by a mutation in the gene encoding mutant huntingtin protein (mHTT). It causes behavioural, cognitive, and motor dysfunctions and no disease-modifying treatment has yet demonstrated efficacy1.
In HD, the selective vulnerability and degeneration of striatal neurons may be caused by the depletion of brain-derived neurotrophic factor (BDNF)2. BDNF is a growth factor implicated in neuronal survival, development, and synaptic plasticity. HD post-mortem brain tissue has been shown to have reduced BDNF3. Murine studies demonstrate that the absence of BDNF leads to early striatal neuronal death and HD phenotypes4,5. BDNF concentration is lower in the striatum of R6/1 and zQ175 mice compared to the wild-type counterparts6,7. This lowered concentration may have been influenced by a wild-type huntingtin-mediated loss of function mechanism. Wild-type huntingtin regulates the transport of BDNF and indirectly promotes the genetic expression of BDNF8,9 and BDNF overexpression produced phenotypic recovery in a murine model10. BDNF and its trophic pathway are targets for therapeutic development11.
BDNF concentration in cerebrospinal fluid (CSF) or blood could be an accessible means of quantifying dysfunction of this pathogenic pathway, could be a useful monitoring or prognosis biomarker, and could elucidate target engagement by therapeutics expected to restore the pathway. BDNF in these fluids has been studied in several neurodegenerative diseases: patients with Parkinson’s and Alzheimer’s disease (AD) have reduced serum BDNF levels12,13, and restoration of BDNF may ameliorate behavioural deficits and neuronal loss in AD models12. Similarly, BDNF deficiency in serum has been observed in HD patients14.
However, BDNF is stored in platelets15 so its concentration in blood-derived products, such as plasma and serum, may not be an accurate reflection of the CNS due to platelet activation and degranulation. Moreover, all previous reports of BDNF levels in CSF in neurodegeneration have used conventional enzyme-linked immunosorbent assays (ELISAs) and have found concentrations below the linear range of the assay, raising doubt as to the validity and accuracy of the reported disease differences16,17,18.
To our knowledge, BDNF has not been successfully quantified in CSF in HD patients19 and no comparison between CSF and plasma levels has been performed using a suitable ultra-sensitive assay.
We therefore compared several immunoassays and quantified BDNF in blood and CSF from HD mutation carriers and healthy controls both cross-sectionally and over a 2-year longitudinal period to determine whether BDNF is a potential biomarker for HD.
Materials and methods
Participants (20 healthy controls, 20 premanifest HD (preHD), and 40 manifest HD) were recruited from the National Hospital for Neurology and Neurosurgery/University College London HD Multidisciplinary Clinic as part of a longitudinal CSF collection initiative (online protocol: https://doi.org/10.5522/04/11828448.v1)20. This was a single-site study affiliated with the HDClarity study(NCT02855476, http://hdclarity.net/) with added optional magnetic resonance imaging (MRI) and 6-week repeated sampling, and with a 24-month longitudinal follow-up. It was conducted according with the Declaration of Helsinki and was approved by the London–Camberwell St Giles Research Ethics Committee. All participants gave written informed consent.
Manifest HD participants were defined as adults having a Unified Huntington’s Disease Rating Scale (UHDRS) diagnostic confidence level (DCL) of 4 and HTT CAG repeat count ≥ 36. PreHD participants had CAG ≥ 40 and DCL < 4. Healthy controls were age- and gender-matched to gene expansion carriers, mostly spouses or gene-negative siblings of HD gene expansion carriers and with no neurological signs or symptoms. Manifest HD participants were staged according to UHDRS total functional capacity21.
The inclusion and exclusion criteria, clinical assessments, blood and CSF collection and processing, and MRI acquisition and processing are described in the online protocol and previous reports20,22. Briefly, participants underwent clinical assessments including the UHDRS subscales. Blood samples were collected into lithium heparin tubes after an overnight fast and were centrifuged at 1300 g for 10 min at 4 °C to produce normal plasma (as opposed to platelet-poor plasma)23 and aliquoted on ice and stored at − 80 °C using a standardised protocol. T1-weighted MRI data were acquired on a 3 T Siemens Prisma scanner as previously described20. Brain volume change was expressed as change per year and adjusted to total intracranial volume.
BDNF was quantified in duplicate in 20 CSF and serum samples from deidentified individuals from a clinical neurochemistry laboratory to compare the sensitivity of commercially available immunoassays: BDNF Emax ImmunoAssay System (Promega, USA), Human BDNF ELISA (Sigma-Aldrich, USA), and Single molecule array (Simoa) Human BDNF Discovery Kit (Quanterix, USA). POLARstar Omega (BMG Labtech, Germany) was used to measure the fluorescent products in the standard ELISAs, whilst an HD-1 Analyzer (Quanterix, USA) was used for the Simoa kit. For Promega and Sigma-Aldrich ELISAs, the limit of detection (LOD) and quantification (LOQ) were calculated from raw absorbance data.
The HD-CSF cohort
Plasma and CSF BDNF from the HD-CSF cohort were quantified in duplicate using the Simoa kit on an HD-1 Analyzer according to manufacturer guidance. Plasma samples were measured at 1:640 and CSF at 1:4 dilution. The lower LOQ and lower LOD were 0.0293 pg/mL and 0.0026 pg/mL, respectively. All measurements were above both. The intra-assay coefficients of variation (CV; calculated as the mean of the CVs for each sample’s duplicate measurements) was 8.30% for CSF (n = 84) and 3.26% for plasma (n = 91). The inter-assay CV (calculated as the mean of the CVs for analogous spiked positive controls provided by the manufacturer and used in each well plate) was 4.39% for CSF (n = 2) and 2.74% for plasma (n = 4). Four (4.8%) CSF samples were only measured once. Quantification was blinded to disease status.
For the HD-CSF cohort, BDNF distribution was assessed for normality, and plasma and CSF BDNF values underwent square root and inverse square transformation, respectively.
General linear models and Pearson’s chi-squared or Fisher’s exact test were performed to assess intergroup differences at baseline and at the 24-month follow-up characteristics.
Potential confounders including age, gender, body mass index (BMI), medication, serum platelet counts, and CSF blood contamination (hemoglobin and erythrocytes), storage duration, and short problem behaviour assessment (PBA-s) subscores were examined through general linear models, Pearson’s correlations or ordinal logistic regressions. Those expected to have a relevant impact on BDNF, either based on reports from the literature, or directly seen in our sample, were included as covariates for subsequent models15,24,25,26,27. All included gender, BMI, anti-depressant, anti-psychotic medication, and age. For plasma we also included sample storage duration and platelet count. For CSF we also included CSF erythrocyte count. As a relevant contributor to HD natural history, CAG repeat length was included in the models.
BDNF intergroup differences were investigated with general linear models. Association in HD mutation carriers with clinical and imaging measures were investigated with Pearson’s partial correlations with bootstrapped bias corrected and accelerated 95% confidence intervals (95%CI). Receiver operating characteristic (ROC) curves were drawn for plasma and CSF BDNF.
To investigate short term stability, two-way mixed effects models intraclass correlations (ICC) were performed between the baseline and optional 6-week samples.
Annualised rates of change in BDNF and clinical measures were calculated by subtracting baseline from follow-up value and dividing by time between samplings. Intergroup differences and associations in HD mutation carriers with clinical and imaging measures were investigated as above.
To study BDNF longitudinal trajectories, we used mixed effects models with age and potential confounders as fixed effects, and random effects for participant (intercept) and age (slope), generated independently for controls and mutation carriers.
All analyses were performed with Stata 15.1 (StataCorp). The significance level was defined as p value < 0.05. No methods for multiplicity correction were used, so any statistically significant outcomes would need to be considered in the context of related statistical tests.
Serum BDNF levels in 20 test samples were in the linear range for tested assays. However, CSF levels were below the LOD in all 20 samples on the Promega assay, while 16 (80%) out of 20 samples were between the LOD and the LOQ on the Sigma-Aldrich assay. In plasma, all tested assays were correlated (Simoa and Promega: r = 0.9200, p < 0.0001; Simoa and Sigma-Aldrich: r = 0.9428, p < 0.0001; Promega and Sigma-Aldrich: r = 0.9175, p < 0.0001). In CSF, Simoa and Sigma-Aldrich showed a weaker association (r = 0.4269, p = 0.0991). The Simoa assay quantified BDNF concentration in blood and CSF within the linear range, and above the LOD and LOQ in all samples. This assay was therefore used for all subsequent analyses in both biofluids.
Cross-sectional analysis of baseline
Demographic characteristics and confounding variables
Demographic and clinical characteristics are summarised in Table 1. The control group was matched to the HD mutation carriers as a whole but was older on average than preHD, which in turn was younger than the HD group. The preHD group had a lower mean BMI than the controls, but did not differ from HD. More manifest HD participants were on medication, including anti-depressants and anti-psychotics.
Plasma and CSF BDNF did not differ by gender (Figure S1). The platelet count in blood did not differ between groups, but it was positively associated with plasma BDNF in HD mutation carriers (Figure S2). In the HD group, the average erythrocyte count was negatively correlated with CSF BDNF concentration (Figure S2).
Storage duration as a BDNF confounder in plasma but not CSF
BDNF levels in baseline plasma samples were substantially higher than in the 24-month follow-up samples (Fig. 1). This was not seen in CSF, suggesting the possibility that BDNF levels were rising artefactually over time in frozen plasma, perhaps due to leakage from small numbers of residual platelets or degradation of pro-BDNF to BDNF. In keeping with this, the time spent in frozen storage was positively associated with plasma BDNF but not CSF BDNF, in controls and HD mutation carriers (Fig. 1). Hence, plasma BDNF analyses were additionally adjusted for sample storage duration.
BDNF levels in Huntington’s disease
Neither plasma nor CSF BDNF differed significantly between groups (Fig. 2). There were no associations between plasma or CSF BDNF and clinical measures, with the sole exception of plasma BDNF which was weakly positively associated with Verbal Fluency—Categorical (r = 0.261, p = 0.015; Figure S3). There were no associations between BDNF and imaging measures, except a weak positive association between CSF BDNF and white matter volume (r = 0.306, p = 0.032; Figure S4). It is of note that no correction for multiplicity was applied.
Plasma and CSF BDNF showed poor ability to distinguish controls from HD mutation carriers (plasma AUC = 0.494, CSF AUC = 0.602; Fig. 2C) and preHD from HD (plasma AUC 0.409, CSF AUC = 0.454; Fig. 2D).
The rate of change in CSF BDNF did not differ between any HD stages (Fig. 3A,B). Longitudinal evaluation of plasma BDNF was limited by its apparent tendency to rise in freezer storage, producing spuriously higher values for baseline samples (Fig. 3C,D), but using the mixed effect model with adjustment for confounders, CSF and plasma BDNF did not change over time in controls or HD mutation carriers (Fig. 3E,F). Overall, baseline BDNF did not predict subsequent change in clinical measures (Figure S5), nor did the rates of change in BDNF (Figure S6).
The conventional ELISAs we tested lacked the sensitivity required to accurately quantify CSF BDNF. With an ultra-sensitive assay, BDNF levels were measurable in both CSF and plasma but did not reflect HD or its progression and were not associated with the examined clinical and imaging measures.
It was notable that the ELISA assays used in previous reports of altered CSF BDNF in neurological disease appear insufficiently sensitive for the purpose. This emphasizes the importance of ensuring the analyte in question lies in the assay’s linear range and urges caution when interpreting previous reports of CSF BDNF as a disease biomarker. To our knowledge, this is therefore the first report of BDNF levels in human CSF using an assay capable of reliably quantifying them.
Unexpectedly, we also found that the storage duration is the major influence upon BDNF level in plasma but not CSF. This diminishes the utility of stored frozen samples for BDNF quantification in plasma and suggests time in storage should be controlled for in future biomarker studies. BDNF is known to be enriched in platelets, and our centrifugation procedure was designed to produce normal as opposed to platelet-poor plasma. The latter may show less influence from platelet-derived BDNF and therefore be a better surrogate for brain BDNF23.
BDNF had no properties suggesting it is a biomarker for HD progression in CSF or plasma. Its level did not differ significantly between controls and HD mutation carriers, or between preHD and HD groups. It had poor classification ability in our ROC analysis and lacked associations with clinical and MRI brain volumetric measures. In the context of a clear lack of groupwise differences, the small number of associations seen among many tests is likely a chance finding and not of biological significance. Neither baseline BDNF level, nor its rate of change, were prognostic for subsequent change in clinical or imaging outcomes. We therefore conclude that BDNF in CSF or plasma is unlikely to be a valid biomarker of HD, in the ‘diagnostic’, ‘monitoring’ or ‘prognostic’ categories according to the FDA’s BEST categorisation.
These negative findings contrast starkly with the performance of other CSF and plasma analytes, most notably neurofilament light and mutant huntingtin proteins, which do differ between groups, rise with progression, and predict subsequent clinical and imaging change20,22,28.
It should be noted that the absence of detectable changes in CSF or plasma does not exclude an important role for BDNF or its trophic pathway in the pathogenesis of HD. The decrease of BDNF might be very region-specific and therefore overwhelmed by generally unaltered BDNF in other regions. Several studies found reduced BDNF in striatum but not cortex in HD models3,7,9. Moreover, if striatal BDNF loss is significant, other gene promotors of the BDNF gene that are not directly modulated by HTT could possibly compensate for the mHTT-induced deficit of BDNF in the cortex29.
In the present study, we did not investigate BDNF isoforms, including its precursor, pro-BDNF. Studying the isoforms of BDNF, including pro-BDNF, could still reveal disease-related changes. Unlike some previous reports, we studied plasma rather than serum, but since plasma is prepared by centrifugation rather than clotting, we reasoned that it was less likely to contain artefactual signals from platelets.
Finally, it is important to note that even though we found BDNF to lack utility as a biomarker of HD in the natural history setting, it is still theoretically possible that a therapeutic intervention could produce detectable and meaningful changes in CSF or plasma BDNF. Our findings may be of value for the design of such trials in which BDNF would serve as a pharmacodynamic biomarker.
The data that support the findings of this study are available from the corresponding author, EJW, upon reasonable request.
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We would like to thank all the participants from the HD community who donated samples and gave their time to take part in this study.
This work was supported by the Medical Research Council UK, the CHDI foundation, the Huntington’s Disease Society of America, the Hereditary Disease Foundation, the Wellcome Trust (Wellcome Collaborative Award In Science 200181/Z/15/Z and Wellcome/EPSRC Centre for Medical Engineering [WT 203148/Z/16/Z]), the Department of Health's NIHR Biomedical Research Centres funding scheme, F. Hoffmann-La Roche Ltd, Horizon 2020 Framework Programme, the Swedish Research Council, the European Research Council, and Swedish State Support for Clinical Research, and the Innovative Medicines Initiative Joint Undertaking under EMIF grant. HZ is a Wallenberg Scholar.
ZAO, LMB, FBR, MF, RT, EBJ, RIS, AH, HZ, EJW are University College London employees. MA is a University College London Hospitals NHS Foundation Trust employee. EDV is a King’s College London employee. LMR has provided consultancy services to GLG, F. Hoffmann-La Roche Ltd, Genentech and Annexon. FBR has provided consultancy services to GLG and F. Hoffmann-La Roche Ltd. RIS has undertaken consultancy services for Ixitech Ltd. HZ has served at scientific advisory boards for Denali, Roche Diagnostics, Wave, Samumed, Siemens Healthineers, Pinteon Therapeutics and CogRx, has given lectures in symposia sponsored by Fujirebio, Alzecure and Biogen, and is a co-founder of Brain Biomarker Solutions in Gothenburg AB (BBS), which is a part of the GU Ventures Incubator Program (outside submitted work). EJW reports grants from Medical Research Council, CHDI Foundation, and F. Hoffmann-La Roche Ltd during the conduct of the study; personal fees from Hoffman La Roche Ltd, Triplet Therapeutics, PTC Therapeutics, Shire Therapeutics, Wave Life Sciences, Mitoconix, Takeda and Loqus23. All honoraria for these consultancies were paid through the offices of UCL Consultants Ltd., a wholly owned subsidiary of University College London. University College London Hospitals NHS Foundation Trust has received funds as compensation for conducting clinical trials for Ionis Pharmaceuticals, Pfizer and Teva Pharmaceuticals.
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Ou, ZY.A., Byrne, L.M., Rodrigues, F.B. et al. Brain-derived neurotrophic factor in cerebrospinal fluid and plasma is not a biomarker for Huntington’s disease. Sci Rep 11, 3481 (2021). https://doi.org/10.1038/s41598-021-83000-x