Abstract
Objective: Alzheimer’s disease (AD) is a complex and severe neurodegenerative disease and still lacks effective methods of diagnosis. Dysfunction of the N-methyl-D-aspartate receptor (NMDAR) has been found to be involved in synapse dysfunction and neurotoxicity of AD mechanisms. d-Serine, an NMDAR receptor coagonist, is reported as a potential new biomarker for AD. However, the results of serum and cerebrospinal fluid (CSF) d-serine levels are conflicting. We conducted a meta-analysis to investigate the serum and CSF d-serine levels in patients with AD. Methods: We searched PubMed, the Cochrane central register of controlled trials, and the Cochrane database of systematic reviews for trials that measured d-serine levels both in patients with AD and in controls. We included controlled trials that analyzed d-serine levels in human samples (e.g., serum and CSF). Studies were pooled using a random-effect model for comparisons between AD and control group. We used effect size (ES; expressed as d-serine levels) in each selected meta-analysis to calculate standardized mean difference (SMD). Positive values indicated increased d-serine levels in AD group. We presented results with 95% confidence intervals (CIs). The heterogeneity of the included trials was evaluated through visually inspecting funnel plots and using the I2 statistic. Moderators of effects were explored using metaregression. Results: Seven trials with more than 1186 participants were included in this meta-analysis. d-serine levels in patients with AD were significantly higher than those in controls (SMD = 0.679, 95% CI = 0.335 to 1.022, p < 0.001). Subgroup analyses showed that the AD group had significantly higher d-serine levels in serum and CSF compared with the control group (SMD = 0.566 (serum) and 1.008 (CSF); 95% CI = 0.183 to 0.948 (serum) and 0.168 to 1.849 (CSF)). Moreover, a metaregression revealed a significant negative association between ES and mean mini-mental state examination score in AD group (slope = −0.1203, p = 0.0004). Conclusions: Our results revealed higher d-serine levels in the serum and CSF of patients with AD relative to the controls. Further studies with a larger sample size and longer follow-up are recommended to clarify this association.
Highlights
Alzheimer’s disease (AD) is a complex and incurable neurodegenerative disease and the most common cause of dementia
One study reported d-serine levels in both serum and cerebrospinal fluid (CSF), and we considered that study as two studies in our analysis (Serum: AD vs. Controls; CSF: AD vs. Controls) [25]
Our meta-analysis revealed that the d-serine levels of patients diagnosed as having AD were significantly higher than those of controls (SMD = 0.679, 95% confidence intervals (CIs) = 0.335 to 1.022, p < 0.001; Figure 2a)
Summary
Alzheimer’s disease (AD) is a complex and incurable neurodegenerative disease and the most common cause of dementia. Diagnostic guidelines include cerebrospinal fluid (CSF) levels of amyloid-β1-42 (Aβ42), total tau protein, and hyperphosphorylated tau (p-tau) [5,6]. G.M.; Bloodgood, B.L.; Townsend, M.; Walsh, D.M.; Selkoe, D.; Sabatini, B.L. Natural Oligomers of the Alzheimer Amyloid- Protein Induce Reversible Synapse Loss by Modulating an NMDA-Type Glutamate Receptor-Dependent Signaling Pathway. C.; Lourenco, M.V.; Vargaslopes, C.; Suemoto, C.; Brandao, C.O.; Reis, T.; Leite, R.E.P.; Laks, J.; Jacobfilho, W.; Pasqualucci, C.A.; et al D-serine levels in Alzheimer’s disease: Implications for novel biomarker development. T.; Miroballo, M.; Casamassa, A.; Mancini, A.; Gaetani, L.; Nisticò, R.; Eusebi, P.; Katane, M.; Homma, H.; Calabresi, P.; et al Cerebrospinal fluid and serum d-serine concentrations are unaltered across the whole clinical spectrum of Alzheimer’s disease.
Sign-in/Register to view highlights & summary Sign-in/Register to access full text options 
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
