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Published on: August 15, 2017
Neuroprotective, cognitive, and immunomodulatory effects of Valproic acid combined with dextromethorphan in bipolar
Chih-Chun Huang1, Nian-Sheng Tzeng2, Yun-Hsuan Chang3
1Department of Psychiatry, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Douliu Branch, Yunlin, Taiwan; Department of Psychiatry, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Abstract:
Valproic acid (VPA) is recognized for its neurotrophic properties and is widely used in psychiatric and peripheral disorders, while dextromethorphan (DM) has demonstrated anti-inflammatory and neuroprotective effects. This study examined whether adjunctive DM provides additional benefits on cognitive or immunomodulatory beyond standard VPA treatment in bipolar disorder (BD). BD aged 20-65 received open-label VPA (500-2500 mg/day; target blood level 50-100 μg/dl) for one week and were then randomized to VPA plus placebo (BDVPA) or VPA plus extended-release DM (BDVPA + DM; 30 or 60 mg/day) for twelve weeks. Neuropsychological measures (Continuous Performance Test, CPT; Wechsler Memory Scale-Revised, WMS-R), symptom severity, cytokines, and BDNF were assessed at baseline and post-treatment. A total of 109 participants (mean age 31.04 years, SD = 10.04) were enrolled; 96 completed cognitive testing and blood sampling (66 BDVPA + DM, 30 BDVPA). Two groups showed no significant differences at baseline in cognition, cytokines, or BDNF. MANOVA showed significant time effects across groups in memory, attention, TNF-α, CRP, IL-8, and BDNF (p < .05), with no group-by-time interactions. Within-group analyses showed modest improvements in several WMS-R and CPT indices in both groups, and small-to-moderate cognitive effect sizes. Both groups showed reductions in selected inflammatory markers and increases in BDNF. Although exploratory within-group patterns suggested slightly larger numerical changes in the BDVPA + DM group, the absence of differential treatment effects limits interpretation. A fully blinded, placebo-controlled trial with long-term follow-up is needed to further clarify whether low-dose DM as an adjunct confers additive neuropsychological or immunomodulatory benefits in BD.
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