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Updated: Oct 15, 2026

Dynamic Digital Biomarkers of Motor and Cognitive Function in Parkinson's Disease
Published on: July 24, 2019
Correlation of peripheral blood BMAL1 level with non-motor symptoms in Parkinson's disease patients
Yanyan Jiang1, Yufei Zhang1, Luoqing Dong1
1Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Objective:
This study aimed to quantify BMAL1 expression in the peripheral blood of patients with Parkinson's disease (PD) and to evaluate its correlation with non-motor symptoms (NMS). We further assessed whether serum interleukin-6 and melatonin levels were associated with BMAL1 expression.
Methods:
This study included 80 patients with PD and 80 age-and sex-matched healthy controls. General clinical information and scores on multiple NMS scales were collected. Peripheral blood BMAL1 expression was quantified using real-time quantitative polymerase chain reaction. Serum levels of melatonin and interleukin-6 were measured using enzyme-linked immunosorbent assay. Spearman's correlation analysis was used to evaluate the associations between BMAL1 expression and the NMS scores.
Results:
Compared to healthy controls, patients with PD exhibited significantly lower peripheral blood BMAL1 expression levels in the morning (p = 0.005). BMAL1 levels were negatively correlated with the NMS Scale score (r = -0.407, p < 0.001). Furthermore, higher BMAL1 levels were associated with better night-time sleep quality and cognitive function, whereas lower BMAL1 levels correlated with more severe anxiety and depression. A weak positive correlation was observed between BMAL1 expression and melatonin levels (r = 0.267, p = 0.017). A significant negative correlation was found between BMAL1 expression and interleukin-6 level (r = -0.603, p < 0.001).
Conclusion:
In this cross-sectional study, peripheral blood BMAL1 expression at a single morning time point was lower in patients with PD and correlated with NMS severity, suggesting a potential pathway involving BMAL1, melatonin, and inflammatory cytokines in NMS pathogenesis. Future studies with multiple time-point measurements are required to validate these findings.
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