SCIENTIFIC HUB

Follow the evidence.

SCIENTIFIC LITERATURE · MED

Correlation of peripheral blood <i>BMAL1</i> level with non-motor symptoms in Parkinson's disease patients.

Front Neurol · 2026-09-28

DOI: 10.3389/fneur.2026.1962167PMID: 42871215

Check source for accessJournal ArticleOriginal source ↗

Research overview

The text below is the source article’s original abstract under a verified reuse license. cc by

ObjectiveThis 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.MethodsThis 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.ResultsCompared 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 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 ConclusionIn 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.

Scientific assessment

01

Research question

Assess the question within the original study’s scope.

02

Methods & sample

Check the source article for study design and sample details.

03

Key findings

An editorially approved findings summary is not yet published for this record.

04

Limitations

Generalizability, bias and clinical meaning require separate assessment.

Methods, samples and clinical conclusions are not inferred from bibliographic metadata.