Key result
Lower serum serotonin linked to ~2% lower odds of calcific aortic valve stenosis.
Why the study?
Calcific aortic valve stenosis lacks pharmacological therapies partly due to incomplete understanding of metabolic alterations and absence of circulating biomarkers for detection.
Is reduced circulating serum serotonin associated with the presence of calcific aortic valve stenosis in adult patients?
Cross-Sectional (n=361)
No
Is reduced circulating serum serotonin associated with the presence of calcific aortic valve stenosis in adult patients?
Odds Ratio: 0.985 (95% CI 0.981–0.99)
p-value: p=<0.001
Reduced circulating serum serotonin is independently associated with the presence of calcific aortic valve stenosis, representing a biologically plausible, novel adjunct biomarker that improves diagnostic discrimination models.
Serum serotonin may enhance CAVS detection models in case-control data; leaves open prospective validation before clinical adoption.
Background: Calcific aortic valve stenosis (CAVS) is the most prevalent valvular heart disease in the elderly, yet no pharmacological therapy can halt its progression, partly due to incomplete understanding of disease-associated metabolic alterations and the lack of circulating biomarkers for disease detection. Objective: We aimed to characterize metabolic alterations associated with CAVS and evaluate a candidate circulating marker for CAVS detection. Methods: In the discovery cohort, patients with severe CAVS and matched controls without aortic valve disease were enrolled. Untargeted serum metabolomics was performed to characterize metabolic profiles. Differential metabolites, pathway enrichment analysis, and machine-learning-based feature prioritization were conducted. Based on pathway-level metabolic annotation, biological evidence, and feasibility of targeted measurement, serotonin was selected as a biologically prioritized, hypothesis-generating candidate and evaluated by ELISA in an independent targeted assessment cohort including controls, non-severe CAVS, and severe CAVS. Associations between serum serotonin levels and CAVS were assessed using multivariable logistic regression, smooth curve analysis, subgroup analyses, and ROC analysis. Results: The discovery cohort included 58 participants [29 with severe CAVS (69.7 ± 7.5 years; 44.8% male) and 29 matched controls (66.8 ± 5.1 years; 58.6% male)]. Untargeted metabolomics identified 70 differential metabolites. KEGG pathway enrichment analysis revealed serotonin-related metabolic annotations, while Random Forest analysis prioritized indoleacrylic acid as a discriminatory metabolite feature. Serotonin was not selected based on individual metabolite ranking but was evaluated based on pathway-level evidence, biological plausibility, and feasibility of targeted measurement. In the independent targeted assessment cohort of 303 individuals (101 controls, 101 non-severe CAVS, and 101 severe CAVS), serum serotonin levels were significantly lower in both non-severe and severe CAVS groups compared with controls, but did not differ between disease severity groups. Multivariable logistic regression adjusted for confounders confirmed its independent inverse association with CAVS. Incorporation of serum serotonin into the clinical model improved discrimination (AUC increased from 0.752 to 0.865), whereas serotonin alone showed moderate diagnostic performance. Conclusion: Reduced circulating serotonin is associated with the presence of CAVS and may represent a biologically plausible candidate adjunct biomarker for disease detection. Further multicenter prospective and mechanistic studies are required to determine its clinical utility and biological significance.
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Gao et al. (2026) conducted a cross-sectional in Calcific aortic valve stenosis (n=361). Serum serotonin vs. Controls (individuals without aortic valve disease) was evaluated on Presence of calcific aortic valve stenosis (OR 0.985, 95% CI 0.981-0.990, p=<0.001). Reduced circulating serum serotonin is independently associated with the presence of calcific aortic valve stenosis (OR 0.985) and significantly improves diagnostic model discrimination.
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