Metabolite Profiling and Cardiovascular Event Risk: a Prospective Study of 3 Population-based Cohorts
Overview
Authors
Affiliations
Background: High-throughput profiling of circulating metabolites may improve cardiovascular risk prediction over established risk factors.
Methods And Results: We applied quantitative nuclear magnetic resonance metabolomics to identify the biomarkers for incident cardiovascular disease during long-term follow-up. Biomarker discovery was conducted in the National Finnish FINRISK study (n=7256; 800 events). Replication and incremental risk prediction was assessed in the Southall and Brent Revisited (SABRE) study (n=2622; 573 events) and British Women's Health and Heart Study (n=3563; 368 events). In targeted analyses of 68 lipids and metabolites, 33 measures were associated with incident cardiovascular events at P<0.0007 after adjusting for age, sex, blood pressure, smoking, diabetes mellitus, and medication. When further adjusting for routine lipids, 4 metabolites were associated with future cardiovascular events in meta-analyses: higher serum phenylalanine (hazard ratio per standard deviation, 1.18; 95% confidence interval, 1.12-1.24; P=4×10(-10)) and monounsaturated fatty acid levels (1.17; 1.11-1.24; P=1×10(-8)) were associated with increased cardiovascular risk, while higher omega-6 fatty acids (0.89; 0.84-0.94; P=6×10(-5)) and docosahexaenoic acid levels (0.90; 0.86-0.95; P=5×10(-5)) were associated with lower risk. A risk score incorporating these 4 biomarkers was derived in FINRISK. Risk prediction estimates were more accurate in the 2 validation cohorts (relative integrated discrimination improvement, 8.8% and 4.3%), albeit discrimination was not enhanced. Risk classification was particularly improved for persons in the 5% to 10% risk range (net reclassification, 27.1% and 15.5%). Biomarker associations were further corroborated with mass spectrometry in FINRISK (n=671) and the Framingham Offspring Study (n=2289).
Conclusions: Metabolite profiling in large prospective cohorts identified phenylalanine, monounsaturated fatty acids, and polyunsaturated fatty acids as biomarkers for cardiovascular risk. This study substantiates the value of high-throughput metabolomics for biomarker discovery and improved risk assessment.
Wu Z, Yang J, Ma Z, Chen Y, Han M, Wu Q J Gastroenterol. 2025; .
PMID: 40074913 DOI: 10.1007/s00535-025-02237-9.
Sun W, Lin R, Li Y, Yao Y, Lu B, Yu Y Front Endocrinol (Lausanne). 2025; 16:1510910.
PMID: 40052157 PMC: 11882422. DOI: 10.3389/fendo.2025.1510910.
Mitu F, Adam C, Richter P, Costache A, Gavril R, Cojocaru C Diagnostics (Basel). 2025; 15(4).
PMID: 40002559 PMC: 11854266. DOI: 10.3390/diagnostics15040408.
Sidorov E, Smith K, Xu C, Sanghera D Neurol Int. 2025; 17(2).
PMID: 39997661 PMC: 11858463. DOI: 10.3390/neurolint17020030.
The Diagnostic Value of Bile Acids and Amino Acids in Differentiating Acute Coronary Syndromes.
Yu Q, Zhao F, Wang S, Jia X, Shen S, Zhao X Int J Gen Med. 2025; 18():179-189.
PMID: 39834909 PMC: 11742763. DOI: 10.2147/IJGM.S499046.