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Metabolite profiling and cardiovascular event risk: a prospective study of 3 population-based cohorts.

Authors :
Würtz P
Havulinna AS
Soininen P
Tynkkynen T
Prieto-Merino D
Tillin T
Ghorbani A
Artati A
Wang Q
Tiainen M
Kangas AJ
Kettunen J
Kaikkonen J
Mikkilä V
Jula A
Kähönen M
Lehtimäki T
Lawlor DA
Gaunt TR
Hughes AD
Sattar N
Illig T
Adamski J
Wang TJ
Perola M
Ripatti S
Vasan RS
Raitakari OT
Gerszten RE
Casas JP
Chaturvedi N
Ala-Korpela M
Salomaa V
Source :
Circulation [Circulation] 2015 Mar 03; Vol. 131 (9), pp. 774-85. Date of Electronic Publication: 2015 Jan 08.
Publication Year :
2015

Abstract

Background: High-throughput profiling of circulating metabolites may improve cardiovascular risk prediction over established risk factors.<br />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).<br />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.<br /> (© 2015 American Heart Association, Inc.)

Details

Language :
English
ISSN :
1524-4539
Volume :
131
Issue :
9
Database :
MEDLINE
Journal :
Circulation
Publication Type :
Academic Journal
Accession number :
25573147
Full Text :
https://doi.org/10.1161/CIRCULATIONAHA.114.013116