Title | Associations between metabolomic compounds and incident heart failure among African Americans: the ARIC Study. |
Publication Type | Journal Article |
Year of Publication | 2013 |
Authors | Zheng, Y, Yu, B, Alexander, D, Manolio, TA, Aguilar, D, Coresh, J, Heiss, G, Boerwinkle, E, Nettleton, JA |
Journal | Am J Epidemiol |
Volume | 178 |
Issue | 4 |
Pagination | 534-42 |
Date Published | 2013 Aug 15 |
ISSN | 1476-6256 |
Keywords | African Americans, Age Distribution, Atherosclerosis, Biomarkers, Comorbidity, Diabetes Mellitus, Female, Follow-Up Studies, Heart Failure, Humans, Hypertension, Kidney Diseases, Male, Metabolomics, Middle Aged, Mississippi, Obesity, Proportional Hazards Models, Sedentary Behavior |
Abstract | Heart failure is more prevalent among African Americans than in the general population. Metabolomic studies among African Americans may efficiently identify novel biomarkers of heart failure. We used untargeted methods to measure 204 stable serum metabolites and evaluated their associations with incident heart failure hospitalization (n = 276) after a median follow-up of 20 years (1987-2008) by using Cox regression in data from 1,744 African Americans aged 45-64 years without heart failure at baseline from the Jackson, Mississippi, field center of the Atherosclerosis Risk in Communities (ARIC) Study. After adjustment for established risk factors, we found that 16 metabolites (6 named with known structural identities and 10 unnamed with unknown structural identities, the latter denoted by using the format X-12345) were associated with incident heart failure (P < 0.0004 based on a modified Bonferroni procedure). Of the 6 named metabolites, 4 are involved in amino acid metabolism, 1 (prolylhydroxyproline) is a dipeptide, and 1 (erythritol) is a sugar alcohol. After additional adjustment for kidney function, 2 metabolites remained associated with incident heart failure (for metabolite X-11308, hazard ratio = 0.75, 95% confidence interval: 0.65, 0.86; for metabolite X-11787, hazard ratio = 1.23, 95% confidence interval: 1.10, 1.37). Further structural analysis revealed X-11308 to be a dihydroxy docosatrienoic acid and X-11787 to be an isoform of either hydroxyleucine or hydroxyisoleucine. Our metabolomic analysis revealed novel biomarkers associated with incident heart failure independent of traditional risk factors. |
DOI | 10.1093/aje/kwt004 |
Alternate Journal | Am. J. Epidemiol. |
PubMed ID | 23788672 |
PubMed Central ID | PMC3736751 |
Grant List | HHSN268201100012C / HL / NHLBI NIH HHS / United States HHSN268201100009I / HL / NHLBI NIH HHS / United States HHSN268201100010C / HL / NHLBI NIH HHS / United States HHSN268201100008C / HL / NHLBI NIH HHS / United States HHSN268201100005G / HL / NHLBI NIH HHS / United States HHSN268201100008I / HL / NHLBI NIH HHS / United States HHSN268201100005C / / PHS HHS / United States HHSN268201100007C / HL / NHLBI NIH HHS / United States HHSN268201100009C / / PHS HHS / United States 3U01HG004402-02S1 / HG / NHGRI NIH HHS / United States HHSN268201100011I / HL / NHLBI NIH HHS / United States HHSN268201100011C / HL / NHLBI NIH HHS / United States 5K01DK082729-04 / DK / NIDDK NIH HHS / United States U01 HG004402 / HG / NHGRI NIH HHS / United States HHSN268201100010C / / PHS HHS / United States HHSN268201100006C / HL / NHLBI NIH HHS / United States HHSN268201100008C / / PHS HHS / United States HHSN268201100012C / / PHS HHS / United States HHSN268201100005I / HL / NHLBI NIH HHS / United States HHSN268201100007C / / PHS HHS / United States HHSN268201100009C / HL / NHLBI NIH HHS / United States HHSN268201100011C / / PHS HHS / United States HHSN268201100005C / HL / NHLBI NIH HHS / United States HHSN268201100007I / HL / NHLBI NIH HHS / United States K01 DK082729 / DK / NIDDK NIH HHS / United States HHSN268201100006C / / PHS HHS / United States |