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Fatty Acid Binding Protein-4 and Risk of Cardiovascular Disease: The Cardiovascular Health Study.

TitleFatty Acid Binding Protein-4 and Risk of Cardiovascular Disease: The Cardiovascular Health Study.
Publication TypeJournal Article
Year of Publication2020
AuthorsEgbuche, O, Biggs, ML, Ix, JH, Kizer, JR, Lyles, MF, Siscovick, DS, Djoussé, L, Mukamal, KJ
JournalJ Am Heart Assoc
Volume9
Issue7
Paginatione014070
Date Published2020 Apr 07
ISSN2047-9980
Abstract<p>Background FABP-4 (fatty acid binding protein-4) is a lipid chaperone in adipocytes and has been associated with prognosis in selected clinical populations. We investigated the associations between circulating FABP-4, risk of incident cardiovascular disease (CVD), and risk of CVD mortality among older adults with and without established CVD. Methods and Results In the Cardiovascular Health Study, we measured FABP4 levels in stored specimens from the 1992-993 visit and followed participants for incident CVD if they were free of prevalent CVD at baseline and for CVD mortality through June 2015. We used Cox regression to estimate hazard ratios for incident CVD and CVD mortality per doubling in serum FABP-4 adjusted for age, sex, race, field center, waist circumference, blood pressure, lipids, fasting glucose, and C-reactive protein. Among 4026 participants free of CVD and 681 with prevalent CVD, we documented 1878 cases of incident CVD and 331 CVD deaths, respectively. In adjusted analyses, FABP-4 was modestly associated with risk of incident CVD (mean, 34.24; SD, 18.90; HR, 1.10 per doubling in FABP-4, 95% CI, 1.00-1.21). In contrast, FABP-4 was more clearly associated with risk of CVD mortality among participants without (HR hazard ratio 1.24, 95% CI, 1.10-1.40) or with prevalent CVD (HR hazard ratio 1.57, 95% CI, 1.24-1.98). These associations were not significantly modified by sex, age, and waist circumference. Conclusions Serum FABP-4 is modestly associated with risk of incident CVD even after adjustment for standard risk factors, but more strongly associated with CVD mortality among older adults with and without established CVD.</p>
DOI10.1161/JAHA.119.014070
Alternate JournalJ Am Heart Assoc
PubMed ID32248728
Grant ListR01 HL094555 / HL / NHLBI NIH HHS / United States
ePub date: 
20/04