| Literature DB >> 33597568 |
Norie Saito1,2, Masato Furuhashi3, Masayuki Koyama1,4, Yukimura Higashiura1, Hiroshi Akasaka5, Marenao Tanaka1, Norihito Moniwa1, Hirofumi Ohnishi1,4, Shigeyuki Saitoh1,6, Nobuyuki Ura7, Kazuaki Shimamoto8, Tetsuji Miura1.
Abstract
Fatty acid-binding protein 4 (FABP4) is secreted from adipose tissue and acts as an adipokine, and an elevated circulating FABP4 level is associated with metabolic disorders and atherosclerosis. However, little is known about the causal link between circulating FABP4 level and mortality in a general population. We investigated the relationship between FABP4 concentration and mortality including cardiovascular death during a 12-year period in subjects of the Tanno-Sobetsu Study, a population-based cohort (n = 721, male/female: 302/419). FABP4 concentration at baseline was significantly higher in female subjects than in male subjects. All-cause death occurred in 123 (male/female: 74/49) subjects, and 34 (male/female: 20/14) and 42 (male/female: 26/16) subjects died of cardiovascular events and cancer, respectively. When divided into 3 groups according to tertiles of FABP4 level at baseline by sex (T1-T3), Kaplan-Meier survival curves showed that there were significant differences in rates of all-cause death and cardiovascular death, but not cancer death, among the groups. Multivariable Cox proportional hazard model analysis with a restricted cubic spline showed that hazard ratio (HR) for cardiovascular death, but not that for all-cause death, significantly increased with a higher FABP4 level at baseline after adjustment of age and sex. The risk of cardiovascular death after adjustment of age, sex, body mass index and levels of brain natriuretic peptide and high-sensitivity C-reactive protein in the 3rd tertile (T3) group (HR: 4.96, 95% confidence interval: 1.20-22.3) was significantly higher than that in the 1st tertile (T1) group as the reference. In conclusion, elevated circulating FABP4 concentration predicts cardiovascular death in a general population.Entities:
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Year: 2021 PMID: 33597568 PMCID: PMC7889640 DOI: 10.1038/s41598-021-83494-5
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379