Fibroblast Growth Factor 23 Is Associated With Subclinical Cerebrovascular Damage The Northern Manhattan Study
Fibroblast Growth Factor 23 Is Associated With Subclinical Cerebrovascular Damage The Northern Manhattan Study
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DOI:
10.1161/strokeaha.115.012379
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发表时间:
2016-04-01
期刊:
影响因子:
8.3
通讯作者:
Wolf, Myles
中科院分区:
文献类型:
--
作者:
Wright, Clinton B.;Shah, Nirav H.;Wolf, Myles
Background and Purpose Elevated fibroblast growth factor 23 (FGF23) regulates phosphate homeostasis and is linked with mortality, cardiovascular events, and stroke. However, the role of FGF23 as a risk factor for subclinical cerebrovascular damage is unclear.Methods We used multivariable linear and logistic regression to evaluate associations between FGF23, continuously and by quartiles, with white matter hyperintensity volume, expressed as percent intracranial volume (%ICV), and subclinical brain infarction (SBI) in a community-based stroke-free sample.Results There were 1170 stroke-free Northern Manhattan Study (NOMAS) participants with FGF23 levels and quantitative magnetic resonance imaging data on white matter hyperintensity volume and SBI. Participants with FGF23 levels in the top quartile (range=85-1425 RU/mL) had greater white matter hyperintensity volume (=0.19 %ICV; 95% CI, 0.04-0.33 %ICV; P=0.01) compared with those in the lowest quartile (range=15-49 RU/mL), adjusted for demographics, vascular risk factors, and estimated glomerular filtration rate. These findings remained significant in those without evidence of chronic kidney disease (estimated glomerular filtration rate