Associations between endogenous sex hormones and FGF-23 among women and men in the Multi-Ethnic Study of Atherosclerosis.
Associations between endogenous sex hormones and FGF-23 among women and men in the Multi-Ethnic Study of Atherosclerosis.
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DOI:
10.1371/journal.pone.0268759
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发表时间:
2022
期刊:
影响因子:
3.7
通讯作者:
中科院分区:
文献类型:
--
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Elevated levels of testosterone and fibroblast growth factor 23 (FGF-23) are both independently associated with a higher risk of cardiovascular disease (CVD). However, the relationship between sex hormones and FGF-23 is not well established. We explored the association between sex hormones and FGF-23 among middle-aged to older men and women in MESA. We studied 3,052 men and 2,868 postmenopausal women free of CVD at the time of enrollment with baseline serum sex hormones [total testosterone (T), free T, estradiol (E2) and sex hormone binding globulin (SHBG)] and intact FGF-23. In sex-stratified analyses, we examined the cross-sectional associations between log-transformed sex hormones (per 1 SD) and log-transformed FGF-23 using multiple linear regression adjusted for socio-demographics, CVD risk factors, estimated glomerular filtration rate and mineral metabolites (25-hydroxyvitamin D, calcium, phosphorus and parathyroid hormone). The mean (SD) age of study participants was 64 (10) years. The median (IQR) of FGF-23 was similar in women and men [38 (30–46) vs 38 (31–47) pg/mL]. In adjusted analyses, among women, 1 SD increment in free T was associated with 3% higher FGF-23 while SHBG was associated with 2% lower FGF-23. In men, 1 SD increment in E2 was associated with 6% higher FGF-23 whereas total T/E2 ratio was associated with 7% lower FGF-23. In conclusion, this exploratory analysis found that a more androgenic sex hormone profile was directly associated with FGF-23 in women and inversely associated with FGF-23 in men. Longitudinal studies are required to determine whether FGF-23 mediates the relationship between sex hormones and CVD risk.
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DOI:
10.1152/ajpgi.00243.2005
发表时间:
2005-12-01
影响因子:
4.5
作者:
Kolek, OI;Hines, ER;Ghishan, FK
通讯作者:
Ghishan, FK
影响因子:
2.7
作者:
Hackbarth, Jennifer S.;Hoyne, Jonathan B.;Singh, Ravinder J.
通讯作者:
Singh, Ravinder J.
影响因子:
5
作者:
CAULEY, JA;GUTAI, JP;POWELL, JG
通讯作者:
POWELL, JG
影响因子:
24
作者:
Ix, Joachim H.;Katz, Ronit;Kestenbaum, Bryan R.;de Boer, Ian H.;Chonchol, Michel;Mukamal, Kenneth J.;Rifkin, Dena;Siscovick, David S.;Sarnak, Mark J.;Shlipak, Michael G.
通讯作者:
Shlipak, Michael G.
影响因子:
37.8
作者:
Mathew JS;Sachs MC;Katz R;Patton KK;Heckbert SR;Hoofnagle AN;Alonso A;Chonchol M;Deo R;Ix JH;Siscovick DS;Kestenbaum B;de Boer IH
通讯作者:
de Boer IH