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:
综合性期刊3区
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--
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睾酮和成纤维细胞生长因子23(FGF-23)水平升高均与心血管疾病(CVD)风险升高独立相关。然而,性激素和FGF-23之间的关系还没有很好地建立。我们探讨了梅萨中老年男性和女性性激素和FGF-23之间的关联。我们研究了3,052名男性和2,868名绝经后女性,在入组时无CVD,基线血清性激素[总睾酮(T),游离T,雌二醇(E2)和性激素结合球蛋白(SHBG)]和完整的FGF-23。在性别分层分析中,我们使用多元线性回归分析了对数转换的性激素(每1 SD)和对数转换的FGF-23之间的横断面相关性,该回归分析针对社会人口统计学、CVD风险因素、估计的肾小球滤过率和矿物质代谢产物(25-羟基维生素D、钙、磷和甲状旁腺激素)进行了调整。研究参与者的平均(SD)年龄为64(10)岁。女性和男性的FGF-23中位数(IQR)相似[38(30-46)vs 38(31-47)pg/mL]。在校正分析中,在女性中,游离T增加1个SD与FGF-23增加3%相关,而SHBG与FGF-23降低2%相关。在男性中,E2增加1 SD与FGF-23升高6%相关,而总T/E2比值与FGF-23降低7%相关。总之,该探索性分析发现,女性中更具雄性激素性的性激素与FGF-23直接相关,而男性中与FGF-23呈负相关。需要进行纵向研究以确定FGF-23是否介导性激素和CVD风险之间的关系。
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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