Channing Laboratory, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Am Heart J. 2011 May;161(5):956-62. doi: 10.1016/j.ahj.2011.02.012.
Fibroblast growth factor 23 (FGF23), parathyroid hormone (PTH), and phosphorus all have been proposed as plasma biomarkers for the development of coronary heart disease (CHD) in individuals with normal renal function.
In a nested case-control study of men in the Health Professionals Follow-up Study, free of diagnosed cardiovascular disease at blood draw, we prospectively examined associations between plasma FGF23, PTH, and phosphorus and risk of CHD. During 10 years of follow-up, 422 men developed nonfatal myocardial infarction or fatal CHD. Controls were selected in a 2:1 ratio and matched for age, date of blood collection, and smoking status.
Mean estimated glomerular filtration rate was 86 mL/min per 1.73 m(2) in cases and controls. At baseline, there were no statistically significant differences between cases and controls in plasma levels of FGF23, PTH, or phosphorus. After adjusting for matching factors, family history of myocardial infarction, body mass index, alcohol consumption, physical activity, history of diabetes mellitus and hypertension, ethnicity, region, plasma 25-hydroxyvitamin D, and other factors, the odds ratios for incident CHD for participants in the highest, compared with lowest, quartiles were 1.03 (95% CI 0.70-1.52, P for trend 0.84) for FGF23, 1.20 (95% CI 0.82-1.76, P trend 0.99) for PTH, and 0.72 (95% CI 0.51-1.02, P trend 0.13) for phosphorus.
Plasma FGF23, PTH, and phosphorus are not associated with the development of incident CHD in men without chronic kidney disease.
成纤维细胞生长因子 23(FGF23)、甲状旁腺激素(PTH)和磷都被提出作为肾功能正常个体发生冠心病(CHD)的血浆生物标志物。
在一项健康专业人员随访研究中,对男性进行了一项嵌套病例对照研究,在采血时无诊断为心血管疾病,我们前瞻性地研究了血浆 FGF23、PTH 和磷与 CHD 风险之间的关系。在 10 年的随访期间,422 名男性发生非致死性心肌梗死或致死性 CHD。对照者按 2:1 的比例选择,并与年龄、采血日期和吸烟状况相匹配。
病例组和对照组的估计肾小球滤过率平均为 86mL/min/1.73m²。在基线时,病例组和对照组之间的血浆 FGF23、PTH 或磷水平没有统计学上的显著差异。在调整了匹配因素、心肌梗死家族史、体重指数、饮酒、体力活动、糖尿病和高血压病史、种族、地区、血浆 25-羟维生素 D 和其他因素后,最高四分位组与最低四分位组相比,发生 CHD 的比值比为 1.03(95%CI 0.70-1.52,P 趋势=0.84),FGF23 为 1.20(95%CI 0.82-1.76,P 趋势=0.99),PTH 为 0.72(95%CI 0.51-1.02,P 趋势=0.13)。
在没有慢性肾病的男性中,血浆 FGF23、PTH 和磷与新发 CHD 无关。