Division of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center at Dallas, Dallas, TX 75390-9047, USA.
Clin Chem. 2012 Jan;58(1):172-82. doi: 10.1373/clinchem.2011.171926. Epub 2011 Nov 7.
Growth differentiation factor 15 (GDF-15) is produced by cardiomyocytes and atherosclerotic lesions under stress conditions. Although higher circulating GDF-15 concentrations are associated with mortality across a spectrum of cardiovascular conditions, the relationship of GDF-15 with atherosclerosis and mortality in the general population remains undefined.
We measured plasma GDF-15 in 3219 participants of the Dallas Heart Study, a population sample of adults ages 30-65 years (55% women, 49% black). GDF-15 was analyzed in prespecified categories (<1200; 1200-1799; and ≥1800 ng/L) and continuously. End points included prevalent coronary artery calcium (CAC>10 Agatston units), increased CAC (CAC≥100 Agatston units) by electron beam computed tomography, and mortality through a median 7.3 years of follow-up (120 deaths, 48 cardiovascular deaths).
Increasing GDF-15 associated with older age, black race, hypertension, diabetes, smoking, left ventricular (LV) mass/body surface area, and worse renal function (P<0.0001 for each). In multivariable models adjusted for traditional risk factors, renal function, and LV mass/body surface area, GDF-15≥1800 ng/L was associated with CAC>10 (odds ratio 2.1; 95% CI 1.2-3.7; P=0.01), CAC≥100 (odds ratio 2.6; 95% CI 1.4-4.9; P=0.002), all-cause mortality (hazard ratio 3.5; 95% CI 2.1-5.9, P<0.0001), and cardiovascular mortality (hazard ratio 2.5; 95% CI 1.1-5.8, P=0.03). Adding log GDF-15 to fully adjusted models modestly improved the c statistic (P=0.025), the integrated discrimination index (0.028; P<0.0001) and the category-less net reclassification index (0.42; P=0.002). These findings remained significant with further adjustment for high-sensitivity C-reactive protein, N-terminal pro-B-type natriuretic peptide, and cardiac troponin T.
GDF-15 is independently associated with subclinical coronary atherosclerosis and mortality, and its potential role for risk stratification in the general population merits further evaluation.
生长分化因子 15(GDF-15)在应激条件下由心肌细胞和动脉粥样硬化病变产生。虽然较高的循环 GDF-15 浓度与各种心血管疾病的死亡率相关,但 GDF-15 与普通人群中的动脉粥样硬化和死亡率的关系仍未确定。
我们在达拉斯心脏研究的 3219 名参与者中测量了血浆 GDF-15,这是一个 30-65 岁成年人的人群样本(55%为女性,49%为黑人)。GDF-15 按预设类别(<1200;1200-1799;和≥1800ng/L)和连续分析。终点包括有症状的冠状动脉钙(CAC>10 个 Agatston 单位)、电子束计算机断层扫描显示 CAC 增加(CAC≥100Agatston 单位)和中位 7.3 年的随访期间的死亡率(120 例死亡,48 例心血管死亡)。
GDF-15 的增加与年龄较大、黑种人、高血压、糖尿病、吸烟、左心室(LV)质量/体表面积和肾功能较差有关(每个因素 P<0.0001)。在调整了传统危险因素、肾功能和 LV 质量/体表面积的多变量模型中,GDF-15≥1800ng/L 与 CAC>10(比值比 2.1;95%CI 1.2-3.7;P=0.01)、CAC≥100(比值比 2.6;95%CI 1.4-4.9;P=0.002)、全因死亡率(风险比 3.5;95%CI 2.1-5.9,P<0.0001)和心血管死亡率(风险比 2.5;95%CI 1.1-5.8,P=0.03)相关。将 log GDF-15 添加到完全调整后的模型中,略微提高了 c 统计量(P=0.025)、综合判别指数(0.028;P<0.0001)和无类别净重新分类指数(0.42;P=0.002)。这些发现仍然具有统计学意义,进一步调整高敏 C 反应蛋白、N 末端 pro-B 型利钠肽和心脏肌钙蛋白 T 后也是如此。
GDF-15 与亚临床冠状动脉粥样硬化和死亡率独立相关,其在普通人群中的风险分层中的潜在作用值得进一步评估。