Department of Epidemiology, Tulane University School of Public Health and Tropical Medicine, New Orleans, LA, USA.
Department of Biostatistics and Epidemiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Atherosclerosis. 2018 Apr;271:53-60. doi: 10.1016/j.atherosclerosis.2018.02.009. Epub 2018 Feb 10.
Coronary artery calcification (CAC) is common among patients with chronic kidney disease (CKD) and predicts the risk for cardiovascular disease (CVD). We examined the associations of novel risk factors with CAC progression among patients with CKD.
Among 1123 CKD patients in the Chronic Renal Insufficiency Cohort (CRIC) Study, CAC was measured in Agatston units at baseline and a follow-up visit using electron beam computed tomography or multidetector computed tomography.
Over an average 3.3-year follow-up, 109 (25.1%) participants without CAC at baseline had incident CAC and 124 (18.0%) participants with CAC at baseline had CAC progression, defined as an annual increase of ≥100 Agatston units. After adjustment for established atherosclerotic risk factors, several novel risk factors were associated with changes in CAC over follow-up. Changes in square root transformed CAC score associated with 1 SD greater level of risk factors were -0.20 (95% confidence interval, -0.31 to -0.10; p < 0.001) for estimated glomerular filtration rate, 0.14 (0.02-0.25; p = 0.02) for 24-h urine albumin, 0.25 (0.15-0.34; p < 0.001) for cystatin C, -0.17 (-0.27 to -0.07; p < 0.001) for serum calcium, 0.14 (0.03-0.24; p = 0.009) for serum phosphate, 0.24 (0.14-0.33; p < 0.001) for fibroblast growth factor-23, 0.13 (0.04-0.23; p = 0.007) for total parathyroid hormone, 0.17 (0.07-0.27; p < 0.001) for interleukin-6, and 0.12 (0.02-0.22; p = 0.02) for tumor necrosis factor-α.
Reduced kidney function, calcium and phosphate metabolism disorders, and inflammation, independent of established CVD risk factors, may progress CAC among CKD patients.
冠状动脉钙化(CAC)在慢性肾脏病(CKD)患者中很常见,可预测心血管疾病(CVD)的风险。我们研究了新型危险因素与 CKD 患者 CAC 进展之间的关系。
在慢性肾功能不全队列研究(CRIC)中,1123 例 CKD 患者基线和随访时使用电子束计算机断层扫描或多排计算机断层扫描进行 CAC 检测,用单位计算 CAC 积分。
平均 3.3 年的随访期间,基线时无 CAC 的 109 例(25.1%)患者发生 CAC 事件,基线时 CAC 阳性的 124 例(18.0%)患者 CAC 进展,定义为 CAC 每年增加≥100 个 Agatston 单位。在调整了已确立的动脉粥样硬化危险因素后,几种新型危险因素与 CAC 随时间的变化相关。与 1 个标准差的风险因素水平升高相关的 CAC 评分变化为估计肾小球滤过率升高 0.20(95%置信区间,-0.31 至-0.10;p<0.001),24 小时尿白蛋白增加 0.14(0.02-0.25;p=0.02),胱抑素 C 增加 0.25(0.15-0.34;p<0.001),血清钙降低 0.17(-0.27 至-0.07;p<0.001),血清磷增加 0.14(0.03-0.24;p=0.009),成纤维细胞生长因子-23 增加 0.24(0.14-0.33;p<0.001),全段甲状旁腺激素增加 0.13(0.04-0.23;p=0.007),白细胞介素-6 增加 0.17(0.07-0.27;p<0.001),肿瘤坏死因子-α增加 0.12(0.02-0.22;p=0.02)。
肾功能降低、钙磷代谢紊乱和炎症,独立于已确立的 CVD 危险因素,可能会使 CKD 患者 CAC 进展。