Martins David, Ani Chizobam, Pan Deyu, Ogunyemi Omolola, Norris Keith
Department of Medicine, Charles Drew University of Medicine and Science, 1731 E 20th Street, Los Angeles, CA 90059, USA.
J Nutr Metab. 2010;2010. doi: 10.1155/2010/167162. Epub 2010 Mar 24.
Background. Renal disease is commonly described as a complication of metabolic syndrome (MetS) but some recent studies suggest that Chronic Kidney disease (CKD) may actually antecede MetS. Few studies have explored the predictive utility of co-clustering CKD with MetS for cardiovascular disease (CVD) mortality. Methods. Data from a nationally representative sample of United States adults (NHANES) was utilized. A sample of 13115 non-pregnant individuals aged >/=35 years, with available follow-up mortality assessment was selected. Multivariable Cox Proportional hazard regression analysis techniques explored the relationship between co-clustered CKD, MetS and CVD mortality. Bayesian analysis techniques tested the predictive accuracy for CVD Mortality of two models using co-clustered MetS and CKD and MetS alone. Results. Co-clustering early and late CKD respectively resulted in statistically significant higher hazard for CVD mortality (HR = 1.80, CI = 1.45-2.23, and HR = 3.23, CI = 2.56-3.70) when compared with individuals with no MetS and no CKD. A model with early CKD and MetS has a higher predictive accuracy (72.0% versus 67.6%), area under the ROC (0.74 versus 0.66), and Cohen's kappa (0.38 versus 0.21) than that with MetS alone. Conclusion. The study findings suggest that the co-clustering of early CKD with MetS increases the accuracy of risk prediction for CVD mortality.
背景。肾脏疾病通常被描述为代谢综合征(MetS)的一种并发症,但最近的一些研究表明,慢性肾脏病(CKD)实际上可能先于MetS出现。很少有研究探讨将CKD与MetS共同聚类对心血管疾病(CVD)死亡率的预测效用。方法。使用了来自美国成年人全国代表性样本(NHANES)的数据。选取了13115名年龄≥35岁的非孕妇个体样本,并进行了随访死亡率评估。多变量Cox比例风险回归分析技术探讨了共同聚类的CKD、MetS与CVD死亡率之间的关系。贝叶斯分析技术测试了使用共同聚类的MetS和CKD以及仅使用MetS的两个模型对CVD死亡率的预测准确性。结果。与无MetS且无CKD的个体相比,分别将早期和晚期CKD与MetS共同聚类导致CVD死亡率的风险在统计学上显著更高(风险比[HR]=1.80,可信区间[CI]=1.45 - 2.23,以及HR = 3.23,CI = 2.56 - 3.70)。与仅使用MetS的模型相比,包含早期CKD和MetS的模型具有更高的预测准确性(72.0%对67.6%)、ROC曲线下面积(0.74对0.66)以及Cohen's kappa值(0.38对0.21)。结论。研究结果表明,早期CKD与MetS共同聚类可提高CVD死亡率风险预测的准确性。