Tsai Wan-Chuan, Wu Hon-Yen, Peng Yu-Sen, Ko Mei-Ju, Wu Ming-Shiou, Hung Kuan-Yu, Wu Kwan-Dun, Chu Tzong-Shinn, Chien Kuo-Liong
From the Department of Internal Medicine (W-CT, H-YW, Y-SP), Far Eastern Memorial Hospital, New Taipei City; Institute of Epidemiology and Preventive Medicine (W-CT, H-YW, K-LC), College of Public Health, National Taiwan University; Department of Internal Medicine (H-YW, Y-SP, M-SW, K-YH, K-DW, T-SC, K-LC); Department of Dermatology (M-JK), National Taiwan University Hospital and College of Medicine; and Department of Dermatology (M-JK), Taipei City Hospital, Taipei, Taiwan.
Medicine (Baltimore). 2016 Mar;95(11):e3013. doi: 10.1097/MD.0000000000003013.
The risk factors influencing the natural course of chronic kidney disease (CKD) are complex and heterogeneous, and few systematic reviews to date have focused on this issue. The aim of the study is to identify the risk factors for disease development and progression in each stage of CKD. We conducted electronic literature searches of PubMed, MEDLINE, Scopus, and the Cochrane Library up to October 15, 2012, for observational studies evaluating the risk factors on the development or progression of CKD. Eligible studies should have collected repeated information that could evaluate changes in renal function. Extracted information from all the included studies was synthesized narratively. Quality assessments were performed using the Newcastle-Ottawa Scale. An exploratory random-effects meta-analysis was performed where feasible to pool effect sizes across studies for a specific risk factor in a specific outcome. We identified 38 cohort studies and 2 case-control studies from 40 articles, with a total of 318,898 participants from 14 countries. The follow-up duration ranged from 1.5 to 16 years. The majority of the included studies were of high quality. The baseline CKD stages of the included studies ranged from normal to later stages, and only 19 studies could be classified into a specific range of CKD stages during follow-up. Three risk factors from studies of the same baseline and follow-up CKD stages were eligible for the exploratory meta-analysis, including male sex, substantial proteinuria, and diabetes. The hazard ratios for the progression from CKD stages 3-5 to end-stage renal disease (ESRD) were 1.37 (95% confidence interval 1.17-1.62), 1.64 (1.01-2.66), and 1.16 (0.98-1.38) for male sex, substantial proteinuria, and diabetes, respectively. In conclusion, our analyses comprehensively summarize the initiating and perpetuating factors for CKD. Male sex and substantial proteinuria are significant perpetuating factors for the progression from late stage CKD to ESRD, and diabetes may play a minor role for the outcome of ESRD among patients with later stages of CKD.
影响慢性肾脏病(CKD)自然病程的危险因素复杂且具有异质性,迄今为止,很少有系统评价关注这一问题。本研究的目的是确定CKD各阶段疾病发生和进展的危险因素。我们对截至2012年10月15日的PubMed、MEDLINE、Scopus和Cochrane图书馆进行了电子文献检索,以查找评估CKD发生或进展危险因素的观察性研究。符合条件的研究应收集能够评估肾功能变化的重复信息。对所有纳入研究提取的信息进行叙述性综合。使用纽卡斯尔-渥太华量表进行质量评估。在可行的情况下,进行探索性随机效应荟萃分析,以汇总特定危险因素在特定结局中的跨研究效应量。我们从40篇文章中确定了38项队列研究和2项病例对照研究,共有来自14个国家的318898名参与者。随访时间为1.5至16年。大多数纳入研究质量较高。纳入研究的基线CKD阶段从正常到晚期不等,只有19项研究可在随访期间分类到特定的CKD阶段范围。来自相同基线和随访CKD阶段研究的三个危险因素符合探索性荟萃分析的条件,包括男性、大量蛋白尿和糖尿病。男性、大量蛋白尿和糖尿病从CKD 3-5期进展至终末期肾病(ESRD)的风险比分别为1.37(95%置信区间1.17-1.62)、1.64(1.01-2.66)和1.16(0.98-1.38)。总之,我们的分析全面总结了CKD的起始和持续因素。男性和大量蛋白尿是晚期CKD进展至ESRD的重要持续因素,而糖尿病在晚期CKD患者的ESRD结局中可能起较小作用。