Protection against death and renal failure by renin-angiotensin system blockers in patients with diabetes and kidney disease

Author:

Shen Jian12,Huang Yan-Mei1,Song Xin-Nan3,Hong Xue-Zhi4,Wang Min1,Ling Wei1,Zhang Xiao-Xi1,Zhao Hai-Lu1

Affiliation:

1. Center for Diabetic Systems Medicine, Guilin Medical University, China

2. Department of pathology, Affiliated Hospital of Guilin Medical University, China

3. Department of Anesthetics, Affiliated Hospital of Guilin Medical University, China

4. Department of Rheumatology and Immunology, Affiliated Hospital of Guilin Medical University, China

Abstract

Introduction: Angiotensin-converting enzyme inhibitors (ACEis) and angiotensin receptor blockers (ARBs) are widely used to block the renin-angiotensin system (RAS). Yet it remains uncertain whether these drugs are equally effective and safe. Methods: Systematic reviews and meta-analyses of ACEis/ARBs in diabetes and kidney disease published in PubMed, Chinese National Knowledge Infrastructure (CNKI) and Wanfang databases were searched for clinical outcomes including all-cause mortality, end-stage renal disease (ESRD), hyperkalemia and cough. Results: Eight meta-analyses included 2177–61,264 patients with follow-up of 6–108 months. RAS blockers reduced mortality (relative risk ratio (RR), 0.90, 95% confidence interval (CI), 0.86–0.95) without heterogeneity. The death protection was significant specifically with ACEis (RR, 0.85, 95% CI, 0.79–0.91), but not with ARBs. Protection against ESRD was homogenously evident by ARBs (RR, 0.79, 95% CI, 0.73–0.87), ACEis (RR, 0.79, 95% , 0.64–0.94), and both (RR, 0.79, 95% CI, 0.73–0.87). Significant side effects were hyperkalemia by ARBs (RR, 2.44, 95% CI, 1.13–5.26), and cough by ACEis (RR, 2.38, 95% CI, 1.75–3.22) Conclusions: In patients with diabetes and kidney disease, ACEis and ARBs are consistently protective for the development of ESRD. Use of ACEis alone additionally reduces deaths and increases the risk for cough. Use of ARBs alone increases the risk for hyperkalemia without additional benefit of death protection.

Publisher

Hindawi Limited

Subject

Endocrinology,Internal Medicine

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