Improvement of clinical outcomes in patients undergoing peritoneal dialysis using hydroxymethylglutaryl-CoA reductase inhibitors: A systematic review and meta-analysis

被引:1
|
作者
Lee, Dan-Ying [1 ,3 ]
Huang, Chi-Jung [2 ]
Yeh, Wan-Yu [2 ]
Sung, Shih-Hsien [2 ,3 ]
Chen, Chen-Huan [3 ,4 ,5 ,6 ]
Cheng, Hao-Min [2 ,3 ,4 ,5 ,6 ,7 ,8 ]
机构
[1] Taipei Vet Gen Hosp, Dept Internal Med, Div Cardiol, Taipei, Taiwan
[2] Taipei Vet Gen Hosp, Ctr Evidence based Med, Taipei, Taiwan
[3] Natl Yang Ming Chiao Tung Univ, Coll Med, Sch Med, Taipei, Taiwan
[4] Natl Yang Ming Chiao Tung Univ, Inst Publ Hlth, Taipei, Taiwan
[5] Natl Yang Ming Chiao Tung Univ, Community Med Res Ctr, Taipei, Taiwan
[6] Taipei Vet Gen Hosp, Dept Med Educ, Taipei, Taiwan
[7] Natl Yang Ming Chiao Tung Univ, PhD Program Interdisciplinary Med PIM, Coll Med, Taipei, Taiwan
[8] Taipei Vet Gen Hosp, Ctr Evidence based Med, 201, Sect 2,Shi Pai Rd, Taipei 112, Taiwan
关键词
All-cause mortality; Cardiovascular disease; Meta-analysis; Peritoneal dialysis; Statin; CHRONIC KIDNEY-DISEASE; C-REACTIVE PROTEIN; STATIN THERAPY; CARDIOVASCULAR EVENTS; RENAL PROTECTION; ATORVASTATIN; SIMVASTATIN; MANAGEMENT; MORTALITY; SURVIVAL;
D O I
10.1097/JCMA.0000000000000840
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background:It is unclear whether hydroxymethylglutaryl-CoA reductase inhibitor (statin) therapy decreases the risk of mortality and cardiovascular disease (CVD) in patients undergoing peritoneal dialysis (PD). Methods:We performed a literature search of PubMed, Cochrane Library, Embase, and other databases for research publications up to June 2022. The outcomes of interest were fatal and nonfatal CVDs, all-cause mortality, and changes in the biochemical profiles. Hazard ratios (HRs) with 95% confidence intervals (CIs) were pooled and synthesized using a random-effects model. The certainty of the evidence was determined using Grading of Recommendations, Assessment, Development, and Evaluation. Results:Nine studies, including 2,933 patients undergoing PD, were included. Among them, three studies, including 2,099 patients, reported all-cause mortality, and three, including 1,571 patients, reported CVDs. In these patients, pooling results of two observational studies (very low-certainty evidence) showed that statin therapy significantly reduced CVDs (HR = 0.67; 95% CI = 0.54-0.84; p = 0.0004). Moreover, statin therapy was associated with significantly reduced low-density lipoprotein cholesterol, total cholesterol, and C-reactive protein levels (very low certainty of evidence). However, the effects of statin therapy on triglyceride, high-density lipoprotein, and albumin levels were not statistically significant. Conclusion:Although statin therapy was associated with significantly reduced low-density lipoprotein cholesterol, total cholesterol, and C-reactive protein levels, the probable beneficial effect of statins on CVD risk in patients undergoing PD could not be concluded firmly. Additional high-quality studies are required to assess the potential beneficial effects of statin therapy in PD patients.
引用
收藏
页码:155 / 165
页数:11
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