Renoprotective effects of coenzyme Q10 supplementation in patients with chronic kidney disease: a protocol for a systematic review

被引:0
|
作者
Abe, Yoshifusa [1 ]
Nishiwaki, Hiroki [2 ]
Suzuki, Taihei [3 ]
Noma, Hisashi [4 ]
Watanabe, Yoshitaka [5 ]
Ota, Erika [6 ]
Hasegawa, Takeshi [3 ,7 ,8 ,9 ]
机构
[1] Showa Univ, Koto Toyosu Hosp, Childrens Med Ctr, Koto Ku, Tokyo, Japan
[2] Showa Univ, Fujigaoka Hosp, Dept Internal Med, Div Nephrol, Yokohama, Kanagawa, Japan
[3] Showa Univ, Dept Internal Med, Div Nephrol, Sch Med, Shinagawa Ku, Tokyo, Japan
[4] Inst Stat Math, Dept Data Sci, Tachikawa, Japan
[5] Showa Univ, Northern Yokohama Hosp, Childrens Med Ctr, Yokohama, Kanagawa, Japan
[6] St Lukes Int Univ, Global Hlth Nursing, Grad Sch Nursing Sci, Chuo Ku, Tokyo, Japan
[7] Showa Univ, Dept Orthoped Surg, Shinagawa Ku, Shinagawa, Kanagawa, Japan
[8] Showa Univ, Grad Sch Med, Dept Hyg Publ Hlth & Prevent Med, Tokyo, Japan
[9] Showa Univ, Res Adm Ctr SURAC, Shinagawa Ku, Shinagawa, Japan
来源
BMJ OPEN | 2024年 / 14卷 / 12期
关键词
Systematic Review; Diabetic nephropathy & vascular disease; Kidney & urinary tract disorders; Q(10);
D O I
10.1136/bmjopen-2024-084088
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Coenzyme Q10 (CoQ10) is a fat-soluble vitamin-like quinone. The plasma levels of CoQ10 are reduced in patients with chronic kidney disease (CKD). CoQ10 supplementation can improve mitochondrial function and decrease oxidative stress in these patients. This systematic review will assess the renoprotective effects of CoQ10 supplementation in patients with CKD. Methods and analysis We will include the following studies: (1) randomised-controlled trials, (2) participants with CKD and (3) participants treated with CoQ10 as an intervention. The systematic review protocol was prepared in accordance with the Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols. MEDLINE, EMBASE, Cochrane Central Register of Controlled Trials and International Clinical Trials Register databases will be searched for articles without language restrictions in December 2024. The authors will be divided into two groups. Two independent authors will screen the titles and abstracts of all reports extracted via an electronic search. After the initial screening, the authors will independently review the full-text articles and perform a directed content analysis of the extracted data. For outcomes measured using continuous scales of measurement, we will adopt standardised mean differences as the effect measures. We will pool the data using the random-effects model. Ethics and dissemination No human participants will be involved in the study. On completion of the analysis, the manuscript will be prepared for publication in a peer-reviewed journal. PROSPERO registration number CRD42021241085.
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页数:4
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