Department of Nephrology, The First Affiliated Hospital of University of South China, Hengyang, China.
Department of Nephrology, The Second Affiliated Hospital of Guangxi Medical University, Nanning, China.
Int Urol Nephrol. 2021 Oct;53(10):2149-2158. doi: 10.1007/s11255-021-02835-5. Epub 2021 Mar 13.
L-carnitine is an amino acid derivative that is thought to be helpful for treating renal anemia in hemodialysis patients. However, the mechanism remains to be fully elucidated.
A literature search was performed on PubMed, Embase, and Cochrane Central Register of Controlled Trials to identify randomized controlled trials (RCTs) and conduct a meta-analysis for investigating the effect of L-carnitine in the treatment of renal anemia in participants receiving hemodialysis.
A total of 18 eligible trials with 1090 participants were included in this study. L-carnitine can significantly increase plasma free L-carnitine levels (mean difference [MD]: 140.53, 95% confidence interval [CI] 102.22-178.85; P < 0.00001), decrease the erythropoietin responsiveness index (ERI; MD: -2.72, 95% CI -3.20 to -2.24; P < 0.00001) and the required erythropoiesis-stimulating agent (ESA) doses (MD: -1.70, 95% CI -2.04 to -1.36; P < 0.00001). However, the use of L-carnitine was not associated with a higher hemoglobin level (MD: 0.18, 95% CI -0.20 to 0.55; P = 0.35) and hematocrit level (MD: 1.07, 95% CI -0.73 to 2.87; P = 0.24). In subgroup analyses, the effects of L-carnitine supplementation on renal anemia in patients on hemodialysis were independent of the treatment duration and intervention routes.
The present meta-analysis indicated that L-carnitine therapy significantly increased plasma L-carnitine concentrations, improved the response to ESA, decreased the required ESA doses in patients receiving hemodialysis, and maintained hemoglobin and hematocrit levels. L-carnitine supplementation should be supported in hemodialysis patients. However, the relationship between L-carnitine treatment and long-term outcomes is still unclear. Further high-quality RCTs are needed to verify our findings.
左旋肉碱是一种氨基酸衍生物,被认为有助于治疗血液透析患者的肾性贫血。然而,其机制仍未完全阐明。
在 PubMed、Embase 和 Cochrane 对照试验中心注册库中进行文献检索,以确定左旋肉碱治疗接受血液透析的患者肾性贫血的随机对照试验(RCT)并进行荟萃分析。
共有 18 项符合条件的试验,涉及 1090 名参与者,纳入本研究。左旋肉碱可显著增加血浆游离左旋肉碱水平(均数差 [MD]:140.53,95%置信区间 [CI] 102.22-178.85;P<0.00001),降低红细胞生成素反应指数(ERI;MD:-2.72,95%CI -3.20 至-2.24;P<0.00001)和所需促红细胞生成素刺激剂(ESA)剂量(MD:-1.70,95%CI -2.04 至-1.36;P<0.00001)。然而,使用左旋肉碱与血红蛋白水平(MD:0.18,95%CI -0.20 至 0.55;P=0.35)和红细胞压积水平(MD:1.07,95%CI -0.73 至 2.87;P=0.24)的升高无关。亚组分析表明,左旋肉碱补充剂对血液透析患者肾性贫血的影响独立于治疗持续时间和干预途径。
本荟萃分析表明,左旋肉碱治疗可显著提高血浆左旋肉碱浓度,改善对 ESA 的反应,降低接受血液透析患者的 ESA 所需剂量,并维持血红蛋白和红细胞压积水平。应支持血液透析患者使用左旋肉碱补充剂。然而,左旋肉碱治疗与长期结局之间的关系仍不清楚。需要进一步的高质量 RCT 来验证我们的发现。