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Review
. 2022 Jun 27;12(7):1053.
doi: 10.3390/jpm12071053.

Impact of l-Carnitine Supplementation on Liver Enzyme Normalization in Patients with Chronic Liver Disease: A Meta-Analysis of Randomized Trials

Affiliations
Review

Impact of l-Carnitine Supplementation on Liver Enzyme Normalization in Patients with Chronic Liver Disease: A Meta-Analysis of Randomized Trials

Hyunwoo Oh et al. J Pers Med. .

Abstract

The effectiveness of l-carnitine in chronic liver disease remains controversial. We conducted this meta-analysis to assess the efficacy of various forms of l-carnitine in the treatment of chronic liver disease.

Methods: We searched the Cochrane Library, EMBASE, KMBASE, and Medline databases for all relevant studies published until April 2022 that examined the ability of l-carnitine or its derivatives to normalize liver enzymes in patients with chronic liver disease. We performed meta-analyses of the proportion of patients with alanine aminotransferase (ALT) normalization and post-treatment serum aspartate aminotransferase (AST) and ALT levels. A random effects model was used for meta-analyses.

Results: Fourteen randomized controlled trials (1217 patients) were included in this meta-analysis. The proportion of patients in whom ALT normalized was higher in the carnitine-orotate treatment group than in the control group (pooled odds ratio (OR), 95% confidence interval (CI) = 4.61 (1.48-14.39)). The proportion of patients in whom ALT normalized was also higher among those who received the carnitine-orotate complex, a combination of carnitine-orotate, biphenyl dimethyl dicarboxylate, and other minor supplementary compounds than in those who did not without significant heterogeneity (pooled OR (95% CI) = 18.88 (7.70-46.27); df = 1; p = 0.51; I2 = 0%). l-carnitine supplementation effectively lowered serum ALT levels compared to controls (pooled mean difference (95% CI) = -11.99 (-22.48 to -1.49)).

Conclusions: l-carnitine supplementation significantly lowered ALT and AST levels and normalized ALT levels in patients with chronic liver disease.

Keywords: acetylcarnitine; carnitine; carnitine-orotate; chronic liver disease.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Study flow diagram.
Figure 2
Figure 2
Forest plot of alanine aminotransferase normalization after carnitine-orotate (or carnitine-orotate complex) versus control treatment. The carnitine–orotate complex includes carnitine-orotate, BDD, and other minor supplementary compounds. The dosage of carnitine-orotate in the included studies in this analysis was 900 mg per day, which is the usual dosage for clinical purposes. * The values in this study were provided by the corresponding author. BDD, biphenyl dimethyl dicarboxylate; M-H, Mantel–Haenszel; CI, confidence interval; df, degrees of freedom.
Figure 3
Figure 3
Forest plot of post-treatment serum AST and ALT levels after l-carnitine (or acetyl-l-carnitine) supplementation versus control treatment. Parentheses following the first author’s name indicate the journal in which the study was published. * Multiple doses were investigated in this study. Data from the maximal dosage group (3 g/day) were used in the analysis. ALT, alanine aminotransferase; AST, aspartate aminotransferase; CI, confidence interval; df, degrees of freedom; IV, inverse variance; SD, standard deviation.

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