Yanfei Li, Yuchen Xie, Chensheng Qiu, Bowen Yu, Fangzheng Yang, Yuanchao Cheng, Weizhen Zhong, Junhua Yuan
Journal: Food & function 2023;14(5):2502-2517
PMID: 36815696
: L-carnitine supplementation has been utilized against glucolipid metabolism disruption. However, to the best of our knowledge, no meta-analysis process has analyzed the effects of L-carnitine supplementation on insulin resistance, fasting blood glucose, lipid metabolism, and liver enzyme levels in adults. : Through the analysis and screening of 12 221 studies, 15 studies were selected from eligible trials for meta-analysis. Meta-analysis was performed in a random effect model with heterogeneity determined by , and subgroup analyses were used to further identify the source of heterogeneity. : The results showed significant effects of L-carnitine on FBG (MD = -4.94 mg dL, 95% CI: -7.07 to -2.82), insulin (MD = -0.99 μU mL, 95% CI: -1.41 to -0.56), HOMA-IR (MD = -0.58, 95% CI: -0.77 to -0.38), TG (MD = -11.22 mg dL, 95% CI: -19.21 to -3.22), TC (MD = -6.45 mg dL, 95% CI: -9.95 to -2.95, LDLc (MD = -8.28 mg dL, 95% CI: -11.08 to -5.47), and ALT (MD = -19.71 IU L, 95% CI: -36.45 to -2.96). However, no significant effect of L-carnitine supplementation was observed in HDLc (MD = -0.77 mg dL, 95% CI: -0.10 to -1.63) or AST (MD = -11.05 IU L, 95% CI: -23.08 to 0.99). The duration of carnitine supplementation was negatively associated with mean differences in FBG, as assessed by meta-regression. : The current meta-analysis revealed that L-carnitine may have favorable effects on glucolipid profile, especially insulin, FBG, HOMA-IR, TG, TC, LDLc, and ALT levels.
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