Department of Gastroenterology, Juntendo University Nerima Hospital, Tokyo 177-8521, Japan.
Department of Cellular and Molecular Function Analysis, Kanazawa University Graduate School of Medical Sciences, Kanazawa 920-8640, Japan.
Nutrients. 2021 Dec 10;13(12):4428. doi: 10.3390/nu13124428.
This study investigated the inhibitory effect of levocarnitine supplementation on sarcopenia progression in hepatocellular carcinoma (HCC) patients treated with lenvatinib. We evaluated the skeletal muscle index (SMI). After propensity score matching for age, sex, modified albumin-bilirubin grade, baseline presence of sarcopenia, and branched-chain amino acid administration, we selected 17 patients who received levocarnitine supplementation after starting lenvatinib therapy and 17 propensity-score-matched patients who did not receive levocarnitine. Sarcopenia was present in 76% of the patients at baseline. Changes in baseline SMI at 6 and 12 weeks of treatment were significantly suppressed in the group with levocarnitine supplementation compared with those without ( = 0.009 and = 0.018, respectively). While there were no significant differences in serum free carnitine levels in cases without levocarnitine supplementation between baseline and after 6 weeks of treatment ( = 0.193), free carnitine levels were significantly higher after 6 weeks of treatment compared with baseline in cases with levocarnitine supplementation ( < 0.001). Baseline SMI and changes in baseline SMI after 6 weeks of treatment were significantly correlated with free carnitine levels (r = 0.359, = 0.037; and r = 0.345, = 0.045, respectively). Levocarnitine supplementation can suppress sarcopenia progression during lenvatinib therapy.
本研究旨在探讨左卡尼汀补充对接受仑伐替尼治疗的肝细胞癌(HCC)患者肌少症进展的抑制作用。我们评估了骨骼肌指数(SMI)。通过对年龄、性别、改良白蛋白-胆红素分级、基线肌少症存在和支链氨基酸给药进行倾向评分匹配后,我们选择了 17 名在开始仑伐替尼治疗后接受左卡尼汀补充的患者和 17 名接受倾向评分匹配但未接受左卡尼汀补充的患者。基线时,76%的患者存在肌少症。与未接受左卡尼汀补充的患者相比,接受左卡尼汀补充的患者在治疗 6 周和 12 周时的基线 SMI 变化明显受到抑制(=0.009 和=0.018,分别)。在未接受左卡尼汀补充的患者中,治疗 6 周时与基线相比,血清游离肉碱水平无显著差异(=0.193),而接受左卡尼汀补充的患者在治疗 6 周后,游离肉碱水平明显高于基线(<0.001)。基线 SMI 和治疗 6 周后基线 SMI 的变化与游离肉碱水平显著相关(r=0.359,=0.037;r=0.345,=0.045,分别)。左卡尼汀补充可抑制仑伐替尼治疗期间肌少症的进展。