Role of Growth Hormone Therapy in Metabolic-Dysfunction-Associated Steatotic Liver Disease: A Systematic Review and Meta-Analysis.

Deep Dutta, Lakshmi Nagendra, Ritin Mohindra, Saptarshi Bhattacharya, Ameya Joshi, Abm Kamrul-Hasan
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Abstract

Multiple observation studies and meta-analysis have linked growth hormone (GH) deficiency with metabolic-dysfunction-associated steatotic liver disease (MASLD). No meta-analysis has analysed the efficacy and safety of GH therapy on different aspects of MASLD. We undertook this meta-analysis to address this gap in knowledge. Electronic databases were searched for RCTs involving patients with MASLD receiving GH therapy. Primary outcome was to evaluate changes in radiologic measures of MASLD (magnetic resonance spectroscopy (MRS) and ultrasonography) and liver enzymes. Secondary outcomes were to evaluate alterations in body composition parameters [dual-energy X-ray absorptiometry (DXA)], lipids, glycaemia and side effects. From initially searched 1047 articles, data from three RCTs (120 patients) which fulfilled all criteria were analysed. After 6 months of GH therapy in MASLD, the per cent reduction in intrahepatic lipid (MRS) was significantly higher with GH as compared to placebo [MD -5.85% (95%CI:-11.41- -0.30); P = 0.04; I2 = 63%]. Visceral adipose tissue (VAT) area reduction (DXA) was significantly higher with GH [MD-9.94 cm2 (95%CI:-19.04- -0.84); P = 0.03; I2 = 0%]. Serum insulin-like growth factor-1 (IGF-1) was significantly raised in MASLD patients receiving GH as compared to placebo [MD +166.86 ng/ml (95%CI: 79.19-254.53); P < 0.0.001; I2 = 90%]. High-sensitivity C-reactive protein (hsCRP) was significantly lower in patients receiving GH [MD -0.89 mg/L (95%CI:-1.40--0.38); P = 0.0.0006; I2 = 0%]. Patients receiving GH had similar changes in triglycerides [MD-1.06 mg/L (95%CI:-20.45-18.34); P = 0.91; I2 = 15%] and fasting glucose [MD -0.56 mg/L (95%CI:-4.67-3.55); P = 0.79; I2 = 39%]. Gamma-glutamyl transpeptidase was significantly lower in patients receiving GH [MD -7.86 U/L (95%CI:-12.46--3.27); P = 0.0008; I2 = 0%]. No increase in new-onset hypothyroidism was noted [OR 5.49 (95%CI: 0.25-121.18); P = 0.28]. Short-term 6-month GH therapy in MASLD is associated with a significant reduction in intrahepatic lipid content, visceral adiposity, GGT and hsCRP without any increased occurrence of dysglycaemia or hypothyroidism.

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生长激素疗法在代谢功能障碍相关性脂肪肝中的作用:系统综述与元分析》。
多项观察研究和荟萃分析显示,生长激素(GH)缺乏症与代谢功能障碍相关性脂肪肝(MASLD)有关。目前还没有荟萃分析对生长激素疗法在 MASLD 不同方面的疗效和安全性进行分析。为了填补这一知识空白,我们进行了这项荟萃分析。我们在电子数据库中搜索了涉及接受 GH 治疗的 MASLD 患者的 RCT。主要结果是评估MASLD的放射学指标(磁共振波谱(MRS)和超声波检查)和肝酶的变化。次要结果是评估身体成分参数[双能X射线吸收测定法(DXA)]、血脂、糖血症和副作用的变化。在初步检索的 1047 篇文章中,对符合所有标准的三项 RCT(120 名患者)的数据进行了分析。MASLD患者在接受6个月的GH治疗后,肝内脂质(MRS)降低的百分比与安慰剂相比明显更高[MD -5.85% (95%CI:-11.41- -0.30);P = 0.04;I2 = 63%]。内脏脂肪组织(VAT)面积减少(DXA)明显高于 GH [MD-9.94 cm2 (95%CI:-19.04- -0.84);P = 0.03;I2 = 0%]。与安慰剂相比,接受 GH 治疗的 MASLD 患者血清胰岛素样生长因子-1(IGF-1)明显升高 [MD +166.86 ng/ml (95%CI: 79.19-254.53); P < 0.0.001; I2 = 90%]。接受 GH 治疗的患者的高敏 C 反应蛋白(hsCRP)显著降低[MD -0.89 mg/L (95%CI:-1.40--0.38); P = 0.0.0006; I2 = 0%]。接受 GH 治疗的患者甘油三酯[MD-1.06 mg/L (95%CI:-20.45-18.34); P = 0.91; I2 = 15%]和空腹血糖[MD -0.56 mg/L (95%CI:-4.67-3.55); P = 0.79; I2 = 39%]的变化相似。接受 GH 治疗的患者γ-谷氨酰转肽酶明显降低[MD -7.86 U/L (95%CI:-12.46--3.27); P = 0.0008; I2 = 0%]。未发现新发甲状腺功能减退症增加[OR 5.49(95%CI:0.25-121.18);P = 0.28]。对 MASLD 进行为期 6 个月的短期 GH 治疗可显著降低肝内脂质含量、内脏脂肪含量、GGT 和 hsCRP,而不会增加血糖异常或甲状腺功能减退的发生率。
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来源期刊
Indian Journal of Endocrinology and Metabolism
Indian Journal of Endocrinology and Metabolism Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.10
自引率
0.00%
发文量
75
期刊介绍: The Indian Journal of Endocrinology and Metabolism (IJEM) aims to function as the global face of Indian endocrinology research. It aims to act as a bridge between global and national advances in this field. The journal publishes thought-provoking editorials, comprehensive reviews, cutting-edge original research, focused brief communications and insightful letters to editor. The journal encourages authors to submit articles addressing aspects of science related to Endocrinology and Metabolism in particular Diabetology. Articles related to Clinical and Tropical endocrinology are especially encouraged. Sub-topic based Supplements are published regularly. This allows the journal to highlight issues relevant to Endocrine practitioners working in India as well as other countries. IJEM is free access in the true sense of the word, (it charges neither authors nor readers) and this enhances its global appeal.
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