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2
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本文引用的文献

1
The combined pioglitazone and topiramate therapy for management of pediatric patients with severe MASLD.吡格列酮联合托吡酯治疗小儿重症 MASLD。
Saudi J Gastroenterol. 2024 Jul 1;30(4):252-259. doi: 10.4103/sjg.sjg_428_23. Epub 2024 May 10.
2
Growth hormone and nonalcoholic fatty liver disease.生长激素与非酒精性脂肪性肝病
Immunometabolism (Cobham). 2023 Jul 27;5(3):e00030. doi: 10.1097/IN9.0000000000000030. eCollection 2023 Jul.
3
Fructose induced KHK-C can increase ER stress independent of its effect on lipogenesis to drive liver disease in diet-induced and genetic models of NAFLD.果糖诱导的 KHK-C 可以增加 ER 应激,而不依赖于其对脂肪生成的影响,从而在饮食诱导和 NAFLD 的遗传模型中驱动肝脏疾病。
Metabolism. 2023 Aug;145:155591. doi: 10.1016/j.metabol.2023.155591. Epub 2023 May 23.
4
Increased GH/IGF-I Axis Activity Relates to Lower Hepatic Lipids and Phosphor Metabolism.生长激素/胰岛素样生长因子-I 轴活性增加与肝内脂质和磷代谢降低有关。
J Clin Endocrinol Metab. 2023 Sep 18;108(10):e989-e997. doi: 10.1210/clinem/dgad206.
5
Ketohexokinase-C regulates global protein acetylation to decrease carnitine palmitoyltransferase 1a-mediated fatty acid oxidation.酮己激酶-C 调节全局蛋白质乙酰化,以降低肉毒碱棕榈酰基转移酶 1a 介导的脂肪酸氧化。
J Hepatol. 2023 Jul;79(1):25-42. doi: 10.1016/j.jhep.2023.02.010. Epub 2023 Feb 21.
6
Dietary Counseling Aimed at Reducing Sugar Intake Yields the Greatest Improvement in Management of Weight and Metabolic Dysfunction in Children with Obesity.饮食咨询旨在减少糖摄入量,可最大程度改善肥胖儿童的体重和代谢功能障碍管理。
Nutrients. 2022 Apr 3;14(7):1500. doi: 10.3390/nu14071500.
7
Randomized placebo-controlled trial of losartan for pediatric NAFLD.随机安慰剂对照试验研究氯沙坦治疗小儿非酒精性脂肪性肝病。
Hepatology. 2022 Aug;76(2):429-444. doi: 10.1002/hep.32403. Epub 2022 Feb 28.
8
High Prevalence of Nonalcoholic Fatty Liver Disease Among Adolescents and Young Adults With Hypopituitarism due to Growth Hormone Deficiency.生长激素缺乏导致的垂体功能减退症青少年和年轻成人中非酒精性脂肪性肝病患病率高。
Endocr Pract. 2021 Nov;27(11):1149-1155. doi: 10.1016/j.eprac.2021.06.003. Epub 2021 Jun 11.
9
Metabolic effects of reduced growth hormone action in fatty liver disease.生长激素作用降低对脂肪肝疾病的代谢影响。
Hepatol Int. 2018 Sep;12(5):474-481. doi: 10.1007/s12072-018-9893-7. Epub 2018 Sep 11.
10
Nonalcoholic fatty liver disease in adult hypopituitary patients with GH deficiency and the impact of GH replacement therapy.成年生长激素缺乏性垂体功能减退症患者的非酒精性脂肪肝及生长激素替代治疗的影响。
Eur J Endocrinol. 2012 Jul;167(1):67-74. doi: 10.1530/EJE-12-0252. Epub 2012 Apr 24.

生长激素治疗使一名肥胖且身材矮小的青少年的肝脏酶水平恢复正常。

Growth Hormone Treatment Normalized Liver Enzymes in an Adolescent with Obesity and Short Statute.

作者信息

Zvekic Mensur, Herbert Maddie, Morales Alba, Softic Samir

机构信息

Northern Kentucky University, Department of Anatomy and Physiology, Highland Heights, KY 41099.

Department of Pediatrics, Division of Adolescent Medicine, University of Kentucky College of Medicine, Lexington, KY. 40536.

出版信息

Ann Pediatr. 2024;7(2). Epub 2024 Aug 7.

PMID:39233776
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11373495/
Abstract

Metabolic Dysfunction Associated Steatotic Liver disease is the most common cause of chronic hepatitis in children and adults. The patients with MASLD have low thyroid hormone activity in the liver. Recent evidence suggests that patients with MASLD may also have haptic growth hormone deficiency. Here, we present a case of a 13-year-old adolescent with obesity and short stature whose liver enzymes normalized with growth hormone therapy. The patient initially presented to the primary care physician's office, revealing a BMI in the 93rd percentile and elevated liver enzymes (ALT = 170 U/L, AST = 94 U/L). Subsequent visits showed a BMI in the 96th percentile, with further elevation in liver enzymes (ALT = 179 U/L, AST = 101 U/L). Following six months of lifestyle intervention, BMI decreased to the 91st percentile, and liver enzymes improved (ALT = 72 U/L, AST = 56 U/L), but did not normalize. Other causes of chronic hepatitis were excluded. Concurrently, screening for short stature revealed delayed bone age, although insulin-like growth factor 1 (IGF1) and insulin-like growth factor-binding protein 3 (IGFB3) levels were normal. Moreover, the patient failed a growth hormone (GH) stimulation test, revealing GH deficiency, corroborated by MRI findings of pituitary hypoplasia. GH therapy was initiated at pubertal doses. Nine months of GH therapy entirely normalized liver enzymes (ALT = 18, AST = 23), and BMI was reduced to the 75th percentile. GH therapy should be further investigated in adolescents with short stature and MASLD.

摘要

代谢功能障碍相关脂肪性肝病是儿童和成人慢性肝炎最常见的病因。患有代谢相关脂肪性肝病的患者肝脏中甲状腺激素活性较低。最近的证据表明,患有代谢相关脂肪性肝病的患者也可能存在生长激素缺乏。在此,我们报告一例13岁肥胖且身材矮小的青少年病例,其肝脏酶水平经生长激素治疗后恢复正常。该患者最初到初级保健医生办公室就诊,发现体重指数(BMI)处于第93百分位,肝脏酶升高(谷丙转氨酶[ALT]=170 U/L,谷草转氨酶[AST]=94 U/L)。随后的就诊显示BMI处于第96百分位,肝脏酶进一步升高(ALT = 179 U/L,AST = 101 U/L)。经过六个月的生活方式干预,BMI降至第91百分位,肝脏酶有所改善(ALT = 72 U/L,AST = 56 U/L),但未恢复正常。排除了慢性肝炎的其他病因。同时,对身材矮小进行筛查发现骨龄延迟,尽管胰岛素样生长因子1(IGF1)和胰岛素样生长因子结合蛋白3(IGFB3)水平正常。此外,患者生长激素(GH)刺激试验未通过,显示生长激素缺乏,垂体发育不全的MRI检查结果证实了这一点。以青春期剂量开始生长激素治疗。九个月的生长激素治疗使肝脏酶完全恢复正常(ALT = 18,AST = 23),BMI降至第75百分位。对于身材矮小和患有代谢相关脂肪性肝病的青少年,应进一步研究生长激素治疗。