Division of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, California.
Department of Medicine, Santa Clara Valley Medical Center, San Jose, California.
Clin Gastroenterol Hepatol. 2019 Oct;17(11):2379-2381. doi: 10.1016/j.cgh.2018.11.024. Epub 2018 Nov 17.
The pathogenetic pathways leading to increasing prevalence of advanced fibrosis in the setting of nonalcoholic fatty liver disease (NAFLD) and resulting in higher rates of liver-related and cardiovascular morbidity and mortality in the United States are multifactorial. The negative health impact of "low-normal" thyroid function, which is defined as a higher level of thyroid-stimulating hormone (TSH) within the euthyroid reference range, may be comparable with overt and subclinical hypothyroidism. We reported a strong association between biopsy-proven advanced fibrosis in NAFLD with increasing TSH levels in a dose-dependent manner even within the euthyroid reference range. To generalize our findings across all ethnicities, we examined the association of both low-normal thyroid function and subclinical hypothyroidism with advanced fibrosis in the US general population.
导致非酒精性脂肪性肝病 (NAFLD) 中晚期纤维化患病率增加的发病途径是多因素的,这导致了美国更高的肝脏相关和心血管发病率和死亡率。“正常低值”甲状腺功能的不良健康影响(定义为促甲状腺激素 (TSH) 在甲状腺功能正常参考范围内的较高水平)可能与明显和亚临床甲状腺功能减退相当。我们报告了在 NAFLD 中,即使在甲状腺功能正常参考范围内,与逐渐增加的 TSH 水平呈剂量依赖性的活检证实的晚期纤维化之间存在强烈关联。为了将我们的发现推广到所有种族,我们在美国普通人群中研究了低正常甲状腺功能和亚临床甲状腺功能减退与晚期纤维化之间的关联。