Division of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, California, USA.
Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.
Am J Gastroenterol. 2020 Sep;115(9):1496-1504. doi: 10.14309/ajg.0000000000000654.
Higher levels of thyroid-stimulating hormone (TSH) in the euthyroid state can negatively affect the metabolic health, including nonalcoholic fatty liver disease (NAFLD). We studied the effect of TSH levels in the setting of normal levels of thyroid hormone on all-cause and cause-specific mortality stratified by NAFLD status.
The National Health and Nutrition Examination Survey (NHANES) III from 1988 to 1994 and NHANES III-linked mortality data through 2015 were used. NAFLD was defined as ultrasonographically diagnosed hepatic steatosis without coexisting liver diseases. Subclinical hypothyroidism was defined as a TSH level over 4.5 mIU/L and "low-normal" thyroid function as higher TSH level (2.5-4.5 mIU/L) within the euthyroid reference range. The Cox proportional hazard model analyzed the all-cause mortality and cause-specific mortality.
In a multivariate logistic regression analysis, individuals with low thyroid function demonstrated an association with NAFLD in a dose-dependent manner. During a median follow-up of 23 years, low thyroid function was associated with increased all-cause mortality only in the univariate model. Low thyroid function was associated with a higher risk for all-cause mortality in individuals with NAFLD and not in those without NAFLD. Furthermore, low thyroid function was associated with a higher risk for cardiovascular mortality in the entire population and among those with NAFLD but demonstrated no association with the non-NAFLD group.
In this large nationally representative sample of American adults, low thyroid function was associated with NAFLD and a predictor of higher risk for all-cause and cardiovascular mortality in individuals with NAFLD.
甲状腺刺激激素(TSH)在甲状腺功能正常状态下的高水平可能会对代谢健康产生负面影响,包括非酒精性脂肪性肝病(NAFLD)。我们研究了在甲状腺激素水平正常的情况下,TSH 水平对所有原因和特定原因死亡率的影响,这些死亡率按 NAFLD 状态分层。
使用了 1988 年至 1994 年的国家健康和营养检查调查(NHANES)III 以及通过 2015 年链接的死亡率数据。NAFLD 定义为超声诊断的无并存肝病的肝脂肪变性。亚临床甲状腺功能减退定义为 TSH 水平超过 4.5 mIU/L,“低正常”甲状腺功能定义为甲状腺功能正常参考范围内较高的 TSH 水平(2.5-4.5 mIU/L)。Cox 比例风险模型分析了全因死亡率和特定原因死亡率。
在多变量逻辑回归分析中,甲状腺功能低下的个体与 NAFLD 呈剂量依赖性相关。在中位数为 23 年的随访期间,仅在单变量模型中,甲状腺功能低下与全因死亡率增加相关。甲状腺功能低下与 NAFLD 患者的全因死亡率风险增加相关,但与无 NAFLD 患者无关。此外,甲状腺功能低下与全人群和 NAFLD 患者的心血管死亡率风险增加相关,但与非 NAFLD 组无关。
在这项美国成年人的大型全国代表性样本中,甲状腺功能低下与 NAFLD 相关,并且是 NAFLD 患者全因和心血管死亡率风险增加的预测因素。