Cho In Young, Chang Yoosoo, Sung Eunju, Kang Jae-Heon, Shin Hocheol, Wild Sarah H, Byrne Christopher D, Ryu Seungho
Department of Family Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Center for Cohort Studies, Total Healthcare Center, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea; Department of Occupational and Environmental Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea; Department of Clinical Research Design and Evaluation, Samsung Advanced Institute for Health Sciences and Technology (SAIHST), Sungkyunkwan University, Seoul, Republic of Korea.
Clin Gastroenterol Hepatol. 2022 Mar;20(3):e583-e599. doi: 10.1016/j.cgh.2021.04.037. Epub 2021 Apr 28.
The study sought to investigate the effect of weight change on hepatic steatosis (HS) incidence with or without liver fibrosis in metabolically healthy overweight or obese individuals.
A cohort of 14,779 metabolically healthy men and women who were overweight or obese (body mass index ≥23 kg/m) and free from HS and an intermediate or high probability of fibrosis at baseline were followed for a median of 5.2 years. Metabolic health was defined as freedom from the components of metabolic syndrome and a homeostatic model assessment of insulin resistance <2.5. Weight changes were calculated as differences from baseline at the next subsequent visit. The outcome was HS incidence, with or without liver fibrosis, as assessed by liver ultrasound and 2 noninvasive fibrosis scores.
During 76,794.6 person-years of follow-up, 3539 cases of HS incidence were identified. The multivariable adjusted hazard ratios (95% confidence intervals) for HS incidence by weight change group, <-5.0%, -5.0%-1.0%, 1.0%-5.0%, and >5.0%, relative to the no weight change group (-0.9% to 0.9%) were 0.52 (0.44-0.60), 0.83 (0.75-0.92), 1.21 (1.10-1.33), and 1.51 (1.36-1.69), respectively. Clinically relevant weight loss of >5% was also associated with a lowered risk of HS with intermediate or high probability of advanced fibrosis. In mediation analyses, associations remained significant, although adjustment for metabolic risk factors was attenuating.
Clinically relevant weight loss was associated with a reduced risk of developing nonalcoholic fatty liver disease with or without intermediate or high probability of advanced fibrosis in metabolically healthy overweight or obese individuals.
本研究旨在调查体重变化对代谢健康的超重或肥胖个体发生肝脂肪变性(HS)(无论有无肝纤维化)的影响。
对14779名代谢健康的超重或肥胖男性和女性(体重指数≥23kg/m²)进行队列研究,这些人在基线时无HS且无肝纤维化中度或高度风险,随访时间中位数为5.2年。代谢健康定义为无代谢综合征成分且胰岛素抵抗的稳态模型评估<2.5。体重变化计算为下次随访时与基线的差值。结局为通过肝脏超声和2种非侵入性纤维化评分评估的有无肝纤维化的HS发生率。
在76794.6人年的随访期间,共确定了3539例HS发生病例。与无体重变化组(-0.9%至0.9%)相比,体重变化组(<-5.0%、-5.0%-1.0%、1.0%-5.0%和>5.0%)发生HS的多变量调整风险比(95%置信区间)分别为0.52(0.44-0.60)、0.83(0.75-0.92)、1.21(1.10-1.33)和1.51(1.36-1.69)。临床上相关的>5%的体重减轻也与晚期纤维化中度或高度风险的HS风险降低相关。在中介分析中,尽管对代谢危险因素的调整减弱了,但关联仍然显著。
临床上相关的体重减轻与代谢健康的超重或肥胖个体发生非酒精性脂肪性肝病(无论有无晚期纤维化中度或高度风险)的风险降低相关。