[探索酒精摄入量与MASLD和MetALD患者全因死亡率之间的关系:一项基于NHANES III数据的研究]。

Q3 Medicine
L Y Jia, F J Rui, X Y Wu, S S Zhou, Y J Chen, C Wu, J P Shi, W H Wu, J Li
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引用次数: 0

摘要

目的:评价代谢功能障碍相关脂肪变性肝病(MASLD)和酒精相关/相关肝病(MetALD)中不同水平的酒精摄入与全因死亡率之间的关系。方法:本研究纳入年龄在20至74岁之间,经超声诊断为肝脂肪变性的参与者。这些数据来自1988年至1994年在美国进行的第三次全国健康和营养检查调查(NHANESⅢ)。通过Cox比例风险回归模型计算多变量校正风险比(aHR)及其95%置信区间(CI),以评估饮酒水平对全因死亡率的影响。参与者根据每日饮酒量分为三组:低、中、高饮酒量组。结果:共纳入受试者2 322例,男性占50.2%(1 166/2 322),中位年龄42.0(31.3 ~ 57.0)岁。在中位随访316.0(270.0-337.0)个月期间,总死亡率为1.48% /人年。三种酒精摄入组的全因死亡率分别为每人年1.38%、1.67%和2.10%。校正协变量后,每日适度饮酒组(校正风险比[aHR]=1.37,95% CI 1.12-1.67,P=0.002)和每日高度饮酒组(aHR=1.45,95% CI 1.17-1.80,P=0.001)与全因死亡率增加独立相关。在糖尿病状态和年龄的亚组分析中,60岁以下的非2型糖尿病(T2DM)参与者的全因死亡率在不同酒精摄入量水平之间存在显著差异,但在60岁以上的非T2DM参与者和所有年龄的T2DM参与者中没有差异。结论:酒精摄入对MASLD和MetALD患者有剂量依赖性的负面影响。全因死亡的风险随着酒精摄入量的增加而显著增加。评估代谢功能障碍相关脂肪变性肝病(MASLD)和酒精相关/相关肝病(MetALD)中不同水平的酒精摄入与全因死亡率之间的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Exploring the relationship between alcohol intake and all-cause mortality in participants with MASLD and MetALD: a study based on NHANES III data].

Objective: To evaluate the association between different levels of alcohol intake and all-cause mortality in metabolic dysfunction-associated steatotic liver disease(MASLD)and alcohol-related/associated liver disease(MetALD). Method: This study included participants aged 20 to 74 who were diagnosed with hepatic steatosis by ultrasound. The data were derived from the Third National Health and Nutrition Examination Survey(NHANES Ⅲ)conducted in the United States from 1988 to 1994. Multivariable-adjusted hazard ratios(aHR)and their 95% confidence intervals(CI)were calculated by Cox proportional risk regression modelling to assess the effect of alcohol consumption levels on all-cause mortality. Participants were categorized into three groups based on daily alcohol intake:low,moderate,and high consumption groups. Results: A total of 2 322 participants were included,with 50.2% males(1 166/2 322),and median age 42.0(31.3-57.0)years. During a median follow up of 316.0(270.0-337.0)months,the overall mortality rate was 1.48% per person-year. The all-cause mortality were 1.38%,1.67% and 2.10% per person-year for those participants in three alcohol intake groups. After adjusting for covariates,daily moderate alcohol intake group(adjusted hazard ratio[aHR]=1.37,95% CI 1.12-1.67,P=0.002),and daily high alcohol intake group(aHR=1.45,95% CI 1.17-1.80,P=0.001),were independently associated with increased all-cause mortality. In subgroup analysis by diabetes status and age,there were significant differences in all-cause mortality across various levels of alcohol intake among non-type 2 diabetes mellitus(T2DM)participants under 60 years old,but not among non-T2DM participants over 60 years old,and T2DM participants of all ages. Conclusion: Alcohol intake has a dose-dependent negative impact on MASLD and MetALD patients. The risk of all-cause mortality significantly increases with higher alcohol intake. To evaluate the association between different levels of alcohol intake and all-cause mortality in metabolic dysfunction-associated steatotic liver disease(MASLD)and alcohol-related/associated liver disease(MetALD).

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中华肝脏病杂志
中华肝脏病杂志 Medicine-Medicine (all)
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1.20
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