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[假设性饮酒干预与肝脂肪变性:一项大型队列的纵向研究]

[Hypothetical Alcohol Consumption Interventions and Hepatic Steatosis: A Longitudinal Study in a Large Cohort].

作者信息

Zhang Ning, Zhang Yuan, Wei Jun, Xiang Yi, Hu Yifan, Xiao Xiong

机构信息

/ ( 610041) Department of Epidemiology and Biostatistics, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu 610041, China.

出版信息

Sichuan Da Xue Xue Bao Yi Xue Ban. 2024 May 20;55(3):653-661. doi: 10.12182/20240560503.

Abstract

OBJECTIVE

Non-alcoholic fatty liver disease (NAFLD) and alcohol-associated fatty liver disease (ALD) are the most common chronic liver diseases. Hepatic steatosis is an early histological subtype of both NAFLD and ALD. Excessive alcohol consumption is widely known to lead to hepatic steatosis and subsequent liver damage. However, reported findings concerning the association between moderate alcohol consumption and hepatic steatosis remain inconsistent. Notably, alcohol consumption as a modifiable lifestyle behavior is likely to change over time, but most previous studies covered alcohol intake only once at baseline. These inconsistent findings from existing studies do not inform decision-making concerning policies and clinical guidelines, which are of greater interest to health policymakers and clinician-scientists. Additionally, recommendations on the types of alcoholic beverages are not available. Usually, assessing the effects of two or more hypothetical alcohol consumption interventions on hepatic steatosis provides answers to questions concerning the population risk of hepatic steatosis if everyone changes from heavy drinking to abstinence, or if everyone keeps on drinking moderately, or if everyone of the drinking population switches from red wine to beer? Thus, we simulated a target trial to estimate the effects of several hypothetical interventions, including changes in the amount of alcohol consumption or the types of alcoholic beverages consumed, on hepatic steatosis using longitudinal data, to inform decisions about alcohol-related policymaking and clinical care.

METHODS

This longitudinal study included 12687 participants from the UK Biobank (UKB), all of whom participated in both baseline and repeat surveys. We excluded participants with missing data related to components of alcohol consumption and fatty liver index (FLI) in the baseline and the repeat surveys, as well as those who had reported liver diseases or cancer at the baseline survey. We used FLI as an outcome indicator and divided the participants into non-, moderate, and heavy drinkers. The surrogate marker FLI has been endorsed by many international organizations' guidelines, such as the European Association for the Study of the Liver. The calculation of FLI was based on laboratory and anthropometric data, including triglyceride, gamma-glutamyl transferase, body mass index, and waist circumference. Participants responded to questions about the types of alcoholic beverages, which were defined in 5 categories, including red wine, white wine/fortified wine/champagne, beer or cider, spirits, and mixed liqueurs, along with the average weekly or monthly amounts of alcohol consumed. Alcohol consumption was defined as pure alcohol consumed per week and was calculated according to the amount of alcoholic beverages consumed per week and the average ethanol content by volume in each alcoholic beverage. Participants were categorized as non-drinkers, moderate drinkers, and heavy drinkers according to the amount of their alcohol consumption. Moderate drinking was defined as consuming no more than 210 g of alcohol per week for men and 140 g of alcohol per week for women. We defined the following hypothetical interventions for the amount of alcohol consumed: sustaining a certain level of alcohol consumption from baseline to the repeat survey (e.g., none to none, moderate to moderate, heavy to heavy) and changing from one alcohol consumption level to another (e.g., none to moderate, moderate to heavy). The hypothetical interventions for the types of alcoholic beverages were defined in a similar way to those for the amount of alcohol consumed (e.g., red wine to red wine, red wine to beer/cider). We applied the parametric g-formula to estimate the effect of each hypothetical alcohol consumption intervention on the FLI. To implement the parametric g-formula, we first modeled the probability of time-varying confounders and FLI conditional on covariates. We then used these conditional probabilities to estimate the FLI value if the alcohol consumption level of each participant was under a specific hypothetical intervention. The confidence interval was obtained by 200 bootstrap samples.

RESULTS

For the alcohol consumption from baseline to the repeat surveys, 6.65% of the participants were sustained non-drinkers, 63.68% were sustained moderate drinkers, and 14.74% were sustained heavy drinkers, while 8.39% changed from heavy drinking to moderate drinking. Regarding the types of alcoholic beverages from baseline to the repeat surveys, 27.06% of the drinkers sustained their intake of red wine. Whatever the baseline alcohol consumption level, the hypothetical interventions for increasing alcohol consumption from the baseline alcohol consumption were associated with a higher FLI than that of the sustained baseline alcohol consumption level. When comparing sustained non-drinking with the hypothetical intervention of changing from non-drinking to moderate drinking, the mean ratio of FLI was 1.027 (95% confidence interval [CI]: 0.997-1.057). When comparing sustained non-drinking with the hypothetical intervention of changing from non-drinking to heavy drinking, the mean ratio of FLI was 1.075 (95% CI: 1.042-1.108). When comparing sustained heavy drinking with the hypothetical intervention of changing from heavy drinking to moderate drinking, the mean ratio of FLI was 0.953 (95% CI: 0.938-0.968). The hypothetical intervention of changing to red wine in the UKB was associated with lower FLI levels, compared with sustained consumption of other types of alcoholic beverages. For example, when comparing sustaining spirits with the hypothetical intervention of changing from spirits to red wine, the mean ratio of FLI was 0.981 (95% CI: 0.948-1.014).

CONCLUSIONS

Regardless of the current level of alcohol consumption, interventions that increase alcohol consumption could raise the risk of hepatic steatosis in Western populations. The findings of this study could inform the formulation of future practice guidelines and health policies. If quitting drinking is challenging, red wine may be a better option than other types of alcoholic beverages in Western populations.

摘要

目的

非酒精性脂肪性肝病(NAFLD)和酒精性脂肪性肝病(ALD)是最常见的慢性肝病。肝脂肪变性是NAFLD和ALD的早期组织学亚型。众所周知,过量饮酒会导致肝脂肪变性及随后的肝损伤。然而,关于适度饮酒与肝脂肪变性之间关联的报道结果仍不一致。值得注意的是,饮酒作为一种可改变的生活方式行为可能会随时间变化,但大多数先前的研究仅在基线时对酒精摄入量进行了一次评估。现有研究中这些不一致的结果无法为卫生政策制定者和临床科学家更感兴趣的政策及临床指南决策提供依据。此外,关于酒精饮料类型的建议也未给出。通常,评估两种或更多假设的饮酒干预对肝脂肪变性的影响,能回答如果每个人从大量饮酒转变为戒酒,或者如果每个人继续适度饮酒,又或者如果饮酒人群中的每个人从饮用红酒改为饮用啤酒,肝脂肪变性的人群风险会怎样等问题。因此,我们模拟了一项目标试验,利用纵向数据估计几种假设干预措施,包括饮酒量的变化或所饮用酒精饮料类型的变化,对肝脂肪变性的影响,以为与酒精相关的政策制定和临床护理提供决策依据。

方法

这项纵向研究纳入了来自英国生物银行(UKB)的12687名参与者,他们均参与了基线调查和重复调查。我们排除了在基线调查和重复调查中与饮酒成分及脂肪肝指数(FLI)相关数据缺失的参与者,以及那些在基线调查中报告有肝病或癌症的参与者。我们将FLI用作结局指标,并将参与者分为不饮酒者、适度饮酒者和大量饮酒者。替代指标FLI已得到许多国际组织指南的认可,如欧洲肝脏研究协会的指南。FLI的计算基于实验室和人体测量数据,包括甘油三酯、γ-谷氨酰转移酶、体重指数和腰围。参与者回答了关于酒精饮料类型的问题,酒精饮料分为5类,包括红酒、白葡萄酒/强化葡萄酒/香槟、啤酒或苹果酒、烈酒以及混合利口酒,同时还包括每周或每月的平均饮酒量。饮酒量定义为每周饮用的纯酒精量,根据每周饮用的酒精饮料量以及每种酒精饮料的平均乙醇体积含量计算得出。根据饮酒量,参与者被分为不饮酒者、适度饮酒者和大量饮酒者。适度饮酒定义为男性每周饮酒不超过210克,女性每周饮酒不超过140克。我们为饮酒量定义了以下假设干预措施:从基线到重复调查维持一定水平的饮酒量(例如,从不饮酒到不饮酒、适度饮酒到适度饮酒、大量饮酒到大量饮酒)以及从一个饮酒水平转变为另一个饮酒水平(例如,从不饮酒到适度饮酒、适度饮酒到大量饮酒)。对酒精饮料类型的假设干预措施定义方式与饮酒量的类似(例如,从饮用红酒到饮用红酒、从饮用红酒到饮用啤酒/苹果酒)。我们应用参数化g公式来估计每种假设饮酒干预对FLI的影响。为实施参数化g公式,我们首先对随时间变化的混杂因素以及基于协变量的FLI概率进行建模。然后,我们使用这些条件概率来估计如果每个参与者的饮酒水平处于特定假设干预下的FLI值。通过200次自助抽样获得置信区间。

结果

从基线到重复调查,6.65%的参与者持续不饮酒,63.68%的参与者持续适度饮酒,14.74%的参与者持续大量饮酒,而8.39%的参与者从大量饮酒转变为适度饮酒。从基线到重复调查,27.06%的饮酒者持续饮用红酒。无论基线饮酒水平如何,与维持基线饮酒量相比,从基线饮酒量增加饮酒量的假设干预与更高的FLI相关。将持续不饮酒与从不饮酒转变为适度饮酒的假设干预进行比较时,FLI的平均比值为1.027(95%置信区间[CI]:0.997 - 1.057)。将持续不饮酒与从不饮酒转变为大量饮酒的假设干预进行比较时,FLI的平均比值为1.075(95% CI:1.042 - 1.108)。将持续大量饮酒与从大量饮酒转变为适度饮酒的假设干预进行比较时,FLI的平均比值为0.953(95% CI:0.938 - 0.968)。与持续饮用其他类型酒精饮料相比,在UKB中转变为饮用红酒的假设干预与较低的FLI水平相关。例如,将持续饮用烈酒与从饮用烈酒转变为饮用红酒的假设干预进行比较时,FLI的平均比值为0.981(95% CI:0.948 - 1.014)。

结论

无论当前饮酒水平如何,增加饮酒量的干预措施可能会增加西方人群肝脂肪变性的风险。本研究结果可为未来实践指南和卫生政策的制定提供依据。如果戒酒具有挑战性,在西方人群中,红酒可能是比其他类型酒精饮料更好的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ec9/11211800/8c1fcdddcab8/scdxxbyxb-55-3-653-1.jpg

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