Suppr超能文献

饮食模式通过代谢组学特征改变代谢相关脂肪性肝病的风险。

Dietary pattern modifies the risk of MASLD through metabolomic signature.

作者信息

Wu Hanzhang, Wei Jiahe, Wang Shuai, Chen Liangkai, Zhang Jihui, Wang Ningjian, Tan Xiao

机构信息

Department of Big Data in Health Science, Zhejiang University School of Public Health, Hangzhou, China. Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.

The Key Laboratory of Intelligent Preventive Medicine of Zhejiang Province, Hangzhou, China.

出版信息

JHEP Rep. 2024 Jun 10;6(8):101133. doi: 10.1016/j.jhepr.2024.101133. eCollection 2024 Aug.

Abstract

BACKGROUND & AIMS: The EAT-Lancet Commission in 2019 advocated a plant-centric diet for health and environmental benefits, but its relation to metabolic dysfunction-associated steatotic liver disease (MASLD) is unclear. We aimed to discover the metabolite profile linked to the EAT-Lancet diet and its association with MASLD risk, considering genetic predisposition.

METHODS

We analyzed data from 105,752 UK Biobank participants with detailed dietary and metabolomic information. We constructed an EAT-Lancet diet index and derived a corresponding metabolomic signature through elastic net regression. A weighted polygenic risk score for MASLD was computed from associated risk variants. The Cox proportional hazards model was employed to estimate hazard ratios (HRs) and 95% CIs for the risk of MASLD (defined as hospital admission or death).

RESULTS

During a median follow-up period of 11.6 years, 1,138 cases of MASLD were documented. Participants in the highest group for the EAT-Lancet diet index had a multivariable HR of 0.79 (95% CI 0.66-0.95) for MASLD compared to the lowest group. The diet's impact was unaffected by genetic predisposition to MASLD ( = 0.42). Moreover, a robust correlation was found between the metabolomic signature and the EAT-Lancet diet index (Pearson r = 0.29; <0.0001). Participants in the highest group for the metabolomic signature had a multivariable HR of 0.46 (95% CI 0.37-0.58) for MASLD, in comparison to those in the lowest group.

CONCLUSIONS

Higher intake of the EAT-Lancet diet and its associated metabolite signature are both linked to a reduced risk of MASLD, independently of traditional risk factors.

IMPACT AND IMPLICATIONS

Our analysis leveraging the UK Biobank study showed higher adherence to the EAT-Lancet diet was associated with a reduced risk of metabolic dysfunction-associated steatotic liver disease (MASLD). We identified a unique metabolite signature comprising 81 metabolites associated with the EAT-Lancet diet, potentially underlying the diet's protective mechanism against MASLD. These findings suggest the EAT-Lancet diet may offer substantial protective benefits against MASLD.

摘要

背景与目的

2019年的《柳叶刀-饮食与健康委员会报告》提倡以植物为主的饮食,认为其对健康和环境有益,但这种饮食与代谢功能障碍相关脂肪性肝病(MASLD)的关系尚不清楚。我们旨在发现与《柳叶刀-饮食与健康委员会报告》饮食相关的代谢物谱及其与MASLD风险的关联,并考虑遗传易感性。

方法

我们分析了来自英国生物银行的105,752名参与者的数据,这些参与者有详细的饮食和代谢组学信息。我们构建了一个《柳叶刀-饮食与健康委员会报告》饮食指数,并通过弹性网回归得出相应的代谢组学特征。根据相关风险变异计算出MASLD的加权多基因风险评分。采用Cox比例风险模型估计MASLD风险(定义为住院或死亡)的风险比(HRs)和95%置信区间(CIs)。

结果

在中位随访期11.6年期间,记录了1138例MASLD病例。与最低组相比,《柳叶刀-饮食与健康委员会报告》饮食指数最高组的参与者患MASLD的多变量HR为0.79(95%CI 0.66-0.95)。该饮食的影响不受MASLD遗传易感性的影响(P=0.42)。此外,在代谢组学特征与《柳叶刀-饮食与健康委员会报告》饮食指数之间发现了很强的相关性(Pearson r=0.29;P<0.0001)。与最低组相比,代谢组学特征最高组的参与者患MASLD的多变量HR为0.46(95%CI 0.37-0.58)。

结论

较高的《柳叶刀-饮食与健康委员会报告》饮食摄入量及其相关的代谢物特征均与MASLD风险降低有关,且独立于传统风险因素。

影响与意义

我们利用英国生物银行研究进行的分析表明,更高程度地遵循《柳叶刀-饮食与健康委员会报告》饮食与代谢功能障碍相关脂肪性肝病(MASLD)风险降低有关。我们确定了一个独特的代谢物特征,包括81种与《柳叶刀-饮食与健康委员会报告》饮食相关的代谢物,这可能是该饮食对MASLD保护机制的潜在基础。这些发现表明,《柳叶刀-饮食与健康委员会报告》饮食可能对MASLD具有显著的保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a495/11286987/508df731795f/ga1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验