Evidence mapPaperPMID 39425782Full record

ArticleDiabetologia2025

Interactions of genes with alcohol consumption affect insulin sensitivity and beta cell function.

Qi Fu, Hao Dai, Sipeng Shen, Yunqiang He, Shuai Zheng, Hemin Jiang, Pan Gu, Min Sun, Xiaowei Zhu, Kuanfeng Xu and 1 more

Abstract read
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In one paragraph

Article in Diabetologia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. MetALD: New Perspectives on an Old Overlooked Disease.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Review
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Qi Fu *Department of Endocrinology and Metabolism, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Hao Dai *Department of Endocrinology and Metabolism, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Sipeng Shen *Department of Biostatistics, Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing, China.
Yunqiang HeDepartment of Endocrinology and Metabolism, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Shuai ZhengDepartment of Endocrinology and Metabolism, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Hemin JiangDepartment of Endocrinology and Metabolism, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Pan GuDepartment of Biostatistics, Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing, China.
Min SunDepartment of Endocrinology and Metabolism, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Xiaowei ZhuDepartment of Endocrinology and Metabolism, the Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi, China. zhuxw@njmu.edu.cn.
Kuanfeng XuDepartment of Endocrinology and Metabolism, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China. bio97xkf@163.com.
Tao YangDepartment of Endocrinology and Metabolism, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China. yangt@njmu.edu.cn.ORCID 0000-0001-6375-3622

Funding

Major Program of Wuxi Medical Center, Nanjing Medical University WXKY202303001National Natural Science Foundation of China 82070803National Natural Science Foundation of China 82100837National Natural Science Foundation of China 82100838National Natural Science Foundation of China 82200888National Natural Science Foundation of China 82370839Natural Science Foundation of Jiangsu Province BK20210959Natural Science Foundation of Jiangsu Province BK20210960Natural Science Foundation of Jiangsu Province BK20220714
6 · The paper itself

Abstract

aims/hypothesisAlcohol consumption has complex effects on diabetes and metabolic disease, but there is widespread heterogeneity within populations and the specific reasons are unclear. Genetic factors may play a role and warrant exploration. The aim of this study was to elucidate genetic variants modulating the impact of alcohol consumption on insulin sensitivity and pancreatic beta cell function within populations presenting normal glucose tolerance (NGT).

methodsWe recruited 4194 volunteers in Nanjing, 854 in Jurong and an additional 5833 in Nanjing for Discovery cohorts 1 and 2 and a Validation cohort, respectively. We performed an OGTT on all participants, establishing a stringent NGT group, and then assessed insulin sensitivity and beta cell function. Alcohol consumption was categorised as abstinent, light-to-moderate (<210 g per week) or heavy (≥210 g per week). After excluding ineligible individuals, an exploratory genome-wide association study identified potential variants interacting with alcohol consumption in 1862 NGT individuals. These findings were validated in an additional cohort of 2169 NGT individuals. Cox proportional hazard regression was further employed to evaluate the effect of the interaction between the potential variants and alcohol consumption on the risk of type 2 diabetes within the UK Biobank cohort.

resultsA significant correlation was observed between drinking levels and insulin sensitivity, accompanied by a consequent inverse relationship with insulin resistance and beta cell insulin secretion after adjusting for confounding factors in NGT individuals. However, no significant associations were noted in the disposition indexes. The interaction of variant rs56221195 with alcohol intake exhibited a pronounced effect on the liver insulin resistance index (LIRI) in the discovery set, corroborated in the validation set (combined p=1.32 × 10 CONCLUSIONS/

interpretationOur findings reveal the effects of the interaction of alcohol and rs56221195 on hepatic insulin sensitivity in NGT individuals. It is imperative to weigh potential benefits and detriments thoughtfully when considering alcohol consumption across diverse genetic backgrounds.

Indexed as

Alcohol DrinkingDiabetes Mellitus, Type 2Insulin ResistanceInsulin-Secreting CellsAdultBlood GlucoseFemaleGenome-Wide Association StudyGlucose Tolerance TestHumansInsulinMaleMiddle AgedPolymorphism, Single NucleotideBlood GlucoseInsulinAlcohol consumptionBeta cell functionGene–environment interactionsInsulin sensitivityType 2 diabetes

Identifiers

PMID39425782

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.