Evidence map›Paper›PMID 41094544›Full record

ArticleCardiovascular diabetology2025

The role of insulin resistance in the longitudinal progression from NAFLD to cardiovascular-kidney-metabolic disease.

Chao Hou, Xiangling Yuan, Min Peng, Xuan Shi, Dahong Yang, Fang Wang, Ke Song, Gelin Xu, Jianzhong Shi

Abstract read
In one paragraph

Article in Cardiovascular diabetology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

9 authors.

Chao Hou *Department of Neurology, Nanjing Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Xiangling Yuan *Guangxi University of Chinese Medicine, Nanning, 530200, Guangxi, China.
Min Peng *Department of Neurology, Institute of Translational Medicine, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People's Hospital, Shenzhen, China.
Xuan ShiDepartment of Geriatric Medicine, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, 321 Zhongshan Rd, Nanjing, 210008, China.
Dahong YangDepartment of Neurology, Xinqiao Hospital and the Second Affiliated Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Fang WangDepartment of Neurology, Shaoxing People's Hospital, Shaoxing, Zhejiang, China.
Ke SongDepartment of Gastroenterology, Liyang People's Hospital, Liyang City, Jiangsu, China.
Gelin XuDepartment of Neurology, Nanjing Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China. xugelin@szseyy.com.
Jianzhong ShiDepartment of Gastroenterology, Liyang People's Hospital, Liyang City, Jiangsu, China. sjz1124sjz@163.com.

Funding

National Natural Science Foundation of China 82401551National Natural Science Foundation of China 82501583National Natural Science Foundation of China U22A20341Shenzhen High-level Hospital Construction Foundation 4004013the China Postdoctoral Science Foundation 2025M772210
6 · The paper itself

Abstract

BACKGROUND AND

objectiveThis study aimed to elucidate the role of insulin resistance in the progression from non-alcoholic fatty liver disease (NAFLD) to cardiovascular-kidney-metabolic (CKM) diseases, and to explore the potential influence of lifestyle factors.

methodsThis study included participants free of NAFLD and CKM diseases from the UK Biobank. Insulin resistance was assessed using the TyG index. CKM diseases include ischemic stroke (IS), ischemic heart disease (IHD), type 2 diabetes (T2D), and chronic kidney disease (CKD). Markov multi-state models were used to assess the associations between the TyG index and disease transitions.

resultsAmong 377,757 participants (median age 57 years), 4949 developed NAFLD over a median follow-up of 13.6 years. Of these, 12.65% progressed to T2D, 9.11% to IHD, 8.63% to CKD, and 4.61% to IS. Elevated TyG levels significantly accelerated transitions from NAFLD to first-onset CKM disease (HR = 1.25, 95% CI 1.05-1.49), double CKM disease (HR = 1.46, 95% CI 1.19-1.80), and triple CKM disease (HR = 1.81, 95% CI 1.28-2.55). Similar progression risk increases were observed for individual CKM components: T2D (HR = 1.41, 95% CI 1.11-1.78), CKD (HR = 1.37, 95% CI 1.08-1.75), and IS (HR = 1.70, 95% CI 1.27-2.27). A J-shaped dose-response relationship was identified. Transitions risk remained pronounced among individuals with healthy sleep and regular physical activity.

conclusionsInsulin resistance independently accelerated the progression from NAFLD to CKM diseases, particularly ischemic stroke. Healthy sleep and regular physical activity failed to offset this detrimental impact.

Indexed as

Cardiovascular DiseasesDiabetes Mellitus, Type 2Insulin ResistanceMyocardial IschemiaNon-alcoholic Fatty Liver DiseaseRenal Insufficiency, ChronicAdultAgedBiomarkersDisease ProgressionFemaleHumansLongitudinal StudiesMaleMiddle AgedPrognosisBiomarkersCardiovascular-kidney-metabolic diseaseNAFLDTyG

Identifiers

PMID41094544
PMCPMC12522269

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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 OpenQuestion graph.