Evidence map›Paper›PMID 25050550›Full record

SynthesisPLoS medicine2014

Association of non-alcoholic fatty liver disease with chronic kidney disease: a systematic review and meta-analysis.

Giovanni Musso, Roberto Gambino, James H Tabibian, Mattias Ekstedt, Stergios Kechagias, Masahide Hamaguchi, Rolf Hultcrantz, Hannes Hagström, Seung Kew Yoon, Phunchai Charatcharoenwitthaya and 23 more

Registry-linked trialOpen access · goldAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in PLoS medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04283942 (Effect of Intermittent Calorie Restriction on Metabolic Dysfunction-Associated Steatotic Liver Disease Patients With Abnormal Glucose Metabolism), which is not on this map. Cited by 347 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
347citing papers in PubMed, 7 pooled it
26.4field-weighted citation impact, top 1% of its field
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.

NCT04283942 nacompletednot on this mapstarted 2020, after this paper: background citation

Effect of Intermittent Calorie Restriction on Metabolic Dysfunction-Associated Steatotic Liver Disease Patients With Abnormal Glucose Metabolism

TypeinterventionalSponsorShanghai Zhongshan HospitalRan2020 to 2021Enrolled60ConditionsFatty Liver Disease, Type 2 Diabetes, Impaired Glucose RegulationArmsIntermittent calorie restriction (ICR), Continuous calorie restriction (CCR)
3 · Its place in the literature

Who cites it

347 citing papers in PubMed, 7 syntheses or guidelines pooled it, 717 citations in OpenAlex.

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287 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

33 authors at 20 institutions in 14 countries.

Giovanni MussoGradenigo Hospital, University of Turin, Turin, Italy.
Roberto GambinoDept. of Medical Sciences, San Giovanni Battista Hospital, University of Turin, Turin, Italy.
James H TabibianDivision of Gastroenterology and Hepatology Mayo Clinic, Rochester, Minnesota, United States of America.
Mattias EkstedtDivision of Gastroenterology and Hepatology, Linköping University, Linköping, Sweden.
Stergios KechagiasDivision of Cardiovascular Medicine, Department of Medical and Health Sciences, Linköping University, Linköping, Sweden.
Masahide HamaguchiDepartment of Experimental Immunology, World Premier International Immunology Frontier Research Center, Osaka University, Osaka, Japan.
Rolf HultcrantzDepartments of Gastroenterology and Hepatology, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Hannes HagströmDepartments of Gastroenterology and Hepatology, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Seung Kew YoonDivision of Hepato-Gastroenterology, Department of Internal Medicine, Kangnam St. Mary Hospital, Catholic University Medical College, Seoul, Korea.
Phunchai CharatcharoenwitthayaDivision of Gastroenterology, Medicine Department, Siriraj Hospital, Mahidol University, Bangkoknoi, Bangkok, Thailand.
Jacob GeorgeStorr Liver Unit, Westmead Millennium Institute, University of Sydney and Department of Gastroenterology and Hepatology, Westmead Hospital, Westmead, New South Wales, Australia.
Francisco BarreraStorr Liver Unit, Westmead Millennium Institute, University of Sydney and Department of Gastroenterology and Hepatology, Westmead Hospital, Westmead, New South Wales, Australia.
Svanhildur HafliðadóttirDept of Gastroenterology and Hepatology, Landspitali University Hospital, Hringbrau, Reykjavik, Iceland.
Einar Stefan BjörnssonDept of Gastroenterology and Hepatology, Landspitali University Hospital, Hringbrau, Reykjavik, Iceland.
Matthew J ArmstrongCentre for Liver Research and NIHR Biomedical Research Unit in Liver Disease, Institute of Biomedical Research, University of Birmingham, Birmingham, United Kingdom.
Laurence J HopkinsCentre for Liver Research and NIHR Biomedical Research Unit in Liver Disease, Institute of Biomedical Research, University of Birmingham, Birmingham, United Kingdom.
Xin GaoDepartment of Endocrinology and Metabolism, Zhongshan Hospital, Fudan University, Shanghai, China.
Sven FrancqueDepartment of Gastroenterology and Hepatology, Antwerp University Hospital, University of Antwerp, Antwerp, Belgium.
An VerrijkenDepartment of Endocrinology, Diabetology and Metabolism, Antwerp University Hospital, University of Antwerp, Antwerp, Belgium.
Yusuf YilmazDepartment of Gastroenterology, Marmara University, School of Medicine, Istanbul, Turkey.
Keith D LindorDivision of Gastroenterology and Hepatology Mayo Clinic, Rochester, Minnesota, United States of America.
Michael CharltonDivision of Gastroenterology and Hepatology Mayo Clinic, Rochester, Minnesota, United States of America.
Robin HaringInstitute of Clinical Chemistry and Laboratory Medicine, Ernst-Moritz-Arndt University Greifswald, Greifswald, Germany.
Markus M LerchDepartment of Medicine A, University Medicine Greifswald, Greifswald, Germany.
Rainer RettigInstitute of Physiology, Ernst-Moritz-Arndt-University Medicine Greifswald, Karlsburg, Germany.
Henry VölzkeInstitute for Community Medicine, Ernst-Moritz-Arndt University Medicine Greifswald, Greifswald, Germany.
Seungho RyuDepartment of Occupational and Environmental Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University, School of Medicine, Seoul, Republic of Korea.
Guolin LiCollege of Life Sciences, Hunan Normal University, Changsha, China.
Linda L WongJohn A. Burns School of Medicine at University of Hawaii, Transplant Institute, Hawaii Medical Center, Honolulu, Hawaii, United States of America.
Mariana MachadoDepartment of Gastroenterology, University Hospital of Santa Maria, Institute of Molecular Medicine, Lisbon, Portugal.
Helena Cortez-PintoDepartment of Gastroenterology, University Hospital of Santa Maria, Institute of Molecular Medicine, Lisbon, Portugal.
Kohichiroh YasuiDepartment of Molecular Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine, Japan.
Maurizio CassaderDept. of Medical Sciences, San Giovanni Battista Hospital, University of Turin, Turin, Italy.
University of Turin · ITHospital de Santa Maria · PTLinköping University · SENational University Hospital of Iceland · ISUniversität Greifswald · DEUniversitätsmedizin Greifswald · DEUniversity of Antwerp · BEWinnMed · USHunan Normal University · CNKangbuk Samsung Hospital · KRKarolinska Institutet · SEKarolinska University Hospital · SEKyoto Prefectural University of Medicine · JPMarmara University · TRMayo Clinic · USNIHR Birmingham Liver Biomedical Research Unit · GBOsaka International University · JPSiriraj Hospital · THThe Catholic University of Korea Seoul St. Mary's Hospital · KRUniversity of Birmingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic kidney disease (CKD) is a frequent, under-recognized condition and a risk factor for renal failure and cardiovascular disease. Increasing evidence connects non-alcoholic fatty liver disease (NAFLD) to CKD. We conducted a meta-analysis to determine whether the presence and severity of NAFLD are associated with the presence and severity of CKD. METHODS AND

findingsEnglish and non-English articles from international online databases from 1980 through January 31, 2014 were searched. Observational studies assessing NAFLD by histology, imaging, or biochemistry and defining CKD as either estimated glomerular filtration rate (eGFR) <60 ml/min/1.73 m2 or proteinuria were included. Two reviewers extracted studies independently and in duplicate. Individual participant data (IPD) were solicited from all selected studies. Studies providing IPD were combined with studies providing only aggregate data with the two-stage method. Main outcomes were pooled using random-effects models. Sensitivity and subgroup analyses were used to explore sources of heterogeneity and the effect of potential confounders. The influences of age, whole-body/abdominal obesity, homeostasis model of insulin resistance (HOMA-IR), and duration of follow-up on effect estimates were assessed by meta-regression. Thirty-three studies (63,902 participants, 16 population-based and 17 hospital-based, 20 cross-sectional, and 13 longitudinal) were included. For 20 studies (61% of included studies, 11 cross-sectional and nine longitudinal, 29,282 participants), we obtained IPD. NAFLD was associated with an increased risk of prevalent (odds ratio [OR] 2.12, 95% CI 1.69-2.66) and incident (hazard ratio [HR] 1.79, 95% CI 1.65-1.95) CKD. Non-alcoholic steatohepatitis (NASH) was associated with a higher prevalence (OR 2.53, 95% CI 1.58-4.05) and incidence (HR 2.12, 95% CI 1.42-3.17) of CKD than simple steatosis. Advanced fibrosis was associated with a higher prevalence (OR 5.20, 95% CI 3.14-8.61) and incidence (HR 3.29, 95% CI 2.30-4.71) of CKD than non-advanced fibrosis. In all analyses, the magnitude and direction of effects remained unaffected by diabetes status, after adjustment for other risk factors, and in other subgroup and meta-regression analyses. In cross-sectional and longitudinal studies, the severity of NAFLD was positively associated with CKD stages. Limitations of analysis are the relatively small size of studies utilizing liver histology and the suboptimal sensitivity of ultrasound and biochemistry for NAFLD detection in population-based studies.

conclusionThe presence and severity of NAFLD are associated with an increased risk and severity of CKD. Please see later in the article for the Editors' Summary.

Indexed as

HumansIncidenceNon-alcoholic Fatty Liver DiseaseRegression AnalysisRenal Insufficiency, ChronicRisk Factors

Identifiers

PMID25050550
PMCPMC4106719
OpenAlexW2168342632

What OpenQuestion holds

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Registered trials

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.