Evidence map›Paper›PMID 30179294›Full record

ArticleLiver international : official journal of the International Association for the Study of the Liver2019

Parental non-alcoholic fatty liver disease increases risk of non-alcoholic fatty liver disease in offspring.

Michelle T Long, Ellen B Gurary, Joseph M Massaro, Jiantao Ma, Udo Hoffmann, Raymond T Chung, Emelia J Benjamin, Rohit Loomba

Abstract read
In one paragraph

Article in Liver international : official journal of the International Association for the Study of the Liver, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.8field-weighted citation impact, top 9% 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.

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

18 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
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  7. Development and Validation of the Nonalcoholic Fatty Liver Disease Familial Risk Score to Detect Advanced Fibrosis: A Prospective, Multicenter Study.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2024
    Article
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  14. Non-Alcoholic Fatty Liver Disease: Metabolic, Genetic, Epigenetic and Environmental Risk Factors.International journal of environmental research and public health · 2021
    Review
  15. Review
  16. Article
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  18. Novel Insights into the Genetic Landscape of Nonalcoholic Fatty Liver Disease.International journal of environmental research and public health · 2019
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Michelle T LongSection of Gastroenterology, Boston Medical Center, Boston University School of Medicine, Boston, Massachusetts.ORCID 0000-0001-6131-3981
Ellen B GuraryDepartment of Biostatistics, Boston University, Boston, Massachusetts.
Joseph M MassaroDepartment of Biostatistics, Boston University, Boston, Massachusetts.
Jiantao MaPopulation Sciences Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland.
Udo HoffmannRadiology Department, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
Raymond T ChungLiver Center, Gastrointestinal Division, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
Emelia J BenjaminDepartment of Epidemiology, Boston University School of Public Health, Boston, Massachusetts.
Rohit LoombaDivision of Gastroenterology, Department of Medicine and Division of Epidemiology, Department of Family and Preventive, University of California at San Diego, La Jolla, California.
Boston University · USHarvard University · USNational Institutes of Health · USUniversity of California San Diego · US

Funding

Project-005UL1TR001430 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BAIR-MERRITT, MEGAN H, CENTER, DAVID M. · 2015 to 2024
$52.3M
IDENTIFICATION OF COMMON GENETIC VARIANTS FOR ATRIAL FIBRILLATION AND PR INTERVALR01HL092577 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI BENJAMIN, EMELIA J., ELLINOR, PATRICK THOMAS · 2009 to 2025
$20.6M
QUS Technology for Diagnosis and Grading of Hepatic Steatosis in NAFLDR01DK106419 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LOOMBA, ROHIT, SIRLIN, CLAUDE B · 2015 to 2019
$3.4M
AFGen Consortium: Atrial Fibrillation Genomics to Functional AnalysesR01HL128914 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BENJAMIN, EMELIA J., ELLINOR, PATRICK THOMAS · 2015 to 2018
$3.1M
Identifying clinical and genetic correlates of hepatic fibrosis from fatty liver disease in the communityK23DK113252 · NIDDK · BOSTON MEDICAL CENTER · PI LONG, MICHELLE T · 2018 to 2022
$944k
NCATS NIH HHS UL1 TR001430NHLBI NIH HHS R01 HL092577NHLBI NIH HHS R01 HL128914NIDDK NIH HHS K23 DK113252NIDDK NIH HHS L30 DK106778NIDDK NIH HHS R01 DK106419
6 · The paper itself

Abstract

BACKGROUND &

aimsLittle is known regarding the risk of hepatic steatosis (HS) among adult children of affected parents. We examined the association between parental and offspring HS in the multigenerational Framingham Heart Study, which characterized HS using computed tomography.

methodsWe performed multivariable logistic regression models adjusted for age, sex, alcohol use, and body mass index to generate the odds of HS according to parental HS. We determined the proportion of participants with HS according to parental HS and the presence or absence of hypertension, diabetes, or obesity (BMI ≥30 kg/m

resultsApproximately 23% (183/785) had at least one parent with HS and 1.1% had two affected parents (9/785). In adjusted models, participants with at least one parent with HS had a nearly two-fold increased odds of HS compared to participants without a parental history of HS (OR 1.86, 95% confidence interval 1.15-3.03). Among participants without hypertension, diabetes, or obesity, a higher proportion had HS if they had a parental history of HS compared to those without (16.1% vs 5.2%, P < 0.001). However, for participants with cardiometabolic risk factors, we did not observe a difference in HS among those with and without parental HS (30.3% vs 28.5%, P = 0.78).

conclusionsIndividuals with a parental history of HS are at increased risk for HS. Specifically, a parental history of HS may be an important factor among those that are otherwise metabolically healthy.

Indexed as

Family HealthParentsAdultBody Mass IndexFemaleGenetic Predisposition to DiseaseHumansLogistic ModelsLongitudinal StudiesMaleMiddle AgedMultivariate AnalysisNon-alcoholic Fatty Liver DiseasePedigreeRisk AssessmentRisk Factorscomputed tomographydisease riskfamilialfatty liver diseaseheritability

Identifiers

PMID30179294
PMCPMC6758911
OpenAlexW2889562911

What OpenQuestion holds

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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 OpenQuestion graph.