Evidence map›Paper›PMID 35047847›Full record

ArticleHGG advances2022

Identification of 90 NAFLD GWAS loci and establishment of NAFLD PRS and causal role of NAFLD in coronary artery disease.

Zong Miao, Kristina M Garske, David Z Pan, Amogha Koka, Dorota Kaminska, Ville Männistö, Janet S Sinsheimer, Jussi Pihlajamäki, Päivi Pajukanta

Open access · goldAbstract read
In one paragraph

Article in HGG advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 4% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

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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 at 3 institutions in 3 countries.

Zong MiaoDepartment of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Kristina M GarskeDepartment of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
David Z PanDepartment of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Amogha KokaDepartment of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Dorota KaminskaDepartment of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Ville MännistöDepartment of Medicine, UEF and Kuopio University Hospital, Kuopio, Finland.
Janet S SinsheimerDepartment of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Jussi PihlajamäkiInstitute of Public Health and Clinical Nutrition UEF, Kuopio, Finland.
Päivi PajukantaDepartment of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
University of California, Los Angeles · USKuopio University Hospital · FIUniversity of Eastern Finland · FI

Funding

Systems genomics of metabolic syndrome traitsP01HL028481 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI REUE, KAREN · 1985 to 2019
$50.2M
Genomics of dyslipidemia in MexicansR01HL095056 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PAJUKANTA, PAIVI · 2009 to 2018
$5.9M
Functional genetic variants for type 2 diabetesU01DK105561 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MOHLKE, KAREN L. · 2015 to 2019
$2.3M
Integrating functional genomics in primary human adipocytes to investigate gene regulatory circuitry for obesogenic cardiovascular traitsF31HL142180 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GARSKE, KRISTINA MARIE · 2018 to 2020
$110k
British Heart Foundation CH/1996001/9454Medical Research Council MC_PC_17228Medical Research Council MC_QA137853NHLBI NIH HHS F31 HL142180NHLBI NIH HHS P01 HL028481NHLBI NIH HHS R01 HL095056NIDDK NIH HHS U01 DK105561
6 · The paper itself

Abstract

The prevalence of non-alcoholic fatty liver disease (NAFLD), now also known as metabolic dysfunction-associated fatty liver disease (MAFLD), is rapidly increasing worldwide due to the ongoing obesity epidemic. However, currently the NALFD diagnosis requires non-readily available imaging technologies or liver biopsy, which has drastically limited the sample sizes of NAFLD studies and hampered the discovery of its genetic component. Here we utilized the large UK Biobank (UKB) to accurately estimate the NAFLD status in UKB based on common serum traits and anthropometric measures. Scoring all individuals in UKB for NAFLD risk resulted in 28,396 NAFLD cases and 108,652 healthy individuals at a >90% confidence level. Using this imputed NAFLD status to perform the largest NAFLD genome-wide association study (GWAS) to date, we identified 94 independent (R

Indexed as

GWASMendelian randomizationNAFLDpolygenic risk scoreUK Biobank

Identifiers

PMID35047847
PMCPMC8756520
OpenAlexW3196959564

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.