Evidence map›Paper›PMID 33532620›Full record

ArticleEndocrinology, diabetes & metabolism2021

Mitochondrial haplogroup G is associated with nonalcoholic fatty liver disease, while haplogroup A mitigates the effects of PNPLA3.

Aaron M Gusdon, You Hui, Jing Chen, Clayton E Mathews, Shen Qu

Open access · goldAbstract read
In one paragraph

Article in Endocrinology, diabetes & metabolism, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. PNPLA3 I148M Interacts With Environmental Triggers to Cause Human Disease.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Review
  3. The Mitochondrial tRNAFrontiers in genetics · 2022
    Article
  4. 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

5 authors at 3 institutions in 2 countries.

Aaron M GusdonDepartment of Neurosurgery Mischer Neuroscience Associates University of Texas Health Science Center at Houston Houston TX USA.ORCID 0000-0002-3350-6601
You HuiDepartment of Endocrinology Shanghai Tenth People's Hospital Tongji University Shanghai China.
Jing ChenDepartment of Pathology, Immunology and Laboratory Medicine University of Florida College of Medicine Gainesville FL USA.
Clayton E MathewsDepartment of Pathology, Immunology and Laboratory Medicine University of Florida College of Medicine Gainesville FL USA.
Shen QuDepartment of Endocrinology Shanghai Tenth People's Hospital Tongji University Shanghai China.ORCID 0000-0003-0811-7070
Tongji University · CNUniversity of Florida · USThe University of Texas Health Science Center at Houston · US

Funding

Project 3P01AI042288 · NIAID · UNIVERSITY OF FLORIDA · PI Todd Michael Brusko · 1997 to 2026
$32.9M
Engineering a Human Microphysiological System for the Characterization of Islet-Immune InteractionsUH3DK122638 · NIDDK · UNIVERSITY OF FLORIDA · PI AGARWAL, ASHUTOSH, BRUSKO, TODD MICHAEL · 2021 to 2023
$3.0M
Engineering a Human Microphysiological System for the Characterization of Islet-Immune InteractionsUG3DK122638 · NIDDK · UNIVERSITY OF FLORIDA · PI AGARWAL, ASHUTOSH, BRUSKO, TODD MICHAEL · 2019 to 2020
$2.1M
NIAID NIH HHS P01 AI042288NIDDK NIH HHS UG3 DK122638NIDDK NIH HHS UH3 DK122638
6 · The paper itself

Abstract

Objectives: Mitochondrial dysfunction plays a pivotal role in the pathogenesis of nonalcoholic fatty liver disease (NAFLD). We hypothesized that mitochondrial DNA (mtDNA) haplogroups affect the risk of NAFLD in Han Chinese patients and interact with PNPLA3 genotypes. Design: NAFLD and control patients were recruited from a tertiary care centre. The mitochondrial genome was amplified in overlapping segments and sequenced. Mitochondrial haplogroups were determined using Mitomaster. Patients: We enrolled 655 NAFLD patients and 504 controls. Results: More NAFLD patients encoded haplogroup G; odds ratio (OR) 1.85 (95% confidence interval [CI] 1.16, 2.80). Subhaplogroup G3 was present more frequently in NAFLD patients (25.8% vs 6.5%). The Conclusion: Haplogroup G was associated with an increased risk of NAFLD

Indexed as

Genetic Predisposition to DiseaseGenotypeHaplotypesAcyltransferasesAsian PeopleDNA, MitochondrialGenetic Association StudiesHumansLipaseMembrane ProteinsMitochondriaNon-alcoholic Fatty Liver DiseasePhospholipases A2, Calcium-IndependentRiskAcyltransferasesDNA, MitochondrialLipaseMembrane ProteinsPhospholipases A2, Calcium-IndependentPNPLA3 protein, humanhaplogroupsmitochondriaNAFLDPNPLA3

Identifiers

PMID33532620
PMCPMC7831202
OpenAlexW3092283163

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.