Evidence map›Paper›PMID 33983957›Full record

ArticlePloS one2021

Common genetic variants associated with obesity in an African-American and Hispanic/Latino population.

Brandon Chalazan, Denada Palm, Arvind Sridhar, Christina Lee, Maria Argos, Martha Daviglus, Jalees Rehman, Sreenivas Konda, Dawood Darbar

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.9field-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

10 citing papers in PubMed, 21 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 2 institutions in 1 country.

Brandon ChalazanDepartment of Medicine, University of Illinois at Chicago, Chicago, Illinois, United States of America.ORCID 0000-0001-5319-6316
Denada PalmDepartment of Medicine, University of Illinois at Chicago, Chicago, Illinois, United States of America.
Arvind SridharDepartment of Medicine, University of Illinois at Chicago, Chicago, Illinois, United States of America.
Christina LeeBroad Institute of MIT and Harvard, Boston, Massachusetts, United States of America.
Maria ArgosDivision of Epidemiology and Biostatics, School of Public Health, University of Illinois at Chicago, Chicago, Illinois, United States of America.
Martha DaviglusDepartment of Medicine, University of Illinois at Chicago, Chicago, Illinois, United States of America.
Jalees RehmanDepartment of Medicine, University of Illinois at Chicago, Chicago, Illinois, United States of America.
Sreenivas KondaDivision of Epidemiology and Biostatics, School of Public Health, University of Illinois at Chicago, Chicago, Illinois, United States of America.
Dawood DarbarDepartment of Medicine, University of Illinois at Chicago, Chicago, Illinois, United States of America.ORCID 0000-0002-4103-5977
University of Illinois Chicago · USBroad Institute · US

Funding

Deciphering the genetic mechanisms of atrial fibrillationR01HL138737 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DARBAR, DAWOOD · 2017 to 2020
$2.6M
Training Program in Personalized Cardiovascular Medicine (TPIPCVM)T32HL139439 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DARBAR, DAWOOD · 2018 to 2022
$2.1M
NHLBI NIH HHS R01 HL138737NHLBI NIH HHS T32 HL139439
6 · The paper itself

Abstract

introductionOver 35% of all adults in the world are currently obese and risk of obesity in racial or ethnic minority groups exist in the US, but the causes of these differences are not all known. As obesity is a leading cause of cardiovascular disease, an improved understanding of risk factors across racial and ethnic groups may improve outcomes.

objectiveThe objective of this study was to determine if susceptibility to obesity is associated with genetic variation in candidate single nucleotide polymorphisms (SNPs) in African Americans and Hispanic/Latinos. MATERIALS AND

methodsWe examined data from 534 African Americans and 557 Hispanic/Latinos participants from the UIC Cohort of Patients, Family and Friends. Participants were genotyped for the top 26 obesity-associated SNPs within FTO, MC4R, TUB, APOA2, APOA5, ADIPOQ, ARL15, CDH13, KNG1, LEPR, leptin, and SCG3 genes.

resultsThe mean (SD) age of participants was 49±13 years, 55% were female, and mean body mass index (BMI) was 31±7.5 kg/m2. After adjusting for age and sex, we found that rs8050136 in FTO (odds ratio [OR] 1.40, 95% confidence interval [CI] 1.1-1.8; P = 0.01) among African Americans and rs2272383 in TUB (OR 1.34, 95% CI 1.04-1.71; P = 0.02) among Hispanic/Latinos were associated with obesity. However, none of the SNPs in multivariable analysis of either AA or H/L cohorts were significant when adjusted for multiple correction.

conclusionsWe show that candidate SNPs in the FTO and TUB genes are associated with obesity in African Americans and Hispanic/Latinos individuals respectively. While the underlying pathophysiological mechanisms by which common genetic variants cause obesity remain unclear, we have identified novel therapeutic targets across racial and ethnic groups.

Indexed as

Adaptor Proteins, Signal TransducingAlpha-Ketoglutarate-Dependent Dioxygenase FTOBlack or African AmericanHispanic or LatinoObesityAdultBody Mass IndexFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedPolymorphism, Single NucleotideAdaptor Proteins, Signal TransducingAlpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, humanTUB protein, human

Identifiers

PMID33983957
PMCPMC8118531
OpenAlexW3162572435

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.