Evidence map›Paper›PMID 27111224›Full record

ArticlePloS one2016

Fine Mapping of the Body Fat QTL on Human Chromosome 1q43.

Brahim Aissani, Howard W Wiener, Kui Zhang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. A longitudinal genome-wide association study of bone mineral density mean and variability in the UK Biobank.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2023
    Article
  3. 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

3 authors at 2 institutions in 1 country.

Brahim AissaniDepartment of Epidemiology, University of Alabama at Birmingham School of Public Health, Birmingham, Alabama, United States of America.
Howard W WienerDepartment of Epidemiology, University of Alabama at Birmingham School of Public Health, Birmingham, Alabama, United States of America.
Kui ZhangDepartment of Mathematical Sciences, Michigan Technological University, Houghton, Michigan, United States of America.
University of Alabama at Birmingham · USMichigan Technological University · US

Funding

Genetic Determinants of Uterine Fibroids in African-American and Caucasian WomenR01HD064398 · NICHD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI AISSANI, BRAHIM · 2010 to 2013
$1.0M
NICHD NIH HHS R01 HD064398
6 · The paper itself

Abstract

introductionEvidence for linkage and association of obesity-related quantitative traits to chromosome 1q43 has been reported in the Quebec Family Study (QFS) and in populations of Caribbean Hispanic ancestries yet no specific candidate locus has been replicated to date.

methodsUsing a set of 1,902 single nucleotide polymorphisms (SNPs) genotyped in 525 African American (AA) and 391 European American (EA) women enrolled in the NIEHS uterine fibroid study (NIEHS-UFS), we generated a fine association map for the body mass index (BMI) across a 2.3 megabase-long interval delimited by RGS7 (regulator of G-protein signaling 7) and PLD5 (Phospholipase D, member 5). Multivariable-adjusted linear regression models were fitted to the data to evaluate the association in race-stratified analyses and meta-analysis.

resultsThe strongest associations were observed in a recessive genetic model and peaked in the 3' end of RGS7 at intronic rs261802 variant in the AA group (p = 1.0 x 10-4) and in meta-analysis of AA and EA samples (p = 9.0 x 10-5). In the EA group, moderate associations peaked at rs6429264 (p = 2.0 x 10-3) in the 2 Kb upstream sequence of RGS7. In the reference populations for the European ancestry in the 1,000 genomes project, rs6429264 occurs in strong linkage disequilibrium (D' = 0.94) with rs1341467, the strongest candidate SNP for total body fat in QFS that failed genotyping in the present study. Additionally we report moderate associations at the 3' end of PLD5 in meta-analysis (3.2 x 10-4 ≤ p ≤ 5.8 x 10-4).

conclusionWe report replication data suggesting that RGS7, a gene abundantly expressed in the brain, might be a putative body fat QTL on human chromosome 1q43. Future genetic and functional studies are required to substantiate our observations and to potentially link them to the neurobehavioral phenotypes associated with the RGS7 region.

Indexed as

Adipose TissueChromosome MappingChromosomes, Human, Pair 1Quantitative Trait LociAdultFemaleHumansMiddle Aged

Identifiers

PMID27111224
PMCPMC4844098
OpenAlexW2344061033

What Socratic holds

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LicenceCC BY
Read underepoch 390

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 Socratic graph.