Evidence map›Paper›PMID 30006737›Full record

Trial reportHuman genetics2018

Admixture mapping and fine-mapping of birth weight loci in the Black Women's Health Study.

Heather M Ochs-Balcom, Holly Shaw, Leah Preus, Julie R Palmer, Stephen A Haddad, Lynn Rosenberg, Edward A Ruiz-Narváez

Abstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Human genetics, 2018. 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 43% 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. Trial
  2. Article
  3. Review
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

7 authors at 3 institutions in 1 country.

Heather M Ochs-BalcomDepartment of Epidemiology and Environmental Health, School of Public Health and Health Professions, University at Buffalo, Buffalo, NY, USA.
Holly ShawDepartment of Epidemiology and Environmental Health, School of Public Health and Health Professions, University at Buffalo, Buffalo, NY, USA.
Leah PreusDepartment of Epidemiology and Environmental Health, School of Public Health and Health Professions, University at Buffalo, Buffalo, NY, USA.
Julie R PalmerSlone Epidemiology Center, Boston University, Boston, MA, USA.
Stephen A HaddadSlone Epidemiology Center, Boston University, Boston, MA, USA.
Lynn RosenbergSlone Epidemiology Center, Boston University, Boston, MA, USA.
Edward A Ruiz-NarváezDepartment of Nutritional Sciences, University of Michigan School of Public Health, 1860 SPH I, 1415 Washington Heights, Ann Arbor, MI, USA. eruiznar@umich.edu.
Boston University · USUniversity at Buffalo, State University of New York · USUniversity of Michigan–Ann Arbor · US

Funding

A Follow-up Study for Causes of Cancer in Black WomenU01CA164974 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Kimberly A. Bertrand, Yvette C Cozier · 2017 to 2026
$24.0M
FOLLOW-UP STUDY FOR CAUSES OF ILLNESS IN BLACK WOMENR01CA058420 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ROSENBERG, LYNN · 1999 to 2013
$20.7M
A Follow-up Study for Causes of Cancer in Black WomenUM1CA164974 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ROSENBERG, LYNN · 2012 to 2017
$13.7M
Gene Polymorphisms in Relation to Cancer in Black WomenR01CA098663 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI PALMER, JULIE R · 2003 to 2012
$5.3M
Weight gain, type 2 diabetes, and factors that affect neuroendocrine functionR01MD007015 · NIMHD · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ROSENBERG, LYNN · 2012 to 2016
$1.4M
American Heart Association 11SDG7390014National Cancer Institute R01CA058420National Cancer Institute UM1CA164974National Institute on Minority Health and Health Disparities (US) R01MD007015NCI NIH HHS R01 CA058420NCI NIH HHS R01 CA098663NCI NIH HHS U01 CA164974NCI NIH HHS UM1 CA164974NIMHD NIH HHS R01 MD007015
6 · The paper itself

Abstract

Several genome-wide association studies (GWAS) have identified genetic variants associated with birth weight. To date, however, most GWAS of birth weight have focused primarily on European ancestry samples even though prevalence of low birth weight is higher among African-Americans. We conducted admixture mapping using 2918 ancestral informative markers in 2596 participants of the Black Women's Health Study, with the goal of identifying novel genomic regions where local African ancestry is associated with birth weight. In addition, we performed a replication analysis of 11 previously identified index single nucleotide polymorphisms (SNPs), and fine-mapped those genetic loci to identify better or new genetic variants associated with birth weight in African-Americans. We found that high African ancestry at 12q14 was associated with low birth weight, and we identified multiple independent birth weight-lowering variants in this genomic region. We replicated the association of a previous GWAS SNP in ADRB1 and our fine-mapping efforts suggested the presence of new birth weight-associated variants in ADRB1, HMGA2, and SLC2A4. Further studies are needed to determine whether birth weight-associated loci can in part explain race-associated birth weight disparities.

Indexed as

Genetic LociPolymorphism, Single NucleotideAdultBirth WeightBlack or African AmericanFemaleGenome-Wide Association StudyGlucose Transporter Type 4HMGA2 ProteinHumansMiddle AgedReceptors, Adrenergic, beta-1ADRB1 protein, humanGlucose Transporter Type 4HMGA2 ProteinHMGA2 protein, humanReceptors, Adrenergic, beta-1SLC2A4 protein, human

Identifiers

PMID30006737
PMCPMC6330255
OpenAlexW2884320664

What Socratic 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 Socratic graph.