Evidence map›Paper›PMID 23543185›Full record

Trial reportHuman genetics2013

Replication of genetic loci for sarcoidosis in US black women: data from the Black Women's Health Study.

Yvette Cozier, Edward Ruiz-Narvaez, Craig McKinnon, Jeffrey Berman, Lynn Rosenberg, Julie Palmer

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Human genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk.American journal of respiratory and critical care medicine · 2015
    Article
  6. Granuloma genes in sarcoidosis: what is new?Current opinion in pulmonary medicine · 2015
    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

6 authors at 1 institution in 1 country.

Yvette CozierSlone Epidemiology Center, Boston University, Boston, USA. yvettec@bu.edu
Edward Ruiz-Narvaez
Craig McKinnon
Jeffrey Berman
Lynn Rosenberg
Julie Palmer
Boston University · US

Funding

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
Sarcoidosis in U.S. Black Women: Genetic and Non-genetic Risk FactorsK01HL088709 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI COZIER, YVETTE C · 2008 to 2012
$590k
NCI NIH HHS CA058420NCI NIH HHS CA098663NCI NIH HHS R01 CA058420NCI NIH HHS R01 CA098663NCI NIH HHS UM1 CA164974NHLBI NIH HHS K01 HL088709NHLBI NIH HHS K01HL088709
6 · The paper itself

Abstract

In the United States, incidence and mortality from sarcoidosis, a chronic, granulomatous disease, are increased in black women. In data from the Black Women's Health Study, a follow-up of US black women, we assessed two SNPs (rs2076530 and rs9268480) previously identified in the BTNL2 gene (chromosome 6p21), of which rs4424066 and rs3817963 are perfect proxies, to determine if they represent independent signals of disease risk. We also assessed whether local ancestry in four genomic regions previously identified through admixture mapping was associated with sarcoidosis. Finally, we assessed the relation of global percent African ancestry to risk. We conducted a nested case-control study of 486 sarcoidosis cases and 943 age- and geography-matched controls. Both BTNL2 SNPs were associated with risk of sarcoidosis in separate models, but in a combined analysis the increased risk was due to the A-allele of the rs3817963 SNP; each copy of the A-allele was associated with a 40 % increase in risk of sarcoidosis (p = 0.02) and was confirmed by our haplotypic analysis. Local African ancestry around the rs30533 ancestry informative marker at chromosome 5q31 was associated with a 29 % risk reduction (p = 0.01). Therefore, we adjusted our analysis of global African ancestry for number of copies of African alleles in rs30533. Subjects in the highest quintile of percent African ancestry had a 54 % increased risk of sarcoidosis. The present results from a population of African-American women support the role of the BTNL2 gene and the 5q31 locus in the etiology of sarcoidosis, and also demonstrate that percent African ancestry is associated with disease risk.

Indexed as

AllelesBlack or African AmericanGenetic LociPolymorphism, Single NucleotideAdultAgedButyrophilinsChromosomes, Human, Pair 5Chromosomes, Human, Pair 6Cohort StudiesFemaleFollow-Up StudiesHumansMembrane GlycoproteinsMiddle AgedRisk FactorsBTNL2 protein, humanButyrophilinsMembrane Glycoproteins

Identifiers

PMID23543185
PMCPMC3746966
OpenAlexW2058629237

What OpenQuestion 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 OpenQuestion graph.