Evidence map›Paper›PMID 26540410›Full record

ReviewPLoS genetics2015

Pleiotropic Effects of Immune Responses Explain Variation in the Prevalence of Fibroproliferative Diseases.

Shirley B Russell, Joan C Smith, Minjun Huang, Joel S Trupin, Scott M Williams

Open access · goldAbstract readReview
In one paragraph

Review in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 25% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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  15. Tumor-Infiltrating Lymphocytes and Colorectal Cancer Survival in African American and Caucasian Patients.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2018
    Article
  16. 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 4 institutions in 1 country.

Shirley B RussellVanderbilt Genetics Institute, Division of Dermatology, Department of Medicine, Vanderbilt University, Nashville, Tennessee, United States of America.
Joan C SmithMeharry Medical College, Nashville, Tennessee, United States of America.
Minjun HuangDepartment of Genetics, Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire, United States of America.
Joel S TrupinMeharry Medical College, Nashville, Tennessee, United States of America.
Scott M WilliamsDepartment of Genetics, Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire, United States of America.
Meharry Medical College · USCase Western Reserve University · USDartmouth College · USVanderbilt University · US

Funding

Quantitative Biology Research InstituteP20GM103534 · NIGMS · DARTMOUTH COLLEGE · PI AMOS, CHRISTOPHER I. · 2012 to 2016
$8.6M
UV, APOPTOSIS, PROTEIN PHOSPHATASE AND SKIN DISEASEP30AR041943 · NIAMS · VANDERBILT UNIVERSITY · PI STRICKLIN, GEORGE PUTNAM · 1994 to 2008
$5.3M
Bioinformatics Strategies for Genome-Wide Association StudiesR01LM010098 · NLM · UNIVERSITY OF PENNSYLVANIA · PI MOORE, JASON H., WILLIAMS, SCOTT MATTHEW · 2009 to 2023
$5.1M
Gene Expression and Variation in Keloid FibroblastsF33AR052241 · NIAMS · MIDDLE TENNESSEE RESEARCH INSTITUTE · PI RUSSELL, SHIRLEY B. · 2005 to 2006
$122k
NIAMS NIH HHS F33 AR052241NIAMS NIH HHS F33AR052241NIAMS NIH HHS P30 AR041943NIAMS NIH HHS P30AR041943NIGMS NIH HHS P20 GM103534NIGMS NIH HHS P20GM103534NLM NIH HHS R01 LM010098NLM NIH HHS R01LM010098
6 · The paper itself

Abstract

Many diseases are differentially distributed among human populations. Differential selection on genetic variants in ancestral environments that coincidentally predispose to disease can be an underlying cause of these unequal prevalence patterns. Selected genes may be pleiotropic, affecting multiple phenotypes and resulting in more than one disease or trait. Patterns of pleiotropy may be helpful in understanding the underlying causes of an array of conditions in a population. For example, several fibroproliferative diseases are more prevalent and severe in populations of sub-Saharan ancestry. We propose that this disparity is due to selection for an enhanced Th2 response that confers resistance to helminthic infections, and concurrently increases susceptibility to fibrosis due to the profibrotic action of Th2 cytokines. Many studies on selection of Th2-related genes for host resistance to helminths have been reported, but the pleiotropic impact of this selection on the distribution of fibrotic disorders has not been explicitly investigated. We discuss the disproportionate occurrence of fibroproliferative diseases in individuals of African ancestry and provide evidence that adaptation of the immune system has shaped the genetic structure of these human populations in ways that alter the distribution of multiple fibroproliferative diseases.

Indexed as

AnimalsBlack PeopleCytokinesDiseaseFibrosisGenetic Predisposition to DiseaseHelminthiasisHumansMicePrevalenceCytokines

Identifiers

PMID26540410
PMCPMC4634921
OpenAlexW2113620675

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.