Evidence map›Paper›PMID 22074755›Full record

ArticleThe journal of pain2011

Potential genetic risk factors for chronic TMD: genetic associations from the OPPERA case control study.

Shad B Smith, Dylan W Maixner, Joel D Greenspan, Ronald Dubner, Roger B Fillingim, Richard Ohrbach, Charles Knott, Gary D Slade, Eric Bair, Dustin G Gibson and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The journal of pain, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 1 pooled it
8.1field-weighted citation impact, top 2% 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

80 citing papers in PubMed, 1 synthesis or guideline pooled it, 209 citations in OpenAlex.

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  20. Clinical aspects of mastication myalgia-an overview.Frontiers in pain research (Lausanne, Switzerland) · 2023
    Review

20 more citing papers are in PubMed but not listed here.

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

14 authors at 7 institutions in 2 countries.

Shad B SmithCenter for Neurosensory Disorders, University of North Carolina at Chapel Hill, North Carolina 27514, USA.
Dylan W Maixner
Joel D Greenspan
Ronald Dubner
Roger B Fillingim
Richard Ohrbach
Charles Knott
Gary D Slade
Eric Bair
Dustin G Gibson
Dmitri V Zaykin
Bruce S Weir
William Maixner
Luda Diatchenko
University of North Carolina at Chapel Hill · USUniversity of Maryland, Baltimore · USBattelle · USNational Institute of Environmental Health Sciences · USUniversity at Buffalo, State University of New York · USUniversity of Florida · USUniversity of Washington · US

Funding

Risk Factors for Onset and Persistence of TMDU01DE017018 · NIDCR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DIATCHENKO, LUDA, FILLINGIM, ROGER B · 2005 to 2016
$35.9M
Vulvar Vestibulitis syndrome (VVS)P01NS045685 · NINDS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ESSICK, GREGORY KENT · 2004 to 2014
$12.5M
Statistical, population genetics and genetic epidemiologyZIAES101866 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI ZAYKIN, DMITRI V · 2009 to 2021
$5.8M
COMT &betaAR Polymorphism &Development of Painful TMDR01DE016558 · NIDCR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DIATCHENKO, LUDA · 2005 to 2009
$1.7M
Contribution of ADA1A polymorphism to persistent pain statesF32DE019057 · NIDCR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SMITH, SHAD BENJAMIN · 2008 to 2010
$149k
Intramural NIH HHSNIDCR NIH HHS DE016558NIDCR NIH HHS F32 DE019057NIDCR NIH HHS F32DE019057NIDCR NIH HHS R01DE016155NIDCR NIH HHS R01 DE016558NIDCR NIH HHS U01 DE017018NIDCR NIH HHS U01DE017018NINDS NIH HHS P01 NS045685NINDS NIH HHS P01NS045685
6 · The paper itself

Abstract

unlabelledGenetic factors play a role in the etiology of persistent pain conditions, putatively by modulating underlying processes such as nociceptive sensitivity, psychological well-being, inflammation, and autonomic response. However, to date, only a few genes have been associated with temporomandibular disorders (TMD). This study evaluated 358 genes involved in pain processes, comparing allelic frequencies between 166 cases with chronic TMD and 1,442 controls enrolled in the OPPERA (Orofacial Pain: Prospective Evaluation and Risk Assessment) study cooperative agreement. To enhance statistical power, 182 TMD cases and 170 controls from a similar study were included in the analysis. Genotyping was performed using the Pain Research Panel, an Affymetrix gene chip representing 3,295 single nucleotide polymorphisms, including ancestry-informative markers that were used to adjust for population stratification. Adjusted associations between genetic markers and TMD case status were evaluated using logistic regression. The OPPERA findings provided evidence supporting previously reported associations between TMD and 2 genes: HTR2A and COMT. Other genes were revealed as potential new genetic risk factors for TMD, including NR3C1, CAMK4, CHRM2, IFRD1, and GRK5. While these findings need to be replicated in independent cohorts, the genes potentially represent important markers of risk for TMD, and they identify potential targets for therapeutic intervention. PERSPECTIVE: Genetic risk factors for TMD pain were explored in the case-control component of the OPPERA cooperative agreement, a large population-based prospective cohort study. Over 350 candidate pain genes were assessed using a candidate gene panel, with several genes displaying preliminary evidence for association with TMD status.

Indexed as

AdolescentAdultAgedCase-Control StudiesChronic PainCohort StudiesFemaleGenetic Association StudiesHumansMaleMiddle AgedMulticenter Studies as TopicProspective StudiesRisk FactorsTemporomandibular Joint DisordersYoung Adult

Identifiers

PMID22074755
PMCPMC3268684
OpenAlexW2023007719

What OpenQuestion holds

Textmetadata
LicenceTDM
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.