Evidence map›Paper›PMID 26081267›Full record

ArticleJournal of endodontics2015

Genetic Variants in Cyclooxygenase-2 Contribute to Post-treatment Pain among Endodontic Patients.

Elizabeth Applebaum, Andrea G Nackley, Eric Bair, William Maixner, Asma A Khan

Abstract read
In one paragraph

Article in Journal of endodontics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 21 citations in OpenAlex.

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  5. 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

5 authors at 1 institution in 1 country.

Elizabeth ApplebaumPrivate Practice, School of Dentistry, University of North Carolina, Chapel Hill, North Carolina.
Andrea G NackleyCenter for Pain Research and Innovation, School of Dentistry, University of North Carolina, Chapel Hill, North Carolina.
Eric BairCenter for Pain Research and Innovation, School of Dentistry, University of North Carolina, Chapel Hill, North Carolina.
William MaixnerCenter for Pain Research and Innovation, School of Dentistry, University of North Carolina, Chapel Hill, North Carolina.
Asma A KhanCenter for Pain Research and Innovation, School of Dentistry, University of North Carolina, Chapel Hill, North Carolina. Electronic address: Asma_Khan@unc.edu.
University of North Carolina at Chapel Hill · 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
Persistent COMT-dependent Pain: Role of beta-adrenergic ReceptorsR01NS072205 · NINDS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI NACKLEY, ANDREA G · 2011 to 2014
$1.4M
NIDCR NIH HHS U01 DE017018NINDS NIH HHS P01 NS045685NINDS NIH HHS R01 NS072205
6 · The paper itself

Abstract

introductionNonsteroidal anti-inflammatory drugs (NSAIDs) have a well-established analgesic efficacy for inflammatory pain. These drugs exert their effect by inhibiting the enzyme cyclooxygenase (COX) and are commonly used for the management of pain after endodontic treatment. There are 2 distinct isoforms of COX: COX-1, which is constitutively expressed, and COX-2, which is primarily induced by inflammation. Previous studies have shown that functional human genetic variants of the COX-2 gene may explain individual variations in acute pain. The present study extends this work by examining the potential contribution of the 2 COX isoforms to pain after endodontic treatment.

methodsNinety-four patients treated by endodontic residents at the University of North Carolina School of Dentistry were enrolled into a prospective cohort study. Data on potential predictors of post-treatment pain were collected, and all patients submitted saliva samples for genetic analysis. Nonsurgical root canal therapy was performed, and participants recorded pain levels for 5 days after.

resultsIn this study, 63% of patients experienced at least mild pain after root canal therapy, and 24% experienced moderate to severe pain. The presence of pretreatment pain was correlated with higher post-treatment pain (P = .01). Elevated heart rate (P = .02) and higher diastolic blood pressure (P = .024) were also correlated with decreased post-treatment pain. Finally, we identified genetic variants in COX-2 (haplotype composed of rs2383515 G, rs5277 G, rs5275 T, and rs2206593 A) associated with post-treatment pain after endodontic treatment (P = .025).

conclusionsUnderstanding the genetic basis of pain after endodontic treatment will advance its prevention and management.

Indexed as

Polymorphism, Single NucleotideAdolescentAdultAgedAged, 80 and overCyclooxygenase 1Cyclooxygenase 2FemaleGenetic Predisposition to DiseaseHaplotypesHumansIncidenceMaleMiddle AgedNorth CarolinaPainCyclooxygenase 1Cyclooxygenase 2PTGS1 protein, humanPTGS2 protein, humanCyclooxygenase-1cyclooxygenase-2odontogenicpostoperative painsingle nucleotide polymorphism

Identifiers

PMID26081267
PMCPMC4519379
OpenAlexW2106069832

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.