Circulating Omega-6 and Omega-3 Polyunsaturated Fatty Acids in Painful Temporomandibular Disorder and Low Back Pain.


Journal

The journal of pain
ISSN: 1528-8447
Titre abrégé: J Pain
Pays: United States
ID NLM: 100898657

Informations de publication

Date de publication:
10 2022
Historique:
received: 10 01 2022
revised: 03 05 2022
accepted: 25 05 2022
pubmed: 14 6 2022
medline: 12 10 2022
entrez: 13 6 2022
Statut: ppublish

Résumé

Preclinical studies demonstrate opposing effects of long-chain polyunsaturated fatty acid (PUFA) metabolites on inflammation and nociception. Omega-6 (n-6) PUFAs amplify both processes while omega-3 (n-3) PUFAs inhibit them. This cross-sectional study examined relationships between PUFAs in circulating erythrocytes and 2 chronic idiopathic pain conditions: temporomandibular disorder (TMD) and low back pain in a community-based sample of 503 U.S. adults. Presence or absence of TMD and low back pain, respectively, were determined by clinical examination and by responses to established screening questions. Liquid chromatography-tandem mass spectrometry quantified PUFAs. In multivariable logistic regression models, a higher ratio of n-6/n-3 long-chain PUFAs was associated with greater odds of TMD (odds ratio ((OR) = 1.75, 95% confidence limits (CL): 1.16, 2.64) and low back pain (OR = 1.63, 95% CL: 1.07, 2.49). Higher levels of the pronociceptive n-6 long-chain arachidonic acid (AA) were associated with a greater probability of both pain conditions for women, but not men. Higher levels of the antinociceptive long-chain n-3 PUFAs eicosapentaenoic and docosahexaenoic acids were associated with a lower probability of both pain conditions for men, but not women. As systemic inflammation is not a hallmark of these conditions, PUFAs may influence idiopathic pain through other mechanisms. PERSPECTIVE: This cross-sectional clinical study found that a higher ratio of circulating n-6/n-3 long-chain PUFAs was associated with greater odds of 2 common chronic overlapping pain conditions. This suggests that the pro and antinociceptive properties of n-6 and n-3 PUFAs, respectively, influence pain independently of their well-established inflammatory pathways.

Identifiants

pubmed: 35697285
pii: S1526-5900(22)00335-2
doi: 10.1016/j.jpain.2022.05.008
pmc: PMC9561056
mid: NIHMS1815304
pii:
doi:

Substances chimiques

Analgesics 0
Arachidonic Acids 0
Fatty Acids, Omega-3 0
Fatty Acids, Omega-6 0
Fatty Acids, Unsaturated 0
Docosahexaenoic Acids 25167-62-8

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1724-1736

Subventions

Organisme : NIA NIH HHS
ID : P30 AG028740
Pays : United States
Organisme : NIDCR NIH HHS
ID : R21 DE029746
Pays : United States

Informations de copyright

Published by Elsevier Inc.

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Auteurs

Anne E Sanders (AE)

Division of Pediatric and Public Health, Adams School of Dentistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina. Electronic address: anne_sanders@unc.edu.

E Diane Weatherspoon (ED)

Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

Brandie M Ehrmann (BM)

Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

Paul S Soma (PS)

Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

Saame R Shaikh (SR)

Department of Nutrition, Gillings School of Global Public Health and School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

John S Preisser (JS)

Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

Richard Ohrbach (R)

Department of Oral Diagnostic Sciences, University at Buffalo, Buffalo, New York.

Roger B Fillingim (RB)

Department of Community Dentistry and Behavioral Science, University of Florida, Gainesville, Florida; Pain Research and Intervention Center of Excellence, Department of Community Dentistry and Behavioral Science, College of Dentistry, University of Florida, Gainesville, Florida.

Gary D Slade (GD)

Division of Pediatric and Public Health, Adams School of Dentistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

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Classifications MeSH