Resistin Is a Novel Marker for Postoperative Pain Intensity.


Journal

Anesthesia and analgesia
ISSN: 1526-7598
Titre abrégé: Anesth Analg
Pays: United States
ID NLM: 1310650

Informations de publication

Date de publication:
03 2019
Historique:
pubmed: 13 4 2018
medline: 25 12 2019
entrez: 13 4 2018
Statut: ppublish

Résumé

Pro- and anti-inflammatory cytokines (adipokines) associated with adipose tissue can modulate inflammatory processes and lead to systemic inflammatory conditions such as metabolic syndrome. In the present pilot study, we investigated 3 major adipokines (leptin, adiponectin, and resistin) and 2 nonspecific proinflammatory cytokines (tumor necrosis factor α and interleukin-6) with regard to their association with postoperative pain intensity. We analyzed a total of 45 single-nucleotide polymorphisms of the adipokines in 57 patients with postlaparotomy pain. We adjusted for multiple testing to reduce the chance of false-positive results by controlling the false discovery rate. Serum levels of the adipokines and proinflammatory cytokines were measured in another 36 patients undergoing laparotomy. A stepwise multiple linear regression analysis using these measurements and opioid dosages as independent variables was performed to explore the factors associated with postoperative pain. Only 1 variant of the resistin gene (rs3745367) demonstrated a significant association with postoperative pain (P < .002). Patients exhibiting homozygosity for the minor alleles (n = 7; numerical rating scale [NRS], 2.3 ± 1.3) demonstrated lower pain intensity compared with those exhibiting homozygosity for the major alleles (n = 29; NRS, 3.8 ± 1.0; P = .004) and heterozygosity for the minor alleles (n = 21; NRS, 4.2 ± 0.8; P < .001). Only serum resistin levels showed a positive association with postoperative pain. A genetic variant of resistin and serum resistin levels were associated with postoperative pain intensity, while other adipokines and cytokines exhibit no such association. Resistin can alter the inflammatory responses in postoperative wounds, although it could be a determinant factor that is independent of inflammatory processes. Resistin may be a novel marker for postoperative pain intensity.

Sections du résumé

BACKGROUND
Pro- and anti-inflammatory cytokines (adipokines) associated with adipose tissue can modulate inflammatory processes and lead to systemic inflammatory conditions such as metabolic syndrome. In the present pilot study, we investigated 3 major adipokines (leptin, adiponectin, and resistin) and 2 nonspecific proinflammatory cytokines (tumor necrosis factor α and interleukin-6) with regard to their association with postoperative pain intensity.
METHODS
We analyzed a total of 45 single-nucleotide polymorphisms of the adipokines in 57 patients with postlaparotomy pain. We adjusted for multiple testing to reduce the chance of false-positive results by controlling the false discovery rate. Serum levels of the adipokines and proinflammatory cytokines were measured in another 36 patients undergoing laparotomy. A stepwise multiple linear regression analysis using these measurements and opioid dosages as independent variables was performed to explore the factors associated with postoperative pain.
RESULTS
Only 1 variant of the resistin gene (rs3745367) demonstrated a significant association with postoperative pain (P < .002). Patients exhibiting homozygosity for the minor alleles (n = 7; numerical rating scale [NRS], 2.3 ± 1.3) demonstrated lower pain intensity compared with those exhibiting homozygosity for the major alleles (n = 29; NRS, 3.8 ± 1.0; P = .004) and heterozygosity for the minor alleles (n = 21; NRS, 4.2 ± 0.8; P < .001). Only serum resistin levels showed a positive association with postoperative pain.
CONCLUSIONS
A genetic variant of resistin and serum resistin levels were associated with postoperative pain intensity, while other adipokines and cytokines exhibit no such association. Resistin can alter the inflammatory responses in postoperative wounds, although it could be a determinant factor that is independent of inflammatory processes. Resistin may be a novel marker for postoperative pain intensity.

Identifiants

pubmed: 29649030
doi: 10.1213/ANE.0000000000003363
doi:

Substances chimiques

Biomarkers 0
Inflammation Mediators 0
RETN protein, human 0
Resistin 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

563-568

Auteurs

Jun Hozumi (J)

From the Departments of Anesthesiology and Pain Relief Center.

Masahiko Sumitani (M)

Pain and Palliative Medicine, The University of Tokyo Hospital, Tokyo, Japan.

Daisuke Nishizawa (D)

Addictive Substance Project, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.

Makoto Nagashima (M)

Department of Surgery, Toho University Medical Center, Sakura Hospital, Chiba, Japan.

Kazutaka Ikeda (K)

Addictive Substance Project, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.

Hiroaki Abe (H)

From the Departments of Anesthesiology and Pain Relief Center.

Ryoji Kato (R)

Department of Surgery, Toho University Medical Center, Sakura Hospital, Chiba, Japan.

Yoshiomi Kusakabe (Y)

From the Departments of Anesthesiology and Pain Relief Center.

Yoshitsugu Yamada (Y)

From the Departments of Anesthesiology and Pain Relief Center.

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Classifications MeSH