Characterization of peritoneal reactive ascites collected from acute appendicitis and small bowel obstruction patients.


Journal

Clinica chimica acta; international journal of clinical chemistry
ISSN: 1873-3492
Titre abrégé: Clin Chim Acta
Pays: Netherlands
ID NLM: 1302422

Informations de publication

Date de publication:
01 Jun 2022
Historique:
received: 10 12 2021
revised: 18 03 2022
accepted: 23 03 2022
pubmed: 30 3 2022
medline: 7 6 2022
entrez: 29 3 2022
Statut: ppublish

Résumé

Pathological abdominal adhesions can cause bowel obstructions. A history of appendectomy (appy) increases patient rehospitalization risk directly related to adhesions. To potentially identify strategies for adhesion treatment, we characterized reactive ascites (rA) collected during appy or adhesiolysis for small bowel obstruction (SBO). This is a non-randomized, prospective observational study recruiting patients with non-perforated appendicitis or SBO from three Level 1 trauma centers in the United States. rA were analyzed via liquid chromatography-mass spectrometry (LC-MS) (n = 31), bead-based quantification cytokines and chemokines (n = 32) and soluble receptors (n = 30), and LC-MS metabolomics (n = 18). LC-MS showed that samples contained albumin, apolipoprotein A1, and transthyretin and that metabolites increased in SBO vs appy rA were biomarkers of oxidative stress. Multi-plex analyses showed levels of 17 cytokines/chemokines and 6 soluble receptors were significantly different in appy vs SBO rA. Top increased proteins in appy compared to SBO rA by 20.14-, 11.53-, and 8.18-fold were granulocyte-colony stimulating factor, C-X-C motif chemokine ligand 10, and interleukin-10, respectively. These data further define pro- and anti-inflammatory mediators and metabolites that may drive formation or perpetuate chronic abdominal adhesions. Future research is to further explore whether attenuation of these factors may decrease pathologic adhesion formation.

Sections du résumé

BACKGROUND BACKGROUND
Pathological abdominal adhesions can cause bowel obstructions. A history of appendectomy (appy) increases patient rehospitalization risk directly related to adhesions. To potentially identify strategies for adhesion treatment, we characterized reactive ascites (rA) collected during appy or adhesiolysis for small bowel obstruction (SBO).
METHODS METHODS
This is a non-randomized, prospective observational study recruiting patients with non-perforated appendicitis or SBO from three Level 1 trauma centers in the United States. rA were analyzed via liquid chromatography-mass spectrometry (LC-MS) (n = 31), bead-based quantification cytokines and chemokines (n = 32) and soluble receptors (n = 30), and LC-MS metabolomics (n = 18).
RESULTS RESULTS
LC-MS showed that samples contained albumin, apolipoprotein A1, and transthyretin and that metabolites increased in SBO vs appy rA were biomarkers of oxidative stress. Multi-plex analyses showed levels of 17 cytokines/chemokines and 6 soluble receptors were significantly different in appy vs SBO rA. Top increased proteins in appy compared to SBO rA by 20.14-, 11.53-, and 8.18-fold were granulocyte-colony stimulating factor, C-X-C motif chemokine ligand 10, and interleukin-10, respectively.
CONCLUSIONS CONCLUSIONS
These data further define pro- and anti-inflammatory mediators and metabolites that may drive formation or perpetuate chronic abdominal adhesions. Future research is to further explore whether attenuation of these factors may decrease pathologic adhesion formation.

Identifiants

pubmed: 35346646
pii: S0009-8981(22)00113-9
doi: 10.1016/j.cca.2022.03.022
pii:
doi:

Substances chimiques

Cytokines 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

126-136

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Melissa A Hausburg (MA)

Trauma Research Department, Swedish Medical Center, 501 E. Hampden, Englewood, CO 80113, United States; Trauma Research Department, St. Anthony Hospital, 11600 W 2nd Pl, Lakewood, CO 80228, United States; Trauma Research Department, Penrose Hospital, 2222 N Nevada Ave, Colorado Springs, CO 80907, United States.

Jennifer M Bocker (JM)

Trauma Services Department, St. Anthony Hospital, 11600 W 2nd Pl, Lakewood, CO 80228, United States.

Robert M Madayag (RM)

Trauma Services Department, St. Anthony Hospital, 11600 W 2nd Pl, Lakewood, CO 80228, United States.

Charles W Mains (CW)

Centura Health Trauma Systems, Centura Health, 9100 E Mineral Circle, Centennial, CO 80112, United States.

Kaysie L Banton (KL)

Trauma Services Deapartment, Swedish Medical Center, 501 E. Hampden, Englewood, CO 80113, United States.

Thaddeus E Liniewicz (TE)

Trauma Services Deapartment, Swedish Medical Center, 501 E. Hampden, Englewood, CO 80113, United States.

Allen Tanner (A)

Trauma Services Department, Penrose Hospital, 2222 N Nevada Ave, Colorado Springs, CO 80907, United States.

Erica Sercy (E)

Trauma Research Department, Swedish Medical Center, 501 E. Hampden, Englewood, CO 80113, United States; Trauma Research Department, St. Anthony Hospital, 11600 W 2nd Pl, Lakewood, CO 80228, United States; Trauma Research Department, Penrose Hospital, 2222 N Nevada Ave, Colorado Springs, CO 80907, United States.

Raphael Bar-Or (R)

Trauma Research Department, Swedish Medical Center, 501 E. Hampden, Englewood, CO 80113, United States; Trauma Research Department, St. Anthony Hospital, 11600 W 2nd Pl, Lakewood, CO 80228, United States; Trauma Research Department, Penrose Hospital, 2222 N Nevada Ave, Colorado Springs, CO 80907, United States.

Jason S Williams (JS)

Trauma Research Department, Swedish Medical Center, 501 E. Hampden, Englewood, CO 80113, United States; Trauma Research Department, St. Anthony Hospital, 11600 W 2nd Pl, Lakewood, CO 80228, United States; Trauma Research Department, Penrose Hospital, 2222 N Nevada Ave, Colorado Springs, CO 80907, United States.

Rebecca J Ryznar (RJ)

Department of Molecular Biology, Rocky Vista University, 8401 S Chambers Rd, Parker, CO 80134, United States.

David Bar-Or (D)

Trauma Research Department, Swedish Medical Center, 501 E. Hampden, Englewood, CO 80113, United States; Trauma Research Department, St. Anthony Hospital, 11600 W 2nd Pl, Lakewood, CO 80228, United States; Trauma Research Department, Penrose Hospital, 2222 N Nevada Ave, Colorado Springs, CO 80907, United States; Department of Molecular Biology, Rocky Vista University, 8401 S Chambers Rd, Parker, CO 80134, United States. Electronic address: davidbme49@gmail.com.

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Classifications MeSH