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Serum sTREM-1 as a surrogate marker of treatment outcome in patients with peptic ulcer disease.

Authors :
Koussoulas V
Giamarellos-Bourboulis EJ
Barbatzas C
Pimentel M
Source :
Digestive diseases and sciences [Dig Dis Sci] 2011 Dec; Vol. 56 (12), pp. 3590-5. Date of Electronic Publication: 2011 Jun 02.
Publication Year :
2011

Abstract

Objective: Soluble triggering receptor expressed on myeloid cells-1 (sTREM-1) is elevated in the gastric juice and in cultures of gastric mucosa of patients with peptic ulcer disease (PUD). Its application as a surrogate marker for the treatment of PUD was assessed.<br />Methods: From 138 eligible patients, 96 were enrolled; 50 with duodenal ulcer, 29 with gastric ulcer and 17 with chronic gastritis. Patients were endoscoped twice; once before treatment and once after treatment. Biopsy specimens were collected for histopathologic estimation of gastritis. Blood was sampled prior to each endoscopy. Serum was collected and sTREM-1 was measured by an enzyme immunoabsorbent assay ( http://www.clinicaltrials.gov identifier NCT00534443).<br />Results: At the end of treatment sTREM-1 was either: (a) below the limit of detection (this occurred in 62 patients and it was accompanied by lacks signs of residual disease in 58 patients, 93.5%); or (b) above the limit of detection (this occurred in 17 patients and it was accompanied by residual disease in 14 patients, 82.3%) (p < 0.0001). Odds ratio for complete healing of peptic ulcer with sTREM-1 below detection limit was 5.30 (95% CI: 1.89-14.83, p < 0.001) compared to serum sTREM-1 above the limit of detection.<br />Conclusions: Serum sTREM-1 below detection limit may effectively distinguish patients who successfully completed therapy for PUD from those with residual disease and apply as a surrogate marker.

Details

Language :
English
ISSN :
1573-2568
Volume :
56
Issue :
12
Database :
MEDLINE
Journal :
Digestive diseases and sciences
Publication Type :
Academic Journal
Accession number :
21633832
Full Text :
https://doi.org/10.1007/s10620-011-1761-4