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Chronic proton pump inhibition therapy in the diagnostic accuracy of serum pepsinogen I and gastrin concentrations to identify pernicious anaemia.

Authors :
Martín-Alcolea M
Rodríguez-Hernández I
Aldea M
Rosas I
Juncà J
Granada ML
Source :
Clinical biochemistry [Clin Biochem] 2017 Jun; Vol. 50 (9), pp. 481-484. Date of Electronic Publication: 2017 Jan 18.
Publication Year :
2017

Abstract

Background: Chronic use of proton pump inhibitors (PPIs) leads to increases in gastrin and pepsinogen-I serum concentrations.<br />Aim: To asses if chronic treatment with PPIs has an effect on serum gastrin and pepsinogen-I concentrations for the diagnosis of pernicious anaemia (PA).<br />Materials and Methods: Serum gastrin and pepsinogen-I were measured in 38 patients with PA and 74 without PA (controls); 17/38 PA patients and 36/74 controls were treated with PPIs. Receiver Operating Curves (ROC) were used to compare diagnostic accuracy of gastrin and pepsinogen-I for PA in patients under chronic treatment with PPIs and in untreated patients.<br />Results: PPI treatment increased pepsinogen-I in patients and in controls, while gastrin increased only in controls. In untreated patients, a pepsinogen-I <8.3ng/mL had 95.2% sensitivity and 100% specificity, whereas a gastrin >115pg/mL had 100% sensitivity and 92.11% specificity for PA diagnosis. In PPI-treated patients, a pepsinogen I<24.1ng/mL had a lower sensitivity (82.4%) but retained 100% specificity, however the best cut-off point for gastrin, 610pg/mL, had a very low sensitivity (58%).<br />Conclusions: PPI chronic treatment decreased the diagnostic accuracy for the studied biomarkers, particularly of gastrin. In PPI-treated patients, serum pepsinogen-I concentrations >24.1ng/mL allowed rejecting a PA diagnosis with 100% specificity.<br /> (Copyright © 2017 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-2933
Volume :
50
Issue :
9
Database :
MEDLINE
Journal :
Clinical biochemistry
Publication Type :
Academic Journal
Accession number :
28109748
Full Text :
https://doi.org/10.1016/j.clinbiochem.2017.01.009