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The value of detecting pepsinogen and gastrin-17 levels in serum for pre-cancerous lesion screening in gastric cancer

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Guang Yu,  Guo-Xiang Wang, Hong-Gang Wang, Fei-Fei Mo, Bin-Bin Tang

Abstract:

The aim of the study was to estimate the value of detecting pepsinogen (PG) I, PGII and gastrin-17 (G-17) levels in serum for chronic atrophic gastritis (CAG) screening and to determine the clinical applicability of combined measurement of serum G-17, pepsinogens (PGI, PGII) and PGI/PGII ratio (PGR) as a screening test for CAG. The PGI, PGII and G-17 levels were detected by ELISA in 68 patients with CAG and 86 healthy volunteers who underwent gastroscopy for gastroduodenal diseases at Taizhou Municipal Hospital between January 2016 and December 2016. Concentrations of all measured serum markers were lower in patients with CAG in comparison to healthy volunteers and achieved statistical significance (p<0.01) in PGI (93.25 vs. 126.98) and PGR (12.67 vs. 17.09). Receiver operating characteristic (ROC) curve analysis revealed the optimal cut-off values for PGI, PGII, PGR and G-17 at 98.10 μg/l, 6.92 ng/l, 15.77 and 1.94 pmol/l, with sensitivities of 72.10%, 58.10%, 61.60% and 59.30%, and specificities of 61.8%, 51.50%, 77.90% and 55.90%, respectively. The areas under the curve (AUCs) of PGI, PGR and G-17 were 0.728, 0.726 and 0.556, respectively. The increase of AUC was observed only in PGR and G-17 combination (0.741) with increased sensitivity (69.10% vs. 61.60%) of screening for CAG, whereas the specificity was reduced (72.10% vs. 77.90%) in comparison to PGR alone. Combination of serum indicators can raise the diagnostic accuracy of CAG in some respects. However, further research including a larger sample size is necessary in order to accurately determine the sensitivity and specificity of combined detection of serum indicators.

Received date: 08/25/2018

Accepted date: 02/20/2019

Ahead of print publish date: 04/25/2019

Issue: 4/2019

Volume: 66

Pages: 637 — 640

Keywords: propepsin, gastrin, chronic atrophic gastritis, pre-canerous lesions,gastric cancer.

DOI: 10.4149/neo_2018_180825N647

Pubmed

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