Serum pepsinogen I, pepsinogen II, and gastrin 17 in relatives of gastric cancer patients: Comparative study with type and severity of gastritis

被引:54
作者
Haj-Sheykholeslami, Arghavan [1 ]
Rakhshani, Naser [1 ,2 ]
Amirzargar, Aliakbar
Rafiee, Reza [3 ]
Shahidi, S. Mehdi [2 ,4 ]
Nikbin, Behrouz
Khosravi, Farideh
Massarrat, Sadegh [1 ]
机构
[1] Shariati Hosp, Digest Dis Res Ctr, Dept Gastroenterol, Tehran, Iran
[2] Univ Tehran, Sina Hosp Med Sch, Tehran, Iran
[3] Shahid Beheshti Univ Med Sci, Dept Pathol, Shohada Hosp, Tehran, Iran
[4] Iran Univ Med Sci, Gastrointestinal & Liver Dis Ctr, Tehran, Iran
关键词
D O I
10.1016/j.cgh.2007.11.016
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: First-degree relatives of gastric cancer patients are at risk for developing precancerous conditions. The aim of this study was to investigate the potential of biomarkers pepsinogen I (PGI), pepsinogen II (PGII), their ratio (PG I:II), as well as gastrin 17 for screening of precancerous conditions and corpus predominant gastritis. MethodS: First-degree relatives of gastric cancer patients underwent endoscopy. Three biopsy specimens from the antrum and 3 from the corpus were evaluated according to the Sydney classification. Serum was taken for the measurement of fasting PGI, PGII, and gastrin 17 by enzyme-linked immunosorbent assay kits. Results: A total of 481 patients were examined (age, 47.8 +/- 6.7 y). With the extension of gastritis, PGII was increased up to 2.5 times (6.6 +/- 2.8 mu g/mL in normal mucosa, 9.5 +/- 6.7 mu g/mL in antral gastritis, and 16.9 +/- 12.4 mu g/mL in corpus-predominant gastritis; P <.01), PGI increased slightly (88.3 +/- 29.4 mu g/ml, in normal mucosa and 111.2 +/- 71.4 mu g/mL in corpus-predominant gastritis), and gastrin 17 was increased substantially in corpus-predominant gastritis (15.3 +/- 19.5 pmol/mL vs 3.8 +/- 5.7 pmol/mL in normal mucosa). By using a cut-off value of 7.5 mu g/mL for PGII, any type of gastritis from normal mucosa can be diagnosed with a sensitivity and specificity of 80%. The sensitivity and specificity of the PG I:II ratio (<= 3) and gastrin 17 (> 17 pmol/mL) together were 9.4% and 99% for screening corpus-predominant gastritis and 14.8% and 97.8%, respectively, for screening intestinal metaplasia in the corpus. Conclusions: PGII is a suitable marker for screening any gastritis from normal mucosa, but neither PGI, the PG I:II ratio, gastrin 17, nor their combination were able to select those with precancerous conditions and corpus-predominant gastritis among the first-degree relatives of gastric cancer patients.
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页码:174 / 179
页数:6
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