PT  - JOURNAL ARTICLE
AU  - A Oksanen
AU  - P Sipponen
AU  - R Karttunen
AU  - A Miettinen
AU  - L Veijola
AU  - S Sarna
AU  - H Rautelin
TI  - Atrophic gastritis and <em>Helicobacter pylori</em> infection in outpatients referred for gastroscopy
AID  - 10.1136/gut.46.4.460
DP  - 2000 Apr 01
TA  - Gut
PG  - 460--463
VI  - 46
IP  - 4
4099  - http://gut.bmj.com/content/46/4/460.short
4100  - http://gut.bmj.com/content/46/4/460.full
SO  - Gut2000 Apr 01; 46
AB  - BACKGROUND Atrophic gastritis has been shown to be one of the long term sequelae ofHelicobacter pylori infection. AIMS To determine the prevalence of atrophic gastritis in outpatients, to study the accuracy of serological methods for revealing atrophy, and to define the association of H pylori infection with atrophic gastritis in these patients. PATIENTS/METHODS A total of 207 consecutive outpatients referred for gastroscopy were included. Biopsy specimens from the antrum and corpus were assessed histologically according to the Sydney system. Serum samples were studied for H pylori IgG and IgA antibodies by enzyme immunoassay, CagA antibodies by immunoblot, pepsinogen I by an immunoenzymometric assay, gastrin by radioimmunoassay, and parietal cell antibodies by indirect immunofluorescence. RESULTS Histological examination revealed atrophic gastritis in 52 (25%) of 207 patients.H pylori and CagA antibodies were strongly associated with atrophic antral gastritis but poorly associated with atrophic corpus gastritis. Low serum pepsinogen I was the most sensitive and specific indicator of moderate and severe atrophic corpus gastritis. All six patients with moderate atrophic corpus gastritis hadH pylori infection but eight of 10 patients with severe atrophic corpus had increased parietal cell antibodies and nine had no signs of H pyloriinfection. CONCLUSIONS Atrophic antral gastritis was strongly associated with CagA positiveH pylori infection. Severe atrophic corpus gastritis was not determined by H pyloritests but low serum pepsinogen I, high gastrin, and parietal cell antibodies may be valuable in detecting these changes.