YOUNG ONSET PEPTIC-ULCER DISEASE AND NONULCER DYSPEPSIA ARE SEPARATE ENTITIES

被引:8
作者
CEDERBERG, A
VARIS, K
SALMI, HA
SIPPONEN, P
HARKONEN, M
SARNA, S
机构
[1] CENT MIL HOSP,MANNERHEIMINTIE 164 A,SF-00300 HELSINKI,FINLAND
[2] MALMINTORI MED CTR,HELSINKI,FINLAND
[3] JORVI HOSP,ESPOO,FINLAND
[4] UNIV HELSINKI,DEPT CLIN CHEM,SF-00100 HELSINKI 10,FINLAND
[5] UNITED LABS,HELSINKI,FINLAND
关键词
PEPTIC ULCER; NONULCER DYSPEPSIA; GASTRITIS; HELICOBACTER-PYLORI; GASTRIC SECRETION; PEPSINOGENS; GASTRIN; ABO-BLOOD GROUPS; LEWISA+ PHENOTYPE; SECRETOR STATUS;
D O I
10.3109/00365529109103985
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The characteristics of peptic ulcer and non-ulcer dyspepsia in young men were studied in 202 consecutive conscripts who attended Central Military Hospital in Helsinki because of long-standing upper abdominal complaints. Active peptic ulceration (APU) was found in 48 patients, inactive peptic ulcer disease (IPU) was diagnosed in 77 patients, non-ulcer dyspepsia (NUD) was diagnosed in 52 patients. In 25 cases the reason for symptoms was another disease, and these patients were excluded from the study. A control series (CON) consisted of 30 symptomless healthy young male volunteers. The likelihood of discriminating between peptic ulcer disease and non-ulcer dyspepsia in a young male patient with dyspepsia are indicated by odds ratios (OR) and its 95% confidence limits (CL 95). Active peptic ulcer disease differs from NUD, e.g., by 1) presence of antrum gastritis, OR 41.5 (CL 95: 10.1-171), 2) Helicobacter pylori in the gastric mucosa, OR 31.0 (7.4-130), 3) Lewis(a+) phenotype, OR 8.9 (1.7-45.4), 4) serum pepsinogen I (S-PGI) > 100-mu-g/l, OR 4.6 (1.7-12.4), 5) non-secretor status, OR 4.3 (1.6-11.6), and 6) O-blood group, OR 3.0 (1.2-7.7). In conclusion, the status of gastroduodenal mucosa, gastric secretion pattern and distribution of some genetic markers in patient series indicate that young onset peptic ulcer and non-ulcer dyspepsia are two separate entities. Helicobacter-positive antrum gastritis is the best determinant of ulcer risk, but also high S-PGI, Lewis(a+) phenotype, non-secretor status and O-blood group are signs of increased risk of peptic ulcer.
引用
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页码:33 / 44
页数:12
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