Circulating anti-Helicobacter pylori immunoglobulin A antibodies and low serum pepsinogen I level are associated with increased risk of gastric cancer

被引:89
作者
Aromaa, A
Kosunen, TU
Knekt, P
Maatela, J
Teppo, L
Heinonen, OP
Harkonen, M
Hakama, MK
机构
[1] SOCIAL INSURANCE INST, HELSINKI, FINLAND
[2] SOCIAL INSURANCE INST, TURKU, FINLAND
[3] HELSINKI UNIV, DEPT BACTERIOL & IMMUNOL, HELSINKI, FINLAND
[4] FINNISH CANC REGISTRY, SF-00170 HELSINKI, FINLAND
[5] HELSINKI UNIV, DEPT PUBL HLTH, HELSINKI, FINLAND
[6] HELSINKI UNIV, DEPT CLIN CHEM, HELSINKI, FINLAND
[7] TAMPERE UNIV, DEPT PUBL HLTH, SF-33101 TAMPERE, FINLAND
关键词
Helicobacter pylori; IgA; IgG; longitudinal studies; pepsinogen; stomach neoplasms;
D O I
10.1093/oxfordjournals.aje.a008901
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Helicobacter pylori infection has been suggested to be associated with an increased risk of gastric cancer, and low levels of serum pepsinogen I (PG I) have been linked to atrophic gastritis, which is a risk factor for gastric cancer, In Finland, 39,268 persons from 25 cohorts participated during 1968-1972 in a health examination survey and were followed for up to 13 years. A nested case-control study was performed on 84 stomach cancer patients identified from the Finnish Cancer Registry and 146 controls matched for age, sex, acid municipality, Serum samples drawn at the baseline study were analyzed. An elevated level of serum anti-H. pylori immunoglobulin A (IgA) antibodies (a titer greater than or equal to 70) and a low serum PG I level (<49 mu g/liter) were associated with an increased risk of gastric cancer. The odds ratios were 2.52 (95% confidence interval (CI) 1.14-5.57) for high IgA and 2.68 (95% CI 1.35-5.30) for low PG I. For high immunoglobulin G (IgG) (greater than or equal to 700), the odds ratio was only 1.50 (95% CI 0.70-3.22). When both high IgA and low PG I were present, the odds ratio was 5.96 (95% CI 2.02-17.57). The association of H. pylori infection with cancer became stronger with longer follow-up times, whereas that of low PG I was strongest at shorter follow-up times, Our findings support the hypothesis that H. pylori infection is a prevalent and potentially preventable cause of gastric cancer. They stress the value of IgA antibody determinations and provide new evidence for a pathogenesis leading from prolonged infection through atrophic gastritis to gastric cancer.
引用
收藏
页码:142 / 149
页数:8
相关论文
共 38 条
  • [1] AROMAA A, 1981, EPIDEMIOLOGY PUBLIC
  • [2] THE COHORT EFFECT AND HELICOBACTER-PYLORI
    BANATVALA, N
    MAYO, K
    MEGRAUD, F
    JENNINGS, R
    DEEKS, JJ
    FELDMAN, RA
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1993, 168 (01) : 219 - 221
  • [3] HELICOBACTER-PYLORI AND THE PATHOGENESIS OF GASTRODUODENAL INFLAMMATION
    BLASER, MJ
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1990, 161 (04) : 626 - 633
  • [4] BLASER MJ, 1994, 7 WORKSH GASTR PATH
  • [5] BRENES F, 1993, AM J GASTROENTEROL, V88, P1870
  • [6] BRESLOW NE, 1980, 32 IARC SCI, V1
  • [7] CORREA P, 1990, CANCER RES, V50, P4737
  • [8] SYSTEMIC AND MUCOSAL HUMORAL RESPONSES TO HELICOBACTER-PYLORI IN GASTRIC-CANCER
    CRABTREE, JE
    WYATT, JI
    SOBALA, GM
    MILLER, G
    TOMPKINS, DS
    PRIMROSE, JN
    MORGAN, AG
    [J]. GUT, 1993, 34 (10) : 1339 - 1343
  • [9] FARINATI F, 1991, ITAL J GASTROENTEROL, V23, P194
  • [10] CYTO-TOXIN PRODUCTION BY CAMPYLOBACTER-PYLORI STRAINS ISOLATED FROM PATIENTS WITH PEPTIC-ULCERS AND FROM PATIENTS WITH CHRONIC GASTRITIS ONLY
    FIGURA, N
    GUGLIELMETTI, P
    ROSSOLINI, A
    BARBERI, A
    CUSI, G
    MUSMANNO, RA
    RUSSI, M
    QUARANTA, S
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1989, 27 (01) : 225 - 226