Role of Helicobacter pylori infection in pernicious anaemia

被引:55
作者
Annibale, B
Lahner, E
Bordi, C
Martino, G
Caruana, P
Grossi, C
Negrini, R
Delle Fave, G
机构
[1] Univ Roma La Sapienza, Policlin Umberto I, Dipartimento Gastroenterol, Med Clin 2, I-00161 Rome, Italy
[2] Univ Parma, I-43100 Parma, Italy
[3] Spedali Civil Brescia, Lab Clin Chem 3, I-25125 Brescia, Italy
关键词
atrophic body gastritis; Helicobacter pylori; pernicious anaemia;
D O I
10.1016/S1590-8658(00)80351-5
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background. Pernicious anaemia is associated with atrophic body gastritis and considered an autoimmune disease. Whether Helicobacter pylori is involved in the induction of pernicious anaemia is uncertain. Aims. To investigate the prevalence of Helicobacter pylori infection in pernicious anaemia patients and to ascertain whether the Helicobacter pylori-positive patients had distinctive clinical and gastric morphofunctional characteristics. Patients and Methods. A series of 81 consecutive pernicious anaemia patients underwent serological functional and endoscopic/histological investigations. Results, A total of 49 (60.5%) patients were Helicobacter pylori-positive (males 61.2% vs females 38.8%). No difference was observed in clinical and morphofunctional characteristics between Helicobacter pylori-positive and negative patients, whereas distinctive functional/histological features between histologically. Helicobacter pylori-positive (n=8) and serologically Helicobacter pylori-positive (n=41) cases were detected. In the histologically Helicobacter pylori-positive group, Pepsinogen I was higher [13 (0-58) vs 5 (0-26) ng/ml; p=0.0025)] and positivity for anti-parietal cell antibodies was lower (42.9% vs 76.9, p=0.0867) Antral histological variables of the gastritis score were significantly higher in the histologically Helicobacter;er pylori-positive than in the serologically Helicobacter pylori-positive patients, but this latter group had a higher score of body atrophy (2.63+/-0.12 vs 1.71+/-0.29; p=0.0051). Body inflammation was also significantly higher in the histologically Helicobacter pylori-positive group (chronic inflammation: 1.43+/-0.2 vs 1.05+/-0.06; p=0.0271; inflammation acitivity: 0.57+/-0.3 vs 0.15+/-0.06, p=0.0220). Antral mucosa was normal in 24/41 (58.5%) of the serologically Helicobacter pylori-positive patients, but only in 1/8 (12.5%) of the histologically Helicobacter pylori-positive patients (p=0.0232). Conclusions. Almost two thirds of pernicious anaemia patients have evidence of Helicobacter pylori, but only those with an active Helicobacter pylori infection have distinctive functional and histological features. These findings support the hypothesis that Helicobacter pylori infection could play a triggering role in a subgroup of pernicious anaemia patients.
引用
收藏
页码:756 / 762
页数:7
相关论文
共 45 条
  • [1] AHMED SA, 1985, AM J PATHOL, V121, P531
  • [2] ANNIBALE B, 1994, ALIMENT PHARM THERAP, V8, P87
  • [3] Atrophic body gastritis: Distinct features associated with Helicobacter pylori infection
    Annibale, B
    Marignani, M
    Azzoni, C
    DAmbra, G
    Caruana, P
    DAdda, T
    DelleFave, G
    Bordi, C
    [J]. HELICOBACTER, 1997, 2 (02) : 57 - 64
  • [4] Annibale B, 2000, ALIMENT PHARM THERAP, V14, P625
  • [5] ANTRAL GASTRIN CELL HYPERFUNCTION IN CHILDREN - A FUNCTIONAL AND IMMUNOCYTOCHEMICAL REPORT
    ANNIBALE, B
    BONAMICO, M
    RINDI, G
    VILLANI, L
    FERRANTE, E
    VANIA, A
    SOLCIA, E
    DELLEFAVE, G
    [J]. GASTROENTEROLOGY, 1991, 101 (06) : 1547 - 1551
  • [6] GASTRITIS - TERMINOLOGY, ETIOLOGY, AND CLINICOPATHOLOGICAL CORRELATIONS - ANOTHER BIASED VIEW
    APPELMAN, HD
    [J]. HUMAN PATHOLOGY, 1994, 25 (10) : 1006 - 1019
  • [7] Bugs on trial:: the case of Helicobacter pylori and autoimmunity
    Appelmelk, BJ
    Faller, G
    Claeys, D
    Kirchner, T
    Vandenbroucke-Grauls, CMJE
    [J]. IMMUNOLOGY TODAY, 1998, 19 (07): : 296 - 299
  • [8] Bordi C, 1997, J PATHOL, V182, P339, DOI 10.1002/(SICI)1096-9896(199707)182:3<339::AID-PATH854>3.0.CO
  • [9] 2-V
  • [10] DELLEFAVE G, 1983, GUT, V24, P231