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The Relationship between Helicobacter pylori and Beta-2 Microglobulin in Humans

H. pylori is related to various gastrointestinal diseases. β (2) Microglobulin (β (2)M) is an intrinsic element of major histocompatibility complex (MHC I). Serum β (2)M level may increase in inflammatory states. The aim of current study is to evaluate the relationship between β (2)M and H. pylori b...

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Detalles Bibliográficos
Autores principales: Yeniova, Abdullah Özgür, Kucukazman, Metin, Ata, Naim, Dal, Kursat, Kefeli, Ayşe, Başyiğit, Sebahat, Aktaş, Bora, Akın, Kadir Okhan, Nazlıgül, Yaşar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163436/
https://www.ncbi.nlm.nih.gov/pubmed/25243160
http://dx.doi.org/10.1155/2014/615089
Descripción
Sumario:H. pylori is related to various gastrointestinal diseases. β (2) Microglobulin (β (2)M) is an intrinsic element of major histocompatibility complex (MHC I). Serum β (2)M level may increase in inflammatory states. The aim of current study is to evaluate the relationship between β (2)M and H. pylori bearing CagA strains. Methods. H. pylori status was determined by histopathology of samples taken from stomach. CagA status and β (2)M level were measured from blood samples of patients. Eradication therapy was administered to the patients with H. pylori infection. β (2) Microglobulin levels were measured before and after treatment. Results. 35 (29.2%) H. pylori(−) patients and 85 (70.8%) H. pylori (+) patients were included in the study. There were 52 (43.3%) patients with CagA negative and 33 (27.5%) patients with CagA positive H. pylori infection. The mean serum β (2)M level was 1.83 mg/L in H. pylori (−) group, 1.76 mg/L in H. pylori (+) CagA (−) group, and 1.93 mg/L in H. pylori and CagA (+) group (P > 0.05). Serum β (2)M levels (1.82 versus 1.64 mg/L P < 0.05) were decreased after eradication. Conclusion. H. pylori and CagA status did not affect β (2)M level. Relationship between low grade systematic inflammation and H. pylori should be investigated to find out new predictors for diseases associated with inflammation.