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Anti-Helicobacter pylori antibody status is associated with cancer mortality: A longitudinal analysis from the Japanese DAIKO prospective cohort study

Paradoxically, patients with advanced stomach cancer who are Helicobacter pylori-positive (HP(+)) have a higher survival rate than those who are HP(-). This finding suggests that HP infection has beneficial effects for cancer treatment. The present study examines whether HP(+) individuals have a low...

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Detalles Bibliográficos
Autores principales: Nishizuka, Satoshi S., Nakatochi, Masahiro, Koizumi, Yuka, Hishida, Asahi, Okada, Rieko, Kawai, Sayo, Sutoh, Yoichi, Koeda, Keisuke, Shimizu, Atsushi, Naito, Mariko, Wakai, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10022139/
https://www.ncbi.nlm.nih.gov/pubmed/36962964
http://dx.doi.org/10.1371/journal.pgph.0001125
Descripción
Sumario:Paradoxically, patients with advanced stomach cancer who are Helicobacter pylori-positive (HP(+)) have a higher survival rate than those who are HP(-). This finding suggests that HP infection has beneficial effects for cancer treatment. The present study examines whether HP(+) individuals have a lower likelihood of death from cancer than those who are HP(-). Prospective cohort data (n = 4,982 subjects enrolled in the DAIKO study between 2008–2010) were used to assess whether anti-HP antibody status was associated with cancer incidence. The median age in the primary registry was 53 years-old (range 35–69 years-old). Over the 8-year observation period there were 234 (4.7%) cancer cases in the cohort and 88 (1.8%) all-cause deaths. Urine anti-HP antibody data was available for all but one participant (n = 4,981; 99.98%). The number of HP(+) and HP(-) individuals was 1,825 (37%) and 3,156 (63%), respectively. Anti-HP antibody distribution per birth year revealed that earlier birth year was associated with higher HP(+) rates. With a birth year-matched cohort (n = 3,376), all-cancer incidence was significantly higher in HP(+) individuals than those who were HP(-) (p = 0.00328), whereas there was no significant difference in the cancer death rate between HP(+) and HP(-) individuals (p = 0.888). Cox regression analysis for prognostic factors revealed that the hazards ratio of HP(+) was 1.59-fold (95%CI 1.17–2.26) higher than HP(-) in all-cancer incidence. Potential systemic effects of HP(+) status may contribute to reduced likelihood of death for patients after an initial diagnosis of cancer.