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Age-Specific Gastric Cancer Risk Indicated by the Combination of Helicobacter Pylori Sero-Status and Serum Pepsinogen Levels Pubmed



Eybpoosh S1, 2 ; Talebkhan Y1 ; Saberi S1 ; Esmaeili M1 ; Oghalaie A1 ; Ebrahimzadeh F1 ; Karimi T1 ; Abdirad A3 ; Nahvijou A4 ; Mohagheghi MA4 ; Hosseini ME5 ; Mohammadi M1
Authors
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Authors Affiliations
  1. 1. HPGC Group, Dept. of Medical Biotechnology, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran
  2. 2. Research Center for Modeling in Health, Institute for Futures Studies in Health, Kerman University of Medical Sciences, Kerman, Iran
  3. 3. Cancer Institute, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Cancer Research Center, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Dept. of Gastroenterology, Amiralam Hospital, Tehran University of Medical Sciences, Tehran, Iran

Source: Iranian Biomedical Journal Published:2015


Abstract

Background: Serologic screening of gastric cancer (GC) by serum pepsinogens (sPG) levels and Helicobacter pylori (Hp) sero-status, though highly informative, has provided heterogeneous results. Here, we have evaluated the modifying effects of demographic factors on the risk impact of Hp sero-status/sPG levels in gastric cancer, with particular emphasis on age. Methods: A cross-sectional study was carried out on 1341 individuals (GC = 578, healthy = 763), who were stratified into two age groups: 35-59 years (middle-aged, n = 830) and ≥ 60 years (60 years-plus, n = 511). Demographic factors and serological states (Hp sero-staus and sPG levels) were recorded by subject interview and serum ELISAs, respectively. Covariate-specific odds ratios were calculated by multivariable logistic regression. Results: Hp infection was consistently associated with increased sPGI and sPGII levels in the 60 year-plus, but not the middle-aged group. The joint examination of the variable states of the three serum biomarkers (Hp serology, sPGI, and sPGI/II ratio), in the 60 year-plus age group, demonstrated a stepwise escalation of risk from the single (sPGIlow; OR = 2.6), to double (sPGIlow/sPGI/IIlow; OR = 3.55, and Hppositive/sPGIlow; OR = 5.0) and ultimately triple (Hppositive/PGIlow/PGI/IIlow; OR = 10.48) positive states, in reference to the triple negatives. However, this pattern was not exhibited in the middle-aged subjects. Conclusion: Age was clearly identified as a modifying factor on the risk projection of the combined states of Hp serology and sPG levels in gastric cancer screening, reflected by the augmented (~10.5 fold) risk of GC in the triple positive (Hppositive/sPGIlow/sPGI/IIlow) 60 year-plus subjects, which was not evident in the middle-aged group. © 2015, Pasteur Institute of Iran. All rights reserved.