Clinically apparent Helicobacter pylori infection and the risk of incident Alzheimer's disease: A population‐based nested case‐control study

Author:

Douros Antonios1234,Ante Zharmaine3,Fallone Carlo A.15,Azoulay Laurent236,Renoux Christel237,Suissa Samy123,Brassard Paul123ORCID

Affiliation:

1. Department of Medicine McGill University Montreal Quebec Canada

2. Department of Epidemiology Biostatistics, and Occupational Health McGill University Montreal Quebec Canada

3. Centre for Clinical Epidemiology, Lady Davis Institute Montreal Quebec Canada

4. Institute of Clinical Pharmacology and Toxicology Charité ‐ Universitätsmedizin Berlin Berlin Germany

5. Division of Gastroenterology McGill University Health Center McGill University Montreal Quebec Canada

6. Gerald Bronfman Department of Oncology McGill University Montreal Quebec Canada

7. Department of Neurology and Neurosurgery McGill University Montreal Quebec Canada

Abstract

AbstractINTRODUCTIONOur population‐based study assessed whether clinically apparent Helicobacter pylori infection (CAHPI) is associated with the risk of Alzheimer's disease (AD).METHODSWe assembled a population‐based cohort of all dementia‐free subjects in the United Kingdom's Clinical Practice Research Datalink (UK CPRD), aged ≥50 years (1988–2017). Using a nested case‐control approach, we matched each newly developed case of AD with 40 controls. Conditional logistic regression estimated odds ratios (ORs) with 95% confidence intervals (CIs) of AD associated with CAHPI compared with no CAHPI during ≥2 years before the index date. We also used salmonellosis as a negative control exposure.RESULTSAmong 4,262,092 dementia‐free subjects, 40,455 developed AD after a mean 11 years of follow‐up. CAHPI was associated with an increased risk of AD (OR, 1.11; 95% CI, 1.01–1.21) compared with no CAHPI. Salmonellosis was not associated with the risk of AD (OR, 1.03; 95% CI, 0.82–1.29).DISCUSSIONCAHPI was associated with a moderately increased risk of AD.Highlights CAHPI was associated with an 11% increased risk of AD in subjects aged ≥50 years. The increase in the risk of AD reached a peak of 24% a decade after CAHPI onset. There was no major effect modification by age or sex. Sensitivity analyses addressing several potential biases led to consistent results.

Funder

Canadian Institutes of Health Research

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology

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