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Hospital-treated infections and subsequent Parkinson's disease risk: a register-based sibling comparison study
Örebro University, School of Medical Sciences. Clinical Epidemiology and Biostatistics, School of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.ORCID iD: 0000-0003-1030-3470
Clinical Epidemiology and Biostatistics, School of Medical Sciences, Faculty of Medicine and Health, Örebro University, 703 62 Örebro, Sweden.ORCID iD: 0000-0002-2088-0530
Örebro University, School of Medical Sciences. Clinical Epidemiology and Biostatistics, School of Medical Sciences, Faculty of Medicine and Health, Örebro University, 703 62 Örebro, Sweden; Nutrition-Gut-Brain Interactions Research Centre, School of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.ORCID iD: 0000-0003-4713-907x
Örebro University, School of Medical Sciences. Nutrition-Gut-Brain Interactions Research Centre, School of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.ORCID iD: 0000-0002-0362-0008
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2024 (English)In: Brain Communications, E-ISSN 2632-1297, Vol. 6, no 2, article id fcae098Article in journal (Refereed) Published
Abstract [en]

Serious infections may result in greater risk of Parkinson's disease. However, high-quality cohort studies focusing on a potential causal role of different types and sites of infection are lacking. Gastrointestinal infections are of a particular interest due to growing evidence implicating gut dysbiosis in Parkinson's disease aetiology. This population-based cohort study used the Swedish Total Population Register to identify individuals born during 1944-77 and resident in Sweden between 1990 and 2018 (N = 3 698 319). Hospital-treated infections at ages 21-30 and 31-40 years were identified from the National Patient Register. Participants were followed to identify Parkinson's disease diagnoses from age 41 years up to December 31, 2018, when the oldest individual reached 75 years. Cox regression with a sibling comparison design to tackle familial genetic and environmental confounding was used to derive hazard ratios and 95% confidence intervals for each infection site, type, or any infections at ages 21-30 and 31-40 years. During a median follow-up of 15.4 years, 8815 unique Parkinson's disease diagnoses were accrued, with a crude rate of 17.3 (95% confidence interval 17.0, 17.7) per 100 000 person-years. After controlling for shared familial factors, hospital-treated gastrointestinal and respiratory infections between 21 and 30 years of age were associated with a greater risk of Parkinson's disease [hazard ratios 1.35 (95% confidence interval: 1.05, 1.75) and 1.45 (95% confidence interval: 1.08, 1.95), respectively]; no association was found for any infections at age 31-40 [hazard ratio 1.05 (95% confidence interval: 0.93, 1.19)]. After adjustment, no statistically significant associations were observed for other sites including genitourinary and skin. These findings suggest that hospital-treated infections of the gastrointestinal tract and lungs, both of which may have an influence on the gut microbiome, by age 30 years may be risk factors for Parkinson's disease.

Place, publisher, year, edition, pages
Oxford University Press, 2024. Vol. 6, no 2, article id fcae098
Keywords [en]
Cohort study, neurodegeneration
National Category
Gerontology, specialising in Medical and Health Sciences
Identifiers
URN: urn:nbn:se:oru:diva-112916DOI: 10.1093/braincomms/fcae098ISI: 001216872600001PubMedID: 38562309Scopus ID: 2-s2.0-85189693358OAI: oai:DiVA.org:oru-112916DiVA, id: diva2:1849737
Funder
Forte, Swedish Research Council for Health, Working Life and Welfare, 2019-01236Nyckelfonden
Note

This study was supported by grants from the Swedish Research Council for Health, Working Life and Welfare (Forte) (grant number 2019-01236), Nyckelfonden and the UK Economic and Social Research Council (ESRC) to the International Centre for Life Course Studies (ES/R008930/1).

Available from: 2024-04-08 Created: 2024-04-08 Last updated: 2024-07-23Bibliographically approved

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Vingeliene, SnieguoleLentjes, MarleenBrummer, Robert J.Fall, KatjaMontgomery, Scott

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