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Mortality among family members of patients with amyotrophic lateral sclerosis: a Swedish register-based study
Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden; Department of Neurology, Karolinska University Hospital, Stockholm, Sweden.
Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Örebro University, School of Medical Sciences. Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.ORCID iD: 0000-0002-6851-3297
Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden; Department of Neurology, Karolinska University Hospital, Stockholm, Sweden.
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2022 (English)In: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, ISSN 2167-8421, E-ISSN 2167-9223, Vol. 23, no 3-4, p. 226-235Article in journal (Refereed) Published
Abstract [en]

Objective: To test two hypotheses: (1) partners of ALS patients have higher mortality due to outcomes related to psychological distress, and (2) parents and siblings of ALS patients have higher mortality due to diseases that co-occur with ALS.

Methods: We performed a nationwide, register-based cohort study in Sweden. We included ALS-free partners, biological parents and full siblings (N = 11,704) of ALS patients, as well as ALS-free partners, biological parents and full siblings (N = 14,460,150) of ALS-free individuals, and followed them during 1961-2013. Hazard ratios (HRs) and 95% confidence intervals (CIs) of overall and cause-specific mortality were derived from Cox regression.

Results: Partners of ALS patients, compared to partners of ALS-free individuals, displayed higher mortality due to external causes (HR 2.14; 95% CI 1.35-3.41), including suicide (HR 2.44; 95% CI 1.09-5.44) and accidents (HR 2.09; 95% CI 1.12-3.90), after diagnosis of the ALS patients. Parents of ALS patients had a slightly higher overall mortality (HR 1.03; 95% CI 1.00-1.07), compared with parents of ALS-free individuals. This was driven by mortality due to dementias and cardiovascular, respiratory, and skin diseases. Parents of ALS patients had, however, lower mortality than parents of ALS-free individuals due to neoplasms. Siblings of ALS patients had higher mortality due to dementias, and digestive and skin diseases.

Conclusions: Increased mortality due to suicide and accidents among partners of ALS patients is likely attributable to severe psychological distress following the ALS diagnosis. Increased mortality due to dementias among parents and full siblings of ALS patients suggests shared mechanisms between neurodegenerative diseases.

Place, publisher, year, edition, pages
Informa Healthcare, 2022. Vol. 23, no 3-4, p. 226-235
Keywords [en]
Amyotrophic lateral sclerosis, family members, mortality, psychological distress, register-based study
National Category
Neurology
Identifiers
URN: urn:nbn:se:oru:diva-93470DOI: 10.1080/21678421.2021.1953075ISI: 000677260400001PubMedID: 34296642Scopus ID: 2-s2.0-85111439743OAI: oai:DiVA.org:oru-93470DiVA, id: diva2:1584493
Funder
Swedish Research Council, 2019-01088European CommissionThe Karolinska Institutet's Research Foundation
Note

Funding agencies:

Bjorklunds Fund

Neuro Sweden

UllaCarin Lindquist Foundation

Available from: 2021-08-12 Created: 2021-08-12 Last updated: 2023-12-08Bibliographically approved

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Larsson, Henrik

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