Mortality rates and proximal causes of death in patients with Lewy body dementia versus Alzheimer's disease: A longitudinal study using secondary care mental health records

Author:

Kershenbaum Anne D.1ORCID,Price Annabel C.12ORCID,Cardinal Rudolf N.12ORCID,Chen Shanquan3ORCID,Fitzgerald James M.1,Lewis Jonathan1ORCID,Moylett Sinéad3ORCID,O’Brien John T.12ORCID

Affiliation:

1. Cambridgeshire and Peterborough NHS Foundation Trust Fulbourn UK

2. University of Cambridge Fulbourn UK

3. Laboratory of Neuroimmunology KU Leuven Leuven Belgium

Abstract

AbstractBackgroundPrevious studies have shown reduced survival in Lewy body dementia (LBD) compared to Alzheimer’s disease (AD), but the reasons for this are not known. We identified cause of death categories accounting for the reduced survival in LBD.MethodsWe linked cohorts of patients with dementia with Lewy bodies (DLB), Parkinson’s disease dementia (PDD) and AD, with proximal cause of death data. We examined mortality by dementia group and hazard ratios for each death category by dementia group in males and females separately. In a specific focus on the dementia group with the highest mortality rate versus reference, we examined cumulative incidence to identify the main causes of death accounting for the excess deaths.ResultsHazard ratios for death were higher in PDD and DLB compared to AD, for both males and females. PDD males had the highest hazard ratio for death across the dementia comparison groups (HR 2.7, 95% CI 2.2–3.3). Compared with AD, hazard ratios for “nervous system” causes of death were significantly elevated in all LBD groups. Additional significant cause‐of‐death categories included aspiration pneumonia, genitourinary causes, other respiratory causes, circulatory and a “symptoms and signs” category in PDD males; other respiratory causes in DLB males; mental disorders in PDD females; and aspiration pneumonia, genitourinary and other respiratory causes in DLB females.ConclusionFurther research and cohort development is required to investigate differences by age group, to extend cohort follow‐up to the whole population and to investigate the risk‐balance of interventions which may differ by dementia group.

Funder

NIHR Cambridge Biomedical Research Centre

Medical Research Council

Publisher

Wiley

Subject

Psychiatry and Mental health,Geriatrics and Gerontology

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