Introduction: Dementia predicts increased mortality. We used case-control and co-twin control models to investigate genetic and shared environmental influences on this association.
Methods: Case-control design, including 987 twins with dementia and 2938 age- and sex-matched controls in the Swedish Twin Registry. Co-twin control design, including 90 monozygotic (MZ) and 288 dizygotic (DZ) twin pairs discordant for dementia. To test for genetic and environmental confounding, differences were examined in mortality risk between twins with dementia and their matched or co-twin controls.
Results: Twins with dementia showed greater mortality risk than age- and sex-matched controls (HR = 2.02 [1.86, 2.18]). Mortality risk is significantly elevated but attenuated substantially in discordant twin pairs, for example, comparing MZ twins with dementia to their co-twin controls (HR = 1.48 [1.08, 2.04]).
Discussion: Findings suggest that genetic factors partially confound the association between dementia and mortality and provide an alternative hypothesis to increased mortality due to dementia itself. Highlights We studied dementia and mortality in twin pairs discordant for dementia. People without dementia outlived people with dementia. Identical twins with dementia and their co-twin controls had similar survival time. Findings suggest genotype may explain the link between dementia and mortality.
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http://dx.doi.org/10.1002/alz.13553 | DOI Listing |
Ann Neurol
December 2024
Department of Neurology, Faculty of Medicine, Juntendo University, Tokyo, Japan.
Objective: Variants in PRKN and PINK1 are the leading cause of early-onset autosomal recessive Parkinson's disease, yet many cases remain genetically unresolved. We previously identified a 7 megabases complex structural variant in a pair of monozygotic twins using Oxford Nanopore Technologies (ONT) long-read sequencing. This study aims to determine if ONT long-read sequencing can detect a second variant in other unresolved early-onset Parkinson's disease (EOPD) cases with 1 heterozygous PRKN or PINK1 variant.
View Article and Find Full Text PDFEur Stroke J
November 2024
Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital, Liverpool, UK.
Introduction: The risk of dementia in patients with stroke-heart syndrome (SHS) remains unexplored.
Patients And Methods: Retrospective analysis using the TriNetX network, including patients with ischaemic stroke from 2010 to 2020. These patients were categorised into two groups: those with SHS (heart failure, myocardial infarction, ventricular fibrillation, or Takotsubo cardiomyopathy within 30 days post-stroke) and those without SHS.
Comput Biol Med
December 2024
Centre for Vision, Speech and Signal Processing, University of Surrey, Guildford, Surrey, United Kingdom; UK Dementia Research Institute Care Research and Technology Centre, Imperial College, London, United Kingdom.
Background: Sensor-based remote health monitoring is increasingly used to detect adverse health in people living with dementia (PLwD) at home, aiming to prevent hospitalizations and reduce caregiver burden. However, home sensor data is often noisy, overly granular, and suffers from unreliable labeling, data drift and high variability between households. Current anomaly detection methods lack generalizability and personalization, often requiring anomaly-free training data and frequent model updates.
View Article and Find Full Text PDFmedRxiv
June 2024
Department of Neurology, Faculty of Medicine, Juntendo University, Tokyo, Japan.
Background: Mutations within the genes and are the leading cause of early onset autosomal recessive Parkinson's disease (PD). However, the genetic cause of most early-onset PD (EOPD) cases still remains unresolved. Long-read sequencing has successfully identified many pathogenic structural variants that cause disease, but this technology has not been widely applied to PD.
View Article and Find Full Text PDFIntroduction: This study investigates the relationship between cognitive functioning and 59 modifiable and intrinsic factors at the cusp of midlife.
Methods: We analyzed data from 1221 participants in the Colorado Adoption/Twin Study of Lifespan behavioral development and cognitive aging (CATSLife; M= 33.20, %Female = 52.
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