Cargando…
Differential effects of sex on longitudinal patterns of cognitive decline in Parkinson’s disease
BACKGROUND: Cognitive impairment is an important and diverse symptom of Parkinson’s disease (PD). Sex is a purported risk variable for cognitive decline in PD, but has not been comprehensively investigated. OBJECTIVES: This cross-sectional and longitudinal study examined sex differences in global an...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8068663/ https://www.ncbi.nlm.nih.gov/pubmed/33399968 http://dx.doi.org/10.1007/s00415-020-10367-8 |
_version_ | 1783683063593566208 |
---|---|
author | Bakeberg, Megan C. Gorecki, Anastazja M. Kenna, Jade E. Jefferson, Alexa Byrnes, Michelle Ghosh, Soumya Horne, Malcolm K. McGregor, Sarah Stell, Rick Walters, Sue Chivers, Paola Winter, Samantha J. Mastaglia, Frank L. Anderton, Ryan S. |
author_facet | Bakeberg, Megan C. Gorecki, Anastazja M. Kenna, Jade E. Jefferson, Alexa Byrnes, Michelle Ghosh, Soumya Horne, Malcolm K. McGregor, Sarah Stell, Rick Walters, Sue Chivers, Paola Winter, Samantha J. Mastaglia, Frank L. Anderton, Ryan S. |
author_sort | Bakeberg, Megan C. |
collection | PubMed |
description | BACKGROUND: Cognitive impairment is an important and diverse symptom of Parkinson’s disease (PD). Sex is a purported risk variable for cognitive decline in PD, but has not been comprehensively investigated. OBJECTIVES: This cross-sectional and longitudinal study examined sex differences in global and domain-specific cognitive performance in a large PD cohort. METHODS: Cognitive function was evaluated using the Addenbrooke’s Cognitive Examination in 392 people with PD (PwP) from the Australian Parkinson’s Disease Registry. The influence of sex on domain-specific cognitive performance was investigated using covariate-corrected generalised linear models. In a repeated measures longitudinal subset of 127 PwP, linear mixed models were used to assess the impact of sex on cognition over time, while accounting for covariates. RESULTS: Cross-sectional-corrected modelling revealed that sex was significantly predictive of cognitive performance, with males performing worse than females on global cognition, and memory and fluency domains. Longitudinally, sex was significantly predictive of cognitive decline, with males exhibiting a greater reduction in global cognition and language, whereas females showed a greater decline in attention/orientation, memory and visuospatial domains, despite starting with higher baseline scores. At follow-up, a significantly higher proportion of males than females fulfilled criteria for mild cognitive impairment or PD dementia. CONCLUSIONS: Sex was revealed as a significant determinant of overall cognitive performance as well as specific cognitive domains, with a differential pattern of decline in male and female participants. Such sex-specific findings appear to explain some of the heterogeneity observed in PD, warranting further investigation of mechanisms underlying this sexual dimorphism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-020-10367-8. |
format | Online Article Text |
id | pubmed-8068663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-80686632021-05-05 Differential effects of sex on longitudinal patterns of cognitive decline in Parkinson’s disease Bakeberg, Megan C. Gorecki, Anastazja M. Kenna, Jade E. Jefferson, Alexa Byrnes, Michelle Ghosh, Soumya Horne, Malcolm K. McGregor, Sarah Stell, Rick Walters, Sue Chivers, Paola Winter, Samantha J. Mastaglia, Frank L. Anderton, Ryan S. J Neurol Original Communication BACKGROUND: Cognitive impairment is an important and diverse symptom of Parkinson’s disease (PD). Sex is a purported risk variable for cognitive decline in PD, but has not been comprehensively investigated. OBJECTIVES: This cross-sectional and longitudinal study examined sex differences in global and domain-specific cognitive performance in a large PD cohort. METHODS: Cognitive function was evaluated using the Addenbrooke’s Cognitive Examination in 392 people with PD (PwP) from the Australian Parkinson’s Disease Registry. The influence of sex on domain-specific cognitive performance was investigated using covariate-corrected generalised linear models. In a repeated measures longitudinal subset of 127 PwP, linear mixed models were used to assess the impact of sex on cognition over time, while accounting for covariates. RESULTS: Cross-sectional-corrected modelling revealed that sex was significantly predictive of cognitive performance, with males performing worse than females on global cognition, and memory and fluency domains. Longitudinally, sex was significantly predictive of cognitive decline, with males exhibiting a greater reduction in global cognition and language, whereas females showed a greater decline in attention/orientation, memory and visuospatial domains, despite starting with higher baseline scores. At follow-up, a significantly higher proportion of males than females fulfilled criteria for mild cognitive impairment or PD dementia. CONCLUSIONS: Sex was revealed as a significant determinant of overall cognitive performance as well as specific cognitive domains, with a differential pattern of decline in male and female participants. Such sex-specific findings appear to explain some of the heterogeneity observed in PD, warranting further investigation of mechanisms underlying this sexual dimorphism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-020-10367-8. Springer Berlin Heidelberg 2021-01-05 2021 /pmc/articles/PMC8068663/ /pubmed/33399968 http://dx.doi.org/10.1007/s00415-020-10367-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Communication Bakeberg, Megan C. Gorecki, Anastazja M. Kenna, Jade E. Jefferson, Alexa Byrnes, Michelle Ghosh, Soumya Horne, Malcolm K. McGregor, Sarah Stell, Rick Walters, Sue Chivers, Paola Winter, Samantha J. Mastaglia, Frank L. Anderton, Ryan S. Differential effects of sex on longitudinal patterns of cognitive decline in Parkinson’s disease |
title | Differential effects of sex on longitudinal patterns of cognitive decline in Parkinson’s disease |
title_full | Differential effects of sex on longitudinal patterns of cognitive decline in Parkinson’s disease |
title_fullStr | Differential effects of sex on longitudinal patterns of cognitive decline in Parkinson’s disease |
title_full_unstemmed | Differential effects of sex on longitudinal patterns of cognitive decline in Parkinson’s disease |
title_short | Differential effects of sex on longitudinal patterns of cognitive decline in Parkinson’s disease |
title_sort | differential effects of sex on longitudinal patterns of cognitive decline in parkinson’s disease |
topic | Original Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8068663/ https://www.ncbi.nlm.nih.gov/pubmed/33399968 http://dx.doi.org/10.1007/s00415-020-10367-8 |
work_keys_str_mv | AT bakebergmeganc differentialeffectsofsexonlongitudinalpatternsofcognitivedeclineinparkinsonsdisease AT goreckianastazjam differentialeffectsofsexonlongitudinalpatternsofcognitivedeclineinparkinsonsdisease AT kennajadee differentialeffectsofsexonlongitudinalpatternsofcognitivedeclineinparkinsonsdisease AT jeffersonalexa differentialeffectsofsexonlongitudinalpatternsofcognitivedeclineinparkinsonsdisease AT byrnesmichelle differentialeffectsofsexonlongitudinalpatternsofcognitivedeclineinparkinsonsdisease AT ghoshsoumya differentialeffectsofsexonlongitudinalpatternsofcognitivedeclineinparkinsonsdisease AT hornemalcolmk differentialeffectsofsexonlongitudinalpatternsofcognitivedeclineinparkinsonsdisease AT mcgregorsarah differentialeffectsofsexonlongitudinalpatternsofcognitivedeclineinparkinsonsdisease AT stellrick differentialeffectsofsexonlongitudinalpatternsofcognitivedeclineinparkinsonsdisease AT walterssue differentialeffectsofsexonlongitudinalpatternsofcognitivedeclineinparkinsonsdisease AT chiverspaola differentialeffectsofsexonlongitudinalpatternsofcognitivedeclineinparkinsonsdisease AT wintersamanthaj differentialeffectsofsexonlongitudinalpatternsofcognitivedeclineinparkinsonsdisease AT mastagliafrankl differentialeffectsofsexonlongitudinalpatternsofcognitivedeclineinparkinsonsdisease AT andertonryans differentialeffectsofsexonlongitudinalpatternsofcognitivedeclineinparkinsonsdisease |