Characterizing the contribution of alcohol use towards neuropsychological profiles in mild cognitive impairment

Guardat en:
Dades bibliogràfiques
Publicat a:Alzheimer's & Dementia vol. 21 (Dec 1, 2025)
Autor principal: Cuperfain, Ari
Altres autors: Pishdadian, Sara, Binns, Malcolm A, Black, Sandra E., Chertkow, Howard, Freedman, Morris, Louis, Janine, Ma, Clement, Masellis, Mario, McLaughlin, Paula M, Ramirez, Joel, Tang‐Wai, David F., Tartaglia, Carmela, Kumar, Sanjeev
Publicat:
John Wiley & Sons, Inc.
Matèries:
Accés en línia:Citation/Abstract
Full Text - PDF
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

MARC

LEADER 00000nab a2200000uu 4500
001 3286416819
003 UK-CbPIL
022 |a 1552-5260 
022 |a 1552-5279 
024 7 |a 10.1002/alz70857_100017  |2 doi 
035 |a 3286416819 
045 0 |b d20251201 
100 1 |a Cuperfain, Ari  |u University of Toronto Temerty Faculty of Medicine, Toronto, ON, Canada, 
245 1 |a Characterizing the contribution of alcohol use towards neuropsychological profiles in mild cognitive impairment 
260 |b John Wiley & Sons, Inc.  |c Dec 1, 2025 
513 |a Journal Article 
520 3 |a Background Excessive alcohol use is known to increase the risk of dementia, however, how alcohol specifically effects cognition in patients with neurocognitive disorders is unclear. In this study, we characterized the effects of excessive alcohol use on cognitive domains in those with mild cognitive impairment (MCI). Method Two multicenter cohorts, the Comprehensive Assessment of Neurodegeneration and Dementia and the Ontario Neurodegenerative Disease Research Initiative, provided data for this study. Participants were diagnosed with MCI due to Alzheimer's disease (AD‐MCI) or cerebro‐vascular disease (V‐MCI), and were categorized based on their current and past alcohol use into ‘zero’, ‘low‐medium’ (less than 1 to 7 standard drinks/week), or ‘high’ (>7 standard drinks/week) alcohol use groups. We generated age‐corrected composite cognitive domain scores for Processing Speed, Memory Encoding, Recall and Recognition, Executive Control, Executive Function, Visuoperceptual, and Language domains, and compared them among the three groups while controlling for sex, pre‐morbid intelligence, and diagnosis. Result The zero alcohol group included 157 participants (females = 48.4%; V‐MCI = 52.2%) with mean (SD) age 71.26 (6.93) years, the low‐medium alcohol group included 213 participants (females = 42.2%; V‐MCI = 44.1%) with mean (SD) age 71.64 (7.77) years, and the high alcohol group included 73 participants (females = 20.5%; V‐MCI = 50.1%) with mean (SD) age 72.23 (7.51) years. The groups differed only in Processing Speed (F(2,407) = 3.298, p =  0.038), Memory Encoding (F(2,394) = 4.689, p =  0.010) and Recall (F(2,403) = 3.997, p =  0.019). Pairwise comparisons revealed a significant difference between the low‐medium and high alcohol groups in both Memory Encoding (p = 0.019) and Recall (p = 0.018), with participants in the high alcohol group demonstrating lower performance. There were no differences between the zero alcohol group and other groups. There were no pairwise differences for Processing Speed. Conclusion In participants with AD‐MCI or V‐MCI, excessive alcohol use is associated with worse memory encoding and retrieval, but not retention. This is consistent with a more dysexecutive memory profile than a typical amnestic cognitive profile. Future studies should investigate underlying mechanisms for these deficits, and their impact on prognosis of the illness. 
653 |a Neurocognition 
653 |a Alcohol use 
653 |a Groups 
653 |a Memory 
653 |a Medical diagnosis 
653 |a Age 
653 |a Dementia 
653 |a Females 
653 |a Executive control 
653 |a Cognition 
653 |a Neuropsychology 
653 |a Cognitive ability 
653 |a Cognitive impairment 
653 |a Intoxication 
653 |a Recall 
653 |a Encoding 
653 |a Drinks 
653 |a Patients 
653 |a Alzheimer's disease 
653 |a Medical prognosis 
653 |a Age groups 
653 |a Encoding (Cognitive process) 
653 |a Retrieval 
653 |a Intelligence 
653 |a Disorders 
653 |a Vascular disease 
653 |a Executive function 
653 |a Disease 
653 |a Profiles 
700 1 |a Pishdadian, Sara  |u Centre for Addiction and Mental Health, Toronto, ON, Canada, 
700 1 |a Binns, Malcolm A  |u Rotman Research Institute, Baycrest Health Sciences, Toronto, ON, Canada, 
700 1 |a Black, Sandra E.  |u Sunnybrook Health Sciences Centre, University of Toronto, Toronto, ON, Canada, 
700 1 |a Chertkow, Howard  |u Rotman Research Institute, Baycrest Health Sciences, Toronto, ON, Canada, 
700 1 |a Freedman, Morris  |u Baycrest Health Sciences, Toronto, ON, Canada, 
700 1 |a Louis, Janine  |u Centre for Addiction and Mental Health, Toronto, ON, Canada, 
700 1 |a Ma, Clement  |u Centre for Addiction and Mental Health, Toronto, ON, Canada, 
700 1 |a Masellis, Mario  |u Sunnybrook Health Sciences Centre, Toronto, ON, Canada, 
700 1 |a McLaughlin, Paula M  |u Nova Scotia Health, Halifax, NS, Canada, 
700 1 |a Ramirez, Joel  |u Sunnybrook Health Sciences Centre, Toronto, ON, Canada, 
700 1 |a Tang‐Wai, David F.  |u Krembil Brain Institute, University Health Network (UHN), Toronto, ON, Canada, 
700 1 |a Tartaglia, Carmela  |u Krembil Brain Institute, University Health Network (UHN), Toronto, ON, Canada, 
700 1 |a Kumar, Sanjeev  |u Centre for Addiction and Mental Health, Toronto, ON, Canada, 
773 0 |t Alzheimer's & Dementia  |g vol. 21 (Dec 1, 2025) 
786 0 |d ProQuest  |t Consumer Health Database 
856 4 1 |3 Citation/Abstract  |u https://www.proquest.com/docview/3286416819/abstract/embedded/L8HZQI7Z43R0LA5T?source=fedsrch 
856 4 0 |3 Full Text - PDF  |u https://www.proquest.com/docview/3286416819/fulltextPDF/embedded/L8HZQI7Z43R0LA5T?source=fedsrch