Alcohol Consumption, Brain Amyloid-β Deposition, and Brain Structural Integrity among Older Adults Free of Dementia

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

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Alcohol Consumption, Brain Amyloid-β Deposition, and Brain Structural Integrity among Older Adults Free of Dementia. / Koch, Manja; Costanzo, Simona; Fitzpatrick, Annette L.; Lopez, Oscar L.; Dekosky, Steven; Kuller, Lewis H.; Price, Julie; MacKey, Rachel H.; Jensen, Majken K.; Mukamal, Kenneth J.

I: Journal of Alzheimer's Disease, Bind 74, Nr. 2, 2020, s. 509-519.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Koch, M, Costanzo, S, Fitzpatrick, AL, Lopez, OL, Dekosky, S, Kuller, LH, Price, J, MacKey, RH, Jensen, MK & Mukamal, KJ 2020, 'Alcohol Consumption, Brain Amyloid-β Deposition, and Brain Structural Integrity among Older Adults Free of Dementia', Journal of Alzheimer's Disease, bind 74, nr. 2, s. 509-519. https://doi.org/10.3233/JAD-190834

APA

Koch, M., Costanzo, S., Fitzpatrick, A. L., Lopez, O. L., Dekosky, S., Kuller, L. H., Price, J., MacKey, R. H., Jensen, M. K., & Mukamal, K. J. (2020). Alcohol Consumption, Brain Amyloid-β Deposition, and Brain Structural Integrity among Older Adults Free of Dementia. Journal of Alzheimer's Disease, 74(2), 509-519. https://doi.org/10.3233/JAD-190834

Vancouver

Koch M, Costanzo S, Fitzpatrick AL, Lopez OL, Dekosky S, Kuller LH o.a. Alcohol Consumption, Brain Amyloid-β Deposition, and Brain Structural Integrity among Older Adults Free of Dementia. Journal of Alzheimer's Disease. 2020;74(2):509-519. https://doi.org/10.3233/JAD-190834

Author

Koch, Manja ; Costanzo, Simona ; Fitzpatrick, Annette L. ; Lopez, Oscar L. ; Dekosky, Steven ; Kuller, Lewis H. ; Price, Julie ; MacKey, Rachel H. ; Jensen, Majken K. ; Mukamal, Kenneth J. / Alcohol Consumption, Brain Amyloid-β Deposition, and Brain Structural Integrity among Older Adults Free of Dementia. I: Journal of Alzheimer's Disease. 2020 ; Bind 74, Nr. 2. s. 509-519.

Bibtex

@article{c7cef6ae80cd4ceebd3a3dcfd5f1df6c,
title = "Alcohol Consumption, Brain Amyloid-β Deposition, and Brain Structural Integrity among Older Adults Free of Dementia",
abstract = "Background: Light to moderate alcohol consumption has been variably associated with lower or higher risk of dementia, but effects on Alzheimer's disease pathology are less clear. Objective: We determined whether late-life alcohol consumption was associated with Alzheimer's disease pathology among older adults. Methods: We assessed the associations of alcohol consumption self-reported in 2000-2002 with brain amyloid-β deposition on PET scans, and white matter lesion and hippocampal volume on MRIs measured 7-9 years later in 189 participants of the Ginkgo Evaluation of Memory Study (age 75-87 years at baseline) who were free of clinical dementia, using multivariable-adjusted and inverse probability-weighted robust linear regression models. Results: Alcohol consumption was not statistically significantly associated with amyloid-β deposition (standardized uptake value ratio difference per drink: -0.013 [95% CI: -0.027, 0.002]). Both non-drinkers and participants consuming ≥1 drink(s)/week had higher white matter lesion volume (% intracranial volume) than did the reference group of those consuming <1 drink/week (differences: 0.25 % [95% CI: 0.01, 0.50]; 0.26 % [95% CI: 0.02, 0.50]). The association of alcohol consumption and hippocampal volume was modified by age (p = 0.02). Among participants younger than 77 years, participants consuming 1-7 drinks/week had larger hippocampal volume compared with participants consuming <1 drink/week. Conclusions: Alcohol consumption was not statistically significantly associated with amyloid-β deposition 7-9 years later. Non-drinking and greater alcohol consumption were associated with higher white matter lesion volume compared with drinking <1 drink/week. Moderate drinking was associated with higher hippocampal volume in younger individuals. Given the selective nature of this population and adverse health effects of excessive alcohol consumption, these findings warrant further investigation, but cannot be translated into clinical recommendations.",
keywords = "Alcohol, brain amyloid-β, epidemiology, hippocampal volume, white matter lesions",
author = "Manja Koch and Simona Costanzo and Fitzpatrick, {Annette L.} and Lopez, {Oscar L.} and Steven Dekosky and Kuller, {Lewis H.} and Julie Price and MacKey, {Rachel H.} and Jensen, {Majken K.} and Mukamal, {Kenneth J.}",
year = "2020",
doi = "10.3233/JAD-190834",
language = "English",
volume = "74",
pages = "509--519",
journal = "Journal of Alzheimer's Disease",
issn = "1387-2877",
publisher = "I O S Press",
number = "2",

}

RIS

TY - JOUR

T1 - Alcohol Consumption, Brain Amyloid-β Deposition, and Brain Structural Integrity among Older Adults Free of Dementia

AU - Koch, Manja

AU - Costanzo, Simona

AU - Fitzpatrick, Annette L.

AU - Lopez, Oscar L.

AU - Dekosky, Steven

AU - Kuller, Lewis H.

AU - Price, Julie

AU - MacKey, Rachel H.

AU - Jensen, Majken K.

AU - Mukamal, Kenneth J.

PY - 2020

Y1 - 2020

N2 - Background: Light to moderate alcohol consumption has been variably associated with lower or higher risk of dementia, but effects on Alzheimer's disease pathology are less clear. Objective: We determined whether late-life alcohol consumption was associated with Alzheimer's disease pathology among older adults. Methods: We assessed the associations of alcohol consumption self-reported in 2000-2002 with brain amyloid-β deposition on PET scans, and white matter lesion and hippocampal volume on MRIs measured 7-9 years later in 189 participants of the Ginkgo Evaluation of Memory Study (age 75-87 years at baseline) who were free of clinical dementia, using multivariable-adjusted and inverse probability-weighted robust linear regression models. Results: Alcohol consumption was not statistically significantly associated with amyloid-β deposition (standardized uptake value ratio difference per drink: -0.013 [95% CI: -0.027, 0.002]). Both non-drinkers and participants consuming ≥1 drink(s)/week had higher white matter lesion volume (% intracranial volume) than did the reference group of those consuming <1 drink/week (differences: 0.25 % [95% CI: 0.01, 0.50]; 0.26 % [95% CI: 0.02, 0.50]). The association of alcohol consumption and hippocampal volume was modified by age (p = 0.02). Among participants younger than 77 years, participants consuming 1-7 drinks/week had larger hippocampal volume compared with participants consuming <1 drink/week. Conclusions: Alcohol consumption was not statistically significantly associated with amyloid-β deposition 7-9 years later. Non-drinking and greater alcohol consumption were associated with higher white matter lesion volume compared with drinking <1 drink/week. Moderate drinking was associated with higher hippocampal volume in younger individuals. Given the selective nature of this population and adverse health effects of excessive alcohol consumption, these findings warrant further investigation, but cannot be translated into clinical recommendations.

AB - Background: Light to moderate alcohol consumption has been variably associated with lower or higher risk of dementia, but effects on Alzheimer's disease pathology are less clear. Objective: We determined whether late-life alcohol consumption was associated with Alzheimer's disease pathology among older adults. Methods: We assessed the associations of alcohol consumption self-reported in 2000-2002 with brain amyloid-β deposition on PET scans, and white matter lesion and hippocampal volume on MRIs measured 7-9 years later in 189 participants of the Ginkgo Evaluation of Memory Study (age 75-87 years at baseline) who were free of clinical dementia, using multivariable-adjusted and inverse probability-weighted robust linear regression models. Results: Alcohol consumption was not statistically significantly associated with amyloid-β deposition (standardized uptake value ratio difference per drink: -0.013 [95% CI: -0.027, 0.002]). Both non-drinkers and participants consuming ≥1 drink(s)/week had higher white matter lesion volume (% intracranial volume) than did the reference group of those consuming <1 drink/week (differences: 0.25 % [95% CI: 0.01, 0.50]; 0.26 % [95% CI: 0.02, 0.50]). The association of alcohol consumption and hippocampal volume was modified by age (p = 0.02). Among participants younger than 77 years, participants consuming 1-7 drinks/week had larger hippocampal volume compared with participants consuming <1 drink/week. Conclusions: Alcohol consumption was not statistically significantly associated with amyloid-β deposition 7-9 years later. Non-drinking and greater alcohol consumption were associated with higher white matter lesion volume compared with drinking <1 drink/week. Moderate drinking was associated with higher hippocampal volume in younger individuals. Given the selective nature of this population and adverse health effects of excessive alcohol consumption, these findings warrant further investigation, but cannot be translated into clinical recommendations.

KW - Alcohol

KW - brain amyloid-β

KW - epidemiology

KW - hippocampal volume

KW - white matter lesions

U2 - 10.3233/JAD-190834

DO - 10.3233/JAD-190834

M3 - Journal article

C2 - 32039843

AN - SCOPUS:85082634961

VL - 74

SP - 509

EP - 519

JO - Journal of Alzheimer's Disease

JF - Journal of Alzheimer's Disease

SN - 1387-2877

IS - 2

ER -

ID: 244969135