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Methods used in 'ALDH2*2 association with longevity and reduced risk of cognitive decline in Japanese-American men'

ALDH2*2 is a loss of function mutation common in East Asian populations associated with facial flushing on exposure to alcohol and increased risk of certain cancers. Conversely, absence of the ALDH2*2 mutation is associated with increased risk of hypertension and cerebral microbleeds, and two recent...

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Autores principales: Sachan, Anubhav Nikunj Singh, Edland, Steven, Chosy, Julia, Launer, Lenore, Seshadri, Sudha, White, Lon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8680691/
http://dx.doi.org/10.1093/geroni/igab046.2515
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author Sachan, Anubhav Nikunj Singh
Edland, Steven
Chosy, Julia
Launer, Lenore
Seshadri, Sudha
White, Lon
author_facet Sachan, Anubhav Nikunj Singh
Edland, Steven
Chosy, Julia
Launer, Lenore
Seshadri, Sudha
White, Lon
author_sort Sachan, Anubhav Nikunj Singh
collection PubMed
description ALDH2*2 is a loss of function mutation common in East Asian populations associated with facial flushing on exposure to alcohol and increased risk of certain cancers. Conversely, absence of the ALDH2*2 mutation is associated with increased risk of hypertension and cerebral microbleeds, and two recent studies report a higher frequency of ALDH2*2 alleles in nonagenarians compared to population control samples. We used survival analysis to investigate the association between ALDH2*2 and risk of cognitive impairment and death after controlling for midlife alcohol consumption and other covariates. Participants are 621 Japanese-American men (72 to 92) enrolled in the Honolulu Asia Aging Study (HAAS) and assessed for cognitive impairment for up to 20 years. Impairment was defined as crossing below a threshold score of 74 on the Cognitive Assessment Screening Instrument (CASI). Age at death was determined by Hawaii state death certificate. Ounces of ethyl alcohol consumed per month was assessed by structured interview (number, frequency, and type of beverage) conducted 25 years prior to baseline cognitive assessment. Persons heterozygous for the ALDH2*2 variant have reduced risk of cognitive impairment and reduced risk of death, compared to homozygote non-carriers. Covarying by alcohol exposure had no effect on observed associations. This study replicates previous findings associating ALDH2*2 with longevity, and provides evidence the protective effect extends to cognition. This poster details the statistical analysis carried out to obtain these results.
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spelling pubmed-86806912021-12-17 Methods used in 'ALDH2*2 association with longevity and reduced risk of cognitive decline in Japanese-American men' Sachan, Anubhav Nikunj Singh Edland, Steven Chosy, Julia Launer, Lenore Seshadri, Sudha White, Lon Innov Aging Abstracts ALDH2*2 is a loss of function mutation common in East Asian populations associated with facial flushing on exposure to alcohol and increased risk of certain cancers. Conversely, absence of the ALDH2*2 mutation is associated with increased risk of hypertension and cerebral microbleeds, and two recent studies report a higher frequency of ALDH2*2 alleles in nonagenarians compared to population control samples. We used survival analysis to investigate the association between ALDH2*2 and risk of cognitive impairment and death after controlling for midlife alcohol consumption and other covariates. Participants are 621 Japanese-American men (72 to 92) enrolled in the Honolulu Asia Aging Study (HAAS) and assessed for cognitive impairment for up to 20 years. Impairment was defined as crossing below a threshold score of 74 on the Cognitive Assessment Screening Instrument (CASI). Age at death was determined by Hawaii state death certificate. Ounces of ethyl alcohol consumed per month was assessed by structured interview (number, frequency, and type of beverage) conducted 25 years prior to baseline cognitive assessment. Persons heterozygous for the ALDH2*2 variant have reduced risk of cognitive impairment and reduced risk of death, compared to homozygote non-carriers. Covarying by alcohol exposure had no effect on observed associations. This study replicates previous findings associating ALDH2*2 with longevity, and provides evidence the protective effect extends to cognition. This poster details the statistical analysis carried out to obtain these results. Oxford University Press 2021-12-17 /pmc/articles/PMC8680691/ http://dx.doi.org/10.1093/geroni/igab046.2515 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of The Gerontological Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstracts
Sachan, Anubhav Nikunj Singh
Edland, Steven
Chosy, Julia
Launer, Lenore
Seshadri, Sudha
White, Lon
Methods used in 'ALDH2*2 association with longevity and reduced risk of cognitive decline in Japanese-American men'
title Methods used in 'ALDH2*2 association with longevity and reduced risk of cognitive decline in Japanese-American men'
title_full Methods used in 'ALDH2*2 association with longevity and reduced risk of cognitive decline in Japanese-American men'
title_fullStr Methods used in 'ALDH2*2 association with longevity and reduced risk of cognitive decline in Japanese-American men'
title_full_unstemmed Methods used in 'ALDH2*2 association with longevity and reduced risk of cognitive decline in Japanese-American men'
title_short Methods used in 'ALDH2*2 association with longevity and reduced risk of cognitive decline in Japanese-American men'
title_sort methods used in 'aldh2*2 association with longevity and reduced risk of cognitive decline in japanese-american men'
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8680691/
http://dx.doi.org/10.1093/geroni/igab046.2515
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