Association of Vascular Risk Scores and Cognitive Performance in a Diverse Cohort: The Multi-Ethnic Study of Atherosclerosis.
Cardiovascular
Cognition
Cognitive aging
Race/ethnicity
Risk factors
Journal
The journals of gerontology. Series A, Biological sciences and medical sciences
ISSN: 1758-535X
Titre abrégé: J Gerontol A Biol Sci Med Sci
Pays: United States
ID NLM: 9502837
Informations de publication
Date de publication:
01 06 2022
01 06 2022
Historique:
received:
20
01
2021
pubmed:
4
7
2021
medline:
7
6
2022
entrez:
3
7
2021
Statut:
ppublish
Résumé
Vascular risk scores are associated with incident dementia. Information regarding their association with cognitive performance and decline in racially/ethnically diverse cohorts is lacking. In 4 392 Multi-Ethnic Study of Atherosclerosis participants (aged 60.1 ± 9.4 years; 53% women; 41% White, 11% Chinese American, 26% African American, 21% Hispanic), we compared associations of Exam 1 (2000-2002) Cardiovascular Risk Factors, Aging, and Incidence of Dementia (CAIDE), Framingham Stroke Risk Profile (FSRP), and atherosclerotic cardiovascular disease pooled cohort equation (ASCVD-PCE) risk scores with Exam 5 (2010-2012) Cognitive Abilities Screening Instrument (CASI), Digit Symbol Coding (DSC), and Digit Span (DS) cognitive test performance using multivariable linear regression, and examined racial/ethnic interactions. In 1 838 participants with repeat CASI data at Exam 6 (2016-2018), we related risk scores to odds of a 1-SD decline in CASI performance using multivariable logistic regression. SD increments in each risk score were associated with worse cognitive performance. CAIDE had stronger associations with CASI performance than the FSRP and ASCVD-PCE, but associations of ASCVD-PCE with the DSC and DS were similar to CAIDE (difference in β [95% CI] = -0.57 [-1.48, 0.34] and -0.21 [-0.43, 0.01], respectively). Race/ethnicity modified associations. For example, associations between CAIDE and CASI were greater in African Americans and Hispanics than in Whites (difference in β = 0.69 [0.02, 1.36] and 1.67 [0.95, 2.39], respectively). Risk scores were comparably associated with decline in CASI performance. Antecedent vascular risk scores are associated with cognitive performance and decline in the 4 most common U.S. racial/ethnic groups, but associations differ among risk scores and by race/ethnicity.
Sections du résumé
BACKGROUND
Vascular risk scores are associated with incident dementia. Information regarding their association with cognitive performance and decline in racially/ethnically diverse cohorts is lacking.
METHOD
In 4 392 Multi-Ethnic Study of Atherosclerosis participants (aged 60.1 ± 9.4 years; 53% women; 41% White, 11% Chinese American, 26% African American, 21% Hispanic), we compared associations of Exam 1 (2000-2002) Cardiovascular Risk Factors, Aging, and Incidence of Dementia (CAIDE), Framingham Stroke Risk Profile (FSRP), and atherosclerotic cardiovascular disease pooled cohort equation (ASCVD-PCE) risk scores with Exam 5 (2010-2012) Cognitive Abilities Screening Instrument (CASI), Digit Symbol Coding (DSC), and Digit Span (DS) cognitive test performance using multivariable linear regression, and examined racial/ethnic interactions. In 1 838 participants with repeat CASI data at Exam 6 (2016-2018), we related risk scores to odds of a 1-SD decline in CASI performance using multivariable logistic regression.
RESULTS
SD increments in each risk score were associated with worse cognitive performance. CAIDE had stronger associations with CASI performance than the FSRP and ASCVD-PCE, but associations of ASCVD-PCE with the DSC and DS were similar to CAIDE (difference in β [95% CI] = -0.57 [-1.48, 0.34] and -0.21 [-0.43, 0.01], respectively). Race/ethnicity modified associations. For example, associations between CAIDE and CASI were greater in African Americans and Hispanics than in Whites (difference in β = 0.69 [0.02, 1.36] and 1.67 [0.95, 2.39], respectively). Risk scores were comparably associated with decline in CASI performance.
CONCLUSIONS
Antecedent vascular risk scores are associated with cognitive performance and decline in the 4 most common U.S. racial/ethnic groups, but associations differ among risk scores and by race/ethnicity.
Identifiants
pubmed: 34216214
pii: 6314276
doi: 10.1093/gerona/glab189
pmc: PMC9159669
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
1208-1215Subventions
Organisme : NIA NIH HHS
ID : L30 AG074138
Pays : United States
Organisme : NHLBI NIH HHS
ID : 75N92020D00007
Pays : United States
Organisme : NHLBI NIH HHS
ID : 75N92020D00001
Pays : United States
Organisme : NIA NIH HHS
ID : K24 AG045334
Pays : United States
Organisme : NHLBI NIH HHS
ID : 75N92020D00005
Pays : United States
Organisme : NHLBI NIH HHS
ID : N01HC95169
Pays : United States
Organisme : NHLBI NIH HHS
ID : 75N92020D00004
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG055606
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG072947
Pays : United States
Organisme : NHLBI NIH HHS
ID : F32 HL146075
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL127659
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG049638
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG059303
Pays : United States
Organisme : NHLBI NIH HHS
ID : 75N92020D00002
Pays : United States
Organisme : NIA NIH HHS
ID : R03 AG064569
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000040
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG058969
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG054069
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001420
Pays : United States
Organisme : NHLBI NIH HHS
ID : 75N92020D00003
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268201500003I
Pays : United States
Organisme : NIA NIH HHS
ID : RF1 AG054474
Pays : United States
Organisme : NHLBI NIH HHS
ID : 75N92020D00006
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001079
Pays : United States
Informations de copyright
© The Author(s) 2021. Published by Oxford University Press on behalf of The Gerontological Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
Références
J Alzheimers Dis. 2017;59(2):695-705
pubmed: 28671114
J Am Coll Cardiol. 1984 Jan;3(1):82-7
pubmed: 6228571
Neurology. 2018 Apr 3;90(14):e1248-e1256
pubmed: 29549223
Stroke. 1991 Mar;22(3):312-8
pubmed: 2003301
Stroke. 2004 Feb;35(2):404-9
pubmed: 14726556
Neurology. 2005 Feb 8;64(3):494-500
pubmed: 15699381
Lancet Neurol. 2006 Sep;5(9):735-41
pubmed: 16914401
Stroke. 2004 Jun;35(6):1264-8
pubmed: 15118167
PLoS One. 2015 Jul 02;10(7):e0132321
pubmed: 26134404
Lancet. 2000 Jul 22;356(9226):279-84
pubmed: 11071182
Neurology. 2013 Apr 2;80(14):1300-6
pubmed: 23547265
Ann Neurol. 2007 May;61(5):403-10
pubmed: 17328068
BMC Cardiovasc Disord. 2019 Sep 14;19(1):213
pubmed: 31521122
Circulation. 2007 Nov 13;116(20):2269-74
pubmed: 17967779
Neurology. 2001 Jun 26;56(12):1683-9
pubmed: 11425934
Neurology. 2005 Jan 25;64(2):277-81
pubmed: 15668425
Alzheimers Dement. 2014 Sep;10(5):562-70
pubmed: 24035147
Arch Neurol. 2005 Oct;62(10):1556-60
pubmed: 16216938
PLoS One. 2014 Dec 05;9(12):e114431
pubmed: 25478916
J Am Geriatr Soc. 2017 Feb;65(2):381-389
pubmed: 27861706
J Womens Health Gend Based Med. 1999 Jul-Aug;8(6):805-13
pubmed: 10495261
J Card Fail. 2017 Jun;23(6):464-475
pubmed: 28433667
Am J Cardiol. 2016 Sep 1;118(5):691-6
pubmed: 27445216
Circulation. 2011 Mar 1;123(8):858-65
pubmed: 21321150
Circulation. 2018 Feb 6;137(6):567-577
pubmed: 29025764
Lancet Neurol. 2011 Sep;10(9):819-28
pubmed: 21775213
Ann Intern Med. 2015 Feb 17;162(4):266-75
pubmed: 25686167
Ann Intern Med. 2007 Oct 16;147(8):573-7
pubmed: 17938396
Postgrad Med. 2016 Nov;128(8):865-868
pubmed: 27701986
J Alzheimers Dis. 2015;44(1):93-101
pubmed: 25190628
J Clin Lipidol. 2015 Sep-Oct;9(5):640-6.e2
pubmed: 26350809
Am J Epidemiol. 2002 Nov 1;156(9):871-81
pubmed: 12397006
Sci Rep. 2017 Sep 28;7(1):12370
pubmed: 28959022
J Am Coll Cardiol. 2014 Jul 1;63(25 Pt B):2935-2959
pubmed: 24239921
Arch Intern Med. 2008 Jun 23;168(12):1270-6
pubmed: 18574083
BMC Neurol. 2008 Apr 22;8:12
pubmed: 18430227
Am J Geriatr Psychiatry. 2015 Jul;23(7):684-97
pubmed: 25704999
BMJ. 2001 Jun 16;322(7300):1447-51
pubmed: 11408299
J Am Geriatr Soc. 2005 Jul;53(7):1101-7
pubmed: 16108925
BMC Cardiovasc Disord. 2014 Nov 20;14:163
pubmed: 25410585