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July 12, 2022; 99 (2) Research Article

Genetic Risk, Midlife Life's Simple 7, and Incident Dementia in the Atherosclerosis Risk in Communities Study

View ORCID ProfileAdrienne Tin, Jan Bressler, Jeannette Simino, Kevin J. Sullivan, Hao Mei, B. Gwen Windham, Michael Griswold, Rebecca F. Gottesman, Eric Boerwinkle, View ORCID ProfileMyriam Fornage, Thomas H. Mosley
First published May 25, 2022, DOI: https://doi.org/10.1212/WNL.0000000000200520
Adrienne Tin
From the Memory Impairment and Neurodegenerative Dementia (MIND) Center and Department of Medicine (A.T., K.J.S., B.G.W., M.G., T.H.M.) and Department of Data Science (J.S., H.M.), University of Mississippi Medical Center, Jackson; Department of Epidemiology (A.T.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Human Genetics Center, School of Public Health (J.B., E.B., M.F.), and Institute of Molecular Medicine, McGovern Medical School (M.F.), University of Texas Health Science Center at Houston; and Stroke Branch (R.F.G.), National Institute of Neurological Disorders and Stroke Intramural Program, National Institutes of Health, Bethesda, MD.
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Jan Bressler
From the Memory Impairment and Neurodegenerative Dementia (MIND) Center and Department of Medicine (A.T., K.J.S., B.G.W., M.G., T.H.M.) and Department of Data Science (J.S., H.M.), University of Mississippi Medical Center, Jackson; Department of Epidemiology (A.T.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Human Genetics Center, School of Public Health (J.B., E.B., M.F.), and Institute of Molecular Medicine, McGovern Medical School (M.F.), University of Texas Health Science Center at Houston; and Stroke Branch (R.F.G.), National Institute of Neurological Disorders and Stroke Intramural Program, National Institutes of Health, Bethesda, MD.
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Jeannette Simino
From the Memory Impairment and Neurodegenerative Dementia (MIND) Center and Department of Medicine (A.T., K.J.S., B.G.W., M.G., T.H.M.) and Department of Data Science (J.S., H.M.), University of Mississippi Medical Center, Jackson; Department of Epidemiology (A.T.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Human Genetics Center, School of Public Health (J.B., E.B., M.F.), and Institute of Molecular Medicine, McGovern Medical School (M.F.), University of Texas Health Science Center at Houston; and Stroke Branch (R.F.G.), National Institute of Neurological Disorders and Stroke Intramural Program, National Institutes of Health, Bethesda, MD.
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Kevin J. Sullivan
From the Memory Impairment and Neurodegenerative Dementia (MIND) Center and Department of Medicine (A.T., K.J.S., B.G.W., M.G., T.H.M.) and Department of Data Science (J.S., H.M.), University of Mississippi Medical Center, Jackson; Department of Epidemiology (A.T.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Human Genetics Center, School of Public Health (J.B., E.B., M.F.), and Institute of Molecular Medicine, McGovern Medical School (M.F.), University of Texas Health Science Center at Houston; and Stroke Branch (R.F.G.), National Institute of Neurological Disorders and Stroke Intramural Program, National Institutes of Health, Bethesda, MD.
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Hao Mei
From the Memory Impairment and Neurodegenerative Dementia (MIND) Center and Department of Medicine (A.T., K.J.S., B.G.W., M.G., T.H.M.) and Department of Data Science (J.S., H.M.), University of Mississippi Medical Center, Jackson; Department of Epidemiology (A.T.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Human Genetics Center, School of Public Health (J.B., E.B., M.F.), and Institute of Molecular Medicine, McGovern Medical School (M.F.), University of Texas Health Science Center at Houston; and Stroke Branch (R.F.G.), National Institute of Neurological Disorders and Stroke Intramural Program, National Institutes of Health, Bethesda, MD.
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B. Gwen Windham
From the Memory Impairment and Neurodegenerative Dementia (MIND) Center and Department of Medicine (A.T., K.J.S., B.G.W., M.G., T.H.M.) and Department of Data Science (J.S., H.M.), University of Mississippi Medical Center, Jackson; Department of Epidemiology (A.T.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Human Genetics Center, School of Public Health (J.B., E.B., M.F.), and Institute of Molecular Medicine, McGovern Medical School (M.F.), University of Texas Health Science Center at Houston; and Stroke Branch (R.F.G.), National Institute of Neurological Disorders and Stroke Intramural Program, National Institutes of Health, Bethesda, MD.
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Michael Griswold
From the Memory Impairment and Neurodegenerative Dementia (MIND) Center and Department of Medicine (A.T., K.J.S., B.G.W., M.G., T.H.M.) and Department of Data Science (J.S., H.M.), University of Mississippi Medical Center, Jackson; Department of Epidemiology (A.T.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Human Genetics Center, School of Public Health (J.B., E.B., M.F.), and Institute of Molecular Medicine, McGovern Medical School (M.F.), University of Texas Health Science Center at Houston; and Stroke Branch (R.F.G.), National Institute of Neurological Disorders and Stroke Intramural Program, National Institutes of Health, Bethesda, MD.
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Rebecca F. Gottesman
From the Memory Impairment and Neurodegenerative Dementia (MIND) Center and Department of Medicine (A.T., K.J.S., B.G.W., M.G., T.H.M.) and Department of Data Science (J.S., H.M.), University of Mississippi Medical Center, Jackson; Department of Epidemiology (A.T.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Human Genetics Center, School of Public Health (J.B., E.B., M.F.), and Institute of Molecular Medicine, McGovern Medical School (M.F.), University of Texas Health Science Center at Houston; and Stroke Branch (R.F.G.), National Institute of Neurological Disorders and Stroke Intramural Program, National Institutes of Health, Bethesda, MD.
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Eric Boerwinkle
From the Memory Impairment and Neurodegenerative Dementia (MIND) Center and Department of Medicine (A.T., K.J.S., B.G.W., M.G., T.H.M.) and Department of Data Science (J.S., H.M.), University of Mississippi Medical Center, Jackson; Department of Epidemiology (A.T.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Human Genetics Center, School of Public Health (J.B., E.B., M.F.), and Institute of Molecular Medicine, McGovern Medical School (M.F.), University of Texas Health Science Center at Houston; and Stroke Branch (R.F.G.), National Institute of Neurological Disorders and Stroke Intramural Program, National Institutes of Health, Bethesda, MD.
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Myriam Fornage
From the Memory Impairment and Neurodegenerative Dementia (MIND) Center and Department of Medicine (A.T., K.J.S., B.G.W., M.G., T.H.M.) and Department of Data Science (J.S., H.M.), University of Mississippi Medical Center, Jackson; Department of Epidemiology (A.T.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Human Genetics Center, School of Public Health (J.B., E.B., M.F.), and Institute of Molecular Medicine, McGovern Medical School (M.F.), University of Texas Health Science Center at Houston; and Stroke Branch (R.F.G.), National Institute of Neurological Disorders and Stroke Intramural Program, National Institutes of Health, Bethesda, MD.
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Thomas H. Mosley
From the Memory Impairment and Neurodegenerative Dementia (MIND) Center and Department of Medicine (A.T., K.J.S., B.G.W., M.G., T.H.M.) and Department of Data Science (J.S., H.M.), University of Mississippi Medical Center, Jackson; Department of Epidemiology (A.T.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Human Genetics Center, School of Public Health (J.B., E.B., M.F.), and Institute of Molecular Medicine, McGovern Medical School (M.F.), University of Texas Health Science Center at Houston; and Stroke Branch (R.F.G.), National Institute of Neurological Disorders and Stroke Intramural Program, National Institutes of Health, Bethesda, MD.
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Genetic Risk, Midlife Life's Simple 7, and Incident Dementia in the Atherosclerosis Risk in Communities Study
Adrienne Tin, Jan Bressler, Jeannette Simino, Kevin J. Sullivan, Hao Mei, B. Gwen Windham, Michael Griswold, Rebecca F. Gottesman, Eric Boerwinkle, Myriam Fornage, Thomas H. Mosley
Neurology Jul 2022, 99 (2) e154-e163; DOI: 10.1212/WNL.0000000000200520

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Abstract

Background and Objectives Higher scores in Life's Simple 7 (LS7), a metric for cardiovascular and brain health, have been associated with lower risk of dementia. It is uncertain whether this association holds among those with high genetic risk of dementia. Our objective is to evaluate the extent that LS7 may offset dementia risk across the range of genetic risk.

Methods Participants in the Atherosclerosis Risk in Communities (ARIC) Study were followed from 1987–1989 to 2019. We derived midlife LS7 scores and generated genetic risk scores (GRS) using genome-wide summary statistics of Alzheimer disease, which have been used to study the genetic risk for dementia. Incident dementia was ascertained based on the criteria of the National Institute on Aging–Alzheimer's Association workgroups and Diagnostic and Statistical Manual of Mental Disorders. The associations of the GRS and LS7 with incident dementia were evaluated using Cox regression.

Results This study included 8,823 European American (EA) and 2,738 African American (AA) participants (mean age at baseline 54 years). We observed 1,603 cases of dementia among EA participants and 631 among AA participants (median follow-up 26.2 years). Higher GRS were associated with higher risk of dementia (EA, hazard ratio [HR] per SD 1.44, 95% CI 1.37, 1.51; AA, HR 1.26, 95% CI 1.16, 1.36). Among EA participants, higher LS7 scores were consistently associated with lower risk of dementia across quintiles of GRS, including the highest quintile (HR per point 0.91, 95% CI 0.87, 0.96). Among AA participants, the associations between LS7 and incident dementia within stratum of GRS had the same direction as among EA participants, although wide CIs and smaller sample sizes limited reliable inferences.

Discussion Across strata of GRS, higher midlife LS7 scores were associated with lower risk of dementia. Larger sample sizes from diverse populations are needed to obtain more reliable estimates of the effects of modifiable health factors on dementia risk within genetic risk strata in each ancestry group.

Glossary

AA=
African American;
AD=
Alzheimer disease;
AHA=
American Heart Association;
ARIC=
Atherosclerosis Risk in Communities;
BioLINCC=
Biologic Specimen and Data Repository Information Coordinating Center;
CVD=
cardiovascular disease;
DSM-5=
Diagnostic and Statistical Manual of Mental Disorders, 5th Edition;
EA=
European American;
FINGER=
Finnish Geriatric Intervention Study to Prevent Cognitive Impairment and Disability;
GRS=
genetic risk scores;
GWAS=
genome-wide association studies;
HR=
hazard ratio;
ICD-9=
International Classification of Diseases–9;
LS7=
Life's Simple 7;
PC=
principal component;
SBP=
systolic blood pressure;
SNP=
single nucleotide polymorphism;
TICS=
Telephone Interview for Cognitive Status

Footnotes

  • Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Submitted and externally peer reviewed. The handling editors were Rawan Tarawneh, MD, and Brad Worrall, MD, MSc.

  • Received October 21, 2021.
  • Accepted in final form February 28, 2022.
  • Written work prepared by employees of the Federal Government as part of their official duties is, under the U.S. Copyright Act, a “work of the United States Government” for which copyright protection under Title 17 of the United States Code is not available. As such, copyright does not extend to the contributions of employees of the Federal Government.
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