Mild Cognitive Impairment that Does Not Progress to Dementia: A Population‐Based Study

Background/Objective In population studies, most individuals with mild cognitive impairment (MCI) do not progress to dementia in the near term, but rather remain stable MCI or revert to normal cognition. Here, we characterized MCI subgroups with different outcomes over 5 years. Setting/Participants...

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Published inJournal of the American Geriatrics Society (JAGS) Vol. 67; no. 2; pp. 232 - 238
Main Authors Ganguli, Mary, Jia, Yichen, Hughes, Tiffany F., Snitz, Beth E., Chang, Chung‐Chou H., Berman, Sarah B., Sullivan, Kevin J., Kamboh, M. Ilyas
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.02.2019
Subjects
Online AccessGet full text
ISSN0002-8614
1532-5415
1532-5415
DOI10.1111/jgs.15642

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Abstract Background/Objective In population studies, most individuals with mild cognitive impairment (MCI) do not progress to dementia in the near term, but rather remain stable MCI or revert to normal cognition. Here, we characterized MCI subgroups with different outcomes over 5 years. Setting/Participants A population‐based cohort (N=1603). Measurements Clinical Dementia Rating (CDR); self‐reported medical conditions, subjective cognitive concerns, self‐rated health, depressive symptoms, blood pressure, medications, blood pressure, APOE genotype, cognitive domain composite scores. Design We compared 3 MCI subgroups who progressed to dementia (n=86), stabilized at MCI (n=384), or reverted to normal (n=252), to those who remained consistently normal (n=881), defining MCI as CDR = 0.5 and dementia as CDR≥1. Using multinomial logistic regression models adjusted for demographics, we examined the associations of each group with selected baseline characteristics. Results With the normal group for reference, worse subjective cognitive concerns, functional impairments, self‐rated health, and depressive symptoms were associated with being in any MCI group. Taking more prescription medications was associated with being in the stable MCI and reverter groups; diabetes and low diastolic blood pressure were associated with stable MCI. The APOE4 genotype was associated with stable and progressive MCI; stroke was associated with progressive MCI. All MCI subgroups were likely to have lower mean composite scores in all cognitive domains and more operationally defined impairments in attention, language, and executive function; reverters were more likely to lack memory and visuospatial impairments. Conclusions MCI subgroups with different 5‐year outcomes had some distinct characteristics suggesting different underlying causes. The progressors, unlike the reverters, had a profile broadly typical of Alzheimer's disease; the stable MCIs had other, including vascular, morbidity. These data shed light on the heterogeneity of MCI in the population. J Am Geriatr Soc 67:232–238, 2019.
AbstractList Background/ObjectiveIn population studies, most individuals with mild cognitive impairment (MCI) do not progress to dementia in the near term, but rather remain stable MCI or revert to normal cognition. Here, we characterized MCI subgroups with different outcomes over 5 years.Setting/ParticipantsA population‐based cohort (N=1603).MeasurementsClinical Dementia Rating (CDR); self‐reported medical conditions, subjective cognitive concerns, self‐rated health, depressive symptoms, blood pressure, medications, blood pressure, APOE genotype, cognitive domain composite scores.DesignWe compared 3 MCI subgroups who progressed to dementia (n=86), stabilized at MCI (n=384), or reverted to normal (n=252), to those who remained consistently normal (n=881), defining MCI as CDR = 0.5 and dementia as CDR≥1. Using multinomial logistic regression models adjusted for demographics, we examined the associations of each group with selected baseline characteristics.ResultsWith the normal group for reference, worse subjective cognitive concerns, functional impairments, self‐rated health, and depressive symptoms were associated with being in any MCI group. Taking more prescription medications was associated with being in the stable MCI and reverter groups; diabetes and low diastolic blood pressure were associated with stable MCI. The APOE4 genotype was associated with stable and progressive MCI; stroke was associated with progressive MCI. All MCI subgroups were likely to have lower mean composite scores in all cognitive domains and more operationally defined impairments in attention, language, and executive function; reverters were more likely to lack memory and visuospatial impairments.ConclusionsMCI subgroups with different 5‐year outcomes had some distinct characteristics suggesting different underlying causes. The progressors, unlike the reverters, had a profile broadly typical of Alzheimer's disease; the stable MCIs had other, including vascular, morbidity. These data shed light on the heterogeneity of MCI in the population. J Am Geriatr Soc 67:232–238, 2019.
In population studies, most individuals with mild cognitive impairment (MCI) do not progress to dementia in the near term, but rather remain stable MCI or revert to normal cognition. Here, we characterized MCI subgroups with different outcomes over 5 years. A population-based cohort (N=1603). Clinical Dementia Rating (CDR); self-reported medical conditions, subjective cognitive concerns, self-rated health, depressive symptoms, blood pressure, medications, blood pressure, APOE genotype, cognitive domain composite scores. We compared 3 MCI subgroups who progressed to dementia (n=86), stabilized at MCI (n=384), or reverted to normal (n=252), to those who remained consistently normal (n=881), defining MCI as CDR = 0.5 and dementia as CDR≥1. Using multinomial logistic regression models adjusted for demographics, we examined the associations of each group with selected baseline characteristics. With the normal group for reference, worse subjective cognitive concerns, functional impairments, self-rated health, and depressive symptoms were associated with being in any MCI group. Taking more prescription medications was associated with being in the stable MCI and reverter groups; diabetes and low diastolic blood pressure were associated with stable MCI. The APOE4 genotype was associated with stable and progressive MCI; stroke was associated with progressive MCI. All MCI subgroups were likely to have lower mean composite scores in all cognitive domains and more operationally defined impairments in attention, language, and executive function; reverters were more likely to lack memory and visuospatial impairments. MCI subgroups with different 5-year outcomes had some distinct characteristics suggesting different underlying causes. The progressors, unlike the reverters, had a profile broadly typical of Alzheimer's disease; the stable MCIs had other, including vascular, morbidity. These data shed light on the heterogeneity of MCI in the population. J Am Geriatr Soc 67:232-238, 2019.
In population studies, most individuals with mild cognitive impairment (MCI) do not progress to dementia in the near term, but rather remain stable MCI or revert to normal cognition. Here, we characterized MCI subgroups with different outcomes over 5 years.BACKGROUND/OBJECTIVEIn population studies, most individuals with mild cognitive impairment (MCI) do not progress to dementia in the near term, but rather remain stable MCI or revert to normal cognition. Here, we characterized MCI subgroups with different outcomes over 5 years.A population-based cohort (N=1603).SETTING/PARTICIPANTSA population-based cohort (N=1603).Clinical Dementia Rating (CDR); self-reported medical conditions, subjective cognitive concerns, self-rated health, depressive symptoms, blood pressure, medications, blood pressure, APOE genotype, cognitive domain composite scores.MEASUREMENTSClinical Dementia Rating (CDR); self-reported medical conditions, subjective cognitive concerns, self-rated health, depressive symptoms, blood pressure, medications, blood pressure, APOE genotype, cognitive domain composite scores.We compared 3 MCI subgroups who progressed to dementia (n=86), stabilized at MCI (n=384), or reverted to normal (n=252), to those who remained consistently normal (n=881), defining MCI as CDR = 0.5 and dementia as CDR≥1. Using multinomial logistic regression models adjusted for demographics, we examined the associations of each group with selected baseline characteristics.DESIGNWe compared 3 MCI subgroups who progressed to dementia (n=86), stabilized at MCI (n=384), or reverted to normal (n=252), to those who remained consistently normal (n=881), defining MCI as CDR = 0.5 and dementia as CDR≥1. Using multinomial logistic regression models adjusted for demographics, we examined the associations of each group with selected baseline characteristics.With the normal group for reference, worse subjective cognitive concerns, functional impairments, self-rated health, and depressive symptoms were associated with being in any MCI group. Taking more prescription medications was associated with being in the stable MCI and reverter groups; diabetes and low diastolic blood pressure were associated with stable MCI. The APOE4 genotype was associated with stable and progressive MCI; stroke was associated with progressive MCI. All MCI subgroups were likely to have lower mean composite scores in all cognitive domains and more operationally defined impairments in attention, language, and executive function; reverters were more likely to lack memory and visuospatial impairments.RESULTSWith the normal group for reference, worse subjective cognitive concerns, functional impairments, self-rated health, and depressive symptoms were associated with being in any MCI group. Taking more prescription medications was associated with being in the stable MCI and reverter groups; diabetes and low diastolic blood pressure were associated with stable MCI. The APOE4 genotype was associated with stable and progressive MCI; stroke was associated with progressive MCI. All MCI subgroups were likely to have lower mean composite scores in all cognitive domains and more operationally defined impairments in attention, language, and executive function; reverters were more likely to lack memory and visuospatial impairments.MCI subgroups with different 5-year outcomes had some distinct characteristics suggesting different underlying causes. The progressors, unlike the reverters, had a profile broadly typical of Alzheimer's disease; the stable MCIs had other, including vascular, morbidity. These data shed light on the heterogeneity of MCI in the population. J Am Geriatr Soc 67:232-238, 2019.CONCLUSIONSMCI subgroups with different 5-year outcomes had some distinct characteristics suggesting different underlying causes. The progressors, unlike the reverters, had a profile broadly typical of Alzheimer's disease; the stable MCIs had other, including vascular, morbidity. These data shed light on the heterogeneity of MCI in the population. J Am Geriatr Soc 67:232-238, 2019.
Background/Objective In population studies, most individuals with mild cognitive impairment (MCI) do not progress to dementia in the near term, but rather remain stable MCI or revert to normal cognition. Here, we characterized MCI subgroups with different outcomes over 5 years. Setting/Participants A population‐based cohort (N=1603). Measurements Clinical Dementia Rating (CDR); self‐reported medical conditions, subjective cognitive concerns, self‐rated health, depressive symptoms, blood pressure, medications, blood pressure, APOE genotype, cognitive domain composite scores. Design We compared 3 MCI subgroups who progressed to dementia (n=86), stabilized at MCI (n=384), or reverted to normal (n=252), to those who remained consistently normal (n=881), defining MCI as CDR = 0.5 and dementia as CDR≥1. Using multinomial logistic regression models adjusted for demographics, we examined the associations of each group with selected baseline characteristics. Results With the normal group for reference, worse subjective cognitive concerns, functional impairments, self‐rated health, and depressive symptoms were associated with being in any MCI group. Taking more prescription medications was associated with being in the stable MCI and reverter groups; diabetes and low diastolic blood pressure were associated with stable MCI. The APOE4 genotype was associated with stable and progressive MCI; stroke was associated with progressive MCI. All MCI subgroups were likely to have lower mean composite scores in all cognitive domains and more operationally defined impairments in attention, language, and executive function; reverters were more likely to lack memory and visuospatial impairments. Conclusions MCI subgroups with different 5‐year outcomes had some distinct characteristics suggesting different underlying causes. The progressors, unlike the reverters, had a profile broadly typical of Alzheimer's disease; the stable MCIs had other, including vascular, morbidity. These data shed light on the heterogeneity of MCI in the population. J Am Geriatr Soc 67:232–238, 2019.
Author Hughes, Tiffany F.
Ganguli, Mary
Snitz, Beth E.
Chang, Chung‐Chou H.
Berman, Sarah B.
Sullivan, Kevin J.
Jia, Yichen
Kamboh, M. Ilyas
AuthorAffiliation 3 Department of Epidemiology, University of Pittsburgh Graduate School of Public Health
1 Department of Psychiatry, University of Pittsburgh School of Medicine
6 Department of Medicine, University of Pittsburgh School of Medicine
7 Department of Human Genetics, University of Pittsburgh of Pittsburgh Graduate School of Public Health
2 Department of Neurology, University of Pittsburgh School of Medicine
4 Department of Biostatistics, University of Pittsburgh of Pittsburgh Graduate School of Public Health
5 Department of Sociology, Anthropology, and Gerontology, Youngstown State University
AuthorAffiliation_xml – name: 3 Department of Epidemiology, University of Pittsburgh Graduate School of Public Health
– name: 7 Department of Human Genetics, University of Pittsburgh of Pittsburgh Graduate School of Public Health
– name: 2 Department of Neurology, University of Pittsburgh School of Medicine
– name: 4 Department of Biostatistics, University of Pittsburgh of Pittsburgh Graduate School of Public Health
– name: 6 Department of Medicine, University of Pittsburgh School of Medicine
– name: 1 Department of Psychiatry, University of Pittsburgh School of Medicine
– name: 5 Department of Sociology, Anthropology, and Gerontology, Youngstown State University
Author_xml – sequence: 1
  givenname: Mary
  orcidid: 0000-0003-2762-7105
  surname: Ganguli
  fullname: Ganguli, Mary
  email: gangulim@upmc.edu
  organization: Graduate School of Public Health, University of Pittsburgh
– sequence: 2
  givenname: Yichen
  surname: Jia
  fullname: Jia, Yichen
  organization: Graduate School of Public Health, University of Pittsburgh
– sequence: 3
  givenname: Tiffany F.
  surname: Hughes
  fullname: Hughes, Tiffany F.
  organization: Youngstown State University
– sequence: 4
  givenname: Beth E.
  surname: Snitz
  fullname: Snitz, Beth E.
  organization: School of Medicine, University of Pittsburgh
– sequence: 5
  givenname: Chung‐Chou H.
  surname: Chang
  fullname: Chang, Chung‐Chou H.
  organization: School of Medicine, University of Pittsburgh
– sequence: 6
  givenname: Sarah B.
  surname: Berman
  fullname: Berman, Sarah B.
  organization: School of Medicine, University of Pittsburgh
– sequence: 7
  givenname: Kevin J.
  surname: Sullivan
  fullname: Sullivan, Kevin J.
  organization: Graduate School of Public Health, University of Pittsburgh
– sequence: 8
  givenname: M. Ilyas
  surname: Kamboh
  fullname: Kamboh, M. Ilyas
  organization: Graduate School of Public Health, University of Pittsburgh
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30444944$$D View this record in MEDLINE/PubMed
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Copyright 2018, Copyright the Author Journal compilation © 2018, The American Geriatrics Society
2018, Copyright the Author Journal compilation © 2018, The American Geriatrics Society.
2019 American Geriatrics Society and Wiley Periodicals, Inc.
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Issue 2
Keywords cognition
epidemiology
aging
Language English
License 2018, Copyright the Author Journal compilation © 2018, The American Geriatrics Society.
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AUTHOR CONTRIBUTIONS. Dr. Ganguli was responsible for study concept and design, study supervision, analysis and interpretation of data, and critical revision of the manuscript for important intellectual content. Ms. Jia was responsible for analysis and interpretation of data, and critical revision of the manuscript for important intellectual content. Dr. Hughes was responsible for interpretation of data, and critical revision of the manuscript for important intellectual content. Dr. Snitz was responsible for interpretation of data, and critical revision of the manuscript for important intellectual content. Dr. Chang was responsible for study supervision, analysis and interpretation of data, and critical revision of the manuscript for important intellectual content. Dr. Berman was responsible for interpretation of data, and critical revision of the manuscript for important intellectual content. Dr. Sullivan was responsible for critical revision of the manuscript for important intellectual content. Dr. Kamboh was responsible for data acquisition and critical revision of the manuscript for important intellectual content. SPONSOR’S ROLE. The National Institute on Aging funded the research grant under which this work was completed. The sponsor had no other role in the design, methods, participant recruitment, data collection, analysis, and preparation of the manuscript.
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Snippet Background/Objective In population studies, most individuals with mild cognitive impairment (MCI) do not progress to dementia in the near term, but rather...
In population studies, most individuals with mild cognitive impairment (MCI) do not progress to dementia in the near term, but rather remain stable MCI or...
Background/ObjectiveIn population studies, most individuals with mild cognitive impairment (MCI) do not progress to dementia in the near term, but rather...
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SubjectTerms Aged
Aged, 80 and over
aging
Alzheimer's disease
Apolipoprotein E
Apolipoprotein E4
Apolipoprotein E4 - analysis
Blood Pressure
Cognition
Cognitive ability
Cognitive Dysfunction - genetics
Cognitive Dysfunction - physiopathology
Cognitive Dysfunction - psychology
Cohort Studies
Dementia
Dementia - epidemiology
Dementia - psychology
Dementia disorders
Demography
Diabetes mellitus
Disease Progression
epidemiology
Executive function
Female
Genotypes
Humans
Logistic Models
Male
Mental depression
Morbidity
Neurodegenerative diseases
Population
Population studies
Population-based studies
Regression analysis
Spatial memory
Stroke - epidemiology
Stroke - psychology
Title Mild Cognitive Impairment that Does Not Progress to Dementia: A Population‐Based Study
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjgs.15642
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Volume 67
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