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 in | Journal of the American Geriatrics Society (JAGS) Vol. 67; no. 2; pp. 232 - 238 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Wiley Subscription Services, Inc
01.02.2019
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Subjects | |
Online Access | Get full text |
ISSN | 0002-8614 1532-5415 1532-5415 |
DOI | 10.1111/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. |
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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 |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30444944$$D View this record in MEDLINE/PubMed |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 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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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 |
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