Marked gender differences in progression of mild cognitive impairment over 8 years
Abstract Introduction This study examined whether, among subjects with mild cognitive impairment (MCI), women progressed at faster rates than men. Methods We examine longitudinal rates of change from baseline in 398 MCI subjects (141 females and 257 males) in the Alzheimer's Disease Neuroimagin...
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Published in | Alzheimer's & dementia : translational research & clinical interventions Vol. 1; no. 2; pp. 103 - 110 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.09.2015
John Wiley & Sons, Inc Elsevier |
Subjects | |
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Abstract | Abstract Introduction This study examined whether, among subjects with mild cognitive impairment (MCI), women progressed at faster rates than men. Methods We examine longitudinal rates of change from baseline in 398 MCI subjects (141 females and 257 males) in the Alzheimer's Disease Neuroimaging Initiative-1, followed for up to 8 years (mean, 4.1 ± 2.5 years) using mixed-effects models incorporating all follow-ups (mean, 8 ± 4 visits). Results Women progressed at faster rates than men on the Alzheimer's disease assessment scale-cognitive subscale (ADAS-Cog; P = .001) and clinical dementia rating-sum of boxes (CDR-SB; P = .003). Quadratic fit for change over time was significant for both ADAS-Cog ( P = .001) and CDR-SB ( P = .004), and the additional acceleration in women was 100% for ADAS-Cog and 143% for CDR-SB. The variability of change was greater in women. The gender effect was greater in apolipoprotein E ( APOE ) ε4 carriers. Discussion Women with MCI have greater longitudinal rates of cognitive and functional progression than men. Studies to confirm and uncover potential mechanisms appear to be warranted. Trial Registration ADNI ClinicalTrials.gov identifier: NCT00106899. |
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AbstractList | This study examined whether, among subjects with mild cognitive impairment (MCI), women progressed at faster rates than men.
We examine longitudinal rates of change from baseline in 398 MCI subjects (141 females and 257 males) in the Alzheimer's Disease Neuroimaging Initiative-1, followed for up to 8 years (mean, 4.1 ± 2.5 years) using mixed-effects models incorporating all follow-ups (mean, 8 ± 4 visits).
Women progressed at faster rates than men on the Alzheimer's disease assessment scale-cognitive subscale (ADAS-Cog; P = .001) and clinical dementia rating-sum of boxes (CDR-SB; P = .003). Quadratic fit for change over time was significant for both ADAS-Cog (P = .001) and CDR-SB (P = .004), and the additional acceleration in women was 100% for ADAS-Cog and 143% for CDR-SB. The variability of change was greater in women. The gender effect was greater in apolipoprotein E (APOE) ε4 carriers.
Women with MCI have greater longitudinal rates of cognitive and functional progression than men. Studies to confirm and uncover potential mechanisms appear to be warranted.
ADNI ClinicalTrials.gov identifier: NCT00106899. Introduction This study examined whether, among subjects with mild cognitive impairment (MCI), women progressed at faster rates than men. Methods We examine longitudinal rates of change from baseline in 398 MCI subjects (141 females and 257 males) in the Alzheimer's Disease Neuroimaging Initiative‐1, followed for up to 8 years (mean, 4.1 ± 2.5 years) using mixed‐effects models incorporating all follow‐ups (mean, 8 ± 4 visits). Results Women progressed at faster rates than men on the Alzheimer's disease assessment scale‐cognitive subscale (ADAS‐Cog; P = .001) and clinical dementia rating‐sum of boxes (CDR‐SB; P = .003). Quadratic fit for change over time was significant for both ADAS‐Cog (P = .001) and CDR‐SB (P = .004), and the additional acceleration in women was 100% for ADAS‐Cog and 143% for CDR‐SB. The variability of change was greater in women. The gender effect was greater in apolipoprotein E (APOE) ε4 carriers. Discussion Women with MCI have greater longitudinal rates of cognitive and functional progression than men. Studies to confirm and uncover potential mechanisms appear to be warranted. Trial Registration ADNI ClinicalTrials.gov identifier: NCT00106899. INTRODUCTIONThis study examined whether, among subjects with mild cognitive impairment (MCI), women progressed at faster rates than men.METHODSWe examine longitudinal rates of change from baseline in 398 MCI subjects (141 Females, 257 Males) in the Alzheimer's Disease Neuroimaging Initiative-1 (ADNI-1), followed for up to 8 years (mean 4.1±2.5 years) using mixed effects models incorporating all follow ups (mean 8±4 visits).RESULTSWomen progressed at faster rates than men on ADAS-Cog (p=0.001) and CDR-SB (p=0.003). Quadratic fit for change over time was significant for both ADAS-Cog (p=0.001) and CDR-SB (p=0.004), and the additional acceleration in women was 100% for ADAS-Cog and 143% for CDR-SB. The variability of change was greater in women. The gender effect was greater in ApoE4 carriers.DISCUSSIONWomen with MCI have greater longitudinal rates of cognitive and functional progression than men. Studies to confirm and uncover potential mechanisms appear to be warranted. IntroductionThis study examined whether, among subjects with mild cognitive impairment (MCI), women progressed at faster rates than men.MethodsWe examine longitudinal rates of change from baseline in 398 MCI subjects (141 females and 257 males) in the Alzheimer's Disease Neuroimaging Initiative‐1, followed for up to 8 years (mean, 4.1 ± 2.5 years) using mixed‐effects models incorporating all follow‐ups (mean, 8 ± 4 visits).ResultsWomen progressed at faster rates than men on the Alzheimer's disease assessment scale‐cognitive subscale (ADAS‐Cog; P = .001) and clinical dementia rating‐sum of boxes (CDR‐SB; P = .003). Quadratic fit for change over time was significant for both ADAS‐Cog (P = .001) and CDR‐SB (P = .004), and the additional acceleration in women was 100% for ADAS‐Cog and 143% for CDR‐SB. The variability of change was greater in women. The gender effect was greater in apolipoprotein E (APOE) ε4 carriers.DiscussionWomen with MCI have greater longitudinal rates of cognitive and functional progression than men. Studies to confirm and uncover potential mechanisms appear to be warranted.Trial RegistrationADNI ClinicalTrials.gov identifier: NCT00106899. Abstract Introduction This study examined whether, among subjects with mild cognitive impairment (MCI), women progressed at faster rates than men. Methods We examine longitudinal rates of change from baseline in 398 MCI subjects (141 females and 257 males) in the Alzheimer's Disease Neuroimaging Initiative-1, followed for up to 8 years (mean, 4.1 ± 2.5 years) using mixed-effects models incorporating all follow-ups (mean, 8 ± 4 visits). Results Women progressed at faster rates than men on the Alzheimer's disease assessment scale-cognitive subscale (ADAS-Cog; P = .001) and clinical dementia rating-sum of boxes (CDR-SB; P = .003). Quadratic fit for change over time was significant for both ADAS-Cog ( P = .001) and CDR-SB ( P = .004), and the additional acceleration in women was 100% for ADAS-Cog and 143% for CDR-SB. The variability of change was greater in women. The gender effect was greater in apolipoprotein E ( APOE ) ε4 carriers. Discussion Women with MCI have greater longitudinal rates of cognitive and functional progression than men. Studies to confirm and uncover potential mechanisms appear to be warranted. Trial Registration ADNI ClinicalTrials.gov identifier: NCT00106899. This study examined whether, among subjects with mild cognitive impairment (MCI), women progressed at faster rates than men. We examine longitudinal rates of change from baseline in 398 MCI subjects (141 Females, 257 Males) in the Alzheimer's Disease Neuroimaging Initiative-1 (ADNI-1), followed for up to 8 years (mean 4.1±2.5 years) using mixed effects models incorporating all follow ups (mean 8±4 visits). Women progressed at faster rates than men on ADAS-Cog (p=0.001) and CDR-SB (p=0.003). Quadratic fit for change over time was significant for both ADAS-Cog (p=0.001) and CDR-SB (p=0.004), and the additional acceleration in women was 100% for ADAS-Cog and 143% for CDR-SB. The variability of change was greater in women. The gender effect was greater in ApoE4 carriers. Women with MCI have greater longitudinal rates of cognitive and functional progression than men. Studies to confirm and uncover potential mechanisms appear to be warranted. |
Author | Rathakrishnan, Bharath G. Lin, Katherine A. Petrella, Jeffrey R. Choudhury, Kingshuk Roy Marks, David M. Doraiswamy, P. Murali |
AuthorAffiliation | c Department of Radiology, Duke University Medical Center, Durham, NC, USA a Department of Psychiatry, Duke University Medical Center, Durham, NC, USA b Duke Institute for Brain Sciences, Duke University, Durham, NC, USA |
AuthorAffiliation_xml | – name: a Department of Psychiatry, Duke University Medical Center, Durham, NC, USA – name: c Department of Radiology, Duke University Medical Center, Durham, NC, USA – name: b Duke Institute for Brain Sciences, Duke University, Durham, NC, USA |
Author_xml | – sequence: 1 fullname: Lin, Katherine A – sequence: 2 fullname: Choudhury, Kingshuk Roy – sequence: 3 fullname: Rathakrishnan, Bharath G – sequence: 4 fullname: Marks, David M – sequence: 5 fullname: Petrella, Jeffrey R – sequence: 6 fullname: Doraiswamy, P. Murali |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26451386$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | The Authors 2015 The Authors 2015 The Authors. Published by Elsevier Inc. on behalf of the Alzheimer's Association. 2015. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2015 The Authors 2015 |
Copyright_xml | – notice: The Authors – notice: 2015 The Authors – notice: 2015 The Authors. Published by Elsevier Inc. on behalf of the Alzheimer's Association. – notice: 2015. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. – notice: 2015 The Authors 2015 |
CorporateAuthor | Alzheimer's Disease Neuroimaging Initiative |
CorporateAuthor_xml | – name: Alzheimer's Disease Neuroimaging Initiative |
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Keywords | Secondary prevention Apolipoprotein ε4 Gender differences Activities of daily living Beta-amyloid prevalence secondary prevention gender differences disease modification |
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publication-title: Neurobiol Aging – volume: 39 start-page: 849 year: 2004 end-page: 854 article-title: Analysis of premature centromere division (PCD) of the X chromosome in Alzheimer patients through the cell cycle publication-title: Exp Gerontol – volume: 34 start-page: 2077.e19 year: 2013 end-page: 2077.e20 article-title: Androgen receptor gene and gender specific Alzheimer's disease publication-title: Neurobiol Aging – volume: 468 start-page: 202 year: 2010 end-page: 206 article-title: Association of the aromatase gene with Alzheimer's disease in women publication-title: Neurosci Lett – volume: 5 start-page: 38 year: 2014 end-page: 40 article-title: Alzheimer disease in post‐menopausal women: Intervene in the critical window period publication-title: J Midlife Health – volume: 31 start-page: 1463 year: 2010 end-page: 1480 article-title: Sex and age differences in atrophic rates: An ADNI study with n1368 MRI scans publication-title: Neurobiol Aging – volume: 62 start-page: 953 year: 2005 end-page: 957 article-title: Sex, apolipoprotein E epsilon 4 status, and hippocampal volume in mild cognitive impairment publication-title: Arch Neurol – volume: 70 start-page: 418 year: 2011 end-page: 426 article-title: Incidence of dementia and cognitive impairment, not dementia in the United States publication-title: Ann Neurol – volume: 73 start-page: 917 year: 2009 end-page: 920 article-title: The X‐chromosome instability phenotype in Alzheimer's disease: A clinical sign of accelerating aging? publication-title: Med Hypotheses – volume: 29 start-page: 1783 year: 2008 end-page: 1794 article-title: The ApoE4 genotype alters the response of microglia and macrophages to 17B‐estradiol publication-title: Neurobiol Aging – volume: 278 start-page: 1349 year: 1997 end-page: 1356 article-title: Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease: A meta‐analysis: APOE and Alzheimer disease meta analysis consortium publication-title: JAMA – volume: 6 start-page: 37 year: 2014 end-page: 48 article-title: Clinical epidemiology of Alzheimer's disease: Assessing sex and gender differences publication-title: Clin Epidemiol – volume: 49 start-page: 1498 year: 1997 end-page: 1504 article-title: Lifetime risk of dementia and Alzheimer's disease. The impact of mortality on risk estimates in the Framingham Study publication-title: Neurology – volume: 13 start-page: 216 year: 1999 end-page: 221 article-title: Evidence for an interaction between apolipoprotein E genotype, gender, and Alzheimer disease publication-title: Alzheimer Dis Assoc Disord – volume: 43 start-page: 1137 year: 2015 end-page: 1148 article-title: Update on the neuroprotective effect of estrogen receptor alpha against Alzheimer's disease publication-title: J Alzheimers Dis – volume: 9 start-page: S39 issue: (1 Suppl) year: 2013 end-page: S44 article-title: Progression of Alzheimer disease as measured by clinical dementia rating sum of boxes scores publication-title: Alzheimers Dement – volume: 140 start-page: 256 year: 1994 end-page: 261 article-title: Estrogen deficiency and risk of Alzheimer's disease in women publication-title: Am J Epidemiol – volume: 80 start-page: 1778 year: 2013 end-page: 1783 article-title: Alzheimer disease in the United States (2010‐2050) estimated using the 2010 census publication-title: Neurology – volume: 62 start-page: 685 year: 2005 end-page: 691 article-title: Sex differences in the clinical manifestations of Alzheimer disease pathology publication-title: Arch Gen Psychiatry – volume: 29 start-page: 610 year: 2014 end-page: 615 article-title: Sex and ESR1 genotype may influence the response to treatment with donepezil and rivastigmine in patients with Alzheimer's disease publication-title: Int J Geriatr Psychiatry – volume: 58 start-page: 803 year: 1996 end-page: 811 article-title: Gender difference in apolipoprotein E‐associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in women publication-title: Am J Hum Genet – volume: 153 start-page: 132 year: 2001 end-page: 136 article-title: Is the risk of developing Alzheimer's disease greater for women than for men? publication-title: Am J Epidemiol – volume: 34 start-page: 989 year: 2012 end-page: 998 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Snippet | Abstract Introduction This study examined whether, among subjects with mild cognitive impairment (MCI), women progressed at faster rates than men. Methods We... This study examined whether, among subjects with mild cognitive impairment (MCI), women progressed at faster rates than men. We examine longitudinal rates of... Introduction This study examined whether, among subjects with mild cognitive impairment (MCI), women progressed at faster rates than men. Methods We examine... IntroductionThis study examined whether, among subjects with mild cognitive impairment (MCI), women progressed at faster rates than men.MethodsWe examine... INTRODUCTIONThis study examined whether, among subjects with mild cognitive impairment (MCI), women progressed at faster rates than men.METHODSWe examine... |
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SubjectTerms | Activities of daily living Age Alzheimer's disease Apolipoprotein ε4 Apolipoproteins Beta-amyloid Cognition & reasoning Cognitive ability Dementia Education Females Gender differences Hypotheses Medical imaging Memory Neurology Normal distribution Older people Other Procedure manuals Secondary prevention |
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Title | Marked gender differences in progression of mild cognitive impairment over 8 years |
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