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Sex and age interact to determine clinicopathologic differences in Alzheimer’s disease

Women reportedly make up two-thirds of Alzheimer’s disease (AD) dementia sufferers. Many estimates regarding AD, however, are based on clinical series lacking autopsy confirmation. The Florida Autopsied Multi-Ethnic (FLAME) cohort was queried for AD cases with a total of 1625 identified ranging in a...

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Autores principales: Liesinger, Amanda M., Graff-Radford, Neill R., Duara, Ranjan, Carter, Rickey E., Hanna Al-Shaikh, Fadi S., Koga, Shunsuke, Hinkle, Kelly M., DiLello, Sarah K., Johnson, McKenna F., Aziz, Adel, Ertekin-Taner, Nilufer, Ross, Owen A., Dickson, Dennis W., Murray, Melissa E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280837/
https://www.ncbi.nlm.nih.gov/pubmed/30219939
http://dx.doi.org/10.1007/s00401-018-1908-x
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author Liesinger, Amanda M.
Graff-Radford, Neill R.
Duara, Ranjan
Carter, Rickey E.
Hanna Al-Shaikh, Fadi S.
Koga, Shunsuke
Hinkle, Kelly M.
DiLello, Sarah K.
Johnson, McKenna F.
Aziz, Adel
Ertekin-Taner, Nilufer
Ross, Owen A.
Dickson, Dennis W.
Murray, Melissa E.
author_facet Liesinger, Amanda M.
Graff-Radford, Neill R.
Duara, Ranjan
Carter, Rickey E.
Hanna Al-Shaikh, Fadi S.
Koga, Shunsuke
Hinkle, Kelly M.
DiLello, Sarah K.
Johnson, McKenna F.
Aziz, Adel
Ertekin-Taner, Nilufer
Ross, Owen A.
Dickson, Dennis W.
Murray, Melissa E.
author_sort Liesinger, Amanda M.
collection PubMed
description Women reportedly make up two-thirds of Alzheimer’s disease (AD) dementia sufferers. Many estimates regarding AD, however, are based on clinical series lacking autopsy confirmation. The Florida Autopsied Multi-Ethnic (FLAME) cohort was queried for AD cases with a total of 1625 identified ranging in age from 53 to 102 years at death. Standard neuropathologic procedures were employed and clinical information was retrospectively collected. Clinicopathologic and genetic data (MAPT and APOE) were stratified by sex. Within the neuropathologically diagnosed AD cohort, the overall number of women and men did not differ. Men were younger at onset of cognitive symptoms, had a shorter disease duration, and more often had atypical (non-amnestic) clinical presentations. The frequency of autopsy-confirmed AD among women and men stratified by age at death revealed an inverse U-shaped curve in men and a U-shaped curve in women, with both curves having inflections at approximately 70 years of age. Regional counts of neurofibrillary tangles differed in women and men, especially when examined by age intervals. Women had overall greater severity of neurofibrillary tangle counts compared to men, especially in the hippocampus. Men were more often classified as hippocampal sparing AD, whereas limbic predominant AD was more common in women. Men and women did not differ in frequency of MAPT haplotype or APOE genotype. Atypical clinical presentations, younger age at onset and shorter disease duration were more frequent in men, suggesting that the lower reported frequency of AD in men may be due to more frequent atypical clinical presentations not recognized as AD. Our data suggest that neuropathologically diagnosed AD cases have the same frequency of women and men, but their clinical presentations and ages at onset tend to differ. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00401-018-1908-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-62808372018-12-26 Sex and age interact to determine clinicopathologic differences in Alzheimer’s disease Liesinger, Amanda M. Graff-Radford, Neill R. Duara, Ranjan Carter, Rickey E. Hanna Al-Shaikh, Fadi S. Koga, Shunsuke Hinkle, Kelly M. DiLello, Sarah K. Johnson, McKenna F. Aziz, Adel Ertekin-Taner, Nilufer Ross, Owen A. Dickson, Dennis W. Murray, Melissa E. Acta Neuropathol Original Paper Women reportedly make up two-thirds of Alzheimer’s disease (AD) dementia sufferers. Many estimates regarding AD, however, are based on clinical series lacking autopsy confirmation. The Florida Autopsied Multi-Ethnic (FLAME) cohort was queried for AD cases with a total of 1625 identified ranging in age from 53 to 102 years at death. Standard neuropathologic procedures were employed and clinical information was retrospectively collected. Clinicopathologic and genetic data (MAPT and APOE) were stratified by sex. Within the neuropathologically diagnosed AD cohort, the overall number of women and men did not differ. Men were younger at onset of cognitive symptoms, had a shorter disease duration, and more often had atypical (non-amnestic) clinical presentations. The frequency of autopsy-confirmed AD among women and men stratified by age at death revealed an inverse U-shaped curve in men and a U-shaped curve in women, with both curves having inflections at approximately 70 years of age. Regional counts of neurofibrillary tangles differed in women and men, especially when examined by age intervals. Women had overall greater severity of neurofibrillary tangle counts compared to men, especially in the hippocampus. Men were more often classified as hippocampal sparing AD, whereas limbic predominant AD was more common in women. Men and women did not differ in frequency of MAPT haplotype or APOE genotype. Atypical clinical presentations, younger age at onset and shorter disease duration were more frequent in men, suggesting that the lower reported frequency of AD in men may be due to more frequent atypical clinical presentations not recognized as AD. Our data suggest that neuropathologically diagnosed AD cases have the same frequency of women and men, but their clinical presentations and ages at onset tend to differ. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00401-018-1908-x) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-09-15 2018 /pmc/articles/PMC6280837/ /pubmed/30219939 http://dx.doi.org/10.1007/s00401-018-1908-x Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Paper
Liesinger, Amanda M.
Graff-Radford, Neill R.
Duara, Ranjan
Carter, Rickey E.
Hanna Al-Shaikh, Fadi S.
Koga, Shunsuke
Hinkle, Kelly M.
DiLello, Sarah K.
Johnson, McKenna F.
Aziz, Adel
Ertekin-Taner, Nilufer
Ross, Owen A.
Dickson, Dennis W.
Murray, Melissa E.
Sex and age interact to determine clinicopathologic differences in Alzheimer’s disease
title Sex and age interact to determine clinicopathologic differences in Alzheimer’s disease
title_full Sex and age interact to determine clinicopathologic differences in Alzheimer’s disease
title_fullStr Sex and age interact to determine clinicopathologic differences in Alzheimer’s disease
title_full_unstemmed Sex and age interact to determine clinicopathologic differences in Alzheimer’s disease
title_short Sex and age interact to determine clinicopathologic differences in Alzheimer’s disease
title_sort sex and age interact to determine clinicopathologic differences in alzheimer’s disease
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280837/
https://www.ncbi.nlm.nih.gov/pubmed/30219939
http://dx.doi.org/10.1007/s00401-018-1908-x
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