author_facet WHITE, LON
PETROVITCH, HELEN
HARDMAN, JOHN
NELSON, JAMES
DAVIS, DARON G.
ROSS, G. WEBSTER
MASAKI, KAMAL
LAUNER, LENORE
MARKESBERY, WILLIAM R.
WHITE, LON
PETROVITCH, HELEN
HARDMAN, JOHN
NELSON, JAMES
DAVIS, DARON G.
ROSS, G. WEBSTER
MASAKI, KAMAL
LAUNER, LENORE
MARKESBERY, WILLIAM R.
author WHITE, LON
PETROVITCH, HELEN
HARDMAN, JOHN
NELSON, JAMES
DAVIS, DARON G.
ROSS, G. WEBSTER
MASAKI, KAMAL
LAUNER, LENORE
MARKESBERY, WILLIAM R.
spellingShingle WHITE, LON
PETROVITCH, HELEN
HARDMAN, JOHN
NELSON, JAMES
DAVIS, DARON G.
ROSS, G. WEBSTER
MASAKI, KAMAL
LAUNER, LENORE
MARKESBERY, WILLIAM R.
Annals of the New York Academy of Sciences
Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants
History and Philosophy of Science
General Biochemistry, Genetics and Molecular Biology
General Neuroscience
author_sort white, lon
spelling WHITE, LON PETROVITCH, HELEN HARDMAN, JOHN NELSON, JAMES DAVIS, DARON G. ROSS, G. WEBSTER MASAKI, KAMAL LAUNER, LENORE MARKESBERY, WILLIAM R. 0077-8923 1749-6632 Wiley History and Philosophy of Science General Biochemistry, Genetics and Molecular Biology General Neuroscience http://dx.doi.org/10.1111/j.1749-6632.2002.tb04794.x <jats:p><jats:bold>A<jats:sc>bstract</jats:sc>: </jats:bold> Clinicopathologic data from 285 autopsies were analyzed. The decedents were long‐standing participants in the Honolulu‐Asia Aging Study, a prospective epidemiologic investigation of stroke, neurodegenerative diseases, and aging. We assessed the prevalence at death of four primary neuropathologic processes using specific microscopic lesions as indicators. An algorithm was developed to assign each decedent to one of six subsets, corresponding to pathologic dominance by microvascular lesions (14% of decedents), Alzheimer lesions (12%), hippocampal sclerosis (5%), cortical Lewy bodies (5%), codominance by two or more primary processes (9%), or without a dominant pathologic process recognized (55%). Definite or probable dementia had been identified in 118 of the decedents. The proportions of men in each subset identified as demented were (in the same order) 57%, 53%, 79%, 57%, 76%, and 25%. In this autopsied panel of older Japanese‐American men, the importance of microvascular lesions as a likely explanation for dementia was nearly equal to that of Alzheimer lesions. The cerebrovascular lesion type most essentially and inclusively related to dementia was multiple microinfarction.</jats:p> Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants Annals of the New York Academy of Sciences
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title Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants
title_unstemmed Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants
title_full Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants
title_fullStr Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants
title_full_unstemmed Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants
title_short Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants
title_sort cerebrovascular pathology and dementia in autopsied honolulu‐asia aging study participants
topic History and Philosophy of Science
General Biochemistry, Genetics and Molecular Biology
General Neuroscience
url http://dx.doi.org/10.1111/j.1749-6632.2002.tb04794.x
publishDate 2002
physical 9-23
description <jats:p><jats:bold>A<jats:sc>bstract</jats:sc>: </jats:bold> Clinicopathologic data from 285 autopsies were analyzed. The decedents were long‐standing participants in the Honolulu‐Asia Aging Study, a prospective epidemiologic investigation of stroke, neurodegenerative diseases, and aging. We assessed the prevalence at death of four primary neuropathologic processes using specific microscopic lesions as indicators. An algorithm was developed to assign each decedent to one of six subsets, corresponding to pathologic dominance by microvascular lesions (14% of decedents), Alzheimer lesions (12%), hippocampal sclerosis (5%), cortical Lewy bodies (5%), codominance by two or more primary processes (9%), or without a dominant pathologic process recognized (55%). Definite or probable dementia had been identified in 118 of the decedents. The proportions of men in each subset identified as demented were (in the same order) 57%, 53%, 79%, 57%, 76%, and 25%. In this autopsied panel of older Japanese‐American men, the importance of microvascular lesions as a likely explanation for dementia was nearly equal to that of Alzheimer lesions. The cerebrovascular lesion type most essentially and inclusively related to dementia was multiple microinfarction.</jats:p>
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author WHITE, LON, PETROVITCH, HELEN, HARDMAN, JOHN, NELSON, JAMES, DAVIS, DARON G., ROSS, G. WEBSTER, MASAKI, KAMAL, LAUNER, LENORE, MARKESBERY, WILLIAM R.
author_facet WHITE, LON, PETROVITCH, HELEN, HARDMAN, JOHN, NELSON, JAMES, DAVIS, DARON G., ROSS, G. WEBSTER, MASAKI, KAMAL, LAUNER, LENORE, MARKESBERY, WILLIAM R., WHITE, LON, PETROVITCH, HELEN, HARDMAN, JOHN, NELSON, JAMES, DAVIS, DARON G., ROSS, G. WEBSTER, MASAKI, KAMAL, LAUNER, LENORE, MARKESBERY, WILLIAM R.
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description <jats:p><jats:bold>A<jats:sc>bstract</jats:sc>: </jats:bold> Clinicopathologic data from 285 autopsies were analyzed. The decedents were long‐standing participants in the Honolulu‐Asia Aging Study, a prospective epidemiologic investigation of stroke, neurodegenerative diseases, and aging. We assessed the prevalence at death of four primary neuropathologic processes using specific microscopic lesions as indicators. An algorithm was developed to assign each decedent to one of six subsets, corresponding to pathologic dominance by microvascular lesions (14% of decedents), Alzheimer lesions (12%), hippocampal sclerosis (5%), cortical Lewy bodies (5%), codominance by two or more primary processes (9%), or without a dominant pathologic process recognized (55%). Definite or probable dementia had been identified in 118 of the decedents. The proportions of men in each subset identified as demented were (in the same order) 57%, 53%, 79%, 57%, 76%, and 25%. In this autopsied panel of older Japanese‐American men, the importance of microvascular lesions as a likely explanation for dementia was nearly equal to that of Alzheimer lesions. The cerebrovascular lesion type most essentially and inclusively related to dementia was multiple microinfarction.</jats:p>
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spelling WHITE, LON PETROVITCH, HELEN HARDMAN, JOHN NELSON, JAMES DAVIS, DARON G. ROSS, G. WEBSTER MASAKI, KAMAL LAUNER, LENORE MARKESBERY, WILLIAM R. 0077-8923 1749-6632 Wiley History and Philosophy of Science General Biochemistry, Genetics and Molecular Biology General Neuroscience http://dx.doi.org/10.1111/j.1749-6632.2002.tb04794.x <jats:p><jats:bold>A<jats:sc>bstract</jats:sc>: </jats:bold> Clinicopathologic data from 285 autopsies were analyzed. The decedents were long‐standing participants in the Honolulu‐Asia Aging Study, a prospective epidemiologic investigation of stroke, neurodegenerative diseases, and aging. We assessed the prevalence at death of four primary neuropathologic processes using specific microscopic lesions as indicators. An algorithm was developed to assign each decedent to one of six subsets, corresponding to pathologic dominance by microvascular lesions (14% of decedents), Alzheimer lesions (12%), hippocampal sclerosis (5%), cortical Lewy bodies (5%), codominance by two or more primary processes (9%), or without a dominant pathologic process recognized (55%). Definite or probable dementia had been identified in 118 of the decedents. The proportions of men in each subset identified as demented were (in the same order) 57%, 53%, 79%, 57%, 76%, and 25%. In this autopsied panel of older Japanese‐American men, the importance of microvascular lesions as a likely explanation for dementia was nearly equal to that of Alzheimer lesions. The cerebrovascular lesion type most essentially and inclusively related to dementia was multiple microinfarction.</jats:p> Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants Annals of the New York Academy of Sciences
spellingShingle WHITE, LON, PETROVITCH, HELEN, HARDMAN, JOHN, NELSON, JAMES, DAVIS, DARON G., ROSS, G. WEBSTER, MASAKI, KAMAL, LAUNER, LENORE, MARKESBERY, WILLIAM R., Annals of the New York Academy of Sciences, Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants, History and Philosophy of Science, General Biochemistry, Genetics and Molecular Biology, General Neuroscience
title Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants
title_full Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants
title_fullStr Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants
title_full_unstemmed Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants
title_short Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants
title_sort cerebrovascular pathology and dementia in autopsied honolulu‐asia aging study participants
title_unstemmed Cerebrovascular Pathology and Dementia in Autopsied Honolulu‐Asia Aging Study Participants
topic History and Philosophy of Science, General Biochemistry, Genetics and Molecular Biology, General Neuroscience
url http://dx.doi.org/10.1111/j.1749-6632.2002.tb04794.x