Association of vascular and degenerative brain pathologies and past medical history from the National Alzheimer’s Coordinating Center Database
Abstract The relationship between past medical histories (PMH) and dementia-related neuropathologies is not well understood. Using the National Alzheimer's Coordinating Center (NACC) database, we explored the relationship between patient-reported PMH and various vascular and degenerative neurop...
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Veröffentlicht in: | Journal of neuropathology and experimental neurology 2023-05, Vol.82 (5), p.390-401 |
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description | Abstract
The relationship between past medical histories (PMH) and dementia-related neuropathologies is not well understood. Using the National Alzheimer's Coordinating Center (NACC) database, we explored the relationship between patient-reported PMH and various vascular and degenerative neuropathologies. We examined the following PMH: transient ischemic attack (TIA), stroke, traumatic brain injury, seizures, hypertension, cardiovascular events, hypercholesterolemia, B12 deficiency, diabetes mellitus, and thyroid disease. We dichotomized the following neuropathologies: atherosclerosis, arteriolosclerosis, cerebral amyloid angiopathy (CAA), Alzheimer disease neuropathology (ADNP), Lewy bodies (LB), hippocampal sclerosis, frontotemporal lobar degeneration (FTLD), and TAR DNA-binding protein-43 (TDP-43). Separate logistic regression models assessed the relationship between the outcome of individual neuropathologies and all PMHs. Additional logistic regressions were stratified by sex to further examine these associations. Hypertension history was associated with an increased likelihood of atherosclerosis (OR = 1.7) and arteriolosclerosis (OR = 1.3), but decreased odds of ADNP (OR = 0.81), CAA (OR = 0.79), and LB (OR = 0.78). History of TIA was associated with an increased likelihood of atherosclerosis (OR = 1.3) and arteriolosclerosis (OR = 1.4) and lower odds of ADNP (OR = 0.72). Seizure history was associated with an increased likelihood of ADNP (OR = 1.9) and lower odds of FTLD (OR = 0.49). Hypertension history was associated with a greater likelihood of vascular pathologies yet a lower likelihood of ADNP and other neurodegenerative pathologies. |
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The relationship between past medical histories (PMH) and dementia-related neuropathologies is not well understood. Using the National Alzheimer's Coordinating Center (NACC) database, we explored the relationship between patient-reported PMH and various vascular and degenerative neuropathologies. We examined the following PMH: transient ischemic attack (TIA), stroke, traumatic brain injury, seizures, hypertension, cardiovascular events, hypercholesterolemia, B12 deficiency, diabetes mellitus, and thyroid disease. We dichotomized the following neuropathologies: atherosclerosis, arteriolosclerosis, cerebral amyloid angiopathy (CAA), Alzheimer disease neuropathology (ADNP), Lewy bodies (LB), hippocampal sclerosis, frontotemporal lobar degeneration (FTLD), and TAR DNA-binding protein-43 (TDP-43). Separate logistic regression models assessed the relationship between the outcome of individual neuropathologies and all PMHs. Additional logistic regressions were stratified by sex to further examine these associations. Hypertension history was associated with an increased likelihood of atherosclerosis (OR = 1.7) and arteriolosclerosis (OR = 1.3), but decreased odds of ADNP (OR = 0.81), CAA (OR = 0.79), and LB (OR = 0.78). History of TIA was associated with an increased likelihood of atherosclerosis (OR = 1.3) and arteriolosclerosis (OR = 1.4) and lower odds of ADNP (OR = 0.72). Seizure history was associated with an increased likelihood of ADNP (OR = 1.9) and lower odds of FTLD (OR = 0.49). Hypertension history was associated with a greater likelihood of vascular pathologies yet a lower likelihood of ADNP and other neurodegenerative pathologies.</description><identifier>ISSN: 0022-3069</identifier><identifier>EISSN: 1554-6578</identifier><identifier>DOI: 10.1093/jnen/nlad020</identifier><identifier>PMID: 36947583</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Alzheimer Disease - pathology ; Alzheimer's disease ; Arteriolosclerosis - pathology ; Atherosclerosis ; Atherosclerosis - complications ; Atherosclerosis - pathology ; Blood circulation disorders ; Brain - pathology ; Complications and side effects ; Degeneration ; Frontotemporal Dementia - pathology ; Humans ; Hypertension ; Hypertension - complications ; Hypertension - pathology ; Ischemic Attack, Transient - pathology ; Medical history ; Nervous system ; Original ; Risk factors ; Statistics ; Transient ischemic attack</subject><ispartof>Journal of neuropathology and experimental neurology, 2023-05, Vol.82 (5), p.390-401</ispartof><rights>The Author(s) 2023. Published by Oxford University Press on behalf of American Association of Neuropathologists, Inc. All rights reserved. For permissions, please email: journals.permissions@oup.com 2023</rights><rights>The Author(s) 2023. Published by Oxford University Press on behalf of American Association of Neuropathologists, Inc. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><rights>COPYRIGHT 2023 Oxford University Press</rights><rights>The Author(s) 2023. Published by Oxford University Press on behalf of American Association of Neuropathologists, Inc. All rights reserved. For permissions, please email: journals.permissions@oup.com</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c512t-6120e2048a7f82dcc1a40048ed051ca0f2ef49017e39f5892e8125be4a3ae8f83</citedby><cites>FETCH-LOGICAL-c512t-6120e2048a7f82dcc1a40048ed051ca0f2ef49017e39f5892e8125be4a3ae8f83</cites><orcidid>0000-0002-9618-6385</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,1584,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36947583$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Scambray, Kiana A</creatorcontrib><creatorcontrib>Nguyen, Hannah L</creatorcontrib><creatorcontrib>Sajjadi, S Ahmad</creatorcontrib><title>Association of vascular and degenerative brain pathologies and past medical history from the National Alzheimer’s Coordinating Center Database</title><title>Journal of neuropathology and experimental neurology</title><addtitle>J Neuropathol Exp Neurol</addtitle><description>Abstract
The relationship between past medical histories (PMH) and dementia-related neuropathologies is not well understood. Using the National Alzheimer's Coordinating Center (NACC) database, we explored the relationship between patient-reported PMH and various vascular and degenerative neuropathologies. We examined the following PMH: transient ischemic attack (TIA), stroke, traumatic brain injury, seizures, hypertension, cardiovascular events, hypercholesterolemia, B12 deficiency, diabetes mellitus, and thyroid disease. We dichotomized the following neuropathologies: atherosclerosis, arteriolosclerosis, cerebral amyloid angiopathy (CAA), Alzheimer disease neuropathology (ADNP), Lewy bodies (LB), hippocampal sclerosis, frontotemporal lobar degeneration (FTLD), and TAR DNA-binding protein-43 (TDP-43). Separate logistic regression models assessed the relationship between the outcome of individual neuropathologies and all PMHs. Additional logistic regressions were stratified by sex to further examine these associations. Hypertension history was associated with an increased likelihood of atherosclerosis (OR = 1.7) and arteriolosclerosis (OR = 1.3), but decreased odds of ADNP (OR = 0.81), CAA (OR = 0.79), and LB (OR = 0.78). History of TIA was associated with an increased likelihood of atherosclerosis (OR = 1.3) and arteriolosclerosis (OR = 1.4) and lower odds of ADNP (OR = 0.72). Seizure history was associated with an increased likelihood of ADNP (OR = 1.9) and lower odds of FTLD (OR = 0.49). Hypertension history was associated with a greater likelihood of vascular pathologies yet a lower likelihood of ADNP and other neurodegenerative pathologies.</description><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer's disease</subject><subject>Arteriolosclerosis - pathology</subject><subject>Atherosclerosis</subject><subject>Atherosclerosis - complications</subject><subject>Atherosclerosis - pathology</subject><subject>Blood circulation disorders</subject><subject>Brain - pathology</subject><subject>Complications and side effects</subject><subject>Degeneration</subject><subject>Frontotemporal Dementia - pathology</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Hypertension - complications</subject><subject>Hypertension - pathology</subject><subject>Ischemic Attack, Transient - pathology</subject><subject>Medical history</subject><subject>Nervous system</subject><subject>Original</subject><subject>Risk factors</subject><subject>Statistics</subject><subject>Transient ischemic attack</subject><issn>0022-3069</issn><issn>1554-6578</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kstu1DAUhiMEokNhxxpZYgEL0tpOnDirajRcpQo2sLbOOMeJR4k92MlIZcUjsOX1eBI8naFQhJAXlv1_5z8XnSx7zOgZo01xvnHozt0ALeX0TrZgQpR5JWp5N1tQynle0Ko5yR7EuKGUNrQp72cnRdWUtZDFIvu2jNFrC5P1jnhDdhD1PEAg4FrSYocOQxJ3SNYBrCNbmHo_-M5ivEa2ECcyYms1DKS3cfLhipjgRzL1SN5f-yZlOXzp0Y4Yfnz9HsnK-9Bal0TXkRW6CQN5CROsIeLD7J6BIeKj432afXr96uPqbX754c271fIy14LxKa8Yp8hpKaE2krdaMyhpemJLBdNADUdTNpTVWDRGyIajZFyssYQCUBpZnGYXB9_tvE7161RFgEFtgx0hXCkPVt1WnO1V53eKUcZqJsrk8PzoEPznGeOkRhs1DgM49HNUvJZNzXgj9sme_oVu_BzSYKIqUr2Sl7QSv6kOBlTWGZ8S672pWtaVLHlqqErU2T-odFocrfYOjU3_twJeHAJ08DEGNDdNMqr2K6T2K6SOK5TwJ38O5gb-tTMJeHYA_Lz9v9VPy7LThw</recordid><startdate>20230501</startdate><enddate>20230501</enddate><creator>Scambray, Kiana A</creator><creator>Nguyen, Hannah L</creator><creator>Sajjadi, S Ahmad</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9618-6385</orcidid></search><sort><creationdate>20230501</creationdate><title>Association of vascular and degenerative brain pathologies and past medical history from the National Alzheimer’s Coordinating Center Database</title><author>Scambray, Kiana A ; Nguyen, Hannah L ; Sajjadi, S Ahmad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c512t-6120e2048a7f82dcc1a40048ed051ca0f2ef49017e39f5892e8125be4a3ae8f83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Alzheimer Disease - pathology</topic><topic>Alzheimer's disease</topic><topic>Arteriolosclerosis - pathology</topic><topic>Atherosclerosis</topic><topic>Atherosclerosis - complications</topic><topic>Atherosclerosis - pathology</topic><topic>Blood circulation disorders</topic><topic>Brain - pathology</topic><topic>Complications and side effects</topic><topic>Degeneration</topic><topic>Frontotemporal Dementia - pathology</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Hypertension - complications</topic><topic>Hypertension - pathology</topic><topic>Ischemic Attack, Transient - pathology</topic><topic>Medical history</topic><topic>Nervous system</topic><topic>Original</topic><topic>Risk factors</topic><topic>Statistics</topic><topic>Transient ischemic attack</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Scambray, Kiana A</creatorcontrib><creatorcontrib>Nguyen, Hannah L</creatorcontrib><creatorcontrib>Sajjadi, S Ahmad</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of neuropathology and experimental neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Scambray, Kiana A</au><au>Nguyen, Hannah L</au><au>Sajjadi, S Ahmad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of vascular and degenerative brain pathologies and past medical history from the National Alzheimer’s Coordinating Center Database</atitle><jtitle>Journal of neuropathology and experimental neurology</jtitle><addtitle>J Neuropathol Exp Neurol</addtitle><date>2023-05-01</date><risdate>2023</risdate><volume>82</volume><issue>5</issue><spage>390</spage><epage>401</epage><pages>390-401</pages><issn>0022-3069</issn><eissn>1554-6578</eissn><abstract>Abstract
The relationship between past medical histories (PMH) and dementia-related neuropathologies is not well understood. Using the National Alzheimer's Coordinating Center (NACC) database, we explored the relationship between patient-reported PMH and various vascular and degenerative neuropathologies. We examined the following PMH: transient ischemic attack (TIA), stroke, traumatic brain injury, seizures, hypertension, cardiovascular events, hypercholesterolemia, B12 deficiency, diabetes mellitus, and thyroid disease. We dichotomized the following neuropathologies: atherosclerosis, arteriolosclerosis, cerebral amyloid angiopathy (CAA), Alzheimer disease neuropathology (ADNP), Lewy bodies (LB), hippocampal sclerosis, frontotemporal lobar degeneration (FTLD), and TAR DNA-binding protein-43 (TDP-43). Separate logistic regression models assessed the relationship between the outcome of individual neuropathologies and all PMHs. Additional logistic regressions were stratified by sex to further examine these associations. Hypertension history was associated with an increased likelihood of atherosclerosis (OR = 1.7) and arteriolosclerosis (OR = 1.3), but decreased odds of ADNP (OR = 0.81), CAA (OR = 0.79), and LB (OR = 0.78). History of TIA was associated with an increased likelihood of atherosclerosis (OR = 1.3) and arteriolosclerosis (OR = 1.4) and lower odds of ADNP (OR = 0.72). Seizure history was associated with an increased likelihood of ADNP (OR = 1.9) and lower odds of FTLD (OR = 0.49). Hypertension history was associated with a greater likelihood of vascular pathologies yet a lower likelihood of ADNP and other neurodegenerative pathologies.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>36947583</pmid><doi>10.1093/jnen/nlad020</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-9618-6385</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alzheimer Disease - pathology Alzheimer's disease Arteriolosclerosis - pathology Atherosclerosis Atherosclerosis - complications Atherosclerosis - pathology Blood circulation disorders Brain - pathology Complications and side effects Degeneration Frontotemporal Dementia - pathology Humans Hypertension Hypertension - complications Hypertension - pathology Ischemic Attack, Transient - pathology Medical history Nervous system Original Risk factors Statistics Transient ischemic attack |
title | Association of vascular and degenerative brain pathologies and past medical history from the National Alzheimer’s Coordinating Center Database |
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