Relationships between Regional Neuronal Loss and Neurofibrillary Changes in the Hippocampal Formation and Duration and Severity of Alzheimer Disease

The total numbers of neurons with and without neurofibrillary changes in the hippocampal subdivisions were estimated in 16 subjects with Alzheimer disease (AD) and in 5 normal elderly controls. On the basis of clinical symptoms, AD patients were subdivided into relatively less (AD-1, Functional Asse...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of neuropathology and experimental neurology 1997-04, Vol.56 (4), p.414-420
Hauptverfasser: BOBINSKI, MACIEJ, WEGIEL, JERZY, TARNAWSKI, MICHAL, BOBINSKI, MARGARET, REISBERG, BARRY, DE LEON, MONY J, MILLER, DOUGLAS C, WISNIEWSKI, HENRYK M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 420
container_issue 4
container_start_page 414
container_title Journal of neuropathology and experimental neurology
container_volume 56
creator BOBINSKI, MACIEJ
WEGIEL, JERZY
TARNAWSKI, MICHAL
BOBINSKI, MARGARET
REISBERG, BARRY
DE LEON, MONY J
MILLER, DOUGLAS C
WISNIEWSKI, HENRYK M
description The total numbers of neurons with and without neurofibrillary changes in the hippocampal subdivisions were estimated in 16 subjects with Alzheimer disease (AD) and in 5 normal elderly controls. On the basis of clinical symptoms, AD patients were subdivided into relatively less (AD-1, Functional Assessment Staging [FAST] stages 7a to 7c) and more severely affected (AD-2, FAST stages 7e to 7f) patient groups. In the AD-1 group relative to controls, the total number of neurons was reduced only in CA1 and in the subiculum. In the AD-2 group, neuronal losses were found in all sectors of the cornu Ammonis and in the subiculum and ranged from 53% in CA3 to 86% in CA1. The dentate gyrus was the only hippocampal subdivision without significant neuronal loss. Within the combined AD patient groups, significant correlations were noted between both clinical stage and duration of AD and both the total number of neurons and the percentage of neurons with neurofibrillary changes in CA1, CA4, and the subiculum. Regression analyses predicted neuronal losses over the maximal observed duration of 22 years of 87% in CA1, 63% in CA4, and 77% in the subiculum. Our data suggest that over the course of AD, continuous neurofibrillary tangle formation and continuous neuronal loss occur in the hippocampal subdivisions. The rate of neuronal loss appears to be similar for CA1, CA4, and the subiculum.
doi_str_mv 10.1097/00005072-199704000-00010
format Article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_78947257</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A536177093</galeid><sourcerecordid>A536177093</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5660-640fe29fe3bc1a2451853b9cdb12b892283279de1bf47d60bbf43636d7eddf93</originalsourceid><addsrcrecordid>eNp1Ul2L1DAULaKs4-hPEIKIb13z0SbN4zDrusKgsO57SNubada0qUnrsP4Of7DZ6TiCYEK4yb3nXJJzkmWI4EuCpXiP0yixoDmRUuAinfK0CH6SrUhZFjkvRfU0W2FMac4wl8-zFzHeJ4jEsrjILiTBmAu6yn7dgtOT9UPs7BhRDdMBYEC3sE857dBnmMNxs_MxIj20S8bYOljndHhA204Pe4jIDmjqAN3YcfSN7sfEufahPzY_Eq_m8PfwFX5AsNMD8gZt3M8ObA8BXdkIOsLL7JnRLsKrU1xnd9cf7rY3-e7Lx0_bzS5vSs5xzgtsgEoDrG6IpkVJqpLVsmlrQutKUloxKmQLpDaFaDmuU2Sc8VZA2xrJ1tm7pe0Y_PcZ4qR6GxtIzxrAz1GJShaCliIB3_wDvPdzSKpERakUjODqsdvlAtprB8oOxk9BN2m20NvGD2Bsym9KxokQWLJEqBZCE5K2AYwag-2TpIpg9eiy-uOyOrusji4n6uvThea6h_ZMPNma6m9PdR0b7UzQQ2PjGUY5wzKps86KBXbwboIQv7n5AEF1oN3Uqf_9MfYbGYHAIg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>229731089</pqid></control><display><type>article</type><title>Relationships between Regional Neuronal Loss and Neurofibrillary Changes in the Hippocampal Formation and Duration and Severity of Alzheimer Disease</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Journals@Ovid Complete</source><creator>BOBINSKI, MACIEJ ; WEGIEL, JERZY ; TARNAWSKI, MICHAL ; BOBINSKI, MARGARET ; REISBERG, BARRY ; DE LEON, MONY J ; MILLER, DOUGLAS C ; WISNIEWSKI, HENRYK M</creator><creatorcontrib>BOBINSKI, MACIEJ ; WEGIEL, JERZY ; TARNAWSKI, MICHAL ; BOBINSKI, MARGARET ; REISBERG, BARRY ; DE LEON, MONY J ; MILLER, DOUGLAS C ; WISNIEWSKI, HENRYK M</creatorcontrib><description>The total numbers of neurons with and without neurofibrillary changes in the hippocampal subdivisions were estimated in 16 subjects with Alzheimer disease (AD) and in 5 normal elderly controls. On the basis of clinical symptoms, AD patients were subdivided into relatively less (AD-1, Functional Assessment Staging [FAST] stages 7a to 7c) and more severely affected (AD-2, FAST stages 7e to 7f) patient groups. In the AD-1 group relative to controls, the total number of neurons was reduced only in CA1 and in the subiculum. In the AD-2 group, neuronal losses were found in all sectors of the cornu Ammonis and in the subiculum and ranged from 53% in CA3 to 86% in CA1. The dentate gyrus was the only hippocampal subdivision without significant neuronal loss. Within the combined AD patient groups, significant correlations were noted between both clinical stage and duration of AD and both the total number of neurons and the percentage of neurons with neurofibrillary changes in CA1, CA4, and the subiculum. Regression analyses predicted neuronal losses over the maximal observed duration of 22 years of 87% in CA1, 63% in CA4, and 77% in the subiculum. Our data suggest that over the course of AD, continuous neurofibrillary tangle formation and continuous neuronal loss occur in the hippocampal subdivisions. The rate of neuronal loss appears to be similar for CA1, CA4, and the subiculum.</description><identifier>ISSN: 0022-3069</identifier><identifier>EISSN: 1554-6578</identifier><identifier>DOI: 10.1097/00005072-199704000-00010</identifier><identifier>PMID: 9100672</identifier><identifier>CODEN: JNENAD</identifier><language>eng</language><publisher>Hagerstown, MD: American Association of Neuropathologists, Inc</publisher><subject>Advertising executives ; Aged ; Aged, 80 and over ; Alzheimer Disease - pathology ; Alzheimer Disease - physiopathology ; Alzheimer's disease ; Analysis ; Biological and medical sciences ; Cell Death ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Female ; Hippocampus - pathology ; Humans ; Male ; Medical research ; Medical sciences ; Neurofibrils - pathology ; Neurology ; Neurons ; Neurons - pathology ; Neurophysiology ; Severity of Illness Index ; Time Factors</subject><ispartof>Journal of neuropathology and experimental neurology, 1997-04, Vol.56 (4), p.414-420</ispartof><rights>1997 American Association of Neuropathologists, Inc</rights><rights>1997 INIST-CNRS</rights><rights>COPYRIGHT 1997 Oxford University Press</rights><rights>Copyright Lippincott Williams &amp; Wilkins Apr 1997</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5660-640fe29fe3bc1a2451853b9cdb12b892283279de1bf47d60bbf43636d7eddf93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=2630928$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9100672$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>BOBINSKI, MACIEJ</creatorcontrib><creatorcontrib>WEGIEL, JERZY</creatorcontrib><creatorcontrib>TARNAWSKI, MICHAL</creatorcontrib><creatorcontrib>BOBINSKI, MARGARET</creatorcontrib><creatorcontrib>REISBERG, BARRY</creatorcontrib><creatorcontrib>DE LEON, MONY J</creatorcontrib><creatorcontrib>MILLER, DOUGLAS C</creatorcontrib><creatorcontrib>WISNIEWSKI, HENRYK M</creatorcontrib><title>Relationships between Regional Neuronal Loss and Neurofibrillary Changes in the Hippocampal Formation and Duration and Severity of Alzheimer Disease</title><title>Journal of neuropathology and experimental neurology</title><addtitle>J Neuropathol Exp Neurol</addtitle><description>The total numbers of neurons with and without neurofibrillary changes in the hippocampal subdivisions were estimated in 16 subjects with Alzheimer disease (AD) and in 5 normal elderly controls. On the basis of clinical symptoms, AD patients were subdivided into relatively less (AD-1, Functional Assessment Staging [FAST] stages 7a to 7c) and more severely affected (AD-2, FAST stages 7e to 7f) patient groups. In the AD-1 group relative to controls, the total number of neurons was reduced only in CA1 and in the subiculum. In the AD-2 group, neuronal losses were found in all sectors of the cornu Ammonis and in the subiculum and ranged from 53% in CA3 to 86% in CA1. The dentate gyrus was the only hippocampal subdivision without significant neuronal loss. Within the combined AD patient groups, significant correlations were noted between both clinical stage and duration of AD and both the total number of neurons and the percentage of neurons with neurofibrillary changes in CA1, CA4, and the subiculum. Regression analyses predicted neuronal losses over the maximal observed duration of 22 years of 87% in CA1, 63% in CA4, and 77% in the subiculum. Our data suggest that over the course of AD, continuous neurofibrillary tangle formation and continuous neuronal loss occur in the hippocampal subdivisions. The rate of neuronal loss appears to be similar for CA1, CA4, and the subiculum.</description><subject>Advertising executives</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer Disease - physiopathology</subject><subject>Alzheimer's disease</subject><subject>Analysis</subject><subject>Biological and medical sciences</subject><subject>Cell Death</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Female</subject><subject>Hippocampus - pathology</subject><subject>Humans</subject><subject>Male</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Neurofibrils - pathology</subject><subject>Neurology</subject><subject>Neurons</subject><subject>Neurons - pathology</subject><subject>Neurophysiology</subject><subject>Severity of Illness Index</subject><subject>Time Factors</subject><issn>0022-3069</issn><issn>1554-6578</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1Ul2L1DAULaKs4-hPEIKIb13z0SbN4zDrusKgsO57SNubada0qUnrsP4Of7DZ6TiCYEK4yb3nXJJzkmWI4EuCpXiP0yixoDmRUuAinfK0CH6SrUhZFjkvRfU0W2FMac4wl8-zFzHeJ4jEsrjILiTBmAu6yn7dgtOT9UPs7BhRDdMBYEC3sE857dBnmMNxs_MxIj20S8bYOljndHhA204Pe4jIDmjqAN3YcfSN7sfEufahPzY_Eq_m8PfwFX5AsNMD8gZt3M8ObA8BXdkIOsLL7JnRLsKrU1xnd9cf7rY3-e7Lx0_bzS5vSs5xzgtsgEoDrG6IpkVJqpLVsmlrQutKUloxKmQLpDaFaDmuU2Sc8VZA2xrJ1tm7pe0Y_PcZ4qR6GxtIzxrAz1GJShaCliIB3_wDvPdzSKpERakUjODqsdvlAtprB8oOxk9BN2m20NvGD2Bsym9KxokQWLJEqBZCE5K2AYwag-2TpIpg9eiy-uOyOrusji4n6uvThea6h_ZMPNma6m9PdR0b7UzQQ2PjGUY5wzKps86KBXbwboIQv7n5AEF1oN3Uqf_9MfYbGYHAIg</recordid><startdate>199704</startdate><enddate>199704</enddate><creator>BOBINSKI, MACIEJ</creator><creator>WEGIEL, JERZY</creator><creator>TARNAWSKI, MICHAL</creator><creator>BOBINSKI, MARGARET</creator><creator>REISBERG, BARRY</creator><creator>DE LEON, MONY J</creator><creator>MILLER, DOUGLAS C</creator><creator>WISNIEWSKI, HENRYK M</creator><general>American Association of Neuropathologists, Inc</general><general>Lippincott Williams &amp; Wilkins</general><general>Oxford University Press</general><scope>IQODW</scope><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>K9.</scope><scope>7X8</scope></search><sort><creationdate>199704</creationdate><title>Relationships between Regional Neuronal Loss and Neurofibrillary Changes in the Hippocampal Formation and Duration and Severity of Alzheimer Disease</title><author>BOBINSKI, MACIEJ ; WEGIEL, JERZY ; TARNAWSKI, MICHAL ; BOBINSKI, MARGARET ; REISBERG, BARRY ; DE LEON, MONY J ; MILLER, DOUGLAS C ; WISNIEWSKI, HENRYK M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5660-640fe29fe3bc1a2451853b9cdb12b892283279de1bf47d60bbf43636d7eddf93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Advertising executives</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Alzheimer Disease - pathology</topic><topic>Alzheimer Disease - physiopathology</topic><topic>Alzheimer's disease</topic><topic>Analysis</topic><topic>Biological and medical sciences</topic><topic>Cell Death</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Female</topic><topic>Hippocampus - pathology</topic><topic>Humans</topic><topic>Male</topic><topic>Medical research</topic><topic>Medical sciences</topic><topic>Neurofibrils - pathology</topic><topic>Neurology</topic><topic>Neurons</topic><topic>Neurons - pathology</topic><topic>Neurophysiology</topic><topic>Severity of Illness Index</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BOBINSKI, MACIEJ</creatorcontrib><creatorcontrib>WEGIEL, JERZY</creatorcontrib><creatorcontrib>TARNAWSKI, MICHAL</creatorcontrib><creatorcontrib>BOBINSKI, MARGARET</creatorcontrib><creatorcontrib>REISBERG, BARRY</creatorcontrib><creatorcontrib>DE LEON, MONY J</creatorcontrib><creatorcontrib>MILLER, DOUGLAS C</creatorcontrib><creatorcontrib>WISNIEWSKI, HENRYK M</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neuropathology and experimental neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BOBINSKI, MACIEJ</au><au>WEGIEL, JERZY</au><au>TARNAWSKI, MICHAL</au><au>BOBINSKI, MARGARET</au><au>REISBERG, BARRY</au><au>DE LEON, MONY J</au><au>MILLER, DOUGLAS C</au><au>WISNIEWSKI, HENRYK M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Relationships between Regional Neuronal Loss and Neurofibrillary Changes in the Hippocampal Formation and Duration and Severity of Alzheimer Disease</atitle><jtitle>Journal of neuropathology and experimental neurology</jtitle><addtitle>J Neuropathol Exp Neurol</addtitle><date>1997-04</date><risdate>1997</risdate><volume>56</volume><issue>4</issue><spage>414</spage><epage>420</epage><pages>414-420</pages><issn>0022-3069</issn><eissn>1554-6578</eissn><coden>JNENAD</coden><abstract>The total numbers of neurons with and without neurofibrillary changes in the hippocampal subdivisions were estimated in 16 subjects with Alzheimer disease (AD) and in 5 normal elderly controls. On the basis of clinical symptoms, AD patients were subdivided into relatively less (AD-1, Functional Assessment Staging [FAST] stages 7a to 7c) and more severely affected (AD-2, FAST stages 7e to 7f) patient groups. In the AD-1 group relative to controls, the total number of neurons was reduced only in CA1 and in the subiculum. In the AD-2 group, neuronal losses were found in all sectors of the cornu Ammonis and in the subiculum and ranged from 53% in CA3 to 86% in CA1. The dentate gyrus was the only hippocampal subdivision without significant neuronal loss. Within the combined AD patient groups, significant correlations were noted between both clinical stage and duration of AD and both the total number of neurons and the percentage of neurons with neurofibrillary changes in CA1, CA4, and the subiculum. Regression analyses predicted neuronal losses over the maximal observed duration of 22 years of 87% in CA1, 63% in CA4, and 77% in the subiculum. Our data suggest that over the course of AD, continuous neurofibrillary tangle formation and continuous neuronal loss occur in the hippocampal subdivisions. The rate of neuronal loss appears to be similar for CA1, CA4, and the subiculum.</abstract><cop>Hagerstown, MD</cop><pub>American Association of Neuropathologists, Inc</pub><pmid>9100672</pmid><doi>10.1097/00005072-199704000-00010</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0022-3069
ispartof Journal of neuropathology and experimental neurology, 1997-04, Vol.56 (4), p.414-420
issn 0022-3069
1554-6578
language eng
recordid cdi_proquest_miscellaneous_78947257
source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Journals@Ovid Complete
subjects Advertising executives
Aged
Aged, 80 and over
Alzheimer Disease - pathology
Alzheimer Disease - physiopathology
Alzheimer's disease
Analysis
Biological and medical sciences
Cell Death
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Female
Hippocampus - pathology
Humans
Male
Medical research
Medical sciences
Neurofibrils - pathology
Neurology
Neurons
Neurons - pathology
Neurophysiology
Severity of Illness Index
Time Factors
title Relationships between Regional Neuronal Loss and Neurofibrillary Changes in the Hippocampal Formation and Duration and Severity of Alzheimer Disease
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T14%3A05%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Relationships%20between%20Regional%20Neuronal%20Loss%20and%20Neurofibrillary%20Changes%20in%20the%20Hippocampal%20Formation%20and%20Duration%20and%20Severity%20of%20Alzheimer%20Disease&rft.jtitle=Journal%20of%20neuropathology%20and%20experimental%20neurology&rft.au=BOBINSKI,%20MACIEJ&rft.date=1997-04&rft.volume=56&rft.issue=4&rft.spage=414&rft.epage=420&rft.pages=414-420&rft.issn=0022-3069&rft.eissn=1554-6578&rft.coden=JNENAD&rft_id=info:doi/10.1097/00005072-199704000-00010&rft_dat=%3Cgale_proqu%3EA536177093%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=229731089&rft_id=info:pmid/9100672&rft_galeid=A536177093&rfr_iscdi=true