Differential involvement of hippocampal subfields in Niemann-Pick type C disease: a case–control study
Hippocampal brain regions are strongly implicated in Niemann Pick type C disease (NPC), but little is known regarding distinct subregions of the hippocampal complex and whether these are equally or differentially affected. To address this gap, we compared volumes of five hippocampal subfields betwee...
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description | Hippocampal brain regions are strongly implicated in Niemann Pick type C disease (NPC), but little is known regarding distinct subregions of the hippocampal complex and whether these are equally or differentially affected. To address this gap, we compared volumes of five hippocampal subfields between NPC and healthy individuals using MRI. To this end, 9 adult-onset NPC cases and 9 age- and gender-matched controls underwent a 3 T T1-weighted MRI scan. Gray matter volumes of the cornu ammonis (CA1, CA2 and CA3), dentate gyrus (DG), subiculum, entorhinal cortex and hippocampal-amygdalar transition area were calculated by integrating MRI-based image intensities with microscopically defined cytoarchitectonic probabilities. Compared to healthy controls, NPC patients showed smaller volumes of the CA1-3 and DG regions bilaterally, with the greatest difference localized to the left DG (Cohen’s
d
= 1.993,
p
= 0.008). No significant associations were shown between hippocampal subfield volumes and key clinical features of NPC, including disease duration, symptom severity and psychosis. The pattern of hippocampal subregional atrophy in NPC differs from those seen in other dementias, which may indicate unique cytoarchitectural vulnerabilities in this earlier-onset disorder. Future MRI studies of hippocampal subfields may clarify its potential as a biomarker of neurodegeneration in NPC. |
doi_str_mv | 10.1007/s11011-021-00782-9 |
format | Article |
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d
= 1.993,
p
= 0.008). No significant associations were shown between hippocampal subfield volumes and key clinical features of NPC, including disease duration, symptom severity and psychosis. The pattern of hippocampal subregional atrophy in NPC differs from those seen in other dementias, which may indicate unique cytoarchitectural vulnerabilities in this earlier-onset disorder. Future MRI studies of hippocampal subfields may clarify its potential as a biomarker of neurodegeneration in NPC.</description><identifier>ISSN: 0885-7490</identifier><identifier>EISSN: 1573-7365</identifier><identifier>DOI: 10.1007/s11011-021-00782-9</identifier><identifier>PMID: 34146215</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adult ; Alzheimer's disease ; Atrophy ; Atrophy - pathology ; Biochemistry ; Biomarkers ; Biomedical and Life Sciences ; Biomedicine ; Brain architecture ; Brain diseases ; Case-Control Studies ; Cortex (entorhinal) ; Dentate gyrus ; Disease control ; Genetic disorders ; Hippocampus ; Hippocampus - diagnostic imaging ; Hippocampus - pathology ; Humans ; Illnesses ; Investigations ; Laboratories ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Mental disorders ; Metabolic Diseases ; Metabolic disorders ; Metabolism ; Neurodegeneration ; Neurology ; Neurosciences ; Niemann-Pick disease ; Niemann-Pick Disease, Type C - diagnostic imaging ; Oncology ; Original Article ; Psychosis ; Subiculum ; Substantia grisea</subject><ispartof>Metabolic brain disease, 2021-10, Vol.36 (7), p.2071-2078</ispartof><rights>Crown 2021</rights><rights>2021. Crown.</rights><rights>Crown 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-b40828bf3a2ddba21d9263d2824ce09d38abbb406d35911153818559fdfc67813</citedby><cites>FETCH-LOGICAL-c375t-b40828bf3a2ddba21d9263d2824ce09d38abbb406d35911153818559fdfc67813</cites><orcidid>0000-0002-7120-6984</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11011-021-00782-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11011-021-00782-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34146215$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wibawa, Pierre</creatorcontrib><creatorcontrib>Kurth, Florian</creatorcontrib><creatorcontrib>Luders, Eileen</creatorcontrib><creatorcontrib>Pantelis, Christos</creatorcontrib><creatorcontrib>Cropley, Vanessa L.</creatorcontrib><creatorcontrib>Di Biase, Maria A.</creatorcontrib><creatorcontrib>Velakoulis, Dennis</creatorcontrib><creatorcontrib>Walterfang, Mark</creatorcontrib><title>Differential involvement of hippocampal subfields in Niemann-Pick type C disease: a case–control study</title><title>Metabolic brain disease</title><addtitle>Metab Brain Dis</addtitle><addtitle>Metab Brain Dis</addtitle><description>Hippocampal brain regions are strongly implicated in Niemann Pick type C disease (NPC), but little is known regarding distinct subregions of the hippocampal complex and whether these are equally or differentially affected. To address this gap, we compared volumes of five hippocampal subfields between NPC and healthy individuals using MRI. To this end, 9 adult-onset NPC cases and 9 age- and gender-matched controls underwent a 3 T T1-weighted MRI scan. Gray matter volumes of the cornu ammonis (CA1, CA2 and CA3), dentate gyrus (DG), subiculum, entorhinal cortex and hippocampal-amygdalar transition area were calculated by integrating MRI-based image intensities with microscopically defined cytoarchitectonic probabilities. Compared to healthy controls, NPC patients showed smaller volumes of the CA1-3 and DG regions bilaterally, with the greatest difference localized to the left DG (Cohen’s
d
= 1.993,
p
= 0.008). No significant associations were shown between hippocampal subfield volumes and key clinical features of NPC, including disease duration, symptom severity and psychosis. The pattern of hippocampal subregional atrophy in NPC differs from those seen in other dementias, which may indicate unique cytoarchitectural vulnerabilities in this earlier-onset disorder. Future MRI studies of hippocampal subfields may clarify its potential as a biomarker of neurodegeneration in NPC.</description><subject>Adult</subject><subject>Alzheimer's disease</subject><subject>Atrophy</subject><subject>Atrophy - pathology</subject><subject>Biochemistry</subject><subject>Biomarkers</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain architecture</subject><subject>Brain diseases</subject><subject>Case-Control Studies</subject><subject>Cortex (entorhinal)</subject><subject>Dentate gyrus</subject><subject>Disease control</subject><subject>Genetic disorders</subject><subject>Hippocampus</subject><subject>Hippocampus - diagnostic imaging</subject><subject>Hippocampus - pathology</subject><subject>Humans</subject><subject>Illnesses</subject><subject>Investigations</subject><subject>Laboratories</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Mental disorders</subject><subject>Metabolic Diseases</subject><subject>Metabolic disorders</subject><subject>Metabolism</subject><subject>Neurodegeneration</subject><subject>Neurology</subject><subject>Neurosciences</subject><subject>Niemann-Pick disease</subject><subject>Niemann-Pick Disease, Type C - diagnostic imaging</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Psychosis</subject><subject>Subiculum</subject><subject>Substantia grisea</subject><issn>0885-7490</issn><issn>1573-7365</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kc1u1DAUhS0EYqaFF2BRWWLTTcDXjmOHHZpSQKqABawtxz-thyRO7WSk2fEOvCFPgiGFSixYWFfW_c651z4IPQPyAggRLzMAAagILYcISav2AdoCF6wSrOEP0ZZIyStRt2SDTnLeE0IYh_Yx2rAa6oYC36Kbi-C9S26cg-5xGA-xP7ihXHH0-CZMUzR6mEorL50Prre5QPhDcIMex-pTMF_xfJwc3mEbstPZvcIam1J_fPtu4jinWKTzYo9P0COv--ye3tVT9OXyzefdu-rq49v3u9dXlWGCz1VXE0ll55mm1naagm1pwyyVtDaOtJZJ3XUFaizjLQBwJkFy3nrrTSMksFN0vvpOKd4uLs9qCNm4vteji0tWlNes5ry8v6DP_0H3cUlj2a5QghIhGs4KRVfKpJhzcl5NKQw6HRUQ9SsHteagSg7qdw6qLaKzO-ulG5z9K_nz8QVgK5BLa7x26X72f2x_AtXvk34</recordid><startdate>20211001</startdate><enddate>20211001</enddate><creator>Wibawa, Pierre</creator><creator>Kurth, Florian</creator><creator>Luders, Eileen</creator><creator>Pantelis, Christos</creator><creator>Cropley, Vanessa L.</creator><creator>Di Biase, Maria A.</creator><creator>Velakoulis, Dennis</creator><creator>Walterfang, Mark</creator><general>Springer US</general><general>Springer Nature B.V</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>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7120-6984</orcidid></search><sort><creationdate>20211001</creationdate><title>Differential involvement of hippocampal subfields in Niemann-Pick type C disease: a case–control study</title><author>Wibawa, Pierre ; Kurth, Florian ; Luders, Eileen ; Pantelis, Christos ; Cropley, Vanessa L. ; Di Biase, Maria A. ; Velakoulis, Dennis ; Walterfang, Mark</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-b40828bf3a2ddba21d9263d2824ce09d38abbb406d35911153818559fdfc67813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Alzheimer's disease</topic><topic>Atrophy</topic><topic>Atrophy - pathology</topic><topic>Biochemistry</topic><topic>Biomarkers</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brain architecture</topic><topic>Brain diseases</topic><topic>Case-Control Studies</topic><topic>Cortex (entorhinal)</topic><topic>Dentate gyrus</topic><topic>Disease control</topic><topic>Genetic disorders</topic><topic>Hippocampus</topic><topic>Hippocampus - diagnostic imaging</topic><topic>Hippocampus - pathology</topic><topic>Humans</topic><topic>Illnesses</topic><topic>Investigations</topic><topic>Laboratories</topic><topic>Magnetic resonance imaging</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Mental disorders</topic><topic>Metabolic Diseases</topic><topic>Metabolic disorders</topic><topic>Metabolism</topic><topic>Neurodegeneration</topic><topic>Neurology</topic><topic>Neurosciences</topic><topic>Niemann-Pick disease</topic><topic>Niemann-Pick Disease, Type C - diagnostic imaging</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Psychosis</topic><topic>Subiculum</topic><topic>Substantia grisea</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wibawa, Pierre</creatorcontrib><creatorcontrib>Kurth, Florian</creatorcontrib><creatorcontrib>Luders, Eileen</creatorcontrib><creatorcontrib>Pantelis, Christos</creatorcontrib><creatorcontrib>Cropley, Vanessa L.</creatorcontrib><creatorcontrib>Di Biase, Maria A.</creatorcontrib><creatorcontrib>Velakoulis, Dennis</creatorcontrib><creatorcontrib>Walterfang, Mark</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>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</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>ProQuest Pharma Collection</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)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</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 One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Metabolic brain disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wibawa, Pierre</au><au>Kurth, Florian</au><au>Luders, Eileen</au><au>Pantelis, Christos</au><au>Cropley, Vanessa L.</au><au>Di Biase, Maria A.</au><au>Velakoulis, Dennis</au><au>Walterfang, Mark</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential involvement of hippocampal subfields in Niemann-Pick type C disease: a case–control study</atitle><jtitle>Metabolic brain disease</jtitle><stitle>Metab Brain Dis</stitle><addtitle>Metab Brain Dis</addtitle><date>2021-10-01</date><risdate>2021</risdate><volume>36</volume><issue>7</issue><spage>2071</spage><epage>2078</epage><pages>2071-2078</pages><issn>0885-7490</issn><eissn>1573-7365</eissn><abstract>Hippocampal brain regions are strongly implicated in Niemann Pick type C disease (NPC), but little is known regarding distinct subregions of the hippocampal complex and whether these are equally or differentially affected. To address this gap, we compared volumes of five hippocampal subfields between NPC and healthy individuals using MRI. To this end, 9 adult-onset NPC cases and 9 age- and gender-matched controls underwent a 3 T T1-weighted MRI scan. Gray matter volumes of the cornu ammonis (CA1, CA2 and CA3), dentate gyrus (DG), subiculum, entorhinal cortex and hippocampal-amygdalar transition area were calculated by integrating MRI-based image intensities with microscopically defined cytoarchitectonic probabilities. Compared to healthy controls, NPC patients showed smaller volumes of the CA1-3 and DG regions bilaterally, with the greatest difference localized to the left DG (Cohen’s
d
= 1.993,
p
= 0.008). No significant associations were shown between hippocampal subfield volumes and key clinical features of NPC, including disease duration, symptom severity and psychosis. The pattern of hippocampal subregional atrophy in NPC differs from those seen in other dementias, which may indicate unique cytoarchitectural vulnerabilities in this earlier-onset disorder. Future MRI studies of hippocampal subfields may clarify its potential as a biomarker of neurodegeneration in NPC.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>34146215</pmid><doi>10.1007/s11011-021-00782-9</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-7120-6984</orcidid></addata></record> |
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subjects | Adult Alzheimer's disease Atrophy Atrophy - pathology Biochemistry Biomarkers Biomedical and Life Sciences Biomedicine Brain architecture Brain diseases Case-Control Studies Cortex (entorhinal) Dentate gyrus Disease control Genetic disorders Hippocampus Hippocampus - diagnostic imaging Hippocampus - pathology Humans Illnesses Investigations Laboratories Magnetic resonance imaging Magnetic Resonance Imaging - methods Mental disorders Metabolic Diseases Metabolic disorders Metabolism Neurodegeneration Neurology Neurosciences Niemann-Pick disease Niemann-Pick Disease, Type C - diagnostic imaging Oncology Original Article Psychosis Subiculum Substantia grisea |
title | Differential involvement of hippocampal subfields in Niemann-Pick type C disease: a case–control study |
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