Delayed Central Nervous System Myelination in the Sudden Infant Death Syndrome
This study was designed to assess whether development of the central nervous system (CNS) is delayed in victims of the sudden infant death syndrome (SIDS). We selected the parameter of myelination because it is a continuously changing and readily accessible marker of CNS development in the SIDS age-...
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Veröffentlicht in: | Journal of neuropathology and experimental neurology 1991-01, Vol.50 (1), p.29-48 |
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creator | Kinney, Hannah C Ann Brody, Betty Finkelstein, Dianne M Vawter, Gordon F Mandell, Frederick Gillies, Floyd H |
description | This study was designed to assess whether development of the central nervous system (CNS) is delayed in victims of the sudden infant death syndrome (SIDS). We selected the parameter of myelination because it is a continuously changing and readily accessible marker of CNS development in the SIDS age-range. We assessed myelination blindly in 61 SIDS and 89 autopsy controls. In 62 sites the degree of myelination was visually graded in myelin-stained histological sections on an ordinal scale of 0-4 using the inferior cerebellar peduncle as an internal standard of degree 3. Cases were stratified by postconceptional age at death and SIDS and controls were compared with respect to myelin degree at each site. Significantly delayed myelination (p < 0.05) occurred in the SIDS group in 25 of the 62 sites examined. Hypomyelination affected fiber systems in which myelination is initiated before or after birth and which myelinate with different tempos and preferentially affect pyramidal and cerebellar (somatomotor) and prefrontal-temporal-limbic (visceromotor) systems. Hypomyelination was not associated with individual clinicopathologic variables in the SIDS group. Somatic growth and brain weight were significantly greater in SIDS than controls. Therefore, we suggest that SIDS is associated with a developmental CNS disorder. Although delayed CNS myelination most likely shares a common antecedent with sudden death and is not its cause, the role of somato- and visceromotor systems in central cardiorespiratory control and arousal warrants further analysis in SIDS. |
doi_str_mv | 10.1097/00005072-199101000-00003 |
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We selected the parameter of myelination because it is a continuously changing and readily accessible marker of CNS development in the SIDS age-range. We assessed myelination blindly in 61 SIDS and 89 autopsy controls. In 62 sites the degree of myelination was visually graded in myelin-stained histological sections on an ordinal scale of 0-4 using the inferior cerebellar peduncle as an internal standard of degree 3. Cases were stratified by postconceptional age at death and SIDS and controls were compared with respect to myelin degree at each site. Significantly delayed myelination (p < 0.05) occurred in the SIDS group in 25 of the 62 sites examined. Hypomyelination affected fiber systems in which myelination is initiated before or after birth and which myelinate with different tempos and preferentially affect pyramidal and cerebellar (somatomotor) and prefrontal-temporal-limbic (visceromotor) systems. Hypomyelination was not associated with individual clinicopathologic variables in the SIDS group. Somatic growth and brain weight were significantly greater in SIDS than controls. Therefore, we suggest that SIDS is associated with a developmental CNS disorder. Although delayed CNS myelination most likely shares a common antecedent with sudden death and is not its cause, the role of somato- and visceromotor systems in central cardiorespiratory control and arousal warrants further analysis in SIDS.</description><identifier>ISSN: 0022-3069</identifier><identifier>EISSN: 1554-6578</identifier><identifier>DOI: 10.1097/00005072-199101000-00003</identifier><identifier>PMID: 1985152</identifier><identifier>CODEN: JNENAD</identifier><language>eng</language><publisher>Hagerstown, MD: American Association of Neuropathologists, Inc</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Birth Weight ; Body Weight ; Brain - pathology ; Central Nervous System - pathology ; Heart Defects, Congenital - pathology ; Humans ; Infant ; Intensive care medicine ; Medical sciences ; Myelin Sheath - ultrastructure ; Organ Size ; Sudden Infant Death - pathology</subject><ispartof>Journal of neuropathology and experimental neurology, 1991-01, Vol.50 (1), p.29-48</ispartof><rights>1991 American Association of Neuropathologists, Inc</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4443-5b48cb9509a9ca322cb15f3649621b2e1e9856b8b3544da5a77232b13547faf3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5417353$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1985152$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kinney, Hannah C</creatorcontrib><creatorcontrib>Ann Brody, Betty</creatorcontrib><creatorcontrib>Finkelstein, Dianne M</creatorcontrib><creatorcontrib>Vawter, Gordon F</creatorcontrib><creatorcontrib>Mandell, Frederick</creatorcontrib><creatorcontrib>Gillies, Floyd H</creatorcontrib><title>Delayed Central Nervous System Myelination in the Sudden Infant Death Syndrome</title><title>Journal of neuropathology and experimental neurology</title><addtitle>J Neuropathol Exp Neurol</addtitle><description>This study was designed to assess whether development of the central nervous system (CNS) is delayed in victims of the sudden infant death syndrome (SIDS). We selected the parameter of myelination because it is a continuously changing and readily accessible marker of CNS development in the SIDS age-range. We assessed myelination blindly in 61 SIDS and 89 autopsy controls. In 62 sites the degree of myelination was visually graded in myelin-stained histological sections on an ordinal scale of 0-4 using the inferior cerebellar peduncle as an internal standard of degree 3. Cases were stratified by postconceptional age at death and SIDS and controls were compared with respect to myelin degree at each site. Significantly delayed myelination (p < 0.05) occurred in the SIDS group in 25 of the 62 sites examined. Hypomyelination affected fiber systems in which myelination is initiated before or after birth and which myelinate with different tempos and preferentially affect pyramidal and cerebellar (somatomotor) and prefrontal-temporal-limbic (visceromotor) systems. Hypomyelination was not associated with individual clinicopathologic variables in the SIDS group. Somatic growth and brain weight were significantly greater in SIDS than controls. Therefore, we suggest that SIDS is associated with a developmental CNS disorder. Although delayed CNS myelination most likely shares a common antecedent with sudden death and is not its cause, the role of somato- and visceromotor systems in central cardiorespiratory control and arousal warrants further analysis in SIDS.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Birth Weight</subject><subject>Body Weight</subject><subject>Brain - pathology</subject><subject>Central Nervous System - pathology</subject><subject>Heart Defects, Congenital - pathology</subject><subject>Humans</subject><subject>Infant</subject><subject>Intensive care medicine</subject><subject>Medical sciences</subject><subject>Myelin Sheath - ultrastructure</subject><subject>Organ Size</subject><subject>Sudden Infant Death - pathology</subject><issn>0022-3069</issn><issn>1554-6578</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtP3DAQx62KCra0H6GSD4hbWj_j-IiWPpAoPcDdmiQTbcBxwHZA--3r7W7pqepcRjPzm4f-Qwjl7BNn1nxmxTQzouLWcsZLVO1S8g1Zca1VVWvTHJEVY0JUktX2hLxL6b4Qlll1TI65bTTXYkVuLtHDFnu6xpAjeHqD8XleEr3dpowT_bFFPwbI4xzoGGjeIL1d-h4DvQoDhEwvEfKm0KGP84TvydsBfMIPB39K7r5-uVt_r65_frtaX1xXnVJKVrpVTddazSzYDqQQXcv1IGtla8FbgRzLfXXbtFIr1YMGY4QULS-hGWCQp-R8P_Yxzk8LpuymMXXoPQQsx7uGyVpYbf4L8prV0ihdwGYPdnFOKeLgHuM4Qdw6ztxOcvdHcvcq-e-ULK0fDzuWdsL-b-Ne41I_O9QhdeCHCKEb0yumFTdS78aoPfYy-4wxPfjlBaPbIPi8cf96uPwFhRKWkQ</recordid><startdate>199101</startdate><enddate>199101</enddate><creator>Kinney, Hannah C</creator><creator>Ann Brody, Betty</creator><creator>Finkelstein, Dianne M</creator><creator>Vawter, Gordon F</creator><creator>Mandell, Frederick</creator><creator>Gillies, Floyd H</creator><general>American Association of Neuropathologists, Inc</general><general>Lippincott Williams & Wilkins</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>199101</creationdate><title>Delayed Central Nervous System Myelination in the Sudden Infant Death Syndrome</title><author>Kinney, Hannah C ; Ann Brody, Betty ; Finkelstein, Dianne M ; Vawter, Gordon F ; Mandell, Frederick ; Gillies, Floyd H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4443-5b48cb9509a9ca322cb15f3649621b2e1e9856b8b3544da5a77232b13547faf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Birth Weight</topic><topic>Body Weight</topic><topic>Brain - pathology</topic><topic>Central Nervous System - pathology</topic><topic>Heart Defects, Congenital - pathology</topic><topic>Humans</topic><topic>Infant</topic><topic>Intensive care medicine</topic><topic>Medical sciences</topic><topic>Myelin Sheath - ultrastructure</topic><topic>Organ Size</topic><topic>Sudden Infant Death - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kinney, Hannah C</creatorcontrib><creatorcontrib>Ann Brody, Betty</creatorcontrib><creatorcontrib>Finkelstein, Dianne M</creatorcontrib><creatorcontrib>Vawter, Gordon F</creatorcontrib><creatorcontrib>Mandell, Frederick</creatorcontrib><creatorcontrib>Gillies, Floyd H</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>Neurosciences Abstracts</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>Kinney, Hannah C</au><au>Ann Brody, Betty</au><au>Finkelstein, Dianne M</au><au>Vawter, Gordon F</au><au>Mandell, Frederick</au><au>Gillies, Floyd H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Delayed Central Nervous System Myelination in the Sudden Infant Death Syndrome</atitle><jtitle>Journal of neuropathology and experimental neurology</jtitle><addtitle>J Neuropathol Exp Neurol</addtitle><date>1991-01</date><risdate>1991</risdate><volume>50</volume><issue>1</issue><spage>29</spage><epage>48</epage><pages>29-48</pages><issn>0022-3069</issn><eissn>1554-6578</eissn><coden>JNENAD</coden><abstract>This study was designed to assess whether development of the central nervous system (CNS) is delayed in victims of the sudden infant death syndrome (SIDS). We selected the parameter of myelination because it is a continuously changing and readily accessible marker of CNS development in the SIDS age-range. We assessed myelination blindly in 61 SIDS and 89 autopsy controls. In 62 sites the degree of myelination was visually graded in myelin-stained histological sections on an ordinal scale of 0-4 using the inferior cerebellar peduncle as an internal standard of degree 3. Cases were stratified by postconceptional age at death and SIDS and controls were compared with respect to myelin degree at each site. Significantly delayed myelination (p < 0.05) occurred in the SIDS group in 25 of the 62 sites examined. Hypomyelination affected fiber systems in which myelination is initiated before or after birth and which myelinate with different tempos and preferentially affect pyramidal and cerebellar (somatomotor) and prefrontal-temporal-limbic (visceromotor) systems. Hypomyelination was not associated with individual clinicopathologic variables in the SIDS group. Somatic growth and brain weight were significantly greater in SIDS than controls. Therefore, we suggest that SIDS is associated with a developmental CNS disorder. Although delayed CNS myelination most likely shares a common antecedent with sudden death and is not its cause, the role of somato- and visceromotor systems in central cardiorespiratory control and arousal warrants further analysis in SIDS.</abstract><cop>Hagerstown, MD</cop><pub>American Association of Neuropathologists, Inc</pub><pmid>1985152</pmid><doi>10.1097/00005072-199101000-00003</doi><tpages>20</tpages></addata></record> |
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subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Birth Weight Body Weight Brain - pathology Central Nervous System - pathology Heart Defects, Congenital - pathology Humans Infant Intensive care medicine Medical sciences Myelin Sheath - ultrastructure Organ Size Sudden Infant Death - pathology |
title | Delayed Central Nervous System Myelination in the Sudden Infant Death Syndrome |
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