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<front>
<journal-meta>
<journal-id journal-id-type="issn">1043-3155</journal-id>
<journal-id journal-id-type="nlm-ta">Pediatr Neurol Briefs</journal-id>
<journal-id journal-id-type="pmc">pedneurbriefs</journal-id>
<journal-id journal-id-type="iso-abbrev">Pediatr Neurol Briefs</journal-id>
<journal-title-group>
<journal-title>Pediatric Neurology Briefs</journal-title>
<abbrev-journal-title>Pediatr Neurol Briefs</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">2166-6482</issn>
<issn pub-type="ppub">1043-3155</issn>
<issn-l>2166-3155</issn-l>
<publisher>
<publisher-name>Pediatric Neurology Briefs Publishers</publisher-name>
<publisher-loc>Chicago, IL, USA</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">PNB-9-23</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-9-3-11</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Demyelinating Disorders</subject>
</subj-group>
<subj-group subj-group-type="Discipline-v2">
<subject>Neurology</subject>
<subject>Pediatrics</subject>
<subject>Nervous System Diseases</subject>
<subject>Child Development</subject>
<subject>Brain Diseases</subject>
<subject>Neurosurgery</subject>
<subject>Child</subject>
<subject>Infant</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Myelin Development in SIDS: MRI Findings</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<contrib-id contrib-id-type="orcid">http://orcid.org/0000-0002-0173-7931</contrib-id>
<name>
<surname>Millichap</surname>
<given-names>J. Gordon</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="AF0001">1</xref>
<xref ref-type="aff" rid="AF0002">2</xref>
<xref ref-type="corresp" rid="cor1">&#x002A;</xref>
</contrib>
</contrib-group>
<aff id="AF0001">
<label>1</label>Division of Neurology, Children&#x0027;s Memorial Hospital, Chicago, IL</aff>
<aff id="AF0002">
<label>2</label>Departments of Pediatrics and Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL</aff>
<author-notes>
<corresp id="cor1"><label>&#x002A;</label>Correspondence: Dr. J. Gordon Millichap, E-mail: <email xlink:href="jgmillichap@northwestern.edu">jgmillichap@northwestern.edu</email>
</corresp>
</author-notes>
<pub-date date-type="pub" publication-format="print">
<month>03</month>
<year>1995</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>06</month>
<year>2016</year>
</pub-date>
<volume>9</volume>
<issue>3</issue>
<fpage>23</fpage>
<lpage>24</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1995 The Author(s)</copyright-statement>
<copyright-year>1995</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
<license-p>This work is licensed under the <uri xlink:href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution 4.0 International License</uri>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<related-article id="R1" related-article-type="commentary-article" ext-link-type="pmid" xlink:href="7862482" vol="95" page="409">
<article-title>Myelin in SIDS: assessment of development and damage using MRI</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>The MRI brain scans of 28 SIDS infants were compared with 14 controls at the Neuropathology Unit, University of Sydney, and the Department of Radiology, Royal Prince Alfred Hospital, New South Wales, Australia.</p>
</abstract>
<kwd-group>
<kwd>MRI Brain Scans</kwd>
<kwd>Myelination</kwd>
<kwd>Densitometer</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>The MRI brain scans of 28 SIDS infants were compared with 14 controls at the Neuropathology Unit, University of Sydney, and the Department of Radiology, Royal Prince Alfred Hospital, New South Wales, Australia. The amount of myelin assessed by densitometer in 21 of 26 sites showed no changes in 15 sites, and a higher rate of myelination in 6 sites, but only in infants older than 8 months. No focal white matter abnormalities were detected. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENT. This MRI investigation failed to confirm the histopathological evidence of delayed myelination in SIDS victims reported from the University of Toronto [<xref ref-type="bibr" rid="CIT0002">2</xref>]. See <underline>Progress in Pediatric Neurology I,</underline> 1991, pp309-310, for a review of mechanisms of SIDS. It was concluded that a central type of respiratory failure or cardiac dysrythmia was involved. A delayed development of the vagus nerve, similar to the finding in an infant with Ondine&#x2019;s curse, was described in the Canadian study.</p>
<p>The Steering Committee of Collaborative Home Infant Monitoring Evaluation reports on a multi-center study aimed at correlating events in infants at increased risk for SIDS, including siblings of prior SIDS victims [<xref ref-type="bibr" rid="CIT0003">3</xref>]. It concluded that siblings are at increased risk for SIDS, and monitoring is cost-effective in sibs of prior SIDS infants.</p>
<p><bold>INTERLEUKIN-6 CSF LEVELS</bold> were increased in 20 infants dying of SIDS in a study reported from the Institute of Forensic Medicine, National Hospital, Oslo, Norway [<xref ref-type="bibr" rid="CIT0004">4</xref>]. The authors suggest that immune activation plays a role in SIDS, and cytokines in the CNS may cause respiratory depression in vulnerable infants.</p>
<p>An increased postneonatal mortality in lower social groups was explained by an association with SIDS in a study from the Department of Epidemiology, National Institute of Public Health, Oslo, Norway. [<xref ref-type="bibr" rid="CIT0005">5</xref>]</p>
<p>A series of articles and an editorial in a recent issue of JAMA address the roles of sleeping position and passive smoking and tobacco exposure through breast milk in the etiology of SIDS. A major factor relating to a decline in SIDS in Tasmania was a reduction in the prevalence of prone sleeping position of infants [<xref ref-type="bibr" rid="CIT0006">6</xref>]. In contrast, routine prone sleeping position was not associated with an increased risk of SIDS in a Southern California study population [<xref ref-type="bibr" rid="CIT0007">7</xref>]. Passive smoking in the same room as infants increased the risk for SIDS in a study at the University of California, San Diego [<xref ref-type="bibr" rid="CIT0008">8</xref>]. An editorial by Willinger M [<xref ref-type="bibr" rid="CIT0009">9</xref>] advises that caregivers should follow AAP recommendations, and parents should be counselled that back or side sleep position is one measure to protect their infant from SIDS, but it is not fool-proof.</p>
</body>
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