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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="ppub">1043-3155</issn>
<issn pub-type="epub">2166-6482</issn>
<issn-l>1043-3155</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-2015-29-8-3</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-29-8-3</article-id>
<article-id pub-id-type="pmid">26933597</article-id>
<article-id pub-id-type="pmcid">PMC4747131</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Perinatal 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>MRI and Motor Outcomes in Children with Cerebral Palsy</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Gaebler-Spira</surname>
<given-names>Deborah</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="AF0001">1</xref>
<xref ref-type="corresp" rid="cor1">&#x002A;</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>McCormick</surname>
<given-names>Kristen</given-names>
</name>
<degrees>DO</degrees>
<xref ref-type="aff" rid="AF0001">1</xref>
</contrib>
</contrib-group>
<aff id="AF0001">
<label>1</label>Rehabilitation Institute of Chicago; and Departments of Pediatrics and Physical Medicine and Rehabilitation, Northwestern University Feinberg School of Medicine, Chicago, IL</aff>
<author-notes>
<corresp id="cor1"><label>&#x002A;</label>Correspondence: Dr. Deborah Gaebler-Spira, E-mail: <email xlink:href="dgaebler@ric.org">dgaebler@ric.org</email>
</corresp>
</author-notes>
<pub-date date-type="pub" publication-format="print">
<month>08</month>
<year>2015</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>07</day>
<month>09</month>
<year>2015</year>
</pub-date>
<volume>29</volume>
<issue>8</issue>
<fpage>60</fpage>
<lpage>60</lpage>
<history>
<date date-type="received">
<day>31</day>
<month>08</month>
<year>2015</year>
</date>
<date date-type="accepted">
<day>05</day>
<month>09</month>
<year>2015</year>
</date>
<date date-type="corrected">
<day>28</day>
<month>03</month>
<year>2016</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2015 The Author(s)</copyright-statement>
<copyright-year>2015</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="doi" xlink:href="10.1016/j.ridd.2015.07.030" vol="45-46" page="178">
<article-title>Relationship between characteristics on magnetic resonance imaging and motor outcomes in children with cerebral palsy and white matter injury.</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Investigators from University of Melbourne, Monash Children&#x0027;s Hospital, Royal Children&#x0027;s Hospital &#x0026; Murdoch Children&#x0027;s Research Institute sought to identify correlation between magnetic resonance imaging (MRI) characteristics including white matter injury (WMI) in children with cerebral palsy (CP) and severity in motor outcomes later in life, irrespective of CP subtype.</p>
</abstract>
<kwd-group>
<kwd>Cerebral Palsy</kwd>
<kwd>Diffusion Tensor Imaging</kwd>
<kwd>GMFM-66</kwd>
<kwd>Structural Connectome</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Investigators from University of Melbourne, Monash Children&#x0027;s Hospital, Royal Children&#x0027;s Hospital &#x0026; Murdoch Children&#x0027;s Research Institute sought to identify correlation between magnetic resonance imaging (MRI) characteristics including white matter injury (WMI) in children with cerebral palsy (CP) and severity in motor outcomes later in life, irrespective of CP subtype. Their goal was to develop a severity classification for WMI that can discriminate children with different levels of functional ability. Data was collected from children seen at Melbourne Children&#x0027;s Campus, in a cohort population from 1999-2008. A total of 272 children were identified from the Victorian Cerebral Palsy Register with a diagnosis of CP and WMI on MRI. Their MRI findings were divided into broad patterns of injury that reflected pathogenesis &#x0026; timing of injury: unilateral, asymmetrical, or symmetrical, then based on location: anterior, mid, and posterior white matter. These data were then analyzed using Chi square tests to assess the strength of association between known Gross Motor Function Classification System (GMFCS) levels and symmetrical WMI, and between motor topography groups for children with symmetrical WMI &#x0026; bilateral CP. There were clear associations between extent of signal abnormality in the worse hemisphere and laterality/symmetry of WMI (p = 0.004), extent/location of WM loss &#x0026; laterality/symmetry (p &#x003C; 0.001), and GMFCS/motor topography and MRI laterality/symmetry (P &#x003C; 0.001). Despite the strong association between MRI symmetry &#x0026; motor topography, there was only 56% agreement between the two. While WMI seen on imaging correlated with physical exam findings in a large majority of patients, physical exam findings correlated with MRI findings less frequently. Overall, it seems that the best model for predicting GMFCS level was MRI laterality/symmetry, extent of WM loss, cerebellar abnormality, and thinning of the corpus callosum (p &#x003C; 0.001). These findings were used by the authors to create a new WMI severity classification for children with CP that could provide valuable predictors of future function to families. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENTARY. This article continues the quest to link structural brain findings to functional
outcome and severity of condition [<xref ref-type="bibr" rid="CIT0002">2</xref>, <xref
ref-type="bibr" rid="CIT0003">3</xref>]. The relationship of structure linked to function is of
increasing importance as the process of targeted neuro-rehabilitation and recovery of the impact of
injury to the neonatal brain is also progressing [<xref ref-type="bibr" rid="CIT0004">4</xref>].
With 56% of variance or severity yet explained, the linkage is still elusive. This is the link
between parent&#x0027;s and neurologist, what is seen on scan and what is expected in real life.</p>
<p>Until a unified approach to reporting MRI findings with validated outcomes in function are used,
the opportunity exists to advance the link, especially with the use of the population-based
registries in Australia, Scandinavia and Europe [<xref ref-type="bibr" rid="CIT0005">5</xref>, <xref
ref-type="bibr" rid="CIT0006">6</xref>, <xref ref-type="bibr" rid="CIT0007">7</xref>]. Population
registry methodology is the most efficient means to this end. Cooperation and collaboration of
registries in the United States would increase available data which could and would advance the
remaining unexplained variance of function seen in this study.</p>
</body>
<back>
<sec>
<title>Disclosures</title>
<p>The author(s) have declared that no competing interests exist.</p>
</sec>
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<sec>
<title>Publisher Note</title>
<p>This article was corrected on 2016 Mar 28. See Pediatr Neurol Briefs. 2016;30(1):e1.
http://dx.doi.org/10.15844/pedneurbriefs-29-8-3-c</p>
</sec>
</back>
</article>
