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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-34-17</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-34-17</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Sleep 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>Iron and Insomnia in Autism Spectrum Disorder</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Donskoy</surname>
<given-names>Innessa</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="aff0001">1</xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Loghmanee</surname>
<given-names>Darius</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="aff0001">1</xref>
<xref ref-type="corresp" rid="cor1">&#x002A;</xref>
</contrib>
</contrib-group>
<aff id="aff0001"><label>1</label>Advocate Children&#x2019;s Hospital, Park Ridge, IL</aff>
<author-notes>
<corresp id="cor1"><label>&#x002A;</label>Correspondence: Dr. Innessa Donskoy, E-mail: <email xlink:href="Innessa.Donskoy@aah.org">Innessa.Donskoy@aah.org</email></corresp>
</author-notes>
<pub-date date-type="pub" publication-format="electronic">
<day>09</day>
<month>12</month>
<year>2020</year>
</pub-date>
<pub-date date-type="collection" publication-format="electronic">
<year>2020</year>
</pub-date>
<volume>34</volume>
<fpage>17</fpage>
<lpage>17</lpage>
<history>
<date date-type="received">
<day>05</day>
<month>03</month>
<year>2020</year>
</date>
<date date-type="accepted">
<day>29</day>
<month>11</month>
<year>2020</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2020 The Author(s)</copyright-statement>
<copyright-year>2020</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.pediatrneurol.2019.07.015" vol="104" page="30">
<article-title>Randomized, Placebo-Controlled Trial of Ferrous Sulfate to Treat Insomnia in Children With Autism Spectrum Disorders</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Investigators from four major Universities studied the impact of iron supplementation on insomnia symptoms in children with Autism Spectrum Disorder (ASD) and ferritin levels not indicative of iron deficiency anemia.</p>
</abstract>
<kwd-group>
<kwd>Autism</kwd>
<kwd>Insomnia</kwd>
<kwd>Restless Legs Syndrome</kwd>
<kwd>Iron</kwd>
<kwd>Ferrous Sulfate</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Investigators from four major Universities studied the impact of iron supplementation on insomnia symptoms in children with Autism Spectrum Disorder (ASD) and ferritin levels not indicative of iron deficiency anemia. The study assessed twenty children who had confirmed ASD, difficulties with sleep onset or maintenance, and ferritin levels 17-50 ng/mL. [<xref ref-type="bibr" rid="cit0001">1</xref>]</p>
<p>COMMENTARY. Sleep disorders are prevalent in children with ASD and have tremendous implications on their physical and social-emotional health [<xref ref-type="bibr" rid="cit0002">2</xref>]. In addition to strengthening positive behavioral patterns surrounding sleep, pediatric neurologists must also consider organic sleep disorders that contribute to sleep challenges. This study focused on children with insomnia and ferritin levels &#x003C;50 ng/mL, a value at which treatment with iron repletion is indicated for Restless Legs Syndrome (RLS) or Periodic Limb Movement Disorder (PLMD) in children [<xref ref-type="bibr" rid="cit0003">3</xref>]. The aim was to assess if difficulties with sleep onset or maintenance would improve with empiric treatment of a ferritin &#x003C;50 ng/mL without a formal sleep disorder. While empiric therapy was not shown to be effective in managing insomnia in the setting of ASD, it highlights the importance of evaluating for at least two independent sleep disorders that may also present with difficulties falling or staying asleep: RLS and PLMD [<xref ref-type="bibr" rid="cit0001">1</xref>].</p>
<p>A reported history of uncomfortable sensations, often in the legs, diagnoses RLS, which are associated with the urge to move and are 1) worse at night, 2) worse at rest, and 3) relieved by movement [<xref ref-type="bibr" rid="cit0003">3</xref>]. Ferritin levels are often empirically treated when &#x003C;50 ng/mL. The lack of an improvement in sleep onset after empiric treatment in this study suggests that the sample may primarily represent children with ASD who do not have RLS. Hopefully, our ability to diagnose RLS in children with ASD will improve in the future to allow for more targeted treatment.</p>
<p>PLMD is diagnosed in children with polysomnography demonstrating &#x003E;5 limb movements/hour with impairment in daytime functioning [<xref ref-type="bibr" rid="cit0004">4</xref>]; a &#x201C;wild sleeper&#x201D; to a parent. Parental observations may also represent Restless Sleep Disorder (RSD), who has subjective reports of sleep movements but no polysomnographic evidence of PLMD [<xref ref-type="bibr" rid="cit0005">5</xref>]. Early findings suggest that these children have decreased iron stores, as well [<xref ref-type="bibr" rid="cit0005">5</xref>]. Arousals with limb movements may also lead to prolonged awakenings if re-initiating sleep is a challenge [<xref ref-type="bibr" rid="cit0006">6</xref>]. Iron testing/treatment follows the RLS pathway. However, as used in this study, actigraphy is not validated to diagnose or assess the response to treatment in PLMD [<xref ref-type="bibr" rid="cit0007">7</xref>]. As with RLS, children with PLMD (or RSD), who could be responders to iron, must be appropriately identified before making therapeutic decisions.</p>
<p>Sleep-focused history taking and formal sleep testing, when indicated, will help identify patients with ASD who could benefit from iron testing and supplementation for the treatment of specific sleep disorders. Selecting these patients out of future studies will help clarify what role, if any, iron can play in managing sleep in this complex population.</p>
<sec sec-type="COI-statement">
<title>Disclosures</title>
<p>The authors have declared that no competing interests exist.</p>
</sec>
</body>
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