Serum melatonin kinetics and long-term melatonin treatment for sleep disorders in Rett syndrome
We studied the circadian rhythm of serum melatonin levels in two patients with classical Rett syndrome having severe sleep disorders; serum melatonin levels were measured before and during melatonin treatment using radioimmnoassay. Patient 1 had a free-running rhythm of sleep-wake cycle from 3 years...
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Veröffentlicht in: | Brain & development (Tokyo. 1979) 1999, Vol.21 (1), p.59-62 |
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creator | Miyamoto, Akie Oki, Junichi Takahashi, Satoru Okuno, Akimasa |
description | We studied the circadian rhythm of serum melatonin levels in two patients with classical Rett syndrome having severe sleep disorders; serum melatonin levels were measured before and during melatonin treatment using radioimmnoassay. Patient 1 had a free-running rhythm of sleep-wake cycle from 3 years of age. At the age of 4 years, the peak time of melatonin was delayed 6 h compared to normal control and the peak value was at the lower limit. Patient 2 had a fragmented sleep pattern accompanied by night screaming from 1 year and 6 months of age. At the age of 10 years, the peak time of melatonin secretion was normal but the peak value was at the lower limit. These patients were given 5 mg melatonin orally prior to bedtime. Exogenous melatonin dramatically improved the sleep-wake cycle in patient 1. In patient 2, exogenous melatonin showed a hypnotic effect but early morning awakenings occurred occasionally. When melatonin treatment was stopped, the sleep disorders recurred and re-administration of 3 mg melatonin was effective in both patients. The effect was maintained over 2 years without any adverse effects. These findings suggests that sleep disorders in patients with Rett syndrome may relate with an impaired secretion of melatonin. |
doi_str_mv | 10.1016/S0387-7604(98)00072-2 |
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Patient 1 had a free-running rhythm of sleep-wake cycle from 3 years of age. At the age of 4 years, the peak time of melatonin was delayed 6 h compared to normal control and the peak value was at the lower limit. Patient 2 had a fragmented sleep pattern accompanied by night screaming from 1 year and 6 months of age. At the age of 10 years, the peak time of melatonin secretion was normal but the peak value was at the lower limit. These patients were given 5 mg melatonin orally prior to bedtime. Exogenous melatonin dramatically improved the sleep-wake cycle in patient 1. In patient 2, exogenous melatonin showed a hypnotic effect but early morning awakenings occurred occasionally. When melatonin treatment was stopped, the sleep disorders recurred and re-administration of 3 mg melatonin was effective in both patients. The effect was maintained over 2 years without any adverse effects. These findings suggests that sleep disorders in patients with Rett syndrome may relate with an impaired secretion of melatonin.</description><identifier>ISSN: 0387-7604</identifier><identifier>EISSN: 1872-7131</identifier><identifier>DOI: 10.1016/S0387-7604(98)00072-2</identifier><identifier>PMID: 10082254</identifier><identifier>CODEN: NTHAA7</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Adolescent ; Biological and medical sciences ; Child ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Female ; Humans ; Kinetics ; Medical sciences ; Melatonin ; Melatonin - blood ; Melatonin - therapeutic use ; Neurology ; Rett syndrome ; Rett Syndrome - complications ; Sleep - drug effects ; Sleep disorder ; Sleep Wake Disorders - drug therapy ; Sleep Wake Disorders - etiology ; Sleep Wake Disorders - physiopathology ; Time Factors ; Treatment Outcome</subject><ispartof>Brain & development (Tokyo. 1979), 1999, Vol.21 (1), p.59-62</ispartof><rights>1999 Elsevier Science B.V.</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c485t-aa8f33870af5df0c36e0bb10d96b3ba13618a3cd83bc3c62e0b868f18eeb4b703</citedby><cites>FETCH-LOGICAL-c485t-aa8f33870af5df0c36e0bb10d96b3ba13618a3cd83bc3c62e0b868f18eeb4b703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0387760498000722$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,4010,27900,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1693830$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10082254$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Miyamoto, Akie</creatorcontrib><creatorcontrib>Oki, Junichi</creatorcontrib><creatorcontrib>Takahashi, Satoru</creatorcontrib><creatorcontrib>Okuno, Akimasa</creatorcontrib><title>Serum melatonin kinetics and long-term melatonin treatment for sleep disorders in Rett syndrome</title><title>Brain & development (Tokyo. 1979)</title><addtitle>Brain Dev</addtitle><description>We studied the circadian rhythm of serum melatonin levels in two patients with classical Rett syndrome having severe sleep disorders; serum melatonin levels were measured before and during melatonin treatment using radioimmnoassay. Patient 1 had a free-running rhythm of sleep-wake cycle from 3 years of age. At the age of 4 years, the peak time of melatonin was delayed 6 h compared to normal control and the peak value was at the lower limit. Patient 2 had a fragmented sleep pattern accompanied by night screaming from 1 year and 6 months of age. At the age of 10 years, the peak time of melatonin secretion was normal but the peak value was at the lower limit. These patients were given 5 mg melatonin orally prior to bedtime. Exogenous melatonin dramatically improved the sleep-wake cycle in patient 1. In patient 2, exogenous melatonin showed a hypnotic effect but early morning awakenings occurred occasionally. When melatonin treatment was stopped, the sleep disorders recurred and re-administration of 3 mg melatonin was effective in both patients. The effect was maintained over 2 years without any adverse effects. These findings suggests that sleep disorders in patients with Rett syndrome may relate with an impaired secretion of melatonin.</description><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Female</subject><subject>Humans</subject><subject>Kinetics</subject><subject>Medical sciences</subject><subject>Melatonin</subject><subject>Melatonin - blood</subject><subject>Melatonin - therapeutic use</subject><subject>Neurology</subject><subject>Rett syndrome</subject><subject>Rett Syndrome - complications</subject><subject>Sleep - drug effects</subject><subject>Sleep disorder</subject><subject>Sleep Wake Disorders - drug therapy</subject><subject>Sleep Wake Disorders - etiology</subject><subject>Sleep Wake Disorders - physiopathology</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><issn>0387-7604</issn><issn>1872-7131</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMlKBDEQhoMoOi6PoOQgoofWpDOdTp9ExA0GBJdzSCfVEu1OxiQjzNubWVBvnqqgvqr6-RA6pOScEsovngkTdVFzMj5txBkhpC6LcgONqMhNTRndRKMfZAftxvieIVpSso12KCGiLKvxCMlnCLMBD9Cr5J11-MM6SFZHrJzBvXdvRYLwF0gBVBrAJdz5gGMPMMXGRh8MhIgz8AQp4Th3JvgB9tFWp_oIB-u6h15vb16u74vJ493D9dWk0GNRpUIp0bGclqiuMh3RjANpW0pMw1vWKso4FYppI1irmeZlngouOioA2nFbE7aHTlZ3p8F_ziAmOdiooe-VAz-LkjecVaJmGaxWoA4-xgCdnAY7qDCXlMiFWbk0KxfaZCPk0qws897R-sGsHcD82VqpzMDxGlBRq74LymkbfzneMMEWQS9XGGQbXxaCjNqC02BsAJ2k8fafJN99aZbC</recordid><startdate>1999</startdate><enddate>1999</enddate><creator>Miyamoto, Akie</creator><creator>Oki, Junichi</creator><creator>Takahashi, Satoru</creator><creator>Okuno, Akimasa</creator><general>Elsevier B.V</general><general>Elsevier Science</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>7X8</scope><scope>8BM</scope></search><sort><creationdate>1999</creationdate><title>Serum melatonin kinetics and long-term melatonin treatment for sleep disorders in Rett syndrome</title><author>Miyamoto, Akie ; Oki, Junichi ; Takahashi, Satoru ; Okuno, Akimasa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c485t-aa8f33870af5df0c36e0bb10d96b3ba13618a3cd83bc3c62e0b868f18eeb4b703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Female</topic><topic>Humans</topic><topic>Kinetics</topic><topic>Medical sciences</topic><topic>Melatonin</topic><topic>Melatonin - blood</topic><topic>Melatonin - therapeutic use</topic><topic>Neurology</topic><topic>Rett syndrome</topic><topic>Rett Syndrome - complications</topic><topic>Sleep - drug effects</topic><topic>Sleep disorder</topic><topic>Sleep Wake Disorders - drug therapy</topic><topic>Sleep Wake Disorders - etiology</topic><topic>Sleep Wake Disorders - physiopathology</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miyamoto, Akie</creatorcontrib><creatorcontrib>Oki, Junichi</creatorcontrib><creatorcontrib>Takahashi, Satoru</creatorcontrib><creatorcontrib>Okuno, Akimasa</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>MEDLINE - Academic</collection><collection>ComDisDome</collection><jtitle>Brain & development (Tokyo. 1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miyamoto, Akie</au><au>Oki, Junichi</au><au>Takahashi, Satoru</au><au>Okuno, Akimasa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum melatonin kinetics and long-term melatonin treatment for sleep disorders in Rett syndrome</atitle><jtitle>Brain & development (Tokyo. 1979)</jtitle><addtitle>Brain Dev</addtitle><date>1999</date><risdate>1999</risdate><volume>21</volume><issue>1</issue><spage>59</spage><epage>62</epage><pages>59-62</pages><issn>0387-7604</issn><eissn>1872-7131</eissn><coden>NTHAA7</coden><abstract>We studied the circadian rhythm of serum melatonin levels in two patients with classical Rett syndrome having severe sleep disorders; serum melatonin levels were measured before and during melatonin treatment using radioimmnoassay. Patient 1 had a free-running rhythm of sleep-wake cycle from 3 years of age. At the age of 4 years, the peak time of melatonin was delayed 6 h compared to normal control and the peak value was at the lower limit. Patient 2 had a fragmented sleep pattern accompanied by night screaming from 1 year and 6 months of age. At the age of 10 years, the peak time of melatonin secretion was normal but the peak value was at the lower limit. These patients were given 5 mg melatonin orally prior to bedtime. Exogenous melatonin dramatically improved the sleep-wake cycle in patient 1. In patient 2, exogenous melatonin showed a hypnotic effect but early morning awakenings occurred occasionally. When melatonin treatment was stopped, the sleep disorders recurred and re-administration of 3 mg melatonin was effective in both patients. The effect was maintained over 2 years without any adverse effects. These findings suggests that sleep disorders in patients with Rett syndrome may relate with an impaired secretion of melatonin.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>10082254</pmid><doi>10.1016/S0387-7604(98)00072-2</doi><tpages>4</tpages></addata></record> |
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subjects | Adolescent Biological and medical sciences Child Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Female Humans Kinetics Medical sciences Melatonin Melatonin - blood Melatonin - therapeutic use Neurology Rett syndrome Rett Syndrome - complications Sleep - drug effects Sleep disorder Sleep Wake Disorders - drug therapy Sleep Wake Disorders - etiology Sleep Wake Disorders - physiopathology Time Factors Treatment Outcome |
title | Serum melatonin kinetics and long-term melatonin treatment for sleep disorders in Rett syndrome |
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