The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy
Abstract Purpose Although it has been reported that some antiepileptic drugs have inducing or inhibiting effects on lamotrigine (LTG) clearance, whether they have the same effects in Asian epilepsy patients as in those in other countries has not been clarified, especially in children. The aim of thi...
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creator | Takeuchi, Tomoya Natsume, Jun Kidokoro, Hiroyuki Ishihara, Naoko Yamamoto, Hiroyuki Azuma, Yoshiteru Ito, Yuji Kurahashi, Naoko Tsuji, Takeshi Suzuki, Motomasa Itomi, Kazuya Yamada, Keitaro Kurahashi, Hirokazu Abe, Shinpei Okumura, Akihisa Maruyama, Koichi Negoro, Tamiko Watanabe, Kazuyoshi Kojima, Seiji |
description | Abstract Purpose Although it has been reported that some antiepileptic drugs have inducing or inhibiting effects on lamotrigine (LTG) clearance, whether they have the same effects in Asian epilepsy patients as in those in other countries has not been clarified, especially in children. The aim of this study was to determine the effects of co-medications on LTG clearance in Japanese children with epilepsy. Methods A total of 342 routine serum concentration measurements of LTG in 102 Japanese epilepsy patients under 20 years of age were reviewed. The dose-corrected concentration (DCC) of LTG was calculated as [concentration]/[dose/(body weight)], and the DCC of LTG was compared by co-medication. The difference in the DCC of LTG was compared between patients with and without valproic acid (VPA) and between those with and without drugs inducing glucuronic acid conjugation (phenytoin (PHT), carbamazepine (CBZ), and phenobarbital (PB)). Results The DCC of LTG was significantly higher in patients on VPA and significantly lower in patients on drugs inducing glucuronic acid conjugation than in patients on LTG monotherapy. The DCC of LTG was significantly higher in patients on CBZ than in patients on PHT or PB. There was no correlation between the DCC of LTG and the concentration of VPA or metabolic inducers within the therapeutic range. Other antiepileptic drugs including clobazam, clonazepam, zonisamide, and levetiracetam had little effect on LTG concentration. Conclusion LTG concentration changes dramatically with concomitant antiepileptic drugs in Japanese children, as previously reported from other countries, and special attention is required. Although the dose of LTG should be adjusted when starting or discontinuing VPA or metabolic inducers, no adjustment is needed when changing the dose of VPA or metabolic inducers in the therapeutic range. |
doi_str_mv | 10.1016/j.braindev.2016.03.004 |
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The aim of this study was to determine the effects of co-medications on LTG clearance in Japanese children with epilepsy. Methods A total of 342 routine serum concentration measurements of LTG in 102 Japanese epilepsy patients under 20 years of age were reviewed. The dose-corrected concentration (DCC) of LTG was calculated as [concentration]/[dose/(body weight)], and the DCC of LTG was compared by co-medication. The difference in the DCC of LTG was compared between patients with and without valproic acid (VPA) and between those with and without drugs inducing glucuronic acid conjugation (phenytoin (PHT), carbamazepine (CBZ), and phenobarbital (PB)). Results The DCC of LTG was significantly higher in patients on VPA and significantly lower in patients on drugs inducing glucuronic acid conjugation than in patients on LTG monotherapy. The DCC of LTG was significantly higher in patients on CBZ than in patients on PHT or PB. There was no correlation between the DCC of LTG and the concentration of VPA or metabolic inducers within the therapeutic range. Other antiepileptic drugs including clobazam, clonazepam, zonisamide, and levetiracetam had little effect on LTG concentration. Conclusion LTG concentration changes dramatically with concomitant antiepileptic drugs in Japanese children, as previously reported from other countries, and special attention is required. Although the dose of LTG should be adjusted when starting or discontinuing VPA or metabolic inducers, no adjustment is needed when changing the dose of VPA or metabolic inducers in the therapeutic range.</description><identifier>ISSN: 0387-7604</identifier><identifier>EISSN: 1872-7131</identifier><identifier>DOI: 10.1016/j.braindev.2016.03.004</identifier><identifier>PMID: 27033151</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject><![CDATA[Adolescent ; Anticonvulsants - administration & dosage ; Anticonvulsants - pharmacokinetics ; Benzodiazepines - administration & dosage ; Carbamazepine - administration & dosage ; Child ; Child, Preschool ; Clonazepam - administration & dosage ; Co-medication ; Drug concentration ; Drug interaction ; Drug Interactions ; Drug Therapy, Combination ; Epilepsy ; Epilepsy - blood ; Epilepsy - drug therapy ; Female ; Humans ; Infant ; Infant, Newborn ; Isoxazoles - administration & dosage ; Japan ; Lamotrigine ; Male ; Neurology ; Phenobarbital - administration & dosage ; Phenytoin - administration & dosage ; Piracetam - administration & dosage ; Piracetam - analogs & derivatives ; Triazines - administration & dosage ; Triazines - pharmacokinetics ; Valproic Acid - administration & dosage ; Young Adult]]></subject><ispartof>Brain & development (Tokyo. 1979), 2016-09, Vol.38 (8), p.723-730</ispartof><rights>The Japanese Society of Child Neurology</rights><rights>2016 The Japanese Society of Child Neurology</rights><rights>Copyright © 2016 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c531t-31240f631b34c4368750e13327235eaa3a2bc8f04f777c5575e22db1fd1fc6d93</citedby><cites>FETCH-LOGICAL-c531t-31240f631b34c4368750e13327235eaa3a2bc8f04f777c5575e22db1fd1fc6d93</cites><orcidid>0000-0002-6006-5258</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.braindev.2016.03.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27033151$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takeuchi, Tomoya</creatorcontrib><creatorcontrib>Natsume, Jun</creatorcontrib><creatorcontrib>Kidokoro, Hiroyuki</creatorcontrib><creatorcontrib>Ishihara, Naoko</creatorcontrib><creatorcontrib>Yamamoto, Hiroyuki</creatorcontrib><creatorcontrib>Azuma, Yoshiteru</creatorcontrib><creatorcontrib>Ito, Yuji</creatorcontrib><creatorcontrib>Kurahashi, Naoko</creatorcontrib><creatorcontrib>Tsuji, Takeshi</creatorcontrib><creatorcontrib>Suzuki, Motomasa</creatorcontrib><creatorcontrib>Itomi, Kazuya</creatorcontrib><creatorcontrib>Yamada, Keitaro</creatorcontrib><creatorcontrib>Kurahashi, Hirokazu</creatorcontrib><creatorcontrib>Abe, Shinpei</creatorcontrib><creatorcontrib>Okumura, Akihisa</creatorcontrib><creatorcontrib>Maruyama, Koichi</creatorcontrib><creatorcontrib>Negoro, Tamiko</creatorcontrib><creatorcontrib>Watanabe, Kazuyoshi</creatorcontrib><creatorcontrib>Kojima, Seiji</creatorcontrib><title>The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy</title><title>Brain & development (Tokyo. 1979)</title><addtitle>Brain Dev</addtitle><description>Abstract Purpose Although it has been reported that some antiepileptic drugs have inducing or inhibiting effects on lamotrigine (LTG) clearance, whether they have the same effects in Asian epilepsy patients as in those in other countries has not been clarified, especially in children. The aim of this study was to determine the effects of co-medications on LTG clearance in Japanese children with epilepsy. Methods A total of 342 routine serum concentration measurements of LTG in 102 Japanese epilepsy patients under 20 years of age were reviewed. The dose-corrected concentration (DCC) of LTG was calculated as [concentration]/[dose/(body weight)], and the DCC of LTG was compared by co-medication. The difference in the DCC of LTG was compared between patients with and without valproic acid (VPA) and between those with and without drugs inducing glucuronic acid conjugation (phenytoin (PHT), carbamazepine (CBZ), and phenobarbital (PB)). Results The DCC of LTG was significantly higher in patients on VPA and significantly lower in patients on drugs inducing glucuronic acid conjugation than in patients on LTG monotherapy. The DCC of LTG was significantly higher in patients on CBZ than in patients on PHT or PB. There was no correlation between the DCC of LTG and the concentration of VPA or metabolic inducers within the therapeutic range. Other antiepileptic drugs including clobazam, clonazepam, zonisamide, and levetiracetam had little effect on LTG concentration. Conclusion LTG concentration changes dramatically with concomitant antiepileptic drugs in Japanese children, as previously reported from other countries, and special attention is required. Although the dose of LTG should be adjusted when starting or discontinuing VPA or metabolic inducers, no adjustment is needed when changing the dose of VPA or metabolic inducers in the therapeutic range.</description><subject>Adolescent</subject><subject>Anticonvulsants - administration & dosage</subject><subject>Anticonvulsants - pharmacokinetics</subject><subject>Benzodiazepines - administration & dosage</subject><subject>Carbamazepine - administration & dosage</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Clonazepam - administration & dosage</subject><subject>Co-medication</subject><subject>Drug concentration</subject><subject>Drug interaction</subject><subject>Drug Interactions</subject><subject>Drug Therapy, Combination</subject><subject>Epilepsy</subject><subject>Epilepsy - blood</subject><subject>Epilepsy - drug therapy</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Isoxazoles - administration & dosage</subject><subject>Japan</subject><subject>Lamotrigine</subject><subject>Male</subject><subject>Neurology</subject><subject>Phenobarbital - administration & dosage</subject><subject>Phenytoin - administration & dosage</subject><subject>Piracetam - administration & dosage</subject><subject>Piracetam - analogs & derivatives</subject><subject>Triazines - administration & dosage</subject><subject>Triazines - pharmacokinetics</subject><subject>Valproic Acid - administration & dosage</subject><subject>Young Adult</subject><issn>0387-7604</issn><issn>1872-7131</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAQhS1ERbeFv1D5yCXpjJ3E4YJAVWlBlThQDpwsxxmzXrJ2sLNF--_r1bYcuHAazei9Gft7jF0g1AjYXW7qIRkfRnqoRelrkDVA84KtsFeiUijxJVuB7FWlOmhO2VnOGwBAgfCKnQoFUmKLK_bjfk2cnCO7ZB4dt7Ha0uitWXwMZRL4ZLZxSf6nD8TtRCaZYIn7wL-Y2QTKZbr205go8D9-WXOa_URz3r9mJ85Mmd481XP2_dP1_dVtdff15vPVx7vKthKXSqJowHUSB9nYRna9aoFQSqGEbMkYacRgeweNU0rZtlUtCTEO6EZ0thvfyXP29rh3TvH3jvKitz5bmqbyuLjLGnvoZd8VY5F2R6lNMedETs_Jb03aawR9wKo3-hmrPmDVIHXBWowXTzd2Q8Hz1_bMsQg-HAVUfvrgKelsPRVQo08FrR6j__-N9_-ssJMPJYnpF-0pb-IuhcJRo85Cg_52CPeQLXYSQBRijwtwoNI</recordid><startdate>20160901</startdate><enddate>20160901</enddate><creator>Takeuchi, Tomoya</creator><creator>Natsume, Jun</creator><creator>Kidokoro, Hiroyuki</creator><creator>Ishihara, Naoko</creator><creator>Yamamoto, Hiroyuki</creator><creator>Azuma, Yoshiteru</creator><creator>Ito, Yuji</creator><creator>Kurahashi, Naoko</creator><creator>Tsuji, Takeshi</creator><creator>Suzuki, Motomasa</creator><creator>Itomi, Kazuya</creator><creator>Yamada, Keitaro</creator><creator>Kurahashi, Hirokazu</creator><creator>Abe, Shinpei</creator><creator>Okumura, Akihisa</creator><creator>Maruyama, Koichi</creator><creator>Negoro, Tamiko</creator><creator>Watanabe, Kazuyoshi</creator><creator>Kojima, Seiji</creator><general>Elsevier B.V</general><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><orcidid>https://orcid.org/0000-0002-6006-5258</orcidid></search><sort><creationdate>20160901</creationdate><title>The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy</title><author>Takeuchi, Tomoya ; Natsume, Jun ; Kidokoro, Hiroyuki ; Ishihara, Naoko ; Yamamoto, Hiroyuki ; Azuma, Yoshiteru ; Ito, Yuji ; Kurahashi, Naoko ; Tsuji, Takeshi ; Suzuki, Motomasa ; Itomi, Kazuya ; Yamada, Keitaro ; Kurahashi, Hirokazu ; Abe, Shinpei ; Okumura, Akihisa ; Maruyama, Koichi ; Negoro, Tamiko ; Watanabe, Kazuyoshi ; Kojima, Seiji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c531t-31240f631b34c4368750e13327235eaa3a2bc8f04f777c5575e22db1fd1fc6d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Anticonvulsants - administration & dosage</topic><topic>Anticonvulsants - pharmacokinetics</topic><topic>Benzodiazepines - administration & dosage</topic><topic>Carbamazepine - administration & dosage</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Clonazepam - administration & dosage</topic><topic>Co-medication</topic><topic>Drug concentration</topic><topic>Drug interaction</topic><topic>Drug Interactions</topic><topic>Drug Therapy, Combination</topic><topic>Epilepsy</topic><topic>Epilepsy - blood</topic><topic>Epilepsy - drug therapy</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Isoxazoles - administration & dosage</topic><topic>Japan</topic><topic>Lamotrigine</topic><topic>Male</topic><topic>Neurology</topic><topic>Phenobarbital - administration & dosage</topic><topic>Phenytoin - administration & dosage</topic><topic>Piracetam - administration & dosage</topic><topic>Piracetam - analogs & derivatives</topic><topic>Triazines - administration & dosage</topic><topic>Triazines - pharmacokinetics</topic><topic>Valproic Acid - administration & dosage</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takeuchi, Tomoya</creatorcontrib><creatorcontrib>Natsume, Jun</creatorcontrib><creatorcontrib>Kidokoro, Hiroyuki</creatorcontrib><creatorcontrib>Ishihara, Naoko</creatorcontrib><creatorcontrib>Yamamoto, Hiroyuki</creatorcontrib><creatorcontrib>Azuma, Yoshiteru</creatorcontrib><creatorcontrib>Ito, Yuji</creatorcontrib><creatorcontrib>Kurahashi, Naoko</creatorcontrib><creatorcontrib>Tsuji, Takeshi</creatorcontrib><creatorcontrib>Suzuki, Motomasa</creatorcontrib><creatorcontrib>Itomi, Kazuya</creatorcontrib><creatorcontrib>Yamada, Keitaro</creatorcontrib><creatorcontrib>Kurahashi, Hirokazu</creatorcontrib><creatorcontrib>Abe, Shinpei</creatorcontrib><creatorcontrib>Okumura, Akihisa</creatorcontrib><creatorcontrib>Maruyama, Koichi</creatorcontrib><creatorcontrib>Negoro, Tamiko</creatorcontrib><creatorcontrib>Watanabe, Kazuyoshi</creatorcontrib><creatorcontrib>Kojima, Seiji</creatorcontrib><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><jtitle>Brain & development (Tokyo. 1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takeuchi, Tomoya</au><au>Natsume, Jun</au><au>Kidokoro, Hiroyuki</au><au>Ishihara, Naoko</au><au>Yamamoto, Hiroyuki</au><au>Azuma, Yoshiteru</au><au>Ito, Yuji</au><au>Kurahashi, Naoko</au><au>Tsuji, Takeshi</au><au>Suzuki, Motomasa</au><au>Itomi, Kazuya</au><au>Yamada, Keitaro</au><au>Kurahashi, Hirokazu</au><au>Abe, Shinpei</au><au>Okumura, Akihisa</au><au>Maruyama, Koichi</au><au>Negoro, Tamiko</au><au>Watanabe, Kazuyoshi</au><au>Kojima, Seiji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy</atitle><jtitle>Brain & development (Tokyo. 1979)</jtitle><addtitle>Brain Dev</addtitle><date>2016-09-01</date><risdate>2016</risdate><volume>38</volume><issue>8</issue><spage>723</spage><epage>730</epage><pages>723-730</pages><issn>0387-7604</issn><eissn>1872-7131</eissn><abstract>Abstract Purpose Although it has been reported that some antiepileptic drugs have inducing or inhibiting effects on lamotrigine (LTG) clearance, whether they have the same effects in Asian epilepsy patients as in those in other countries has not been clarified, especially in children. The aim of this study was to determine the effects of co-medications on LTG clearance in Japanese children with epilepsy. Methods A total of 342 routine serum concentration measurements of LTG in 102 Japanese epilepsy patients under 20 years of age were reviewed. The dose-corrected concentration (DCC) of LTG was calculated as [concentration]/[dose/(body weight)], and the DCC of LTG was compared by co-medication. The difference in the DCC of LTG was compared between patients with and without valproic acid (VPA) and between those with and without drugs inducing glucuronic acid conjugation (phenytoin (PHT), carbamazepine (CBZ), and phenobarbital (PB)). Results The DCC of LTG was significantly higher in patients on VPA and significantly lower in patients on drugs inducing glucuronic acid conjugation than in patients on LTG monotherapy. The DCC of LTG was significantly higher in patients on CBZ than in patients on PHT or PB. There was no correlation between the DCC of LTG and the concentration of VPA or metabolic inducers within the therapeutic range. Other antiepileptic drugs including clobazam, clonazepam, zonisamide, and levetiracetam had little effect on LTG concentration. Conclusion LTG concentration changes dramatically with concomitant antiepileptic drugs in Japanese children, as previously reported from other countries, and special attention is required. Although the dose of LTG should be adjusted when starting or discontinuing VPA or metabolic inducers, no adjustment is needed when changing the dose of VPA or metabolic inducers in the therapeutic range.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>27033151</pmid><doi>10.1016/j.braindev.2016.03.004</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-6006-5258</orcidid></addata></record> |
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subjects | Adolescent Anticonvulsants - administration & dosage Anticonvulsants - pharmacokinetics Benzodiazepines - administration & dosage Carbamazepine - administration & dosage Child Child, Preschool Clonazepam - administration & dosage Co-medication Drug concentration Drug interaction Drug Interactions Drug Therapy, Combination Epilepsy Epilepsy - blood Epilepsy - drug therapy Female Humans Infant Infant, Newborn Isoxazoles - administration & dosage Japan Lamotrigine Male Neurology Phenobarbital - administration & dosage Phenytoin - administration & dosage Piracetam - administration & dosage Piracetam - analogs & derivatives Triazines - administration & dosage Triazines - pharmacokinetics Valproic Acid - administration & dosage Young Adult |
title | The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy |
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