Thermolabile polymorphism of carnitine palmitoyltransferase 2: A genetic risk factor of overall acute encephalopathy.
Identifieur interne : 000339 ( Main/Exploration ); précédent : 000338; suivant : 000340Thermolabile polymorphism of carnitine palmitoyltransferase 2: A genetic risk factor of overall acute encephalopathy.
Auteurs : Akiko Shibata [Japon] ; Mariko Kasai [Japon] ; Ai Hoshino [Japon] ; Taku Miyagawa [Japon] ; Hiroshi Matsumoto [Japon] ; Gaku Yamanaka [Japon] ; Kenjiro Kikuchi [Japon] ; Ichiro Kuki [Japon] ; Akira Kumakura [Japon] ; Shinya Hara [Japon] ; Takashi Shiihara [Japon] ; Sawako Yamazaki [Japon] ; Masayasu Ohta [Japon] ; Takanori Yamagata [Japon] ; Jun-Ichi Takanashi [Japon] ; Masaya Kubota [Japon] ; Akira Oka [Japon] ; Masashi Mizuguchi [Japon]Source :
- Brain & development [ 1872-7131 ] ; 2019.
Descripteurs français
- KwdFr :
- Allèles, Carnitine O-palmitoyltransferase (déficit), Carnitine O-palmitoyltransferase (génétique), Crises épileptiques, Encéphalite, Encéphalopathies (génétique), Enfant d'âge préscolaire, Facteurs de risque, Femelle, Fréquence d'allèle (génétique), Génotype, Humains, Japon, Mâle, Nourrisson, Polymorphisme génétique (génétique), Étude d'association pangénomique (), Études cas-témoins.
- MESH :
- déficit : Carnitine O-palmitoyltransferase.
- génétique : Carnitine O-palmitoyltransferase, Encéphalopathies, Fréquence d'allèle, Polymorphisme génétique.
- Allèles, Crises épileptiques, Encéphalite, Enfant d'âge préscolaire, Facteurs de risque, Femelle, Génotype, Humains, Japon, Mâle, Nourrisson, Étude d'association pangénomique, Études cas-témoins.
- Wicri :
- geographic : Japon.
English descriptors
- KwdEn :
- Alleles, Brain Diseases (genetics), Carnitine O-Palmitoyltransferase (deficiency), Carnitine O-Palmitoyltransferase (genetics), Case-Control Studies, Child, Preschool, Encephalitis, Female, Gene Frequency (genetics), Genome-Wide Association Study (methods), Genotype, Humans, Infant, Japan, Male, Polymorphism, Genetic (genetics), Risk Factors, Seizures.
- MESH :
- chemical , deficiency : Carnitine O-Palmitoyltransferase.
- geographic : Japan.
- genetics : Brain Diseases, Carnitine O-Palmitoyltransferase, Gene Frequency, Polymorphism, Genetic.
- methods : Genome-Wide Association Study.
- Alleles, Case-Control Studies, Child, Preschool, Encephalitis, Female, Genotype, Humans, Infant, Male, Risk Factors, Seizures.
Abstract
Acute encephalopathy is an acute brain dysfunction after preceding infection, consisting of multiple syndromes. Some syndromes, such as acute encephalopathy with biphasic seizures and late reduced diffusion (AESD), are severe with poor outcome, whereas others, such as clinically mild encephalitis/encephalopathy with reversible splenial lesion (MERS), are mild with favorable outcome. Previous study reported the association of the thermolabile polymorphism in Carnitine Palmitoyltransferase 2 (CPT2) gene and severe syndromes of acute encephalopathy. To further explore the pathogenetic role of CPT2 in acute encephalopathy, we conducted a case-control association study of a typical thermolabile CPT2 polymorphism, rs2229291, in 416 patients of acute encephalopathy, including both severe and mild syndromes.
DOI: 10.1016/j.braindev.2019.07.008
PubMed: 31351739
Affiliations:
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Le document en format XML
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<author><name sortKey="Kikuchi, Kenjiro" sort="Kikuchi, Kenjiro" uniqKey="Kikuchi K" first="Kenjiro" last="Kikuchi">Kenjiro Kikuchi</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Thermolabile polymorphism of carnitine palmitoyltransferase 2: A genetic risk factor of overall acute encephalopathy.</title>
<author><name sortKey="Shibata, Akiko" sort="Shibata, Akiko" uniqKey="Shibata A" first="Akiko" last="Shibata">Akiko Shibata</name>
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<author><name sortKey="Kasai, Mariko" sort="Kasai, Mariko" uniqKey="Kasai M" first="Mariko" last="Kasai">Mariko Kasai</name>
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<author><name sortKey="Hoshino, Ai" sort="Hoshino, Ai" uniqKey="Hoshino A" first="Ai" last="Hoshino">Ai Hoshino</name>
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<author><name sortKey="Miyagawa, Taku" sort="Miyagawa, Taku" uniqKey="Miyagawa T" first="Taku" last="Miyagawa">Taku Miyagawa</name>
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<author><name sortKey="Matsumoto, Hiroshi" sort="Matsumoto, Hiroshi" uniqKey="Matsumoto H" first="Hiroshi" last="Matsumoto">Hiroshi Matsumoto</name>
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<author><name sortKey="Yamanaka, Gaku" sort="Yamanaka, Gaku" uniqKey="Yamanaka G" first="Gaku" last="Yamanaka">Gaku Yamanaka</name>
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<author><name sortKey="Kikuchi, Kenjiro" sort="Kikuchi, Kenjiro" uniqKey="Kikuchi K" first="Kenjiro" last="Kikuchi">Kenjiro Kikuchi</name>
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<author><name sortKey="Kuki, Ichiro" sort="Kuki, Ichiro" uniqKey="Kuki I" first="Ichiro" last="Kuki">Ichiro Kuki</name>
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<author><name sortKey="Kumakura, Akira" sort="Kumakura, Akira" uniqKey="Kumakura A" first="Akira" last="Kumakura">Akira Kumakura</name>
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<author><name sortKey="Hara, Shinya" sort="Hara, Shinya" uniqKey="Hara S" first="Shinya" last="Hara">Shinya Hara</name>
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<author><name sortKey="Shiihara, Takashi" sort="Shiihara, Takashi" uniqKey="Shiihara T" first="Takashi" last="Shiihara">Takashi Shiihara</name>
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<author><name sortKey="Yamazaki, Sawako" sort="Yamazaki, Sawako" uniqKey="Yamazaki S" first="Sawako" last="Yamazaki">Sawako Yamazaki</name>
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<country xml:lang="fr">Japon</country>
<wicri:regionArea>Department of Pediatrics, Niigata Minami Hospital, Niigata</wicri:regionArea>
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<author><name sortKey="Ohta, Masayasu" sort="Ohta, Masayasu" uniqKey="Ohta M" first="Masayasu" last="Ohta">Masayasu Ohta</name>
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<wicri:regionArea>Department of Pediatrics, Aiseikai Memorial Ibaraki Welfare Medical Center, Ibaraki</wicri:regionArea>
<wicri:noRegion>Ibaraki</wicri:noRegion>
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</author>
<author><name sortKey="Yamagata, Takanori" sort="Yamagata, Takanori" uniqKey="Yamagata T" first="Takanori" last="Yamagata">Takanori Yamagata</name>
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<wicri:regionArea>Department of Pediatrics, Jichi Medical University, Tochigi</wicri:regionArea>
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<author><name sortKey="Takanashi, Jun Ichi" sort="Takanashi, Jun Ichi" uniqKey="Takanashi J" first="Jun-Ichi" last="Takanashi">Jun-Ichi Takanashi</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Pediatrics, Tokyo Women's Medical University Yachiyo Medical Center, Chiba, Japan.</nlm:affiliation>
<country xml:lang="fr">Japon</country>
<wicri:regionArea>Department of Pediatrics, Tokyo Women's Medical University Yachiyo Medical Center, Chiba</wicri:regionArea>
<wicri:noRegion>Chiba</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Kubota, Masaya" sort="Kubota, Masaya" uniqKey="Kubota M" first="Masaya" last="Kubota">Masaya Kubota</name>
<affiliation wicri:level="3"><nlm:affiliation>Division of Neurology, National Center for Child Health and Development, Tokyo, Japan.</nlm:affiliation>
<country xml:lang="fr">Japon</country>
<wicri:regionArea>Division of Neurology, National Center for Child Health and Development, Tokyo</wicri:regionArea>
<placeName><settlement type="city">Tokyo</settlement>
<region type="région">Région de Kantō</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Oka, Akira" sort="Oka, Akira" uniqKey="Oka A" first="Akira" last="Oka">Akira Oka</name>
<affiliation wicri:level="4"><nlm:affiliation>Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.</nlm:affiliation>
<country xml:lang="fr">Japon</country>
<wicri:regionArea>Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, Tokyo</wicri:regionArea>
<placeName><settlement type="city">Tokyo</settlement>
<region type="région">Région de Kantō</region>
</placeName>
<orgName type="university">Université de Tokyo</orgName>
</affiliation>
</author>
<author><name sortKey="Mizuguchi, Masashi" sort="Mizuguchi, Masashi" uniqKey="Mizuguchi M" first="Masashi" last="Mizuguchi">Masashi Mizuguchi</name>
<affiliation wicri:level="4"><nlm:affiliation>Department of Developmental Medical Sciences, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.</nlm:affiliation>
<country xml:lang="fr">Japon</country>
<wicri:regionArea>Department of Developmental Medical Sciences, Graduate School of Medicine, The University of Tokyo, Tokyo</wicri:regionArea>
<placeName><settlement type="city">Tokyo</settlement>
<region type="région">Région de Kantō</region>
</placeName>
<orgName type="university">Université de Tokyo</orgName>
</affiliation>
</author>
</analytic>
<series><title level="j">Brain & development</title>
<idno type="eISSN">1872-7131</idno>
<imprint><date when="2019" type="published">2019</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Alleles</term>
<term>Brain Diseases (genetics)</term>
<term>Carnitine O-Palmitoyltransferase (deficiency)</term>
<term>Carnitine O-Palmitoyltransferase (genetics)</term>
<term>Case-Control Studies</term>
<term>Child, Preschool</term>
<term>Encephalitis</term>
<term>Female</term>
<term>Gene Frequency (genetics)</term>
<term>Genome-Wide Association Study (methods)</term>
<term>Genotype</term>
<term>Humans</term>
<term>Infant</term>
<term>Japan</term>
<term>Male</term>
<term>Polymorphism, Genetic (genetics)</term>
<term>Risk Factors</term>
<term>Seizures</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Allèles</term>
<term>Carnitine O-palmitoyltransferase (déficit)</term>
<term>Carnitine O-palmitoyltransferase (génétique)</term>
<term>Crises épileptiques</term>
<term>Encéphalite</term>
<term>Encéphalopathies (génétique)</term>
<term>Enfant d'âge préscolaire</term>
<term>Facteurs de risque</term>
<term>Femelle</term>
<term>Fréquence d'allèle (génétique)</term>
<term>Génotype</term>
<term>Humains</term>
<term>Japon</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Polymorphisme génétique (génétique)</term>
<term>Étude d'association pangénomique ()</term>
<term>Études cas-témoins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="deficiency" xml:lang="en"><term>Carnitine O-Palmitoyltransferase</term>
</keywords>
<keywords scheme="MESH" type="geographic" xml:lang="en"><term>Japan</term>
</keywords>
<keywords scheme="MESH" qualifier="déficit" xml:lang="fr"><term>Carnitine O-palmitoyltransferase</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Brain Diseases</term>
<term>Carnitine O-Palmitoyltransferase</term>
<term>Gene Frequency</term>
<term>Polymorphism, Genetic</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Carnitine O-palmitoyltransferase</term>
<term>Encéphalopathies</term>
<term>Fréquence d'allèle</term>
<term>Polymorphisme génétique</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Genome-Wide Association Study</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Alleles</term>
<term>Case-Control Studies</term>
<term>Child, Preschool</term>
<term>Encephalitis</term>
<term>Female</term>
<term>Genotype</term>
<term>Humans</term>
<term>Infant</term>
<term>Male</term>
<term>Risk Factors</term>
<term>Seizures</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Allèles</term>
<term>Crises épileptiques</term>
<term>Encéphalite</term>
<term>Enfant d'âge préscolaire</term>
<term>Facteurs de risque</term>
<term>Femelle</term>
<term>Génotype</term>
<term>Humains</term>
<term>Japon</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Étude d'association pangénomique</term>
<term>Études cas-témoins</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr"><term>Japon</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Acute encephalopathy is an acute brain dysfunction after preceding infection, consisting of multiple syndromes. Some syndromes, such as acute encephalopathy with biphasic seizures and late reduced diffusion (AESD), are severe with poor outcome, whereas others, such as clinically mild encephalitis/encephalopathy with reversible splenial lesion (MERS), are mild with favorable outcome. Previous study reported the association of the thermolabile polymorphism in Carnitine Palmitoyltransferase 2 (CPT2) gene and severe syndromes of acute encephalopathy. To further explore the pathogenetic role of CPT2 in acute encephalopathy, we conducted a case-control association study of a typical thermolabile CPT2 polymorphism, rs2229291, in 416 patients of acute encephalopathy, including both severe and mild syndromes.</div>
</front>
</TEI>
<affiliations><list><country><li>Japon</li>
</country>
<region><li>Région de Kantō</li>
</region>
<settlement><li>Tokyo</li>
</settlement>
<orgName><li>Université de Tokyo</li>
</orgName>
</list>
<tree><country name="Japon"><region name="Région de Kantō"><name sortKey="Shibata, Akiko" sort="Shibata, Akiko" uniqKey="Shibata A" first="Akiko" last="Shibata">Akiko Shibata</name>
</region>
<name sortKey="Hara, Shinya" sort="Hara, Shinya" uniqKey="Hara S" first="Shinya" last="Hara">Shinya Hara</name>
<name sortKey="Hoshino, Ai" sort="Hoshino, Ai" uniqKey="Hoshino A" first="Ai" last="Hoshino">Ai Hoshino</name>
<name sortKey="Kasai, Mariko" sort="Kasai, Mariko" uniqKey="Kasai M" first="Mariko" last="Kasai">Mariko Kasai</name>
<name sortKey="Kikuchi, Kenjiro" sort="Kikuchi, Kenjiro" uniqKey="Kikuchi K" first="Kenjiro" last="Kikuchi">Kenjiro Kikuchi</name>
<name sortKey="Kubota, Masaya" sort="Kubota, Masaya" uniqKey="Kubota M" first="Masaya" last="Kubota">Masaya Kubota</name>
<name sortKey="Kuki, Ichiro" sort="Kuki, Ichiro" uniqKey="Kuki I" first="Ichiro" last="Kuki">Ichiro Kuki</name>
<name sortKey="Kumakura, Akira" sort="Kumakura, Akira" uniqKey="Kumakura A" first="Akira" last="Kumakura">Akira Kumakura</name>
<name sortKey="Matsumoto, Hiroshi" sort="Matsumoto, Hiroshi" uniqKey="Matsumoto H" first="Hiroshi" last="Matsumoto">Hiroshi Matsumoto</name>
<name sortKey="Miyagawa, Taku" sort="Miyagawa, Taku" uniqKey="Miyagawa T" first="Taku" last="Miyagawa">Taku Miyagawa</name>
<name sortKey="Mizuguchi, Masashi" sort="Mizuguchi, Masashi" uniqKey="Mizuguchi M" first="Masashi" last="Mizuguchi">Masashi Mizuguchi</name>
<name sortKey="Ohta, Masayasu" sort="Ohta, Masayasu" uniqKey="Ohta M" first="Masayasu" last="Ohta">Masayasu Ohta</name>
<name sortKey="Oka, Akira" sort="Oka, Akira" uniqKey="Oka A" first="Akira" last="Oka">Akira Oka</name>
<name sortKey="Shiihara, Takashi" sort="Shiihara, Takashi" uniqKey="Shiihara T" first="Takashi" last="Shiihara">Takashi Shiihara</name>
<name sortKey="Takanashi, Jun Ichi" sort="Takanashi, Jun Ichi" uniqKey="Takanashi J" first="Jun-Ichi" last="Takanashi">Jun-Ichi Takanashi</name>
<name sortKey="Yamagata, Takanori" sort="Yamagata, Takanori" uniqKey="Yamagata T" first="Takanori" last="Yamagata">Takanori Yamagata</name>
<name sortKey="Yamanaka, Gaku" sort="Yamanaka, Gaku" uniqKey="Yamanaka G" first="Gaku" last="Yamanaka">Gaku Yamanaka</name>
<name sortKey="Yamazaki, Sawako" sort="Yamazaki, Sawako" uniqKey="Yamazaki S" first="Sawako" last="Yamazaki">Sawako Yamazaki</name>
</country>
</tree>
</affiliations>
</record>
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