Hypomethylation of the dopamine transporter (DAT) gene promoter is associated with hyperphagia-related behavior in Prader-Willi syndrome: A case-control study.

Wieting, Jelte; Jahn, Kirsten; Eberlein, Christian K; Bleich, Stefan; Frieling, Helge; Deest, Maximilian

Wieting, Jelte; Jahn, Kirsten; Eberlein, Christian K; Bleich, Stefan; Frieling, Helge; Deest, Maximilian.

Afiliação

Wieting J; Hannover Medical School, Department of Psychiatry, Social Psychiatry and Psychotherapy, Carl-Neuberg-Str. 1, 30625 Hannover, Germany. Electronic address: wieting.jelte@mh-hannover.de.
Jahn K; Hannover Medical School, Department of Psychiatry, Social Psychiatry and Psychotherapy, Carl-Neuberg-Str. 1, 30625 Hannover, Germany.
Eberlein CK; Hannover Medical School, Department of Psychiatry, Social Psychiatry and Psychotherapy, Carl-Neuberg-Str. 1, 30625 Hannover, Germany.
Bleich S; Hannover Medical School, Department of Psychiatry, Social Psychiatry and Psychotherapy, Carl-Neuberg-Str. 1, 30625 Hannover, Germany.
Frieling H; Hannover Medical School, Department of Psychiatry, Social Psychiatry and Psychotherapy, Carl-Neuberg-Str. 1, 30625 Hannover, Germany.
Deest M; Hannover Medical School, Department of Psychiatry, Social Psychiatry and Psychotherapy, Carl-Neuberg-Str. 1, 30625 Hannover, Germany.

Behav Brain Res ; 450: 114494, 2023 07 26.

Article em En | MEDLINE | ID: mdl-37182741

Assuntos

Síndrome de Prader-Willi; Humanos; Síndrome de Prader-Willi/genética; Síndrome de Prader-Willi/complicações; Síndrome de Prader-Willi/tratamento farmacológico; Epigênese Genética; Estudos de Casos e Controles; Proteínas da Membrana Plasmática de Transporte de Dopamina/genética; Proteínas da Membrana Plasmática de Transporte de Dopamina/metabolismo; Hiperfagia/genética; Hiperfagia/metabolismo; Regiões Promotoras Genéticas/genética

Palavras-chave

Appetite regulation; Dopamine receptor D2; Dopamine transporter; Hyperphagia; Methylation; Prader-Willi syndrome

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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Behav Brain Res Ano de publicação: 2023 Tipo de documento: Article

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