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Difference in brain surface area between first-episode familial and sporadic schizophrenia and its association with COMT gene polymorphisms / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 259-263, 2015.
Article Dans Chinois | WPRIM | ID: wpr-239491
ABSTRACT
<p><b>OBJECTIVE</b>To assess the association of impairment of surface area of first-episode schizophrenia(SZ) with polymorphisms of COMT gene, and the difference in the impaired patterns between familial patients with schizophrenia(FPS) and sporadic patients with schizophrenia(SPS).</p><p><b>METHODS</b>Ninety-eight patients with first-episode SZ(FPS=40, SPS=58) and 78 healthy controls were recruited. COMT gene was genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Participants were scanned for 3.0T magnetic resonance images. Freesurfer software was used to analyze the difference in brain surface area between SZ and controls, its association with COMT genotypes, and the difference between SPS, FPS and control groups. Multiple tests were corrected using a Monte Carlo simulation at P<0.05.</p><p><b>RESULTS</b>Compared with controls, SZ showed decreased surface area in right occipital cortex and left prefrontal cortex. No association was found between COMT polymorphisms and whole brain area difference. Among the three subgroups, SPS showed smaller left prefrontal area compared with both FPS and control groups. Patients with SPS also showed significant area reduction in right occipital lobe compared with controls.</p><p><b>CONCLUSION</b>Surface area impairment can be found in those with first-episode SZ, but without association with COMT gene polymorphisms. The SPS have more severe area impairment than FPS, indicating that SPS and FPS may be attributed to different etiological mechanisms.</p>
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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Schizophrénie / Polymorphisme de restriction / Encéphale / Imagerie diagnostique / Imagerie par résonance magnétique / Radiographie / Catechol O-methyltransferase / Génétique Type d'étude: Etude diagnostique / Étude pronostique Limites du sujet: Adulte / Femelle / Humains / Mâle langue: Chinois Texte intégral: Chinese Journal of Medical Genetics Année: 2015 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Schizophrénie / Polymorphisme de restriction / Encéphale / Imagerie diagnostique / Imagerie par résonance magnétique / Radiographie / Catechol O-methyltransferase / Génétique Type d'étude: Etude diagnostique / Étude pronostique Limites du sujet: Adulte / Femelle / Humains / Mâle langue: Chinois Texte intégral: Chinese Journal of Medical Genetics Année: 2015 Type: Article