TY - JOUR
T1 - The drug-naïve OCD patients imaging genetics, cognitive and treatment response study
T2 - Methods and sample description
AU - Hoexter, Marcelo Queiroz
AU - Shavitt, Roseli Gedanke
AU - D'Alcante, Carina Chaubet
AU - Cecconii, Janaina Philippi
AU - Diniz, Juliana Belo
AU - Belotto-Silva, Cristina
AU - Hounie, Ana Gabriela
AU - Borcato, Sonia
AU - Moraes, Ivanil
AU - Joaquim, Marines Alves
AU - Cappi, Carolina
AU - Sampaio, Aline Santos
AU - De Mathis, Maria Alice
AU - Batistuzzo, Marcelo Camargo
AU - Lopes, Antonio Carlos
AU - Rosa, Ana Claudia F
AU - Muniz, Renan Kawano
AU - Marques, Andrea Horvath
AU - Santos, Luciana Cristina
AU - Taub, Anita
AU - Duran, Fábio Luís De Souza
AU - Dougherty, Darin Dean
AU - Filho Busatto, Geraldo
AU - Bressan, Rodrigo Affonseca
AU - Miguel, Euripedes Constantino
PY - 2009/12
Y1 - 2009/12
N2 - OBJECTIVE: To describe a protocol that was based on an integrative neurobiological model of scientific investigation to better understand the pathophysiology of obsessive-compulsive disorder and to present the clinical and demographic characteristics of the sample. METHOD: A standardized research protocol that combines different methods of investigation (genetics, neuropsychology, morphometric magnetic resonance imaging and molecular neuroimaging of the dopamine transporter) obtained before and after treatment of drug-naïve adult obsessive-compulsive disorder patients submitted to a sequentially allocated 12-week clinical trial with a selective serotonin reuptake inhibitor (fluoxetine) and group cognitive-behavioral therapy. RESULTS: Fifty-two treatment-naïve obsessive-compulsive disorder patients entered the clinical trial (27 received fluoxetine and 25 received group cognitive-behavioral therapy). At baseline, 47 blood samples for genetic studies, 50 neuropsychological evaluations, 50 morphometrical magnetic resonance images and 48 TRODAT-1 single-photon emission computed tomography (SPECT) exams were obtained. After 12 weeks, 38 patients completed the protocol (fluoxetine = 20 and GCBT = 18). Thirty-eight neuropsychological evaluations, 31 morphometrical magnetic resonance images and 34 TRODAT-1 SPECT exams were obtained post-treatment. Forty-one healthy controls matched for age, gender, socioeconomic status, level of education and laterality were submitted to the same research procedures at baseline. CONCLUSION: The comprehensive treatment response protocol applied in this project allowing integration on genetic, neuropsychological, morphometrical and molecular imaging of the dopamine transporter data in drugnaïve patients has the potential to generate important original information on the neurobiology of obsessivecompulsive disorder, and at the same time be clinically meaningful.
AB - OBJECTIVE: To describe a protocol that was based on an integrative neurobiological model of scientific investigation to better understand the pathophysiology of obsessive-compulsive disorder and to present the clinical and demographic characteristics of the sample. METHOD: A standardized research protocol that combines different methods of investigation (genetics, neuropsychology, morphometric magnetic resonance imaging and molecular neuroimaging of the dopamine transporter) obtained before and after treatment of drug-naïve adult obsessive-compulsive disorder patients submitted to a sequentially allocated 12-week clinical trial with a selective serotonin reuptake inhibitor (fluoxetine) and group cognitive-behavioral therapy. RESULTS: Fifty-two treatment-naïve obsessive-compulsive disorder patients entered the clinical trial (27 received fluoxetine and 25 received group cognitive-behavioral therapy). At baseline, 47 blood samples for genetic studies, 50 neuropsychological evaluations, 50 morphometrical magnetic resonance images and 48 TRODAT-1 single-photon emission computed tomography (SPECT) exams were obtained. After 12 weeks, 38 patients completed the protocol (fluoxetine = 20 and GCBT = 18). Thirty-eight neuropsychological evaluations, 31 morphometrical magnetic resonance images and 34 TRODAT-1 SPECT exams were obtained post-treatment. Forty-one healthy controls matched for age, gender, socioeconomic status, level of education and laterality were submitted to the same research procedures at baseline. CONCLUSION: The comprehensive treatment response protocol applied in this project allowing integration on genetic, neuropsychological, morphometrical and molecular imaging of the dopamine transporter data in drugnaïve patients has the potential to generate important original information on the neurobiology of obsessivecompulsive disorder, and at the same time be clinically meaningful.
KW - Cognition
KW - Genetics
KW - Imaging
KW - Obsessive-compulsive disorder
KW - Treatment outcome
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U2 - 10.1590/S1516-44462009000400011
DO - 10.1590/S1516-44462009000400011
M3 - Article
C2 - 20098825
AN - SCOPUS:77149136771
SN - 1516-4446
VL - 31
SP - 349
EP - 353
JO - Revista Brasileira de Psiquiatria
JF - Revista Brasileira de Psiquiatria
IS - 4
ER -