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Chunk #66 — Methods — Second Replication Cohort

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A genome-wide investigation of SNPs and CNVs in schizophrenia.
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The sample comprised a total of 918 subjects of whom 394 (mean age±SD 43.5±12.8 years, range 19–80) had a DSM-IV-TR [50] diagnosis of schizophrenia and 524 (mean age±SD 47.3±29.7 years, range 19–87) were healthy controls. Patients and controls were of Caucasian ancestry for at least two generations, lived in northern Italy, were unrelated to other participants, and fulfilled predefined group-specific inclusion and exclusion criteria. The different subtypes of schizophrenia were observed as follows: paranoid 61.9%, undifferentiated 17.0%, residual 10.4%, disorganized 9.4%, catatonic 1.3%. The patients were enrolled from those voluntarily admitted to the Brescia IRCCS Fatebenefratelli. The inclusion criteria were a DSM-IV-TR diagnosis of schizophrenia [54] and a level of understanding and attention judged sufficient to give true informed consent; a lifetime comorbidity with other DSM-IV-TR Axis I disorders was an exclusion criterion. All participants underwent detailed clinical interviews, implemented, when required, by DSM-IV-TR adjusted versions of the Structural Clinical Interview for DSM-IV Axis I Disorders. Moreover, to attribute the schizophrenia subtype, a checklist of the symptoms dominating the clinical picture at the screening visit and in the previous 4 weeks was used.