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Chunk #6 — Methods — Sample and measures

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The association of polygenic risk for schizophrenia, bipolar disorder, and depression with neural connectivity in adolescents and young adults: examining developmental and sex differences.
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COGA’s prospective study began data collection in 2004 and ended in 2019. Details of data collection and procedures have been published33. Briefly, offspring from families affected with AUD and community comparison families from the COGA study were enrolled when they were aged 12–22, with new subjects added as they reached the age of 12. Subjects were assessed ~every 2 years with a comprehensive battery that includes the Semi-Structured Assessment for the Genetics of Alcoholism (SSAGA)34,35 assessing substance use and related disorders, neurocognitive performance, and a neurophysiological battery that includes resting-state EEG. Owing to the majority European ancestry (EA) of the PGC SCZ GWAS, our analytic sample comprises EA individuals with genotypic and EEG data from at least three assessments (N = 1426 offspring from 913 EA families, with a mean of 3.5 assessments). Among them, the median age at first interview was 15.6 (Range = 12–26), 51.6% were female, 17.8% met criteria for DSM-IV Alcohol Dependence, and 41% had a family history of AUD. Experimental protocols were approved by each site’s IRB, and informed consent was obtained from all participants, including parental permission from participants aged 18 years or younger.