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. Author manuscript; available in PMC: 2018 May 7.
Published in final edited form as: Mol Psychiatry. 2017 Nov 7;23(5):1293–1302. doi: 10.1038/mp.2017.200

Table 2.

Sample characteristics of discovery cohorts of European-American and European-Australian (EA) individuals included in meta-analysis (CATS, COGA-cc, COGA-f, OZALC+, SAGE), replication cohort (Yale-Penn) and neuroimaging extension (DNS) samples. Only individuals with a lifetime history of ever using cannabis are included.

Study Ncase Ncontrols Median age % Male % Alcohol dependent % Nicotine dependent % Cocaine dependent % Opioid dependent
Discovery Samples
CATS 799 813 36 57.5 % 38.8 % 60.2 % 24.8 % 76.1 %
COGA-cc 311 593 40 60.1 % 79.4 % 49.0 % 34.4 % 13.3 %
COGA-f 368 894 36 50.6 % 47.0 % 40.3 % 13.9 % 5.7 %
OZALC 357 3094 43 51.7 % 40.2 % 50.7 % 0.4 % 0.5 %
SAGE 245 1041 38 46.4 % 55.0 % 53.4 % 25.2 % 9.3 %
Replication Samples
Yale-Penn EA 781 1591 38 57.7 % 74.2% 77.3 % 78.9 % 62.0 %
Yale-Penn AA 896 1905 42 54.6 % 59.9 % 57.5 % 75.6 % 21.2 %
Neuroimaging Sample
DNS - - 19 46.7% 6.3% 0% 0% 0%

CATS: Comorbidity and Trauma Study; COGA-cc: Case-control component of the Collaborative Study of the Genetics of Alcoholism, COGA-f: family-based component of the Collaborative Study of the Genetics of Alcoholism; OZALC+: Australian alcohol, nicotine and trauma studies; SAGE: Study of Addictions: Genes and Environment; DNS: Duke Neurogenetics Study.