TY - JOUR
T1 - Sibling Aggregation for Psychopathology in Offspring of Opiate Addicts
T2 - Effects of Parental Comorbidity
AU - Rende, Richard
AU - Weissman, Myrna M.
N1 - Funding Information:
This work was supported by National Institutes of Health Grant DA07201 awarded to Myrna M. Weissman and an Aaron Diamond Postdoctoral Fellowship in the Biomedical and Social Sciences, a National Alliance on Research on Schizophrenia and Affective Disorders Young Investigator Award, and a Mentored Research Scientist Development Award (MH01559) given to Richard Rende.
PY - 1999
Y1 - 1999
N2 - Applied a new analytic approach within the high-risk paradigm, the analysis of sibling aggregation, to identify homogeneous subtypes of familial risk for psychopathology and addiction. All sibling pairs participating in a study of offspring of opiate-addicted parents were identified and their aggregation for psychiatric disorders was determined usingpairwise odds ratios, an analytic technique used in genetic epidemiology. Sibling aggregation was most notable for depressive and anxiety disorders but only in the presence of comorbid depressive disorders in the parents. Parental comorbid alcoholism did not impact sibling aggregation. We emphasize methodological implications of this approach for addressing issues of phenotypic and etiologic heterogeneity in the study of developmental risk for substance abuse.
AB - Applied a new analytic approach within the high-risk paradigm, the analysis of sibling aggregation, to identify homogeneous subtypes of familial risk for psychopathology and addiction. All sibling pairs participating in a study of offspring of opiate-addicted parents were identified and their aggregation for psychiatric disorders was determined usingpairwise odds ratios, an analytic technique used in genetic epidemiology. Sibling aggregation was most notable for depressive and anxiety disorders but only in the presence of comorbid depressive disorders in the parents. Parental comorbid alcoholism did not impact sibling aggregation. We emphasize methodological implications of this approach for addressing issues of phenotypic and etiologic heterogeneity in the study of developmental risk for substance abuse.
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U2 - 10.1207/S15374424jccp280306
DO - 10.1207/S15374424jccp280306
M3 - Article
C2 - 10446683
AN - SCOPUS:0033190935
SN - 1537-4416
VL - 28
SP - 342
EP - 348
JO - Journal of Clinical Child and Adolescent Psychology
JF - Journal of Clinical Child and Adolescent Psychology
IS - 3
ER -