In a cross-national study, we propose to investigate etiological heterogeneity in autism by focussing on disorders in the first degree relatives of autistic probands which may be genetically associated with autism and thus, may represent a genetic predisposition to autism. 220 families will be ascertained through a school-aged autistic child (110 from each site). The autistic probands will be stratified by sex and IQ, and characterized according to their early environmental history, and clinical features and tested for fragile-X. Their first degree relatives will be examined to detect cognitive abnormalities (mental retardation, language delay and reading disability), abnormalities of social relatedness, and the major psychiatric disorders, (affective disorder and schizophrenia). The first degree relatives of 80 children with Down's syndrome (40 at each site), matched on relevant variables, and the first degree relatives of 40 adopted autistic children, (20 at each site), will be similarly studied to establish base rates of the proposed """"""""associated"""""""" abnormalities as they occur in families of children handicapped by a condition known to be genetically absent from the other family members. The major hypotheses of the study are that mental retardation, language delay, reading disability, and abnormalities of social relatedness, but not the major psychiatric disorders, will be more common among the family members of autistic probands than among the family members controls; that within the families of autistic children, these abnormalities will be less frequent among family members of autistic probands who suffered from environmental injuries (infectious or traumatic); that the abnormalities of reading ability, language delay and social relatedness will be more common among family members of autistic probands with higher IQa (""""""""pure autism""""""""), and that mental retardation, on the other hand, will be more common among family members of autistic probands with low IQs; and finally, that Fragile-X will explain some but not all of the familial loading in autism.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH039936-02
Application #
3377724
Study Section
(PCBA)
Project Start
1986-04-01
Project End
1989-03-31
Budget Start
1987-05-01
Budget End
1988-03-31
Support Year
2
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Mazefsky, Carla A; Folstein, Susan E; Lainhart, Janet E (2008) Overrepresentation of mood and anxiety disorders in adults with autism and their first-degree relatives: what does it mean? Autism Res 1:193-7
Folstein, S E; Santangelo, S L; Gilman, S E et al. (1999) Predictors of cognitive test patterns in autism families. J Child Psychol Psychiatry 40:1117-28
Lainhart, J E; Piven, J; Wzorek, M et al. (1997) Macrocephaly in children and adults with autism. J Am Acad Child Adolesc Psychiatry 36:282-90
Piven, J; Wzorek, M; Landa, R et al. (1994) Personality characteristics of the parents of autistic individuals. Psychol Med 24:783-95
Lainhart, J E; Folstein, S E (1994) Affective disorders in people with autism: a review of published cases. J Autism Dev Disord 24:587-601
Piven, J; Simon, J; Chase, G A et al. (1993) The etiology of autism: pre-, peri- and neonatal factors. J Am Acad Child Adolesc Psychiatry 32:1256-63
Landa, R; Piven, J; Wzorek, M M et al. (1992) Social language use in parents of autistic individuals. Psychol Med 22:245-54
Piven, J; Nehme, E; Simon, J et al. (1992) Magnetic resonance imaging in autism: measurement of the cerebellum, pons, and fourth ventricle. Biol Psychiatry 31:491-504
Folstein, S E; Piven, J (1991) Etiology of autism: genetic influences. Pediatrics 87:767-73
Landa, R; Folstein, S E; Isaacs, C (1991) Spontaneous narrative-discourse performance of parents of autistic individuals. J Speech Hear Res 34:1339-45

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