Hereditary factors play a significant role in the etiology of autism. In addition to autism, abnormalities which are milder, but qualitatively similar to behaviors which define autism (i.e, particular personality, language and cognitive characteristics, and psychiatric disorders), have been shown to aggregate in relatives of autistic individuals. Clarification of the boundaries of phenotypic expression of the underlying genetic liability to autism is a critical preliminary step to further genetic analyses of this disorder. In addition, the finding that social deficits in the relatives of autistic probands, evident in measures of both personality and language, may be biologically-based and etiologically-related to particular cognitive disabilities and psychiatric disorders, is of importance beyond the significance these findings have for understanding the etiology of autism. This is an application for a Scientist Development Award for Clinicians. During the award period, the candidate proposes an organized program of training and supervised research. Training will focus on learning to assess and measure behaviors (i.e., language, personality and cognitive) hypothesized to define a """"""""lesser variant"""""""" in autism and to develop a critical fund of knowledge in quantitative, medical and molecular genetics for examining the role of genetic factors in complex childhood neuropsychiatric disorders.
The specific aims of the research portion of this award include: 1) estimation of the frequency of disorders that may be genetically associated with autism in first-degree relatives of autistic and Down syndrome probands and 2) definition of the characteristics of a """"""""lesser variant"""""""" in autism for use in future genetic studies of this disorder by investigating the pattern of disorders among first-degree autism relatives. A variety of behavioral measures will be used to assess the first-degree relatives of autistic probands from multiple-incidence autism families and Down syndrome probands, in a case/control family study.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Unknown (K20)
Project #
1K20MH001028-01
Application #
3088956
Study Section
Child Psychopathology and Treatment Review Committee (CPT)
Project Start
1992-09-01
Project End
1997-08-31
Budget Start
1992-09-01
Budget End
1993-08-31
Support Year
1
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of Iowa
Department
Type
Schools of Medicine
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Piven, J; Palmer, P (1999) Psychiatric disorder and the broad autism phenotype: evidence from a family study of multiple-incidence autism families. Am J Psychiatry 156:557-63
Baker, P; Piven, J; Sato, Y (1998) Autism and tuberous sclerosis complex: prevalence and clinical features. J Autism Dev Disord 28:279-85
Piven, J; Bailey, J; Ranson, B J et al. (1998) No difference in hippocampus volume detected on magnetic resonance imaging in autistic individuals. J Autism Dev Disord 28:105-10
Piven, J; Palmer, P; Jacobi, D et al. (1997) Broader autism phenotype: evidence from a family history study of multiple-incidence autism families. Am J Psychiatry 154:185-90
Piven, J; Saliba, K; Bailey, J et al. (1997) An MRI study of autism: the cerebellum revisited. Neurology 49:546-51
Piven, J; Bailey, J; Ranson, B J et al. (1997) An MRI study of the corpus callosum in autism. Am J Psychiatry 154:1051-6
Piven, J (1997) The biological basis of autism. Curr Opin Neurobiol 7:708-12
Piven, J; Palmer, P (1997) Cognitive deficits in parents from multiple-incidence autism families. J Child Psychol Psychiatry 38:1011-21
Piven, J; Harper, J; Palmer, P et al. (1996) Course of behavioral change in autism: a retrospective study of high-IQ adolescents and adults. J Am Acad Child Adolesc Psychiatry 35:523-9
Piven, J; Arndt, S; Bailey, J et al. (1996) Regional brain enlargement in autism: a magnetic resonance imaging study. J Am Acad Child Adolesc Psychiatry 35:530-6

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