SNP analyses of growth factor genes EGF, TGFβ-1, and HGF reveal haplotypic association of EGF with autism

• DOI: 10.1016/j.bbrc.2007.06.051
• Publication Date: 2007-06-19T11:09:18Z
• Authors: Takao Toyoda; Kazuhiko Nakamura; Kazuo Yamada; Ismail Thanseem; Ayyappan Anitha; Shiro Suda; Masatsugu Tsujii; Yoshimi Iwayama; Eiji Hattori; Tomoko Toyota; Taishi Miyachi; Yasuhide Iwata; Katsuaki Suzuki; Hideo Matsuzaki; Masayoshi Kawai; Yoshimoto Sekine; Kenji Tsuchiya; Gen-ichi Sugihara; Yasuomi Ouchi; Toshiro Sugiyama; Nori Takei; Takeo Yoshikawa; Norio Mori
• Keywords: Genetic Association

Autism is a pervasive neurodevelopmental disorder diagnosed in early childhood. Growth factors have been found to play a key role in the cellular differentiation and proliferation of the central and peripheral nervous systems. Epidermal growth factor (EGF) is detected in several regions of the developing and adult brain, where, it enhances the differentiation, maturation, and survival of a variety of neurons. Transforming growth factor-beta (TGFbeta) isoforms play an important role in neuronal survival, and the hepatocyte growth factor (HGF) has been shown to exhibit neurotrophic activity. We examined the association of EGF, TGFbeta1, and HGF genes with autism, in a trio association study, using DNA samples from families recruited to the Autism Genetic Resource Exchange; 252 trios with a male offspring scored for autism were selected for the study. Transmission disequilibrium test revealed significant haplotypic association of EGF with autism. No significant SNP or haplotypic associations were observed for TGFbeta1 or HGF. Given the role of EGF in brain and neuronal development, we suggest a possible role of EGF in the pathogenesis of autism.