Evidence for an association with the serotonin transporter promoter region polymorphism and autism

✍ Scribed by Yirmiya, Nurit ;Pilowsky, Tammy ;Nemanov, Lubov ;Arbelle, Shoshana ;Feinsilver, Temira ;Fried, Iris ;Ebstein, Richard P.

• Publisher: John Wiley and Sons
• Year: 2001
• Tongue: English
• Weight: 75 KB
• Volume: 105
• Category: Article
• ISSN: 0148-7299
• DOI: 10.1002/ajmg.1365

✦ Synopsis

We have examined three functional polymorphisms, serotonin transporter promoter region polymorphism (5-HTTLPR), dopamine D4 exon III repeat region (DRD4), and catechol-O-methyltransferase (COMT), in a small family-based design toward identifying candidate genes that confer risk for autism. A significant excess of the long/long 5-HTTLPR genotype was observed (likelihood ratio = 7.18; P = 0.027; 2 df; n = 33 families) as well as preferential transmission of the long allele of the 5-HTTLPR (TDT chi-square = 5.44; P<0.025; 1 df). No association was observed between the COMT and DRD4 polymorphisms and autism in this sample. Some previous studies have observed linkage between autism and the 5-HTTLPR polymorphism and the current results are similar to those first reported by Klauck et al. [1997: Hum Genet 100:224-229; 1997: Hum Mol Genet 6:2233-2238]. Additionally, elevated serotonin levels have been consistently found in 30%-50% of autistic patients and may represent a marker for familial autism. Hyperserotonemia in autism appears to be due to enhanced 5-HT uptake, as free 5-HT levels are normal and the current report of an excess of the long/long 5-HTTLPR genotype in autism could provide a partial molecular explanation for high platelet serotonin content in autism.