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A study on the polymorphism of IL-1Ra86bp,IL-1βexon5 gene and cognitive function in han chinese with TS

Published online by Cambridge University Press:  16 April 2020

H.F. Chang
Affiliation:
Changning Mental Health Center, Shanghai, China The Affiliated Hospital of Bio-X Center of Shanghai Jiaotong University, Shanghai, China
W.D. Ji
Affiliation:
Changning Mental Health Center, Shanghai, China
Y. Li
Affiliation:
Changning Mental Health Center, Shanghai, China
B.Y. Guo
Affiliation:
Jiading Mental Health Center, Shanghai, China
D.L. Yang
Affiliation:
Changning Mental Health Center, Shanghai, China

Abstract

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Background and aims:

Tourette's syndrome (TS) is a childhood-onset neuro- psychiatric disorder characterised by multiple motor and vocal tics lasting more than one year. An immune-mediated mechanism involving molecular mimicry has been proposed for PANDAS (Paediatric autoimmune neuropsychiatric disorders associated with streptococcal infection). PANDAS may offer a new way to explore the pathogens of GTS. IL-1Ra86bp,IL-1βexon5 gene Polymorphism and Cognitive Function are studied in 86 Children with Tourette's Syndrome.

Methods:

In the present study, we genotyped a large multiplex sample of GTS affected children for polymorphisms in IL-1Ra86bp,IL-1βexon5 genes. Associations were tested by the transmission disequilibrium test (TDT). 86 Han Chinese children with GTS were tested using a set of neuropsychological test(Stroop test, trail making test, verbal fluency test, modified Wisconsin Card sorting test) and compared with 51 healthy control group to understand the relationship between cognitive deficits and genetics.

Results:

No evidence for transmission disequilibrium was found for polymorphisms of IL-1 Ra86bp,IL-1 βexon5 gene in this GTS sample. The frequency of 410bp/240bp genotype and 240bp allele in combined ADHD were significantly different from GTS alone. Compared with normal children, The GTS group showed impairment on almost all psychological measures. No evidence show significantly difference among IL-1Ra86bp, IL-1βexon5 gene Polymorphism and Cognitive Function.

Conclusions:

For the GTS+ADHD group, the 240bp allele of IL-1Ra gene Polymorphism perhaps is another risk factor.GTS patient has memory, attention and executive function defect, these defects may have something to do with the prefrontal dopamine disfunction.

Type
Poster Session 2: Organic Mental Disorders and Memory and Cognitive Dysfunctions
Copyright
Copyright © European Psychiatric Association 2007
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