Serotonin transporter promoter variants: Analysis in Indian autistic and control population

被引:33
作者
Guhathakurta, Subhrangshu
Ghosh, Sagarmoy
Sinha, Swagata
Chatterjee, Anindita
Ahmed, Shabina
Chowdhury, Susanta Roy
Gangopadhyay, Prasanta Kumar
Ghosh, Saurabh
Singh, Manoranjan
Usha, Rajamma
机构
[1] Manovikas Biomed Res & Diagnost Ctr, Kolkata 700107, W Bengal, India
[2] Univ Calcutta, Coll Sci & Technol, Dept Microbiol, Kolkata 700019, W Bengal, India
[3] Manovikas Kendra Rehabil & Res Inst Handicapped, Kolkata 700107, W Bengal, India
[4] Assam Autism Fdn, Gauhati 781005, India
[5] Indian Inst Chem Biol, Div Human Genet & Genom, Kolkata 700032, W Bengal, India
[6] Bangus Inst Neurol, Dept Neuromed, Kolkata 700025, W Bengal, India
[7] Indian Stat Inst, Human Genet Unit, Kolkata 700108, W Bengal, India
关键词
serotonin transporter; S-HTTLPR; Indian population; autism; genetic association; meta-analysis;
D O I
10.1016/j.brainres.2006.03.078
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Serotonin transporter (5-HTT) is a transmembrane protein belonging to Na+/Cl- dependent membrane transporter family and transports S-HT across the membranes of presynaptic neurons. 5-HTT-linked polymorphic region (S-HTTLPR) gained much interest because of the differential regulation of expression and activity of 5-HTT by its various genotypes. A population-based study has been conducted on 5-HTTLPR with 358 individuals, which included 79 autistic probands, 136 parents, and 143 controls from two subpopulations of east and northeast regions of India. The genotypic frequencies of all the groups conform to Hardy-Weinberg equilibrium. With the finding of efficacy of serotonin reuptake inhibitors in ameliorating ritualistic behavior in autistic disorder, 5-HTT emerged as a putative candidate gene for autism and association studies have been carried out in different ethnic populations. But these studies were inconclusive due to conflicting results on association. Because such a study has never been performed in the Indian population, we have tested the possible involvement of 5-HTTLPR polymorphism with autism. The present study failed to establish any association or linkage of 5-HTTLPR with autism in the Indian population by case-control studies (chi(2) = 1.314, P = 0.63) and family-based approaches (TDT chi(2) = 0.22, P = 0.64 and HHRR-chi(2) = 0.25, P = 0.61). However, when a meta-analysis of all the available TDT data, inclusive of the present study is carried out, we observed a significant preferential transmission of S-allele from parents to the affected offspring (chi(2) = 7.51, P = 0.006) indicating an association of 5-HTTLPR with autism. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:28 / 35
页数:8
相关论文
共 46 条
[1]  
Amara S G, 1991, Curr Opin Neurobiol, V1, P84, DOI 10.1016/0959-4388(91)90014-X
[2]   DETERMINATION OF SEROTONIN IN WHOLE-BLOOD, PLATELET-RICH PLASMA, PLATELET-POOR PLASMA AND PLASMA ULTRAFILTRATE [J].
ANDERSON, GM ;
FEIBEL, FC ;
COHEN, DJ .
LIFE SCIENCES, 1987, 40 (11) :1063-1070
[3]   Presence of multiple functional polyadenylation signals and a single nucleotide polymorphism in the 3′ untranslated region of the human serotonin transporter gene [J].
Battersby, S ;
Ogilvie, AD ;
Blackwood, DHR ;
Shen, SB ;
Muqit, MMK ;
Muir, WJ ;
Teague, P ;
Goodwin, GM ;
Harmar, AJ .
JOURNAL OF NEUROCHEMISTRY, 1999, 72 (04) :1384-1388
[4]   Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder [J].
Betancur, C ;
Corbex, M ;
Spielewoy, C ;
Philippe, A ;
Laplanche, JL ;
Launay, JM ;
Gillberg, C ;
Mouren-Siméoni, MC ;
Hamon, M ;
Giros, B ;
Nosten-Bertrand, M ;
Leboyer, M .
MOLECULAR PSYCHIATRY, 2002, 7 (01) :67-71
[5]   Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population [J].
Conroy, J ;
Meally, E ;
Kearney, G ;
Fitzgerald, M ;
Gill, M ;
Gallagher, L .
MOLECULAR PSYCHIATRY, 2004, 9 (06) :587-593
[6]  
Cook EH, 1997, MOL PSYCHIATR, V2, P247
[7]   FREE SEROTONIN IN PLASMA - AUTISTIC-CHILDREN AND THEIR 1ST-DEGREE RELATIVES [J].
COOK, EH ;
LEVENTHAL, BL ;
FREEDMAN, DX .
BIOLOGICAL PSYCHIATRY, 1988, 24 (04) :488-491
[8]   Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism [J].
Coutinho, AM ;
Oliveira, G ;
Morgadinho, T ;
Fesel, C ;
Macedo, TR ;
Bento, C ;
Marques, C ;
Ataíde, A ;
Miguel, T ;
Borges, L ;
Vicente, AM .
MOLECULAR PSYCHIATRY, 2004, 9 (03) :264-271
[9]  
de Oliveira JRM, 1998, AM J MED GENET, V81, P225, DOI 10.1002/(SICI)1096-8628(19980508)81:3<225::AID-AJMG4>3.0.CO
[10]  
2-V