No Association Between a Common Single Nucleotide Polymorphism, rs4141463, in the MACROD2 Gene and Autism Spectrum Disorder

被引：27

作者：

Curran, Sarah ^{[1
]}

Bolton, Patrick ^{[1
,2
]}

Rozsnyai, Kinga ^{[2
]}

Chiocchetti, Andreas ^{[3
]}

Klauck, Sabine M. ^{[3
]}

Duketis, Eftichia ^{[4
]}

Poustka, Fritz ^{[4
]}

Schlitt, Sabine ^{[4
]}

Freitag, Christine M. ^{[5
]}

Lee, Irene ^{[6
]}

Muglia, Pierandrea ^{[7
]}

Poot, Martin ^{[8
]}

Staal, Wouter ^{[9
]}

de Jonge, Maretha V. ^{[9
]}

Ophoff, Roel A. ^{[10
]}

Lewis, Cathryn ^{[2
]}

Skuse, David ^{[6
]}

Mandy, Will ^{[11
]}

Vassos, Evangelos ^{[2
]}

Fossdal, Ragnheidur ^{[12
]}

Magnusson, Pall ^{[13
]}

Hreidarsson, Stefan ^{[14
]}

Saemundsen, Evald ^{[14
]}

Stefansson, Hreinn ^{[12
]}

Stefansson, Kari ^{[12
]}

Collier, David ^{[2
]}

机构：

[1] Kings Coll London, Dept Child & Adolescent Psychiat, Inst Psychiat, London WC2R 2LS, England

[2] Kings Coll London, Inst Psychiat, SGDP Res Ctr, London SE5 8AF, England

[3] German Canc Res Ctr, Div Mol Genome Anal, Heidelberg, Germany

[4] Goethe Univ Frankfurt, Dept Child & Adolescent Psychiat Psychosomat & Ps, Frankfurt, Germany

[5] Saarland Univ Hosp, Dept Child & Adolescent Psychiat, Saarbrucken, Germany

[6] UCL, Inst Child Hlth, Behav & Brain Sci Unit, London, England

[7] Univ Toronto, Toronto, ON M5S 1A1, Canada

[8] Univ Med Ctr Utrecht, Dept Med Genet, Utrecht, Netherlands

[9] UMC Utrecht, Dept Child & Adolescent Psychiat, Utrecht, Netherlands

[10] UMC Utrecht, Univ Calif Los Angeles, Utrecht, Netherlands

[11] UCL, Res Dept Clin Educ & Hlth Psychol, London, England

[12] deCode Genet, Reykjavik, Iceland

[13] Landspitali Univ Hosp, Reykjavik, Iceland

[14] State Diagnost & Counseling Ctr, Kopavogur, Iceland

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS | 2011年 / 156B卷 / 06期

基金：

英国医学研究理事会;

关键词：

autism; autism spectrum; genetic association; common genetic risk variants; MACROD2; GENOME-WIDE ASSOCIATION; PATERNAL-AGE; LINKAGE; VARIANTS; REVEALS; RISK; INDIVIDUALS; MUTATIONS; C20ORF133; CHILDREN;

D O I：

10.1002/ajmg.b.31201

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

The Autism Genome Project (AGP) Consortium recently reported genome-wide significant association between autism and an intronic single nucleotide polymorphism marker, rs4141463, within the MACROD2 gene. In the present study we attempted to replicate this finding using an independent case-control design of 1,170 cases with autism spectrum disorder (ASD) (874 of which fulfilled narrow criteria for Autism (A)) from five centers within Europe (UK, Germany, the Netherlands, Italy, and Iceland), and 35,307 controls. The combined sample size gave us a non-centrality parameter (NCP) of 11.9, with 93% power to detect allelic association of rs4141463 at an alpha of 0.05 with odds ratio of 0.84 (the best odds ratio estimate of the AGP Consortium data), and for the narrow diagnosis of autism, an NCP of 8.9 and power of 85%. Our case-control data were analyzed for association, stratified by each center, and the summary statistics were combined using the meta-analysis program, GWAMA. This resulted in an odds ratio (OR) of 1.03 (95% CI 0.944-1.133), with a P-value of 0.5 for ASD and OR of 0.99 (95% CI 0.88-1.11) with P-value = 0.85 for the Autism(A) sub-group. Therefore, this study does not provide support for the reported association between rs4141463 and autism. (C) 2011 Wiley-Liss, Inc.

引用

页码：633 / 639

页数：7

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