You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


Advertisement

ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | RSS | Access Rights | Sign In


  Vol. 163 No. 10, October 2009 TABLE OF CONTENTS
  Online Only
 •  Online First Table of
Contents
  Article
 •Online Features
 This Article
 •Full text
 •PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Citing articles on Web of Science (25)
 •Contact me when this article is cited
 Related Content
 •Related article
 •Similar articles in this journal
 Topic Collections
 •Pediatrics
 •Child Development
 •Psychiatry
 •Autism
 •Child Psychiatry
 •Genetics
 •Genetic Disorders
 •Alert me on articles by topic
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Delicious Add to Digg Add to Facebook Add to Reddit Add to Technorati Add to Twitter What's this?

Characteristics and Concordance of Autism Spectrum Disorders Among 277 Twin Pairs

Rebecca E. Rosenberg, MD, MPH; J. Kiely Law, MD, MPH; Gayane Yenokyan, MS; John McGready, PhD; Walter E. Kaufmann, MD; Paul A. Law, MD, MPH

Arch Pediatr Adolesc Med. 2009;163(10):907-914. doi:10.1001/archpediatrics.2009.98

Objectives  To examine patterns of autism spectrum disorder (ASD) inheritance and other features in twin pairs by zygosity, sex, and specific ASD diagnosis.

Design  Cross-sectional study.

Setting  Internet-based autism registry for US residents.

Participants  Survey results from 277 twin pairs (210 dizygotic [DZ] and 67 monozygotic [MZ]) aged 18 years or younger with at least 1 affected twin.

Main Exposures  Zygosity and sex.

Outcome Measures  Concordance within twin pairs of diagnosis, natural history, and results from standardized autism screening.

Results  Pairwise ASD concordance was 31% for DZ and 88% for MZ twins. Female and male MZ twins were 100% and 86% concordant, respectively, and DZ twin pairs with at least 1 female were less likely to be concordant (20%) than were male-male DZ twin pairs (40%). The hazard ratio for ASD diagnosis of the second twin after a first-twin diagnosis was 7.48 for MZ vs DZ twins (95% confidence interval, 3.8-14.7). Affected DZ individual twins had an earlier age at first parental concern and more frequent diagnoses of intellectual disability than did MZ twins; MZ twins had a higher prevalence of bipolar disorder and Asperger syndrome and higher concordance of the latter. Results of autism screening correlated with parent-reported ASD status in more than 90% of cases.

Conclusions  Our data support greater ASD concordance in MZ vs DZ twins. Overall higher functioning, psychiatric comorbidity, and Asperger syndrome concordance among affected MZ vs DZ twins may also suggest differential heritability for different ASDs. For families in which one MZ twin is diagnosed with ASD, the second twin is unlikely to receive an ASD diagnosis after 12 months. In addition, Internet parent report of ASD status is valid.


Author Affiliations: Department of Medical Informatics (Drs Rosenberg, J. K. Law, and P. A. Law) and Center for Genetic Disorders of Cognition and Behavior, Kennedy Krieger Institute (Dr Kaufmann), The Johns Hopkins Medical Institutions; Departments of Pediatrics (Drs J. K. Law and P. A. Law) and Psychiatry, Neurology, Pathology, and Radiology (Dr Kaufmann), The Johns Hopkins University School of Medicine; and Department of Biostatistics, Bloomberg School of Public Health, The Johns Hopkins University (Ms Yenokyan and Dr McGready), Baltimore, Maryland.



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Delicious Delicious   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?

RELATED ARTICLE

This Month in Archives of Pediatrics & Adolescent Medicine
Arch Pediatr Adolesc Med. 2009;163(10):878.
FULL TEXT  


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Is Autism, at Least in Part, a Disorder of Fetal Programming?
Szatmari
Arch Gen Psychiatry 2011;68:1091-1092.
FULL TEXT  

Gain-of-function glutamate receptor interacting protein 1 variants alter GluA2 recycling and surface distribution in patients with autism
Mejias et al.
Proc. Natl. Acad. Sci. USA 2011;108:4920-4925.
ABSTRACT | FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | PHYSICIAN JOBS | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2009 American Medical Association. All Rights Reserved.