Essential versus complex autism: definition of fundamental prognostic subtypes - PubMed (original) (raw)
. 2005 Jun 1;135(2):171-80.
doi: 10.1002/ajmg.a.30590.
Affiliations
- PMID: 15887228
- DOI: 10.1002/ajmg.a.30590
Essential versus complex autism: definition of fundamental prognostic subtypes
J H Miles et al. Am J Med Genet A. 2005.
Abstract
Heterogeneity within the autism diagnosis obscures the genetic basis of the disorder and impedes our ability to develop effective treatments. We found that by using two readily available tests, autism can be divided into two subgroups, "essential autism" and "complex autism," with different outcomes and recurrence risks. Complex autism consists of individuals in whom there is evidence of some abnormality of early morphogenesis, manifested by either significant dysmorphology or microcephaly. The remainder have "essential autism." From 1995 to 2001, 260 individuals who met DSM-IV criteria for autistic disorder were examined. Five percent (13/260) were microcephalic and 16% (41/260) had significant physical anomalies. Individually, each trait predicted a poorer outcome. Together they define the "complex autism" subgroup, comprising 20% (46/233) of the total autism population. Individuals with complex autism have lower IQs (P=0.006), more seizures (P=0.0008), more abnormal EEGs (46% vs. 30%), more brain abnormalities by MRI (28% vs. 13%). Everyone with an identifiable syndrome was in the complex group. Essential autism defines the more heritable group with higher sib recurrence (4% vs. 0%), more relatives with autism (20% vs. 9%), and higher male to female ratio (6.5:1 vs. 3.2:1). Their outcome was better with higher IQs (P=0.02) and fewer seizures (P=0.0008). They were more apt to develop autism with a regressive onset (43% vs. 23%, P=0.02). Analysis of the features predictive of poor outcome (IQ<55, functionally non-verbal) showed that microcephaly was 100% specific but only 14% sensitive; the presence of physical anomalies was 86% specific and 34% sensitive. The two tests combined yielded 87% specificity, 47% sensitivity, and an odds ratio of 4.8:1 for poor outcome. Separating essential from complex autism should be the first diagnostic step for children with autism spectrum disorders as it allows better prognostication and counseling. Definition of more homogeneous populations should increase power of research analyses.
Copyright (c) 2005 Wiley-Liss, Inc.
Similar articles
- Modeling clinical outcome of children with autistic spectrum disorders.
Coplan J, Jawad AF. Coplan J, et al. Pediatrics. 2005 Jul;116(1):117-22. doi: 10.1542/peds.2004-1118. Pediatrics. 2005. PMID: 15995041 - Value of a clinical morphology examination in autism.
Miles JH, Hillman RE. Miles JH, et al. Am J Med Genet. 2000 Apr 10;91(4):245-53. Am J Med Genet. 2000. PMID: 10766977 - Head circumference is an independent clinical finding associated with autism.
Miles JH, Hadden LL, Takahashi TN, Hillman RE. Miles JH, et al. Am J Med Genet. 2000 Dec 11;95(4):339-50. Am J Med Genet. 2000. PMID: 11186888 - The genetics of autism.
Muhle R, Trentacoste SV, Rapin I. Muhle R, et al. Pediatrics. 2004 May;113(5):e472-86. doi: 10.1542/peds.113.5.e472. Pediatrics. 2004. PMID: 15121991 Review. - Autistic children: diagnosis and clinical features.
Rapin I. Rapin I. Pediatrics. 1991 May;87(5 Pt 2):751-60. Pediatrics. 1991. PMID: 1708491 Review.
Cited by
- Neuroimaging of autism.
Verhoeven JS, De Cock P, Lagae L, Sunaert S. Verhoeven JS, et al. Neuroradiology. 2010 Jan;52(1):3-14. doi: 10.1007/s00234-009-0583-y. Epub 2009 Dec 24. Neuroradiology. 2010. PMID: 20033797 Review. - Syndromic autism spectrum disorders: moving from a clinically defined to a molecularly defined approach.
Fernandez BA, Scherer SW. Fernandez BA, et al. Dialogues Clin Neurosci. 2017 Dec;19(4):353-371. doi: 10.31887/DCNS.2017.19.4/sscherer. Dialogues Clin Neurosci. 2017. PMID: 29398931 Free PMC article. Review. - Comorbidity clusters in autism spectrum disorders: an electronic health record time-series analysis.
Doshi-Velez F, Ge Y, Kohane I. Doshi-Velez F, et al. Pediatrics. 2014 Jan;133(1):e54-63. doi: 10.1542/peds.2013-0819. Epub 2013 Dec 9. Pediatrics. 2014. PMID: 24323995 Free PMC article. - Immune regulation of neurodevelopment at the mother-foetus interface: the case of autism.
Sotgiu S, Manca S, Gagliano A, Minutolo A, Melis MC, Pisuttu G, Scoppola C, Bolognesi E, Clerici M, Guerini FR, Carta A. Sotgiu S, et al. Clin Transl Immunology. 2020 Nov 13;9(11):e1211. doi: 10.1002/cti2.1211. eCollection 2020. Clin Transl Immunology. 2020. PMID: 33209302 Free PMC article. Review. - Anhedonia and Hyperhedonia in Autism and Related Neurodevelopmental Disorders.
Dichter GS, Rodriguez-Romaguera J. Dichter GS, et al. Curr Top Behav Neurosci. 2022;58:237-254. doi: 10.1007/7854_2022_312. Curr Top Behav Neurosci. 2022. PMID: 35397066
MeSH terms
LinkOut - more resources
Full Text Sources
Miscellaneous