The 'Fractionable Autism Triad': A Review of Evidence from Behavioural, Genetic, Cognitive and Neural Research

被引:336
作者
Happe, Francesca [1 ]
Ronald, Angelica [2 ]
机构
[1] Kings Coll London, Inst Psychiat, MRC Social Genet & Dev Psychiat Ctr, London WC2R 2LS, England
[2] Birkbeck Coll, Ctr Brain & Cognit Dev, London, England
基金
英国医学研究理事会;
关键词
Autism; Autism spectrum disorders; Cognitive theories; Fractionation; Twin studies;
D O I
10.1007/s11065-008-9076-8
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Autism is diagnosed on the basis of a triad of impairments in social interaction, communication, and flexible imaginative functions (with restricted and repetitive behaviors and interests; RRBIs). There has been a strong presumption that these different features of the syndrome are strongly intertwined and proceed from a common cause at the genetic, cognitive and neural levels. In this review we examine evidence for an alternative approach, considering the triad as lamely 'fractionable'. We present evidence from Our own twin Studies, and review relevant literature on autism and autistic-like traits in other groups. We Suggest that largely independent genes may operate on social skills/impairments, communication abilities, and RRBIs, requiring a change in molecular-genetic research approaches. At the cognitive level, we suggest that satisfactory accounts exist for each of the triad domains, but no single unitary account can explain both social and nonsocial features of autism. We discuss the implications of the fractionable-triad approach for both diagnosis and future research directions.
引用
收藏
页码:287 / 304
页数:18
相关论文
共 150 条
[1]   The neuroanatomy of autism:: a voxel-based whole brain analysis of structural scans [J].
Abell, F ;
Krams, M ;
Ashburner, J ;
Passingham, R ;
Friston, KJ ;
Frackowiak, R ;
Happé, F ;
Frith, C ;
Frith, U .
NEUROREPORT, 1999, 10 (08) :1647-1651
[2]   Advances in autism genetics: on the threshold of a new neurobiology [J].
Abrahams, Brett S. ;
Geschwind, Daniel H. .
NATURE REVIEWS GENETICS, 2008, 9 (05) :341-355
[3]   Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families [J].
Alarcón, M ;
Cantor, RM ;
Liu, JJ ;
Gilliam, TC ;
Geschwind, DH .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (01) :60-71
[4]   Meeting of minds: the medial frontal cortex and social cognition [J].
Amodio, DM ;
Frith, CD .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (04) :268-277
[5]  
[Anonymous], 1984, NOT OUR GENES BIOL I
[6]   A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism [J].
Arking, Dan E. ;
Cutler, David J. ;
Brune, Camille W. ;
Teslovich, Tanya M. ;
West, Kristen ;
Ikeda, Morna ;
Rea, Alexis ;
Guy, Moltu ;
Lin, Shin ;
Cook, Edwin H., Jr. ;
Chakravarti, Aravinda .
AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (01) :160-164
[7]  
AUSTIN EJ, 2005, PERSONALITY IN PRESS
[8]   The Autism Spectrum Quotient: Children's Version (AQ-Child) [J].
Auyeung, Bonnie ;
Baron-Cohen, Simon ;
Wheelwright, Sally ;
Allison, Carrie .
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 2008, 38 (07) :1230-1240
[9]   AUTISM AS A STRONGLY GENETIC DISORDER - EVIDENCE FROM A BRITISH TWIN STUDY [J].
BAILEY, A ;
LECOUTEUR, A ;
GOTTESMAN, I ;
BOLTON, P ;
SIMONOFF, E ;
YUZDA, E ;
RUTTER, M .
PSYCHOLOGICAL MEDICINE, 1995, 25 (01) :63-77
[10]  
Baron-Cohen S. E., 2000, UNDERSTANDING OTHER