60
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Sexually dimorphic facial features vary according to level of autistic-like traits in the general population

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          In a recent study, Bejerot et al. observed that several physical features (including faces) of individuals with an autism spectrum disorder (ASD) were more androgynous than those of their typically developed counterparts, suggesting that ASD may be understood as a ‘gender defiant’ disorder. These findings are difficult to reconcile with the hypermasculinisation account, which proposes that ASD may be an exaggerated form of cognitive and biological masculinity. The current study extended these data by first identifying six facial features that best distinguished males and females from the general population and then examining these features in typically developing groups selected for high and low levels of autistic-like traits.

          Methods

          In study 1, three-dimensional (3D) facial images were collected from 208 young adult males and females recruited from the general population. Twenty-three facial distances were measured from these images and a gender classification and scoring algorithm was employed to identify a set of six facial features that most effectively distinguished male from female faces. In study 2, measurements of these six features were compared for groups of young adults selected for high ( n = 46) or low ( n = 66) levels of autistic-like traits.

          Results

          For each sex, four of the six sexually dimorphic facial distances significantly differentiated participants with high levels of autistic-like traits from those with low trait levels. All four features were less masculinised for high-trait males compared to low-trait males. Three of four features were less feminised for high-trait females compared to low-trait females. One feature was, however, not consistent with the general pattern of findings and was more feminised among females who reported more autistic-like traits. Based on the four significantly different facial distances for each sex, discriminant function analysis correctly classified 89.7% of the males and 88.9% of the females into their respective high- and low-trait groups.

          Conclusions

          The current data provide support for Bejerot et al.’s androgyny account since males and females with high levels of autistic-like traits generally showed less sex-typical facial features than individuals with low levels of autistic-like traits.

          Related collections

          Most cited references56

          • Record: found
          • Abstract: not found
          • Article: not found

          Die „Autistischen Psychopathen” im Kindesalter

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            2nd to 4th digit ratios, fetal testosterone and estradiol.

            The ratio of 2nd to 4th digit length (2D:4D) is sexually dimorphic (mean 2D:4D is lower in males than females) and is thought to be fixed early in development. 2D:4D has been reported to be related to fetal growth, hand preference, autism, Asperger's syndrome, sperm counts, family size, age at myocardial infarction in men and breast cancer in women. There is indirect evidence that 2D:4D is established in utero and is negatively related to prenatal testosterone and positively with prenatal estradiol. However, there are no studies which show direct relationships between fetal testosterone (FT), fetal estradiol (FE) and 2D:4D. To investigate the relationships between 2D:4D ratios and FT and FE from amniotic fluid. Cohort study. 33 children. Radioimmunoassays of FT and FE obtained from routine amniocentesis; 2D:4D ratios calculated from 2nd and 4th digit length of the right and left hands at age 2 years. A significant negative association between right 2D:4D ratio and FT/FE ratio, which was independent of sex. These preliminary findings lend support to an association between low 2D:4D and high levels of FT relative to FE, and high 2D:4D with low FT relative to FE.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Fetal testosterone and autistic traits.

              Studies of amniotic testosterone in humans suggest that fetal testosterone (fT) is related to specific (but not all) sexually dimorphic aspects of cognition and behaviour. It has also been suggested that autism may be an extreme manifestation of some male-typical traits, both in terms of cognition and neuroanatomy. In this paper, we examine the possibility of a link between autistic traits and fT levels measured in amniotic fluid during routine amniocentesis. Two instruments measuring number of autistic traits (the Childhood Autism Spectrum Test (CAST) and the Child Autism Spectrum Quotient (AQ-Child)) were completed by these women about their children (N=235), ages 6-10 years. Intelligence Quotient (IQ) was measured in a subset of these children (N=74). fT levels were positively associated with higher scores on the CAST and AQ-Child. This relationship was seen within sex as well as when the sexes were combined, suggesting this is an effect of fT rather than of sex per se. No relationships were found between overall IQ and the predictor variables, or between IQ and CAST or AQ-Child. These findings are consistent with the hypothesis that prenatal androgen exposure is related to children exhibiting more autistic traits. These results need to be followed up in a much larger sample to test if clinical cases of ASC have elevated fT.
                Bookmark

                Author and article information

                Contributors
                zulqarnain.gilani@uwa.edu.au
                diana.tan@research.uwa.edu.au
                suzanna.russell-smith@uwa.edu.au
                murray.maybery@uwa.edu.au
                ajmal.mian@uwa.edu.au
                peter.eastwood@health.wa.gov.au
                faisal.shafait@uwa.edu.au
                mithran.goonewardene@uwa.edu.au
                andrew.whitehouse@telethonkids.org.au
                Journal
                J Neurodev Disord
                J Neurodev Disord
                Journal of Neurodevelopmental Disorders
                BioMed Central (London )
                1866-1947
                1866-1955
                15 April 2015
                15 April 2015
                2015
                : 7
                : 1
                : 14
                Affiliations
                [ ]School of Computer Science and Software Engineering, University of Western Australia, 35 Stirling Highway, Crawley, 6009 Perth, WA Australia
                [ ]Neurocognitive Development Unit, School of Psychology, University of Western Australia, 35 Stirling Highway, Crawley, 6009 Perth, WA Australia
                [ ]School of Anatomy, Physiology and Human Biology, University of Western Australia, 35 Stirling Highway, Crawley, 6009 Perth, WA Australia
                [ ]School of Dentistry/Oral Health Centre of Western Australia, University of Western Australia, 35 Stirling Highway, Crawley, 6009 Perth, WA Australia
                [ ]Telethon Kids Institute, University of Western Australia, 100 Roberts Road, Subiaco, 6008 Perth, WA Australia
                Article
                9109
                10.1186/s11689-015-9109-6
                4404287
                25901187
                b450f159-38c3-41db-a088-036d47b483c7
                © Gilani et al.; licensee BioMed Central. 2015

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 18 August 2014
                : 2 April 2015
                Categories
                Research
                Custom metadata
                © The Author(s) 2015

                Neurosciences
                autism,autism spectrum disorder,hypermasculinisation,gender defiant disorder,facial features,masculinity,femininity,raine study

                Comments

                Comment on this article