Department of Mental Health Sciences, University College London, London, UK
Department of Psychiatry, University of Vermont College of Medicine, Burlington, Vermont, Canada
Kings College London, London, UK
Psychiatric and Neurodevelopmental Genetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA
Correspondence: David Pauls, Psychiatric and Neurodevelopmental Genetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, Harvard Medical School, 185 Cambridge Street, Boston, MA 02114 USA. Email: dpauls{at}pngu.mgh.harvard.edu
None. Funding detailed in Acknowledgements.
Background
Tourette syndrome is a heterogeneous familial disorder for which the genetic mechanisms are unknown. A better characterisation of the phenotype may help identify susceptibility genes.
Aims
To extend previous factor-analytic studies of the syndrome.
Method
Symptom data from 410 people with Tourette syndrome were included in agglomerative hierarchical cluster and principal components analyses.
Results
Five factors were observed, characterised by: (1) socially inappropriate behaviours and other complex vocal tics; (2) complex motor tics; (3) simple tics; (4) compulsive behaviours; and (5) touching self. Individuals with co-occurring attention-deficit hyperactivity disorder had significantly higher factor scores on Factors 1 and 3, whereas individuals with co-occurring obsessive–compulsive disorder and behaviours had significantly higher factor scores for Factors 1–4.
Conclusions
These findings add to the growing body of evidence that Tourette syndrome is not a unitary condition and can be disaggregated into more homogeneous symptom components.
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