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MF.03 The Gilles de la Tourette Syndrome behavioural spectrum: a factor analysis of 639 patients

Identifieur interne : 000077 ( Main/Exploration ); précédent : 000076; suivant : 000078

MF.03 The Gilles de la Tourette Syndrome behavioural spectrum: a factor analysis of 639 patients

Auteurs : A E Cavanna ; H D Critchley ; M. Orth ; J S Stern ; M-B Young ; M M Robertson

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RBID : ISTEX:AA97E8A0A1E55B4E52A67F51E17C8471F521F9AC

Abstract

Aims Recent studies using quantitative methods, such as principal-component factor analysis, hierarchical cluster analysis and latent class analysis, have suggested that Gilles de la Tourette syndrome (GTS) should no longer be considered a unitary condition as in current classification systems. We set out to identify quantitative components of GTS symptomatology using a large, well characterised cohort of singleton individuals with GTS, in order to inform future genetic studies with more homogeneous phenotypes. Methods Principal-component factor analysis with oblique rotation was used to analyse symptom data from a sample of 639 patients recruited at two tertiary referral centres using identical schedules during the period 1980–2008. Results Three Factors were identified: (1) complex motor tics and echo-paliphenomena; (2) attention-deficit and hyperactivity symptoms plus aggressive behaviours; (3) complex vocal tics and coprophenomena. Obsessive compulsive behaviours loaded significantly on the first two Factors. The three Factors accounted for 48.5% of the total symptomatic variance. Conclusions GTS is a phenotypically heterogeneous condition encompassing tics, tic-related symptoms and associated behavioural problems. Our results, coupled with previous findings, identified a clinical continuum of complex involuntary movements, hyperactivity/impulsivity symptoms, and semantically relevant utterances and gestures. A better characterisation of the GTS phenotypes will help to identify susceptibility genes.

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DOI: 10.1136/jnnp-2011-300504.14


Affiliations:


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<div type="abstract">Aims Recent studies using quantitative methods, such as principal-component factor analysis, hierarchical cluster analysis and latent class analysis, have suggested that Gilles de la Tourette syndrome (GTS) should no longer be considered a unitary condition as in current classification systems. We set out to identify quantitative components of GTS symptomatology using a large, well characterised cohort of singleton individuals with GTS, in order to inform future genetic studies with more homogeneous phenotypes. Methods Principal-component factor analysis with oblique rotation was used to analyse symptom data from a sample of 639 patients recruited at two tertiary referral centres using identical schedules during the period 1980–2008. Results Three Factors were identified: (1) complex motor tics and echo-paliphenomena; (2) attention-deficit and hyperactivity symptoms plus aggressive behaviours; (3) complex vocal tics and coprophenomena. Obsessive compulsive behaviours loaded significantly on the first two Factors. The three Factors accounted for 48.5% of the total symptomatic variance. Conclusions GTS is a phenotypically heterogeneous condition encompassing tics, tic-related symptoms and associated behavioural problems. Our results, coupled with previous findings, identified a clinical continuum of complex involuntary movements, hyperactivity/impulsivity symptoms, and semantically relevant utterances and gestures. A better characterisation of the GTS phenotypes will help to identify susceptibility genes.</div>
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