Skip to main content

Advertisement

Log in

Quality of life in young people with Tourette syndrome: a controlled study

  • Original Communication
  • Published:
Journal of Neurology Aims and scope Submit manuscript

Abstract

Quality of life (QoL) may be adversely affected by Tourette syndrome (TS). Although the core symptoms of this complex neurodevelopmental disorder are tics, patients often present with an array of behavioural difficulties, such as co-morbid obsessive compulsive disorder (OCD) or attention deficit hyperactivity disorder (ADHD). In this study we investigated whether young people with TS exhibited poorer QoL in comparison to healthy individuals and an epilepsy control group. We also analysed whether greater tic severity or co-morbid OCD and\or ADHD led to greater differences in perceived QoL. The Youth Quality of Life Instrument-Research Version (Edwards et al. in J Adolesc 25:275–286, 2002) was used to assess QoL and a range of clinical scales were administered to assess anxiety, depression and other behavioural symptoms. TS was associated with significant differences in aspects of QoL related to home and social activities, involving peer and family interactions. Patients with more severe tics reported a greater negative impact on QoL. Patients with TS and no associated diagnoses (pure TS) presented with lower QoL scores in the environment domain, poorer perceived QoL in general, and depressive features. Co-morbid OCD appeared to exert a greater impact on self and relationship QoL domains. The presence of both OCD and ADHD as co-morbidities led to more widespread problems. In conclusion, TS can be associated with poorer perceived QoL. Although social aspects of QoL may be more vulnerable to TS in general, co-morbid conditions make an important contribution in determining which aspects of QoL are most affected in the individual.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. American Psychiatric Association (2000) Diagnostic and statistical manual of mental disorders (4th edn: text revision; DSM-IV-TR). American Psychiatric Association, Washington DC

    Book  Google Scholar 

  2. Robertson MM (2000) Tourette syndrome, associated conditions and the complexities of treatment. Brain 123:425–462

    Article  PubMed  Google Scholar 

  3. Cavanna AE, Servo S, Monaco F, Robertson MM (2009) The behavioral spectrum of Gilles de la Tourette syndrome. J Neuropsychiatry Clin Neurosci 21:13–23

    PubMed  Google Scholar 

  4. Erenberg G, Cruse RP, Rothner DA (1987) The natural history of Tourette’s syndrome: a follow-up study. Ann Neurol 22:383–385

    Article  CAS  PubMed  Google Scholar 

  5. Piacentini J, Bergman RL, Keller M, McCracken JT (2003) Functional impairment in children and adolescents with obsessive-compulsive disorder. J Child Adolesc Psychopharm 13(Suppl.1):S61–S69

    Article  Google Scholar 

  6. Storch EA, Merlo LJ, Lack C, Milsom VA, Geffken GR, Goodman WK, Murphy TK (2007) Quality of life in youth with Tourette’s syndrome and chronic tic disorder. J Clin Child Adolesc Psychol 36:217–227

    Article  PubMed  Google Scholar 

  7. Cutler D, Murphy T, Gilmour J, Heyman I (2009) The quality of life of young people with Tourette syndrome. Child 35:496–504

    CAS  Google Scholar 

  8. Elstner K, Selai CE, Trimble MR, Robertson MM (2001) Quality of life (QoL) of patients with Gilles de la Tourette syndrome. Acta Psychiatrica Scand 103:52–59

    Article  CAS  Google Scholar 

  9. Packer LE (2005) Tic-related school problems: impact of functioning, accommodations and interventions. Behav Mod 29:876–899

    Article  Google Scholar 

  10. Champion LM, Fulton WA, Shady GA (1988) Tourette syndrome and social functioning in a Canadian population. Neurosci Biobehav Rev 12:255–257

    Article  CAS  PubMed  Google Scholar 

  11. Bernard BA, Stebbins GT, Siegel S, Schultz TM, Hays C, Morrissey MJ, Leurgans S, Goetz CG (2009) Determinants of Quality of Life in Children with Tourette syndrome. Mov Disord 24:1070–1073

    Article  PubMed  Google Scholar 

  12. Edwards TC, Hueber CE, Connell FA, Patrick DL (2002) Adolescent quality of life, part I: conceptual and measurement model. J Adolesc 25:275–286

    Article  PubMed  Google Scholar 

  13. Patrick DL, Edwards TC, Topolski T (2002) Adolescent quality of life part II: initial validation of a new instrument. J Adolesc 25:287–300

    Article  PubMed  Google Scholar 

  14. Robertson MM, Eapen V (1996) The National Hospital Interview Schedule for the assessment of Gilles de la Tourette syndrome and related behaviours. Int J Methods Psychiatry Res 6:203–226

    Article  Google Scholar 

  15. March JS, Parker JDA, Sullivan K, Stallings P, Conners CK (1997) The Multidimensional Anxiety Scales for Children (MASC): Factor structure, reliability and validity. J Am Acad Child Adolesc Psychiatry 36:544–552

    Google Scholar 

  16. Kovacs M (1992) Children’s Depression Inventory (CDI). Multihealth Systems, Inc., New York

    Google Scholar 

  17. Scahill L, Riddle MA, McSwiggin-Harden M, Ort SI, King RA, Goodman WK, Cicchetti D, Leckman JF (1997) Children’s Yale-Brown Obsessive Compulsive Scale: reliability and validity. J Am Acad Child Adolesc Psychiatry 36:844–852

    Article  CAS  PubMed  Google Scholar 

  18. Conners CK (1973) Rating scales for use in drug studies with children. Psychopharmacology Bulletin: Pharmacotherapy with children. Government Printing Office, Washington, DC

    Google Scholar 

  19. Achenbach T, Edelbrock C (1983) Manual for the child behavior checklist and revised child behavior profile. University of Vermont Department of Psychiatry, Burlington

    Google Scholar 

  20. Leckman JF, Riddle MA, Hardin MT, Ort SI, Swartz KL, Stevenson J, Cohen D (1989) The Yale Global Tic Severity Scale: initial testing of a clinician rated scale of tic severity. J Am Acad Child Adolesc Psychiatry 28:566–577

    Article  CAS  PubMed  Google Scholar 

  21. Stokes A, Bawden HN, Bachman JE, Booley JM, Campfield PR (1991) Peer problems in Tourette’s disorder. Pediatrics 87:936–942

    CAS  PubMed  Google Scholar 

  22. Cavanna AE, Schrag A, Morley D, Orth M, Robertson MM, Joyce E, Critchley HD, Selai C (2008) The Gilles de la Tourette syndrome-quality of life scale (GTS-QOL): development and validation. Neurology 71:1410–1416

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

The authors are grateful to Dr Tari Topolski for the useful discussions. MMR and AEC are funded by Tourettes Action-UK.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to A. E. Cavanna.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Eddy, C.M., Rizzo, R., Gulisano, M. et al. Quality of life in young people with Tourette syndrome: a controlled study. J Neurol 258, 291–301 (2011). https://doi.org/10.1007/s00415-010-5754-6

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00415-010-5754-6

Keywords

Navigation