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04-12-2019 | Original Paper | Uitgave 3/2020 Open Access

The Profiles and Correlates of Psychopathology in Adolescents and Adults with Williams, Fragile X and Prader–Willi Syndromes

Tijdschrift:: Journal of Autism and Developmental Disorders > Uitgave 3/2020

Auteurs:: R. Royston, C. Oliver, P. Howlin, A. Dosse, P. Armitage, J. Moss, J. Waite

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The online version of this article (https://doi.org/10.1007/s10803-019-04317-1) contains supplementary material, which is available to authorized users.

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Abstract

Psychopathology is prevalent in Williams (WS), fragile X (FXS) and Prader–Willi (PWS) syndromes. However, little is known about the potential correlates of psychopathology in these groups. A questionnaire study was completed by 111 caregivers of individuals with WS (n = 35); FXS (n = 50) and PWS (n = 26). Mean age was 26 years (range 12–57 years); 74 (67%) were male. Multiple regression analyses indicated that higher rates of health problems and sensory impairments predicted higher psychopathology in WS (p < .0001). In PWS, poorer adaptive ability predicted higher overall psychiatric disturbance (p = .001), generalised anxiety (p = .006) and hyperactivity (p = .003). There were no significant predictors in FXS. This study highlights dissociations in the potential risk markers of psychopathology between genetic syndromes. Implications for intervention are discussed.

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American Psychiatric Association. (2013). Diagnostic and statistical manual of mental disorders (5th ed.). Arlington, VA: American Psychiatric Publishing.

Austin, P. C., & Steyerberg, E. W. (2015). The number of subjects per variable required in linear regression analyses. Journal of Clinical Epidemiology, 68(6), 627–636. PubMed

Baranek, G. T., David, F. J., Poe, M. D., Stone, W. L., & Watson, L. R. (2006). Sensory experiences questionnaire: Discriminating sensory features in young children with autism, developmental delays, and typical development. Journal of Child Psychology and Psychiatry, 47(6), 591–601. PubMed

Bartholomay, K. L., Lee, C. H., Bruno, J. L., Lightbody, A. A., & Reiss, A. L. (2019). Closing the gender gap in fragile X syndrome: Review on females with FXS and preliminary research findings. Brain Sciences, 9(1), 11. PubMedCentral

Butler, M. G., Bittel, D. C., Kibiryeva, N., Talebizadeh, Z., & Thompson, T. (2004). Behavioral differences among subjects with Prader–Willi syndrome and type I or type II deletion and maternal disomy. Pediatrics, 113(3), 565–573. PubMedPubMedCentral

Cassidy, S. B., & Driscoll, D. J. (2009). Prader–Willi syndrome. European Journal of Human Genetics, 17(1), 3. PubMed

Cassidy, S. B., Schwartz, S., Miller, J. L., & Driscoll, D. J. (2011). Prader–Willi syndrome. Genetics in Medicine, 14(1), 10–26. PubMed

Cassidy, S. B., Schwartz, S., Miller, J. L., & Driscoll, D. J. (2012). Prader–Willi syndrome. Genetics in Medicine, 14(1), 10. PubMed

Clark, L. A., Watson, D., & Reynolds, S. (1995). Diagnosis and classification of psychopathology: Challenges to the current system and future directions. Annual Review of Psychology, 46(1), 121–153. PubMed

Coffee, B., Keith, K., Albizua, I., Malone, T., Mowrey, J., Sherman, S. L., et al. (2009). Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA. The American Journal of Human Genetics, 85(4), 503–514. PubMed

Cohen, J. (1988). Statistical power analysis for the behavioral sciences (2nd ed.). Hillsdale: Lawrence Erlbaum.

Cordeiro, L., Ballinger, E., Hagerman, R., & Hessl, D. (2011). Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: Prevalence and characterization. Journal of Neurodevelopmental Disorders, 3(1), 57. PubMed

Crawford, H., Waite, J., & Oliver, C. (2017). Diverse profiles of anxiety related disorders in fragile X, Cornelia de Lange and Rubinstein-Taybi syndromes. Journal of Autism and Developmental Disorders, 47(12), 3728–3740. PubMedPubMedCentral

Dodd, H. F., & Porter, M. A. (2009). Psychopathology in Williams syndrome: The effect of individual differences across the life span. Journal of Mental Health Research in Intellectual Disabilities, 2(2), 89–109.

Dunn, O. J. (1964). Multiple comparisons using rank sums. Technometrics, 6(3), 241–252.

Dykens, E. M. (2004). Maladaptive and compulsive behavior in Prader–Willi syndrome: New insights from older adults. American Journal on Mental Retardation, 109(2), 142–153. PubMed

Dykens, E. M., & Cassidy, S. B. (1995). Correlates of maladaptive behavior in children and adults with Prader–Willi syndrome. American Journal of Medical Genetics Part A, 60(6), 546–549.

Dykens, E. M., & Kasari, C. (1997). Maladaptive behavior in children with Prader–Willi syndrome, Down syndrome, and nonspecific mental retardation. American Journal on Mental Retardation, 102(3), 228–237. PubMed

Dykens, E., & Shah, B. (2003). Psychiatric disorders in Prader–Willi syndrome. CNS Drugs, 17(3), 167–178. PubMed

Einfeld, S. L., Smith, A., Durvasula, S., Florio, T., & Tonge, B. J. (1999). Behavior and emotional disturbance in Prader–Willi syndrome. American Journal of Medical Genetics, 82(2), 123–127. PubMed

Einfeld, S. L., & Tonge, B. J. (1995). The developmental behavior checklist: The development and validation of an instrument to assess behavioral and emotional disturbance in children and adolescents with mental retardation. Journal of Autism and Developmental Disorders, 25(2), 81–104. PubMed

Einfeld, S. L., Tonge, B. J., & Florio, T. (1997). Behavioral and emotional disturbance in individuals with Williams syndrome. American Journal on Mental Retardation, 102(1), 45–53. PubMed

Esbensen, A. J., Rojahn, J., Aman, M. G., & Ruedrich, S. (2003). Reliability and validity of an assessment instrument for anxiety, depression, and mood among individuals with mental retardation. Journal of Autism and Developmental Disorders, 33(6), 617–629. PubMed

Ethridge, L. E., White, S. P., Mosconi, M. W., Wang, J., Byerly, M. J., & Sweeney, J. A. (2016). Reduced habituation of auditory evoked potentials indicate cortical hyper-excitability in fragile X syndrome. Translational Psychiatry, 6(4), e787. PubMedPubMedCentral

Ewart, A. K., Morris, C. A., Atkinson, D., Jin, W., Sternes, K., Spallone, P., et al. (1993). Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome. Nature Genetics, 5(1), 11. PubMed

Field, A. (2013). Discovering statistics using IBM SPSS statistics. Los Angeles: Sage.

Garber, K. B., Visootsak, J., & Warren, S. T. (2008). Fragile X syndrome. European Journal of Human Genetics, 16(6), 666–672. PubMed

Hall, S. S., Arron, K., Sloneem, J., & Oliver, C. (2008). Health and sleep problems in Cornelia de Lange syndrome: A case control study. Journal of Intellectual Disability Research, 52(5), 458–468. PubMed

Hatton, D. D., Hooper, S. R., Bailey, D. B., Skinner, M. L., Sullivan, K. M., & Wheeler, A. (2002). Problem behavior in boys with fragile X syndrome. American Journal of Medical Genetics, 108(2), 105–116. PubMed

Hessl, D., Dyer-Friedman, J., Glaser, B., Wisbeck, J., Barajas, R. G., Taylor, A., et al. (2001). The influence of environmental and genetic factors on behavior problems and autistic symptoms in boys and girls with fragile X syndrome. Pediatrics, 108(5), e88–e88. PubMed

Hilton, C., Graver, K., & LaVesser, P. (2007). Relationship between social competence and sensory processing in children with high functioning autism spectrum disorders. Research in Autism Spectrum Disorders, 1(2), 164–173.

Hofmann, S. G., & Bitran, S. (2007). Sensory-processing sensitivity in social anxiety disorder: Relationship to harm avoidance and diagnostic subtypes. Journal of Anxiety Disorders, 21(7), 944–954. PubMed

Humes, L. E., Busey, T. A., Craig, J., & Kewley-Port, D. (2013). Are age-related changes in cognitive function driven by age-related changes in sensory processing? Attention, Perception, & Psychophysics, 75(3), 508–524.

Jones, W., Bellugi, U., Lai, Z., Chiles, M., Reilly, J., Lincoln, A., et al. (2000). II. Hypersociability in Williams syndrome. Journal of Cognitive Neuroscience, 12(1), 30–46. PubMed

Keiding, N., & Louis, T. A. (2016). Perils and potentials of self-selected entry to epidemiological studies and surveys. Journal of the Royal Statistical Society: Series A (Statistics in Society), 179(2), 319–376.

Kolacz, J., Raspa, M., Heilman, K. J., & Porges, S. W. (2018). Evaluating sensory processing in fragile X syndrome: Psychometric analysis of the brain body center sensory scales (BBCSS). Journal of Autism and Developmental Disorders, 48(6), 2187–2202. PubMed

Lesniak-Karpiak, K., Mazzocco, M. M., & Ross, J. L. (2003). Behavioral assessment of social anxiety in females with Turner or fragile X syndrome. Journal of Autism and Developmental Disorders, 33(1), 55–67. PubMed

Levitin, D. J., Cole, K., Lincoln, A., & Bellugi, U. (2005). Aversion, awareness, and attraction: Investigating claims of hyperacusis in the Williams syndrome phenotype. Journal of Child Psychology and Psychiatry, 46(5), 514–523. PubMed

Leyfer, O. T., Woodruff-Borden, J., Klein-Tasman, B. P., Fricke, J. S., & Mervis, C. B. (2006). Prevalence of psychiatric disorders in 4 to 16-year-olds with Williams syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 141(6), 615–622.

Li, K. Z., & Lindenberger, U. (2002). Relations between aging sensory/sensorimotor and cognitive functions. Neuroscience and Biobehavioral Reviews, 26(7), 777–783. PubMed

Little, L. M., Freuler, A. C., Houser, M. B., Guckian, L., Carbine, K., David, F. J., et al. (2011). Psychometric validation of the sensory experiences questionnaire. American Journal of Occupational Therapy, 65(2), 207–210. PubMed

Maenner, M. J., Smith, L. E., Hong, J., Makuch, R., Greenberg, J. S., & Mailick, M. R. (2013). Evaluation of an activities of daily living scale for adolescents and adults with developmental disabilities. Disability and Health Journal, 6(1), 8–17. PubMed

Matson, J. L., & Shoemaker, M. E. (2011). Psychopathology and intellectual disability. Current Opinion in Psychiatry, 24(5), 367–371. PubMed

Mazzocco, M. M. (2000). Advances in research on the fragile X syndrome. Mental Retardation and Developmental Disabilities Research Reviews, 6(2), 96–106. PubMed

McLennan, Y., Polussa, J., Tassone, F., & Hagerman, R. (2011). Fragile X syndrome. Current Genomics, 12(3), 216–224. PubMedPubMedCentral

Mohr, C., Tonge, B. J., & Einfeld, S. L. (2005). The development of a new measure for the assessment of psychopathology in adults with intellectual disability. Journal of Intellectual Disability Research, 49(7), 469–480. PubMed

Oakes, A., Thurman, A. J., McDuffie, A., Bullard, L. M., Hagerman, R. J., & Abbeduto, L. (2016). Characterising repetitive behaviours in young boys with fragile X syndrome. Journal of Intellectual Disability Research, 60(1), 54–67. PubMed

Pober, B. R., & Morris, C. A. (2007). Diagnosis and management of medical problems in adults with Williams-Beuren syndrome. American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 145(3), 280–290.

Reddy, L. A., & Pfeiffer, S. I. (2007). Behavioral and emotional symptoms of children and adolescents with Prader–Willi syndrome. Journal of Autism and Developmental Disorders, 37(5), 830–839. PubMed

Riby, D. M., Kirk, H., Hanley, M., & Riby, L. M. (2014). Stranger danger awareness in Williams syndrome. Journal of Intellectual Disability Research, 58(6), 572–582. PubMed

Rogers, S. J., Hepburn, S., & Wehner, E. (2003). Parent reports of sensory symptoms in toddlers with autism and those with other developmental disorders. Journal of Autism and Developmental Disorders, 33(6), 631–642. PubMed

Royston, R., Howlin, P., Waite, J., & Oliver, C. (2017). Anxiety disorders in Williams syndrome contrasted with intellectual disability and the general population: A systematic review and meta-analysis. Journal of Autism and Developmental Disorders, 47(12), 3765–3777. PubMed

Royston, R., Waite, J., & Howlin, P. (2019). Williams syndrome: Recent advances in our understanding of cognitive, social and psychological functioning. Current Opinion in Psychiatry, 32(2), 60–66. PubMed

Saldarriaga, W., Tassone, F., González-Teshima, L. Y., Forero-Forero, J. V., Ayala-Zapata, S., & Hagerman, R. (2014). Fragile X syndrome. Colombia Médica, 45(4), 190–198. PubMed

Sanislow, C. A., Pine, D. S., Quinn, K. J., Kozak, M. J., Garvey, M. A., Heinssen, R. K., et al. (2010). Developing constructs for psychopathology research: Research domain criteria. Journal of Abnormal Psychology, 119(4), 631. PubMed

Soni, S., Whittington, J., Holland, A. J., Webb, T., Maina, E. N., Boer, H., et al. (2008). The phenomenology and diagnosis of psychiatric illness in people with Prader–Willi syndrome. Psychological Medicine, 38(10), 1505–1514. PubMed

Stauder, J. E., Brinkman, M. J., & Curfs, L. M. (2002). Multi-modal P3 deflation of event-related brain activity in Prader–Willi syndrome. Neuroscience Letters, 327(2), 99–102. PubMed

Stinton, C., Elison, S., & Howlin, P. (2010). Mental health problems in adults with Williams syndrome. American Journal on Intellectual and Developmental Disabilities, 115(1), 3–18. PubMed

Strømme, P., Bjømstad, P. G., & Ramstad, K. (2002). Prevalence estimation of Williams syndrome. Journal of Child Neurology, 17(4), 269–271. PubMed

Taffe, J. R., Tonge, B. J., Gray, K. M., & Einfeld, S. L. (2008). Extracting more information from behaviour checklists by using components of mean based scores. International Journal of Methods in Psychiatric Research, 17(4), 232–240. PubMed

Tomczak, M., & Tomczak, E. (2014). The need to report effect size estimates revisited. An overview of some recommended measures of effect size. Trends in Sport Sciences, 21(1), 19–25.

Uljarević, M., Labuschagne, I., Bobin, R., Atkinson, A., & Hocking, D. R. (2018). Brief report: The impact of sensory hypersensitivity and intolerance of uncertainty on anxiety in Williams syndrome. Journal of Autism and Developmental Disorders. https://doi.org/10.1007/s10803-018-3631-9. CrossRefPubMed

Vasa, R. A., Kalb, L., Mazurek, M., Kanne, S., Freedman, B., Keefer, A., et al. (2013). Age-related differences in the prevalence and correlates of anxiety in youth with autism spectrum disorders. Research in Autism Spectrum Disorders, 7(11), 1358–1369.

Watson, D. (2005). Rethinking the mood and anxiety disorders: A quantitative hierarchical model for DSM-V. Journal of Abnormal Psychology, 114(4), 522. PubMed

Woodruff-Borden, J., Kistler, D. J., Henderson, D. R., Crawford, N. A., & Mervis, C. B. (2010). Longitudinal course of anxiety in children and adolescents with Williams syndrome. American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 154(2), 277–290.

Titel: The Profiles and Correlates of Psychopathology in Adolescents and Adults with Williams, Fragile X and Prader–Willi Syndromes
Auteurs:: R. Royston
C. Oliver
P. Howlin
A. Dosse
P. Armitage
J. Moss
J. Waite
Publicatiedatum: 04-12-2019
DOI: https://doi.org/10.1007/s10803-019-04317-1
Uitgeverij: Springer US
Tijdschrift: Journal of Autism and Developmental Disorders
Uitgave 3/2020
Print ISSN: 0162-3257
Elektronisch ISSN: 1573-3432

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