Skip to main content
Log in

The Effect of Predictive Testing in Adult-Onset Neurodegenerative Diseases on Social and Personal Life

  • Original Research
  • Published:
Journal of Genetic Counseling

Abstract

Follow-up studies on predictive testing for hereditary neurodegenerative diseases mainly focussed on psychological outcomes. We investigated whether the social and personal life of mutation carriers differ negatively from non-carriers and untested at-risk individuals. Asymptomatic individuals (≥ 35 years) who received a genetic test result for Huntington’s disease, frontotemporal dementia or Alzheimer’s disease more than 2 years before the onset of the study and untested subjects at 50% risk were invited to complete a questionnaire and an additional questionnaire with extra or adjusted items. Of the 283 selected individuals, 115 returned a positive informed consent (response rate 39.6%). Of these, 17 carriers, 30 non-carriers and 27 untested persons (n = 74) fulfilled the criteria and completed both questionnaires. We found no significant differences in employment, financial situation and lifestyle or anxiety and depression between carriers and non-carriers or untested individuals at risk. Carriers were more often single and childless, though these differences were not significant. The findings of this study suggest that the result of predictive testing on adult-onset neurodegenerative diseases does not have a large negative effect on social and personal life, although these observations should be interpreted with caution because of the small number of participants and low response rate.

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.

Fig. 1

Similar content being viewed by others

References

  • Almqvist, E. W., Brinkman, R. R., Wiggins, S., & Hayden, M. R. (2003). Psychological consequences and predictors of adverse events in the first 5 years after predictive testing for Huntington's disease. Clinical Genetics, 64, 300–309.

    Article  PubMed  CAS  Google Scholar 

  • Baker, M., Mackenzie, I. R., Pickering-Brown, S. M., Gass, J., Rademakers, R., Lindholm, C., et al. (2006). Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature, 442, 916–919.

    Article  PubMed  CAS  Google Scholar 

  • Bjelland, I., Dahl, A. A., Haug, T. T., & Neckelmann, D. (2002). The validity of the hospital anxiety and depression scale. An updated literature review. Journal of Psychosomatic Research, 52, 69–77.

    Article  PubMed  Google Scholar 

  • Bombard, Y., Penziner, E., Suchowersky, O., Guttman, M., Paulsen, J. S., Bottorff, J. L., et al. (2008). Engagement with genetic discrimination: concerns and experiences in the context of Huntington disease. European Journal of Human Genetics, 16, 279–289.

    Article  PubMed  Google Scholar 

  • Clark, R. F., Hutton, M., Fuldner, M., Froelich, S., Karran, E., Talbot, C., et al. (1995). The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families. Alzheimer’s Disease Collaborative Group. Nature Genetics, 11, 219–222.

    Article  CAS  Google Scholar 

  • Cruts, M., Gijselinck, I., Van der Zee, J., Engelborghs, S., Wils, H., Pirici, D., et al. (2006). Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature, 442, 920–924.

    Article  PubMed  CAS  Google Scholar 

  • Dejesus-Hernandez, M., Mackenzie, I. R., Boeve, B. F., Boxer, A. L., Baker, M., Rutherford, N. J., et al. (2011). Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron, 72, 245–256.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • Dopper, E. G., Rombouts, S. A., Jiskoot, L. C., den Heijer, T., de Graaf, J. R., de Koning, I., et al. (2014). Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia. Neurology, 83, e19–e26.

    Article  PubMed  Google Scholar 

  • Erwin, C., Williams, J. K., Juhl, A. R., Mengeling, M., Mills, J. A., Bombard, Y., et al. (2010). Perception, experience, and response to genetic discrimination in Huntington disease: the international RESPOND-HD study. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 153B, 1081–1093.

    Google Scholar 

  • Gandek, B., Ware, J. E., Aaronson, N. K., Apolone, G., Bjorner, J. B., Brazier, J. E., et al. (1998). Cross-validation of item selection and scoring for the SF-12 Health Survey in nine countries: results from the IQOLA Project. International Quality of Life Assessment. Journal of Clinical Epidemiology, 51, 1171–1178.

    PubMed  CAS  Google Scholar 

  • Goate, A., Chartier-Harlin, M. C., Mullan, M., Brown, J., Crawford, F., Fidani, L., et al. (1991). Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer’s disease. Nature, 349, 704–706.

    Article  PubMed  CAS  Google Scholar 

  • Hutton, M., Lendon, C. L., Rizzu, P., Baker, M., Froelich, S., Houlden, H., et al. (1998). Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature, 393, 702–705.

    Article  PubMed  CAS  Google Scholar 

  • MacDonald, M. E., Ambrose, C. M., Duyao, M. P., Myers, R. H., Lin, C., Srinidhi, L., et al. (1993). A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. Cell, 72, 971–983.

    Article  Google Scholar 

  • Morrison, P. J., Harding-Lester, S., & Bradley, A. (2011). Uptake of Huntington disease predictive testing in a complete population. Clinical Genetics, 80, 281–286.

    Article  PubMed  CAS  Google Scholar 

  • Paulsen, J. S., Nance, M., Kim, J. I., Carlozzi, N. E., Erwin, C., Goh, A., et al. (2013). A review of quality of life after predictive testing for and earlier identification of neurodegenerative diseases. Progress in Neurobiology, 110, 2–28.

    Article  PubMed  Google Scholar 

  • Penziner, E., Williams, J. K., Erwin, C., Bombard, Y., Wallis, A., Beglinger, L. J., et al. (2008). Perceptions of discrimination among persons who have undergone predictive testing for Huntington’s disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147, 320–325.

    Article  Google Scholar 

  • Renton, A. E., Majounie, E., Waite, A., Simon-Sanchez, J., Rollinson, S., Gibbs, J. R., et al. (2011). A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron, 72(2), 257–268. https://doi.org/10.1016/j.neuron.2011.09.010.

  • Riedijk, S. R., Niermeijer, M. F. N., Dooijes, D., & Tibben, A. (2009). A decade of genetic counseling in frontotemporal dementia affected families: few counseling requests and much familial opposition to testing. Journal of Genetic Counseling, 18, 350–356.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • Sherrington, R., Rogaev, E. I., Liang, Y., Rogaeva, E. A., Levesque, G., Ikeda, M., et al. (1995). Cloning of a gene bearing missense mutations in early-onset familial Alzheimer’s disease. Nature, 375, 754–760.

    Article  PubMed  CAS  Google Scholar 

  • Spillantini, M. G., Murrell, J. R., Goedert, M., Farlow, M. R., Klug, A., & Ghetti, B. (1998). Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. Proceedings of the National Academy of Sciences of the United States of America, 95, 7737–7741.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • Spinhoven, P., Ormel, J., Sloekers, P. P., Kempen, G. I., Speckens, A. E., & Van Hemert, A. M. (1997). A validation study of the Hospital Anxiety and Depression Scale (HADS) in different groups of Dutch subjects. Psychological Medi cine, 27, 363–370.

    Article  CAS  Google Scholar 

  • Statistics Netherlands (2016) [online publication]. Retrieved from http://statline.cbs.nl/Statweb/?LA=en

  • Steinbart, E. J., Smith, C. O., Poorkaj, P., & Bird, T. D. (2001). Impact of DNA testing for early-onset familial Alzheimer disease and frontotemporal dementia. Archives of Neurology, 58, 1828–1831.

    Article  PubMed  CAS  Google Scholar 

  • Tibben, A. (2007). Predictive testing for Huntington’s disease. Brain Research Bulletin, 72, 165–171.

    Article  PubMed  Google Scholar 

  • Timman, R., Roos, R., Maat-Kievit, A., & Tibben, A. (2004). Adverse effects of predictive testing for Huntington disease underestimated: long-term effects 7-10 years after the test. Health Psychology, 23, 189–197.

    Article  PubMed  Google Scholar 

  • Williams, J. K., Erwin, C., Juhl, A. R., Mengeling, M., Bombard, Y., Hayden, M. R., et al. (2010). In their own words: reports of stigma and genetic discrimination by people at risk for Huntington disease in the International RESPOND-HD study. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 153B, 1150–1159.

    Google Scholar 

  • Zigmond, A. S., & Snaith, R. P. (1983). The hospital anxiety and depression scale. Acta Psychiatrica Scandinavia, 67, 361–370.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank Reinier Timman and Lidewij Henneman for their advice on the design of the study and the questionnaires. This work was conducted to fulfill a degree requirement.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Anneke Kievit.

Ethics declarations

Conflicts of Interest

PC, JvS, YP, AT, HM and AK declare that they have no conflict of interest.

Human Studies and Informed Consent

All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2000 (5). Informed consent was obtained from all patients for being included in the study.

Animal Studies

No animals have been used in this study.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Cohn-Hokke, P.E., van Swieten, J.C., Pijnenburg, Y.A.L. et al. The Effect of Predictive Testing in Adult-Onset Neurodegenerative Diseases on Social and Personal Life. J Genet Counsel 27, 947–954 (2018). https://doi.org/10.1007/s10897-017-0195-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10897-017-0195-3

Keywords

Navigation