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Implications of genetic risk information in families with a high density of bipolar disorder: an exploratory study

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  • Meiser, Bettina
  • Mitchell, Philip B.
  • McGirr, H.
  • Van Herten, M.
  • Schofield, Peter R.

Abstract

While major susceptibility genes for bipolar disorder are yet to be identified, the opportunity exists to systematically ascertain the important issues and societal implications of genetic risk determination for bipolar disorder prior to these technological advances becoming widely available. This study explores, in a sample of families with a high density of bipolar disorder: (i) attitudes to predictive genetic and prenatal testing, using different risk frames; (ii) attributions for bipolar disorder, in particular the degree to which a genetic model is endorsed; and (iii) the impact of these attributions on the perceived stigma of bipolar disorder. A qualitative methodology was selected as most appropriate as no previous research has examined this issue. Participants were ascertained through a molecular genetics study of bipolar disorder. In-depth interviews were conducted with 21 members of families with a high density of bipolar disorder. Most participants reported being interested in genetic testing if it gave a definitive answer, while expressed interest in testing was lower if it gave a probable answer only. Almost all stressed that a genetic susceptibility and environmental factors interacted. Most participants felt that a genetic explanation was likely to decrease the stigma associated with bipolar disorder as it shifted the locus of control and responsibility away from the individual towards the role of heredity. Findings indicate that expressed interest in genetic testing depends on the certainty imparted by the test. Results suggest that families with bipolar disorder are likely to benefit psychologically from information about the genetic basis of bipolar disorder.

Suggested Citation

  • Meiser, Bettina & Mitchell, Philip B. & McGirr, H. & Van Herten, M. & Schofield, Peter R., 2005. "Implications of genetic risk information in families with a high density of bipolar disorder: an exploratory study," Social Science & Medicine, Elsevier, vol. 60(1), pages 109-118, January.
  • Handle: RePEc:eee:socmed:v:60:y:2005:i:1:p:109-118
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    References listed on IDEAS

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    1. Mechanic, David & McAlpine, Donna & Rosenfield, Sarah & Davis, Diane, 1994. "Effects of illness attribution and depression on the quality of life among persons with serious mental illness," Social Science & Medicine, Elsevier, vol. 39(2), pages 155-164, July.
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    1. Kvaale, Erlend P. & Gottdiener, William H. & Haslam, Nick, 2013. "Biogenetic explanations and stigma: A meta-analytic review of associations among laypeople," Social Science & Medicine, Elsevier, vol. 96(C), pages 95-103.
    2. Shostak, Sara & Zarhin, Dana & Ottman, Ruth, 2011. "What's at stake? Genetic information from the perspective of people with epilepsy and their family members," Social Science & Medicine, Elsevier, vol. 73(5), pages 645-654, September.
    3. Raman Deep Pattanayak & Rajesh Sagar, 2012. "A qualitative study of perceptions related to family risk of bipolar disorder among patients and family members from India," International Journal of Social Psychiatry, , vol. 58(5), pages 463-469, September.
    4. de Vries, Jantina & Jallow, Muminatou & Williams, Thomas N. & Kwiatkowski, Dominic & Parker, Michael & Fitzpatrick, Raymond, 2012. "Investigating the potential for ethnic group harm in collaborative genomics research in Africa: Is ethnic stigmatisation likely?," Social Science & Medicine, Elsevier, vol. 75(8), pages 1400-1407.
    5. Faure, Marlyn C. & Matshabane, Olivia P. & Marshall, Patricia & Appelbaum, Paul S. & Stein, Dan J. & Engel, Mark E. & de Vries, Jantina, 2019. "Does genetics matter for disease-related stigma? The impact of genetic attribution on stigma associated with rheumatic heart disease in the Western Cape, South Africa," Social Science & Medicine, Elsevier, vol. 243(C).
    6. Easter, Michele M., 2012. "“Not all my fault”: Genetics, stigma, and personal responsibility for women with eating disorders," Social Science & Medicine, Elsevier, vol. 75(8), pages 1408-1416.

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