Psychosocial impact of Von Hippel-Lindau disease: Levels and sources of distress
Von Hippel-Lindau disease (VHL) is a hereditary tumor susceptibility syndrome, characterized by an increased risk of developing multiple benign and malignant tumors at various sites and ages with limited preventive options. This study evaluates the prevalence of distress among VHL family members and factors associated significantly with such distress.Forty-eight families with a VHL mutation were identified via the nine family cancer clinics in the Netherlands. In total, 171 family members (carriers, 50% at-risk, non-carriers) were approached, of whom 123 (72%) completed a self-report questionnaire. Approximately 40% of the VHL family members reported clinically relevant levels of distress, approaching 50% among the carriers and, possibly even more striking, 36% among the non-carriers. Having lost a first degree relative due to VHL during adolescence (OR 11.2; 95% CI 1.4-86.9) was related significantly to heightened levels of distress. Approximately, only one-third of those who reported heightened levels of distress had received professional psychosocial support. A substantial percentage of family members experience clinically relevant levels of distress. We would recommend the introduction of a procedure for screening for distress in this vulnerable population. Special attention should be paid to those individuals who have lost a close relative due to VHL during adolescence.
|Keywords||Distress, Lindau disease, Psychosocial impact, Quality of life, Von Hippel, Worries|
|Persistent URL||dx.doi.org/10.1111/j.1399-0004.2010.01333.x, hdl.handle.net/1765/27306|
|Journal||Clinical Genetics: an international journal of genetics and molecular medicine|
Lammens, C.R.M, Bleiker, E.M.A, Verhoef, S, Hes, F.J, Ausems, M.G.E.M, Majoor-Krakauer, D.F, … Aaronson, K. (2010). Psychosocial impact of Von Hippel-Lindau disease: Levels and sources of distress. Clinical Genetics: an international journal of genetics and molecular medicine, 77(5), 483–491. doi:10.1111/j.1399-0004.2010.01333.x