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Braz. J. Psychiatry (São Paulo, 1999, Impr.) ; 38(2): 113-120, Apr.-June 2016. tab
Article in English | LILACS | ID: lil-784298

ABSTRACT

Objective: To study anxiety as a variable of the mid- and long-term psychological impact of pre-symptomatic testing for three autosomal dominant late-onset disorders – Huntington’s disease (HD), Machado-Joseph disease (MJD) and familial amyloid polyneuropathy (FAP) TTR V30M – in a Portuguese sample. Methods: This cross-sectional study included 203 participants: 170 (83.7%) underwent pre-symptomatic testing for FAP, 29 (14.3%) for HD, and 4 (2%) for MJD. Of the 203 participants, 73 (36.0%) were asymptomatic carriers, 29 (14.5%) were symptomatic carriers, 9 (4.5%) were diagnosed with FAP and had a liver transplant, and 89 (44.5%) were non-carriers. Most were women (58.1%) and married (66.5%). The anxiety variable was assessed using the Zung Self-Rating Anxiety Scale (SAS). Results: The anxiety scores were higher for symptomatic carriers and for those who underwent psychological support consultations over the years. For symptomatic carriers, the mean scores were superior to 40 points, which reflects clinical anxiety. Conclusion: Although it was not possible to differentiate between the mid- and long-term psychological impacts, this study supports the conclusion that the proximity to the age of symptoms onset might be a trigger for anxiety.


Subject(s)
Humans , Male , Female , Adult , Aged , Anxiety/diagnosis , Huntington Disease/psychology , Machado-Joseph Disease/psychology , Amyloid Neuropathies, Familial/psychology , Asymptomatic Diseases/psychology , Anxiety/classification , Anxiety/psychology , Portugal , Time Factors , Cross-Sectional Studies , Predictive Value of Tests , Surveys and Questionnaires , Huntington Disease/diagnosis , Machado-Joseph Disease/diagnosis , Amyloid Neuropathies, Familial/diagnosis , Middle Aged
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