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Long-term negative Psychological Impact of Presymptomatic Testing for Huntington’s Disease

dc.contributor.authorLeite, Ângela Maria Teixeira
dc.contributor.authorDinis, Maria Alzira Pimenta
dc.contributor.authorPinto, Susana Maria Lêdo da Silva
dc.contributor.authorPinto, Ana Manuela Baldaia Carvalho
dc.contributor.authorGomes, Ana Isabel Pinheiro
dc.contributor.authore Sousa, Hélder Fernando Pedrosa
dc.date.accessioned2019-09-13T14:52:58Z
dc.date.available2019-09-13T14:52:58Z
dc.date.issued2017
dc.descriptionhttp://sherpa.ac.uk/romeo/issn/2422-8419/pt_PT
dc.description.abstractPresymptomatic Testing (PST) for Huntington’s disease (HD) is available since 1986 and its impact on carriers and non-carriers is not yet fully clear. It is important to understand its psychological impact so that the PST protocols are best suited to the subjects at-risk. Preventing a negative psychological impact is the ultimate purpose of the genetic counselling process. This study addresses the long-term negative psychological impact assessment of PST for HD. The sample consisted of 29 subjects that were 50% at-risk for HD, and had performed the PST for at least three years ago. Participants answered the sociodemographic questionnaire and the Brief Symptom Inventory, the Zung Self-Rating Anxiety Scale, and the Beck Depression Inventory. Although most of the sample does not present clinically significant psychopathology values, 6 subjects present a Positive Symptoms Distress Index value which is equal to or greater than 1.7; 7 subjects present a value which is equal to or greater than 40 of anxiety; and 7 subjects present mild depression. Symptomatic carriers, who underwent the PST less time ago, present worse psychopathological symptoms, depression and anxiety. Subjects with this profile should have a more intense and personalized psychological and social support, aiming to prevent the risk of suicide and to improve the quality of their lives.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationAPA: Leite, Â. M. T., Dinis, M. A. P., Pinto, S. M. L. d. S., Pinto, A. M. B. C., Gomes, A. I. P., & e Sousa, H. F. P. (2017). Long-term negative Psychological Impact of Presymptomatic Testing for Huntington’s Disease. Journal of Health, Medicine and Nursing, 34, 1-9.pt_PT
dc.identifier.issn2422-8419
dc.identifier.urihttp://hdl.handle.net/10284/7869
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherInternational Peer Reviewed Journal and Book Publishingpt_PT
dc.relation.publisherversionhttps://iiste.org/Journals/index.php/JHMN/article/view/35145pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectPresymptomatic Testing (PST)pt_PT
dc.subjectPreditive genetic testingpt_PT
dc.subjectHuntington´s Disease (HD)pt_PT
dc.subjectLong-term Psychological Impactpt_PT
dc.subjectLate-onset diseasept_PT
dc.titleLong-term negative Psychological Impact of Presymptomatic Testing for Huntington’s Diseasept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage9pt_PT
oaire.citation.startPage1pt_PT
oaire.citation.titleJournal of Health, Medicine and Nursingpt_PT
oaire.citation.volume34pt_PT
person.familyNameDinis
person.givenNameMaria Alzira Pimenta
person.identifier493603
person.identifier.ciencia-id4710-147D-FDAF
person.identifier.orcid0000-0002-2198-6740
person.identifier.ridF-3309-2011
person.identifier.scopus-author-id55539804000
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublication1e85592a-e8e2-4aea-bd8e-1007c94388c0
relation.isAuthorOfPublication.latestForDiscovery1e85592a-e8e2-4aea-bd8e-1007c94388c0

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