G02 Decision-making in predictive testing in huntington’s disease

Federica Terenzi, C. Ferrari, C. Bartolozzi, F. Rotella, E. Ghelli, Eleonora Mascherini, E. Volpi, S. Latorraca, S. Bagnoli, B. Nacmias, S. Piacentini, S. Sorbi
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Abstract

Objective The protocol for genetic test in at-risk individuals for Huntington Disease provides a neurological examination and a psychiatric evaluation before to begin the psychological counseling, that provides to engage the client in at least two or more psychological session aimed to support the decision-making process. The present study investigated the at-risk subjects’ decision to engage psychological counselling and to carry out genetic test. Materials The collected data were obtained through the recruitment of people with HD and their families within the European Huntington’s Disease Network (EHDN). Using the EHDN Registry, data on clinical signs and symptoms of HD are collected together with the family history of the disease and the data obtained by neurocognitive tests and self-report questionnaires. Methods One hundred and three individuals at risk for Huntington Disease have been included in the study, obtained from clinical data collected from 2007 and 2017 at the HD Center in Careggi Teaching Hospital. Data were manually retrieved from clinical records and included in a database for analyses. Results Forty-four (42.7%) subjects, out of 103 at-risk individuals, decided to start the protocol and engaged on psychological counselling about decision making for genetic test. Thirty-one (70.4%) subjects, out of 44 subjects who undertook the protocol, decided to carry out genetic test,while thirteen (30.6%) subjects decided to temporarily stop the psychological counselling. Within our sample, 18 females (58%) have undergone genetic test, among them 13 (72,2%) were in reproductive period (average age of 29,4 years). Discussion The study examined changes in decision-making for and against the predictive genetic test for Huntington’s disease during psychological counselling. Our data highlight that a high proportion of subjects changed the initial decision of having the genetic test after psychological counselling, preferring uncertainty to the chance of a negative result.
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G02亨廷顿氏病预测检测中的决策
目的:亨廷顿病高危人群基因检测方案在心理咨询开始前提供神经学检查和精神病学评估,并提供至少两次或两次以上的心理咨询,以支持决策过程。本研究调查了高危受试者参与心理咨询和进行基因测试的决定。收集的数据是通过招募欧洲亨廷顿病网络(EHDN)中的亨廷顿舞蹈症患者及其家庭获得的。使用EHDN Registry,收集HD的临床体征和症状数据、疾病家族史以及通过神经认知测试和自我报告问卷获得的数据。方法将103名亨廷顿病高危人群纳入研究,这些数据来自Careggi教学医院亨廷顿病中心2007年至2017年收集的临床数据。人工从临床记录中检索数据,并将其纳入数据库进行分析。结果103名高危人群中有44人(42.7%)决定启动基因检测方案,并参与了基因检测决策的心理咨询。接受方案的44名受试者中,31名(70.4%)受试者决定进行基因检测,13名(30.6%)受试者决定暂时停止心理咨询。在我们的样本中,有18名女性(58%)接受了基因检测,其中13名(72.2%)处于育龄期(平均年龄29.4岁)。该研究调查了心理咨询期间支持和反对亨廷顿氏病预测性基因检测的决策变化。我们的数据强调,很大比例的受试者在心理咨询后改变了进行基因检测的最初决定,他们更喜欢不确定性,而不是阴性结果的可能性。
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