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Posttraumatic growth in Huntington disease: Measuring the effects of genetic testing and disease on positive psychological change.

机译:亨廷顿病的创伤后生长:测量基因测试和疾病对积极心理变化的影响。

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摘要

Huntington disease (HD) is a genetically transmitted fatal neurodegenerative condition that currently has no cure. The symptoms of HD are manifested as cognitive declines, neuropsychiatric disturbances, and motor dysfunction. An autosomal dominant genetic defect is responsible for the onset of HD, which means that the children of an affected parent have a 50% chance of inheriting the disease. Predictive genetic testing for HD has been available since 1993, and a positive test result means that a person will develop HD with 100% certainty. People who have the HD-gene expansion, but have not yet manifested unequivocal motor signs, are said to be in the prodromal phase of HD. A number of studies have examined concerns about the utility of genetic testing and its negative psychological consequences for gene-expanded and non-expanded individuals (e.g., traumatization, suicidal ideation). Although research has understandably focused on the potential for distress, there has been some evidence suggesting that individuals may actually experience psychological growth related to a receiving a genetic test result (e.g., improved relationships, pursuing new opportunities). The aim of the present study was to understand the relationship between genetic testing, prodromal HD symptoms, and posttraumatic growth (PTG).;Participants were recruited through the multinational PREDICT-HD study (Jane Paulsen, PI) and they completed the Posttraumatic Growth Inventory (PTGI; Tedeschi & Calhoun, 1996) to assess permanent positive psychological change as a result of learning about their HD-gene status. The Symbol Digit Modalities Test (Smith, 1991), Unified Huntington's Disease Rating Scale Motor Exam (Huntington's Study Group, 1996), and the SCl-90-R Depression subscale (Derogatis, 1994) were also completed. A total of 82 gene-expanded patients and 37 non-expanded patients took part in this study.;Results revealed that gene-expanded and non-expanded individuals reported experiencing PTG, particularly in their appreciation for life and ability to relate to others. Gene-expanded and non-expanded participants did not differ in the amount of growth they reported, which indicated that the outcome of genetic testing was not related to how much growth people experienced. Age and gender were associated with PTG, with younger participants and women reporting the most growth. The amount of time elapsed since genetic testing, estimated proximity to a diagnosis of HD, and the clinical characteristics of prodromal HD were not related to PTG. In conclusion, people experience positive psychological change as result of genetic testing for HD. The findings of this study have important implications for future research and for mental health professionals assisting people through the genetic counseling process.
机译:亨廷顿病(HD)是目前无法治愈的遗传性致命性神经退行性疾病。 HD的症状表现为认知能力下降,神经精神障碍和运动功能障碍。常染色体显性遗传缺陷是导致HD发病的原因,这意味着患病父母的孩子有50%的机会遗传该疾病。自1993年以来就可以进行HD的预测性基因检测,检测结果呈阳性意味着一个人可以100%的确定性发展HD。具有HD基因扩展功能但尚未表现出明确的运动体征的人们被称为HD的前驱阶段。许多研究检查了对基因检测的效用及其对基因扩增和未扩增个体的负面心理后果(例如创伤,自杀意念)的担忧。虽然研究可以理解地集中在潜在的困扰上,但是有一些证据表明,个体可能实际上会因接受基因检测结果而经历心理成长(例如,改善人际关系,寻求新机会)。本研究的目的是了解基因检测,前驱高清症状和创伤后生长(PTG)之间的关系。通过多国PREDICT-HD研究(Jane Paulsen,PI)招募了参与者,他们完成了创伤后生长清单(PTGI; Tedeschi&Calhoun,1996),以评估由于了解其高清基因状态而产生的永久性积极的心理变化。还完成了符号数字模态测试(Smith,1991年),亨廷顿舞蹈症统一疾病等级量表汽车考试(Huntington研究组,1996年)和SCl-90-R抑郁量表(Derogatis,1994年)。共有82位基因扩增患者和37位非扩增患者参加了该研究。结果显示,基因扩增和未扩增个体报告患有PTG,尤其是他们对生活的欣赏和与他人的联系能力。基因扩增和非扩增参与者报告的生长量没有差异,这表明基因测试的结果与人们经历的生长量无关。年龄和性别与PTG相关,年轻的参与者和女性报告的增长最多。自基因检测以来经过的时间量,估计的接近HD诊断水平以及前驱HD的临床特征与PTG无关。总之,通过高清基因测试,人们会经历积极的心理变化。这项研究的结果对未来的研究以及通过基因咨询过程协助人们的精神卫生专业人员具有重要意义。

著录项

  • 作者单位

    The University of Iowa.;

  • 授予单位 The University of Iowa.;
  • 学科 Counseling Psychology.;Neurosciences.;Genetics.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 191 p.
  • 总页数 191
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:44:47

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