首页> 美国卫生研究院文献>Journal of Medical Genetics >Adverse psychological events occurring in the first year after predictive testing for Huntingtons disease. The Canadian Collaborative Study Predictive Testing.
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Adverse psychological events occurring in the first year after predictive testing for Huntingtons disease. The Canadian Collaborative Study Predictive Testing.

机译:在对亨廷顿氏病进行预测测试后的第一年发生了不良的心理事件。加拿大合作研究预测测试。

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摘要

A total of 135 participants in the Canadian predictive testing programme for HD were followed for at least one year in one of four study groups: increased risk (n = 37), decreased risk ( n = 58), uninformative (n = 17), or not tested (n = 23). Clinical criteria for an adverse event were a suicide attempt or formulation of a suicide attempt plan, psychiatric hospitalisation, depression lasting longer than two months, a marked increase in substance abuse, and the breakdown of important relationships. Quantitative criteria, as measured by changes on the General Severity Index of the Symptom Checklist 90-R and the Beck Depression Inventory, were also used to identify people who had adverse events. Twenty of the 135 participants (14.8%) had an adverse event. There were no significant differences between those with or without an adverse event with respect to age, sex, marital status, education, psychiatric history, general psychiatric distress, or social supports at baseline. However, evidence for depression was associated with an increased frequency of adverse events (p < 0.04). The adverse events were similar and seen with equivalent frequency in those receiving an increased risk or decreased risk and persons at risk who did not receive a modification of risk. However, a significant difference was found in the timing of adverse events for the increased and decreased risk groups (p < 0.0002). In the increased risk group all of the adverse events occurred within 10 days after results whereas, in the decreased risk group, all of the adverse events occurred six months or later after reviewing test results. These results suggest that people entering into predictive testing with some evidence of clinical depression warrant special vigilance and also suggest that counselling and support should be available for all participants in predictive testing irrespective of the direction of test results.
机译:在四个研究组之一中,对加拿大HD预测性测试计划中的135名参与者进行了至少一年的随访:风险增加(n = 37),风险降低(n = 58),信息不足(n = 17),或未经测试(n = 23)。不良事件的临床标准是自杀未遂或制定自杀未遂计划,精神病住院,持续超过两个月的抑郁症,药物滥用显着增加以及重要关系破裂。通过症状检查表90-R的一般严重性指数和贝克抑郁量表的变化来衡量的定量标准也用于识别发生不良事件的人。 135名参与者中有20名(14.8%)有不良事件。在基线时,有或没有不良事件的人在年龄,性别,婚姻状况,受教育程度,精神病史,一般精神病困扰或社会支持方面均无显着差异。但是,抑郁的证据与不良事件发生频率增加相关(p <0.04)。不良事件相似,在风险增加或风险降低的人以及未接受风险改变的风险人中,发生频率相同。但是,对于增加和降低的风险组,不良事件发生的时间有显着差异(p <0.0002)。在高风险组中,所有不良事件均在结果后10天内发生,而在低风险组中,所有不良事件均在检查测试结果后的6个月或更晚时间内发生。这些结果表明,在进行带有某些临床抑郁症证据的预测性测试的人时,应格外警惕,并建议对于预测性测试的所有参与者,无论测试结果的方向如何,都应提供咨询和支持。

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