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[对14名要求进行遗传性神经肌肉疾病预测性基因检测的个体的分析]

[Analysis of 14 individuals who requested predictive genetic testing for hereditary neuromuscular diseases].

作者信息

Yoshida Kunihiro, Tamai Mariko, Kubota Takeo, Kawame Hiroshi, Amano Naoji, Ikeda Shu-ichi, Fukushima Yoshimitsu

机构信息

Division of Clinical and Molecular Genetics, Shinshu University Hospital, Third Department of Internal Medicine, Shinshu University School of Medicine.

出版信息

Rinsho Shinkeigaku. 2002 Feb;42(2):113-7.

Abstract

Predictive genetic testing for hereditary neuromuscular diseases is a delicate issue for individuals at risk and their families, as well as for medical staff because these diseases are often late-onset and intractable. Therefore careful pre- and post-test genetic counseling and psychosocial support should be provided along with such genetic testing. The Division of Clinical and Molecular Genetics was established at our hospital in May 1996 to provide skilled professional genetic counseling. Since its establishment, 14 individuals have visited our clinic to request predictive genetic testing for hereditary neuromuscular diseases (4 for myotonic dystrophy, 6 for spinocerebellar ataxia, 3 for Huntington's disease, and 1 for Alzheimer's disease). The main reasons for considering testing were to remove uncertainty about the genetic status and to plan for the future. Nine of 14 individuals requested testing for making decisions about a forthcoming marriage or pregnancy (family planning). Other reasons raised by the individuals included career or financial planning, planning for their own health care, and knowing the risk for their children. At the first genetic counseling session, all of the individuals expressed hopes of not being a gene carrier and of escaping from fear of disease, and seemed not to be mentally well prepared for an increased-risk result. To date, 7 of the 14 individuals have received genetic testing and only one, who underwent predictive genetic testing for spinocerebellar ataxia, was given an increased-risk result. The seven individuals including the one with an increased-risk result, have coped well with their new knowledge about their genetic status after the testing results were disclosed. None of them has expressed regret. In pre-test genetic counseling sessions, we consider it quite important not only to determine the psychological status of the individual, but also to make the individual try to anticipate the changes in his/her life upon receiving an increased-risk or a decreased-risk result. Sufficient time should be taken to build a good relationship between the individual and his/her family and the medical staff during pre-test counseling sessions. This will help the individuals feel satisfied with their own decisions for the future, whether they receive genetic testing or not.

摘要

对遗传性神经肌肉疾病进行预测性基因检测,对于有患病风险的个体及其家人,乃至医护人员来说,都是一个棘手的问题,因为这些疾病往往发病较晚且难以治疗。因此,在进行此类基因检测的同时,应提供仔细的检测前和检测后基因咨询以及心理社会支持。我院临床与分子遗传学部门于1996年5月成立,旨在提供专业的基因咨询服务。自成立以来,已有14人前来我院门诊,要求对遗传性神经肌肉疾病进行预测性基因检测(4人检测强直性肌营养不良,6人检测脊髓小脑共济失调,3人检测亨廷顿舞蹈症,1人检测阿尔茨海默病)。考虑进行检测的主要原因是消除对基因状况的不确定性并为未来做规划。14人中,有9人要求检测以决定即将到来的婚姻或生育(计划生育)。个体提出的其他原因包括职业或财务规划、自身医疗保健规划以及了解子女患病风险。在首次基因咨询时,所有个体都表示希望自己不是基因携带者并摆脱对疾病的恐惧,而且似乎对风险增加的检测结果没有做好心理准备。迄今为止,14人中有7人接受了基因检测,只有1名接受脊髓小脑共济失调预测性基因检测的个体检测结果显示风险增加。包括这名风险增加的个体在内的7人,在检测结果公布后,都很好地应对了关于自身基因状况的新知识。他们中没有人表示后悔。在检测前的基因咨询中,我们认为不仅要确定个体的心理状态,而且要让个体尝试预想在收到风险增加或降低的检测结果后其生活的变化,这一点非常重要。在检测前的咨询过程中,应花足够的时间在个体及其家人与医护人员之间建立良好的关系。这将有助于个体对自己未来的决定感到满意,无论他们是否接受基因检测。

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