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本文引用的文献

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An inventory for measuring depression.一份用于测量抑郁的量表。
Arch Gen Psychiatry. 1961 Jun;4:561-71. doi: 10.1001/archpsyc.1961.01710120031004.
2
CAG repeat size and clinical presentation in Huntington's disease.亨廷顿舞蹈症中CAG重复序列长度与临床表现
Neurology. 1994 Jun;44(6):1137-43. doi: 10.1212/wnl.44.6.1137.
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A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats.亨廷顿舞蹈症突变的全球研究。测量CAG重复序列的敏感性和特异性。
N Engl J Med. 1994 May 19;330(20):1401-6. doi: 10.1056/NEJM199405193302001.
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Diagnosis of Huntington disease: a model for the stages of psychological response based on experience of a predictive testing program.亨廷顿病的诊断:基于一项预测性检测项目经验的心理反应阶段模型。
Am J Med Genet. 1993 Sep 1;47(3):368-74. doi: 10.1002/ajmg.1320470314.
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Incidence and prevalence of Huntington's disease in Olmsted County, Minnesota (1950 through 1989).明尼苏达州奥尔姆斯特德县亨廷顿氏病的发病率与患病率(1950年至1989年)
Arch Neurol. 1994 Jul;51(7):696-8. doi: 10.1001/archneur.1994.00540190076018.
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Proceed with care: direct predictive testing for Huntington disease.谨慎行事:亨廷顿舞蹈症的直接预测性检测
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Predictive genetic diagnosis.预测性基因诊断
Am J Hum Genet. 1994 Oct;55(4):603-5.
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Neurology. 1994 Aug;44(8):1369-73. doi: 10.1212/wnl.44.8.1369.
9
A polymorphic DNA marker genetically linked to Huntington's disease.一种与亨廷顿舞蹈症基因连锁的多态性DNA标记。
Nature. 1983;306(5940):234-8. doi: 10.1038/306234a0.
10
Huntington disease: functional capacities in patients treated with neuroleptic and antidepressant drugs.亨廷顿病:接受抗精神病药物和抗抑郁药物治疗患者的功能能力
Neurology. 1981 Oct;31(10):1333-5. doi: 10.1212/wnl.31.10.1333.

DNA检测对亨廷顿舞蹈病症状患者的情感及功能影响。

Emotional and functional impact of DNA testing on patients with symptoms of Huntington's disease.

作者信息

Jankovic J, Beach J, Ashizawa T

机构信息

Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

J Med Genet. 1995 Jul;32(7):516-8. doi: 10.1136/jmg.32.7.516.

DOI:10.1136/jmg.32.7.516
PMID:7562962
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1050542/
Abstract

The potential impact of DNA testing on asymptomatic subjects at risk for Huntington's disease (HD) has been addressed by numerous studies, but the effect of revealing the genetic results to patients with a clinically established diagnosis of HD has not been previously evaluated. We studied 36 patients, with equal distribution of men and women, mean age 53.9 (SD 12.3) years (range 25-76) and mean duration of symptoms of 11.2 (SD 7.7) years (range 2-33), whose clinical diagnosis of HD was confirmed by expanded CAG repeats (> 40). Coping strategies and depression levels were assessed before the results of DNA testing were imparted. The assessments were repeated two weeks and three months after the results were explained to the patients and their relatives and were compared to the baseline assessments. This group of HD patients was compared with 10 patients who had similar symptoms but the diagnosis of HD was excluded by normal CAG repeats (< 30). Although some patients with HD expressed a subjective reaction to the positive result (four were "surprised", one was "frustrated", and one "devastated"), there were no differences in any psychological scores including Beck Depression Inventory, functional capacity, symptom interference, independence scale, and other measures of mood and behaviour two weeks and three months later. Similarly, no change was noted in any of these measures in the non-HD group. These results suggest that mood and coping strategies are unaffected by DNA confirmation of diagnosis in symptomatic patients with HD.

摘要

多项研究探讨了DNA检测对有患亨廷顿舞蹈症(HD)风险的无症状个体的潜在影响,但此前尚未评估向临床确诊为HD的患者披露基因检测结果的影响。我们研究了36例患者,男女比例均等,平均年龄53.9(标准差12.3)岁(范围25 - 76岁),平均症状持续时间为11.2(标准差7.7)年(范围2 - 33年),其HD的临床诊断经扩展的CAG重复序列(> 40)得以证实。在告知DNA检测结果之前,对患者的应对策略和抑郁水平进行了评估。在向患者及其亲属解释检测结果后的两周和三个月,重复进行评估,并与基线评估进行比较。将这组HD患者与10例有类似症状但因CAG重复序列正常(< 30)而排除HD诊断的患者进行比较。尽管一些HD患者对阳性结果表达了主观反应(4人“感到惊讶”,1人“感到沮丧”,1人“深受打击”),但在两周和三个月后,包括贝克抑郁量表、功能能力、症状干扰、独立量表以及其他情绪和行为指标在内的任何心理评分均无差异。同样,非HD组的这些指标也未出现任何变化。这些结果表明,对于有症状的HD患者,DNA确诊对其情绪和应对策略没有影响。