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本文引用的文献

1
The elusive ideal of inclusiveness: lessons from a worldwide survey of neurologists on the ethical issues raised by whole-genome sequencing.包容性这一难以捉摸的理想:来自一项针对全球神经科医生关于全基因组测序引发的伦理问题的调查的经验教训。
BMC Med Ethics. 2017 Apr 11;18(1):28. doi: 10.1186/s12910-017-0187-8.
2
Genetic testing among Spanish pediatric neurologists: Knowledge, attitudes and practices.西班牙儿科神经科医生的基因检测:知识、态度与实践
Eur J Med Genet. 2017 Feb;60(2):124-129. doi: 10.1016/j.ejmg.2016.11.007. Epub 2016 Nov 25.
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Mutations in HECW2 are associated with intellectual disability and epilepsy.HECW2基因的突变与智力残疾和癫痫有关。
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Ethical issues in consumer genome sequencing: Use of consumers' samples and data.消费者基因组测序中的伦理问题:消费者样本和数据的使用。
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Neurologist Comfort in the Use of Next-Generation Sequencing Diagnostics: Current State and Future Prospects.神经科医生对使用下一代测序诊断技术的信心:现状与未来前景
JAMA Neurol. 2016 Jun 1;73(6):621-2. doi: 10.1001/jamaneurol.2016.0168.
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The Future of Next-Generation Sequencing in Neurology.神经病学中下一代测序的未来
JAMA Neurol. 2015 Sep;72(9):971-2. doi: 10.1001/jamaneurol.2015.1076.
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Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.全基因组测序在癌症遗传学诊所中的诊断与发现应用。
EBioMedicine. 2015 Jan;2(1):74-81. doi: 10.1016/j.ebiom.2014.12.003.
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Reporting incidental findings in genomic scale clinical sequencing--a clinical laboratory perspective: a report of the Association for Molecular Pathology.基因组规模临床测序中偶然发现的报告——临床实验室视角:分子病理学协会报告
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Movement disorders in 2014. Genetic advances spark a revolution in dystonia phenotyping.2014 年的运动障碍。遗传学进展引发了肌张力障碍表型的革命。
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神经科医生在临床环境中使用全基因组测序的实践与观点:一项基于网络的调查。

Practices and views of neurologists regarding the use of whole-genome sequencing in clinical settings: a web-based survey.

作者信息

Jaitovich Groisman Iris, Hurlimann Thierry, Shoham Amir, Godard Béatrice

机构信息

Groupe de recherche Omics-Ethics, Institut de recherche en santé publique, Université de Montréal, Montreal, Quebec, Canada.

Département de psychologie, Faculté des arts et des sciences, Université de Montréal, Montreal, Quebec, Canada.

出版信息

Eur J Hum Genet. 2017 Jun;25(7):801-808. doi: 10.1038/ejhg.2017.64. Epub 2017 May 10.

DOI:10.1038/ejhg.2017.64
PMID:28488681
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5520076/
Abstract

The use of Whole-Genome Sequencing (WGS) in clinical settings has brought up a number of controversial scientific and ethical issues. The application of WGS is of particular relevance in neurology, as many conditions are difficult to diagnose. We conducted a worldwide, web-based survey to explore neurologists' views on the benefits of, and concerns regarding, the clinical use of WGS, as well as the resources necessary to implement it. Almost half of the 204 neurologists in the study treated mostly adult patients (48%), while the rest mainly children (37.3%), or both (14.7%). Epilepsy (73%) and headaches (57.8%) were the predominant conditions treated. Factor analysis brought out two profiles: neurologists who would offer WGS to their patients, and those who would not, or were not sure in which circumstances it should be offered. Neurologists considering the use of WGS as bringing more benefits than drawbacks currently used targeted genetic testing (P<0.05) or treated mainly children (P<0.05). WGS' benefits were directed towards the patients, while its risks were of a financial and legal nature. Furthermore, there was a correlation between respondents' current use of genetic tests and an anticipation of increased use in the future (P<0.001). However, over half of respondents did not feel sufficiently informed to use WGS in their practice (53.5%). Our results highlight gaps in education, organization, and funding to support the use of WGS in neurology, and draw attention to the need for resources that could strongly contribute to more straightforward diagnoses and possibly better treatment of neurological conditions.

摘要

在临床环境中使用全基因组测序(WGS)引发了一些具有争议性的科学和伦理问题。WGS的应用在神经病学领域尤为重要,因为许多病症难以诊断。我们开展了一项全球性的网络调查,以探究神经科医生对于WGS临床应用的益处、担忧以及实施所需资源的看法。参与研究的204名神经科医生中,近一半主要治疗成年患者(48%),其余主要治疗儿童(37.3%),或两者都治疗(14.7%)。治疗的主要病症为癫痫(73%)和头痛(57.8%)。因子分析得出两种类型:愿意向患者提供WGS的神经科医生,以及不愿意或不确定应在何种情况下提供WGS的医生。认为使用WGS利大于弊的神经科医生目前使用靶向基因检测(P<0.05)或主要治疗儿童(P<0.05)。WGS的益处是针对患者的,而其风险则具有财务和法律性质。此外,受访者目前使用基因检测的情况与未来使用量增加的预期之间存在相关性(P<0.001)。然而,超过一半的受访者认为自己没有足够的信息在临床实践中使用WGS(53.5%)。我们的研究结果凸显了在教育、组织和资金方面存在的差距,这些差距阻碍了WGS在神经病学中的应用,并提请注意需要一些资源,这些资源能够有力地促进更直接的诊断,并可能改善对神经系统疾病的治疗。