[基因的临床可操作性:罕见疾病的概念和对肌病的首次客观评估]。

IF 0.6 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL M S-medecine Sciences Pub Date : 2024-11-01 Epub Date: 2024-11-18 DOI:10.1051/medsci/2024128
Emmanuelle Pion, Gisèle Bonne, Antonio Atalaia, Emmanuelle Salort-Campana, Svetlana Gorokhova, Shahram Attarian, Mireille Cossée, Martin Krahn
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引用次数: 0

摘要

高通量测序引入了 "可操作基因 "的概念。这些基因与疾病相关,而这些疾病有特定的治疗或护理方法。因此,准确的基因诊断对于启动干预措施以预防或延缓罕见疾病的发展至关重要。高通量测序大大提高了基因分析的能力,但也导致分析请求的增加,延长了获得结果所需的时间。因此,有必要确定分析的优先次序,尤其是在怀疑涉及 "可操作基因 "的情况下。就肌病而言,法国的一项全国性研究已经发现了 63 个可采取行动的基因,这些基因与疾病有关,可以对这些疾病进行有针对性的治疗和/或优先护理,从而改善病人的预后。尽管取得了进展,但许多罕见疾病仍然没有特定的治疗方法,这凸显了医学遗传学研究和创新的持续重要性。
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[The clinical actionability of genes: A concept for rare diseases and the first objective assessment for myopathies].

High-throughput sequencing has introduced the concept of "actionable genes". These genes are linked to diseases for which specific treatments or care exist. Accurate genetic diagnosis is therefore crucial for initiating interventions that can prevent or delay the progression of rare diseases. High-throughput sequencing has considerably increased the capacities of genetic analyses, but it has also led to an increase in requests for analyses, lengthening the time taken to obtain results. It is becoming necessary to prioritize analyses, especially when "actionable genes" are suspected to be implicated. In the case of myopathies, a French national study has identified 63 actionable genes, implicated in diseases for which a targeted treatment and/or priority care can be initiated, thereby improving the patient's prognosis. Despite advances, many rare diseases remain without specific treatments, underlining the continuing importance of research and innovation in medical genetics.

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来源期刊
M S-medecine Sciences
M S-medecine Sciences 医学-医学:研究与实验
CiteScore
0.80
自引率
14.30%
发文量
182
审稿时长
4-8 weeks
期刊介绍: m/s offers high-quality review articles in French, covering all areas of biomedical and health research, in a monthly magazine format (10 issues / year). m/s is read by the whole French-speaking community, in France but also in Belgium, Switzerland, Canada, Morocco, Algeria, Tunisia etc. m/s is not a primary publication, and thus will not consider unpublished data. Most articles are invited by the Editors, but spontaneous proposals are welcomed. Each issue combines news and views on the most recent scientific publications, as well as broadly accessible and updated review articles on a specific topic, and essays on science and society, history of science, public health, or reactions to published articles. Each year, m/s also publishes one or two thematic issues focused on a research topic of high interest. All review articles and essays are peer-reviewed.
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