Host/genetic factors associated with COVID-19 call for precision medicine.

IF 5.1 4区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Precision Clinical Medicine Pub Date : 2020-07-21 eCollection Date: 2020-09-01 DOI:10.1093/pcmedi/pbaa026
Alain R Thierry
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引用次数: 20

Abstract

If the current rate of infection are to be better managed, and future waves of infection kept at bay, it is absolutely necessary that the conditions and mechanisms of exposure to Severe Acute Respiratory Syndrome-Coronavirus 2 (SARS-CoV-2) be better understood, as well as the downstream severe or lethal clinical complications. While the identification of notable comorbidities has now helped to define broad risk groups, the idiosyncratic responses of individual patients can generate unexpected clinical deterioration that is difficult to predict from initial clinical features. Thus, physicians caring for patients with COVID-19 face clinical dilemmas on a daily basis. The ability to decipher individual predispositions to SARS-CoV-2 infection or severe illness, in light of variations in host immunological and inflammatory responses, in particular as a result of genetic variations, would be of great benefit in infection management. To this end, this work associates the description of COVID-19 clinical complications, comorbidities, sequelae, and environmental and genetic factors. We also give examples of underlying genomic susceptibility to COVID-19, especially with regard to the newly reported link between the disease and the unbalanced formation of neutrophil extracellular traps. As a consequence, we propose that the host/genetic factors associated with COVID-19 call for precision medicine in its treatment. This is to our knowledge the first article describing elements towards precision medicine for patients with COVID-19.

与COVID-19相关的宿主/遗传因素需要精准医疗。
如果要更好地控制当前的感染率,并遏制未来的感染浪潮,就绝对有必要更好地了解严重急性呼吸综合征-冠状病毒2 (SARS-CoV-2)暴露的条件和机制,以及下游严重或致命的临床并发症。虽然对显著合并症的识别现在有助于确定广泛的风险群体,但个体患者的特殊反应可能产生意想不到的临床恶化,这很难从最初的临床特征来预测。因此,照顾COVID-19患者的医生每天都面临临床困境。根据宿主免疫和炎症反应的变化(特别是由于遗传变异),破译个体对SARS-CoV-2感染或严重疾病的易感性的能力,将对感染管理大有裨益。为此,本工作将COVID-19临床并发症、合并症、后遗症以及环境和遗传因素的描述联系起来。我们还列举了对COVID-19潜在的基因组易感性的例子,特别是关于新报道的疾病与中性粒细胞细胞外陷阱不平衡形成之间的联系。因此,我们建议,与COVID-19相关的宿主/遗传因素需要精准医学治疗。据我们所知,这是第一篇描述COVID-19患者精准医疗要素的文章。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Precision Clinical Medicine
Precision Clinical Medicine MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
10.80
自引率
0.00%
发文量
26
审稿时长
5 weeks
期刊介绍: Precision Clinical Medicine (PCM) is an international, peer-reviewed, open access journal that provides timely publication of original research articles, case reports, reviews, editorials, and perspectives across the spectrum of precision medicine. The journal's mission is to deliver new theories, methods, and evidence that enhance disease diagnosis, treatment, prevention, and prognosis, thereby establishing a vital communication platform for clinicians and researchers that has the potential to transform medical practice. PCM encompasses all facets of precision medicine, which involves personalized approaches to diagnosis, treatment, and prevention, tailored to individual patients or patient subgroups based on their unique genetic, phenotypic, or psychosocial profiles. The clinical conditions addressed by the journal include a wide range of areas such as cancer, infectious diseases, inherited diseases, complex diseases, and rare diseases.
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