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哮喘个性化医学的新方法:我们在哪里?

New approaches to personalized medicine for asthma: where are we?

机构信息

Channing Laboratory, Department of Medicine, Brigham and Women's Hospital, Boston, Mass 02115, USA.

出版信息

J Allergy Clin Immunol. 2012 Feb;129(2):327-34. doi: 10.1016/j.jaci.2011.12.971.

Abstract

Access to an electronic medical record is essential for personalized medicine. Currently, only 40% of US physicians have such access, but this is rapidly changing. It is expected that 100,000 Americans will have their whole genome sequenced in 2012. The cost of such sequencing is rapidly dropping, and is estimated to be $1000 by 2013. These technological advances will make interpretation of whole genome sequence data a major clinical challenge for the foreseeable future. At present, a relatively small number of genes have been identified to determine drug treatment response phenotypes for asthma. It is anticipated that this will dramatically increase over the next 10 years as personalized medicine becomes more of a reality for asthma patients.

摘要

获取电子病历对于个性化医疗至关重要。目前,只有 40%的美国医生能够获得这种访问权限,但这一情况正在迅速改变。预计 2012 年将有 10 万名美国人对其整个基因组进行测序。这种测序的成本正在迅速下降,预计到 2013 年将降至 1000 美元。这些技术进步将使全基因组序列数据的解释成为可预见的未来的主要临床挑战。目前,已经确定了相对较少的基因来确定哮喘药物治疗反应表型。预计在未来 10 年,随着个性化医疗成为哮喘患者的现实,这一数字将大幅增加。

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