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骨质疏松症的药物遗传学的未来。

The future of pharmacogenetics for osteoporosis.

机构信息

Metabolic Bone Unit, Department of Surgery & Translation Medicine, University of Florence, Florence, Italy.

出版信息

Pharmacogenomics. 2013 Apr;14(6):641-53. doi: 10.2217/pgs.13.40.

Abstract

The possibility to predict the outcome of medical treatments, both in terms of efficacy and development of adverse effects, is the main goal of modern personalized medicine. The principal aim of pharmacogenetics is to design specific predictive genetic tests, to be performed prior to any drug treatment, and to tailor the therapy for each patient based on the results of these tests. Few pharmacogenetic tests are today validated and commonly applied in clinical practice, and none in the area of osteoporosis and bone disorders. Surely, the complex regulation of bone metabolism and the involvement of numerous different molecular pathways makes it difficult to individuate responsible genes and polymorphisms involved in the modulation of anti-osteoporotic drug response and, subsequently, in designing specific predictive analyses.

摘要

预测医疗效果和不良反应的可能性是现代个性化医学的主要目标。药物遗传学的主要目标是设计特定的预测性遗传检测,在进行任何药物治疗之前进行,并根据这些检测结果为每个患者定制治疗方案。如今,只有少数药物遗传学检测经过验证并在临床实践中广泛应用,而在骨质疏松症和骨骼疾病领域则没有。当然,骨骼代谢的复杂调节以及众多不同分子途径的参与使得确定参与调节抗骨质疏松药物反应的相关基因和多态性变得困难,从而难以设计特定的预测分析。

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