The future of pharmacogenetics for osteoporosis

被引:2
作者
Marini, Francesca [1 ]
Brandi, Maria Luisa [1 ]
机构
[1] Univ Florence, Dept Surg & Translat Med, Metab Bone Unit, Florence, Italy
关键词
bone metabolism; individual drug response; osteoporosis; pharmacogenetics; BONE-MINERAL-DENSITY; VITAMIN-D-RECEPTOR; HORMONE-REPLACEMENT THERAPY; COLIA1; SP1; POLYMORPHISM; BINDING-SITE POLYMORPHISM; LARGE-SCALE ANALYSIS; POSTMENOPAUSAL WOMEN; GENE POLYMORPHISMS; JAPANESE WOMEN; ALPHA GENE;
D O I
10.2217/PGS.13.40
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
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.
引用
收藏
页码:641 / 653
页数:13
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