Using Personalized Medicine in the Management of Diabetes Mellitus

被引:6
|
作者
Elk, Nina [1 ]
Iwuchukwu, Otito F. [2 ]
机构
[1] Fairleigh Dickinson Univ, Div Pharm Practice, Sch Pharm, 230 Pk Ave,M SP1-01, Florham Pk, NJ 07932 USA
[2] Fairleigh Dickinson Univ, Div Pharmaceut Sci, Sch Pharm, 230 Pk Ave,M SP1-01, Florham Pk, NJ 07932 USA
来源
PHARMACOTHERAPY | 2017年 / 37卷 / 09期
关键词
pharmacogenomics; diabetes; monogenic diabetes syndrome; maturity-onset diabetes of the young; oral glucose lowering agents; CHANNEL SUBUNIT KIR6.2; THERAPEUTIC RESPONSE; GENETIC ARCHITECTURE; E23K VARIANT; ACTIVATING MUTATIONS; SEVERE HYPOGLYCEMIA; SER1369ALA VARIANT; SECONDARY FAILURE; INCREASED RISK; KCNJ11; E23K;
D O I
10.1002/phar.1976
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Diabetes mellitus is a worldwide problem with an immense pharmacoeconomic burden. The multifactorial and complex nature of the disease lends itself to personalized pharmacotherapeutic approaches to treatment. Variability in individual risk and subsequent development of diabetes has been reported in addition to differences in response to the many oral glucose lowering therapies currently available for diabetes pharmacotherapy. Pharmacogenomic studies have attempted to uncover the heritable components of individual variability in risk susceptibility and response to pharmacotherapy. We review the current pharmacogenomics evidence as it relates to common oral glucose lowering therapies and how they can be utilized in the management of polygenic and monogenic forms of diabetes. Evidence supports the use of genetic testing and personalized approaches to the treatment of monogenic diabetes of the young. The data are not as robust for the current application of pharmacogenetic approaches to the treatment of polygenic type 2 diabetes mellitus, but there are suggestions as to future applications in this regard. We reviewed pertinent primary literature sources as well as current evidence-based guidelines on diabetes management.
引用
收藏
页码:1131 / 1149
页数:19
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