Pharmacogenetics and pharmacogenomics of sexual dysfunction: current status, gaps and potential applications

被引:2
作者
Abdel-Hamid, Ibrahim A. [1 ]
Andersson, Karl-Erik [2 ]
机构
[1] Mansoura Fac Med, Sexual Med Unit, Dept Androl, Mansoura, Egypt
[2] Wake Forest Univ, Wake Forest Inst Regenerat Med, Winston Salem, NC 27109 USA
关键词
androgens; PDE5; inhibitors; pharmacogenetics; pharmacogenomics; phosphodiesterase-5; serotonin reuptake inhibitors; sexual dysfunction; SSRIs; ANDROGEN RECEPTOR GENE; NITRIC-OXIDE SYNTHASE; ANGIOTENSIN-CONVERTING ENZYME; SUBUNIT 825T ALLELE; CYCLIC-NUCLEOTIDE PHOSPHODIESTERASES; TESTOSTERONE REPLACEMENT THERAPY; REPEAT LENGTH POLYMORPHISM; HUMAN CGMP-BINDING; PREMATURE EJACULATION; ERECTILE DYSFUNCTION;
D O I
10.2217/PGS.09.104
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although treatment of different types of sexual dysfunction has improved in the past decade with the introduction of phosphodiesterase type 5 inhibitors and selective serotonin reuptake inhibitors, response rates to these targeted therapies are variable. There are a number of studies in the published literature that provide proof-of-concept that genetic variation contributes to the variable response. Pharmacogenomics will most likely be one part of our therapeutic armamentarium in the future and will provide a stronger scientific basis for optimizing drug therapy on the basis of each patient's genetic constitution. This article will review English language medical literature on the state-of-the-art genetic polymorphisms of drug targets, transporters and signaling molecules as well as pharmacogenetic studies of sexual dysfunction and suggested possible applications. Collectively, the data demonstrate that pharmacogenomics in the field of sexual medicine is still in its infancy. More research will provide further intriguing new discoveries in years to come.
引用
收藏
页码:1625 / 1644
页数:20
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