Pharmacogenetic considerations for migraine therapies

被引:16
作者
Capi, Matilde [1 ]
Gentile, Giovanna [2 ]
Lionetto, Luana [3 ]
Salerno, Gerardo [2 ,4 ]
Cipolla, Fabiola [2 ]
Curto, Martina [4 ]
Borro, Marina [2 ]
Martelletti, Paolo [4 ,5 ]
机构
[1] St Andrea Hosp, Lab Clin Chem, Rome, Italy
[2] Sapienza Univ Rome, Dept Neurosci Mental Hlth & Sensory Organs NESMOS, Rome, Italy
[3] IRCCS, IDI, Adv Mol Diagnost Unit, Rome, Italy
[4] Sapienza Univ Rome, Dept Clin & Mol Med, Via Grottarossa 1035, I-00189 Rome, Italy
[5] St Andrea Hosp, Reg Referral Headache Ctr, Rome, Italy
关键词
Migraine; pharmacogenetics; polymorphisms; CYP; drug response; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; CLINICAL-RELEVANCE; POLYMORPHISM; PHARMACOKINETICS; GLUCURONIDATION; INHIBITION; GUIDELINE; VARIANTS; ASPIRIN; CYP2D6;
D O I
10.1080/17425255.2018.1541452
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Migraine is a common neurological disorder with a complex pathophysiology. It has been estimated that incidence between adults of current headache disorder is about 50%. Different studies show that this condition has an important and complex genetic component in response to drug therapy. Areas covered: This review shows and summarizes the importance of the polymorphisms associated with the major antimigraine drug metabolizing enzymes. The research of bibliographic databases has involved only published peer-reviewed articles from indexed journals. Expert opinion: Pharmacogenetics is based on the identification of polymorphism and promises personalized therapy with efficacy and reduction of adverse events. The association between genotype and an altered metabolizer status could guide clinical decision to evade concomitant treatments and adverse events. The introduction of routine genetic testing could help to choose the efficacy drug on the individual and genetic profile.
引用
收藏
页码:1161 / 1167
页数:7
相关论文
共 60 条
[1]  
Agúndez JAG, 2009, EXPERT OPIN DRUG MET, V5, P607, DOI [10.1517/17425250902970998 , 10.1517/17425250902970998]
[2]  
[Anonymous], 2005, NEUROLOGICAL DISORDE
[3]  
[Anonymous], 2009, DRUG CLASS REV BETA
[4]   Recent advances in migraine therapy [J].
Antonaci, Fabio ;
Ghiotto, Natascia ;
Wu, Shizheng ;
Pucci, Ennio ;
Costa, Alfredo .
SPRINGERPLUS, 2016, 5
[5]   Molecular genetics of CYP2D6:: Clinical relevance with focus on psychotropic drugs [J].
Bertilsson, L ;
Dahl, ML ;
Dalén, P ;
Al-Shurbaji, A .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2002, 53 (02) :111-122
[6]   The pathophysiology of migraine: Year 2005 [J].
Buzzi M.G. ;
Moskowitz M.A. .
The Journal of Headache and Pain, 2005, 6 (3) :105-111
[7]  
Catella-Lawson F, 1999, J PHARMACOL EXP THER, V289, P735
[8]   Cardiovascular Pharmacogenomics-Implications for Patients With CKD [J].
Cavallari, Larisa H. ;
Mason, Darius L. .
ADVANCES IN CHRONIC KIDNEY DISEASE, 2016, 23 (02) :82-90
[9]   Role of cortical spreading depression in the pathophysiology of migraine [J].
Cui, Yilong ;
Kataoka, Yosky ;
Watanabe, Yasuyoshi .
NEUROSCIENCE BULLETIN, 2014, 30 (05) :812-822
[10]  
Dean Laura, 2012, NATL CTR BIOTECHNOLO