Why pharmacokinetic differences among oral triptans have little clinical importance: a comment

被引:32
作者
Ferrari, Anna [1 ]
Tiraferri, Ilaria [2 ]
Neri, Laura [3 ]
Sternieri, Emilio [1 ]
机构
[1] Univ Modena & Reggio Emilia, Div Toxicol & Clin Pharmacol, Headache & Drug Abuse Inter Dep Res Ctr, I-41100 Modena, Italy
[2] Univ Modena & Reggio Emilia, Sch Med Toxicol, I-41100 Modena, Italy
[3] Univ Modena & Reggio Emilia, Sch Clin Pharmacol, I-41100 Modena, Italy
关键词
Acute treatment; Disposition; Headache; Pharmacokinetics; Triptan; Variability; MIGRAINE HEADACHE RECURRENCE; HEALTHY-VOLUNTEERS; SUMATRIPTAN PHARMACOKINETICS; 5-HT1B/1D AGONISTS; RECEPTOR AGONISTS; POOLED ANALYSIS; RIZATRIPTAN; TOLERABILITY; EFFICACY; THERAPY;
D O I
10.1007/s10194-010-0258-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Triptans, selective 5-HT1B/1D receptor agonists, are specific drugs for the acute treatment of migraine that have the same mechanism of action. Here, it is discussed why the differences among kinetic parameters of oral triptans have proved not to be very important in clinical practice. There are three main reasons: (1) the differences among the kinetic parameters of oral triptans are smaller than what appears from their average values; (2) there is a large inter-subject, gender-dependent, and intra-subject (outside/during the attack) variability of kinetic parameters related to the rate and extent of absorption, i.e., those which are considered as critical for the response; (3) no dose-concentration-response curves have been defined and it is, therefore, impossible both to compare the kinetics of triptans, and to verify the objective importance of kinetic differences; (4) the importance of kinetic differences is outweighed by non-kinetic factors of variability of response to triptans. If no oral formulations are found that can allow more predictable pharmacokinetics, the same problems will probably also arise with new classes of drugs for the acute treatment of migraine.
引用
收藏
页码:5 / 12
页数:8
相关论文
共 73 条
  • [1] Adelman J U, 2001, Clin Cornerstone, V4, P53, DOI 10.1016/S1098-3597(01)90039-0
  • [2] Gastric stasis occurs in spontaneous, visually induced, and interictal migraine
    Aurora, Sheena
    Kori, Shashidhar
    Barrodale, Patricia
    Nelsen, Andrew
    McDonald, Susan
    [J]. HEADACHE, 2007, 47 (10): : 1443 - 1446
  • [3] Headache recurrence and treatment
    Sheena K. Aurora
    John Dempsey
    [J]. Current Treatment Options in Neurology, 2002, 4 (5) : 335 - 342
  • [4] Satisfaction with current migraine therapy: Experience from 3 centers in US and Sweden
    Bigal, Marcelo
    Rapoport, Alan
    Aurora, Sheena
    Sheftell, Fred
    Tepper, Stewart
    Dahlof, Carl
    [J]. HEADACHE, 2007, 47 (04): : 475 - 479
  • [5] A CORRELATION BETWEEN SEVERITY OF MIGRAINE AND DELAYED GASTRIC-EMPTYING MEASURED BY AN EPIGASTRIC IMPEDANCE METHOD
    BOYLE, R
    BEHAN, PO
    SUTTON, JA
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1990, 30 (03) : 405 - 409
  • [6] Migraine and Functional Impairment
    Brandes, Jan Lewis
    [J]. CNS DRUGS, 2009, 23 (12) : 1039 - 1045
  • [7] Clinical pharmacokinetics of frovatriptan
    Buchan, P
    Keywood, C
    Wade, A
    Ward, C
    [J]. HEADACHE, 2002, 42 : S54 - S62
  • [8] Elevated Saliva Calcitonin Gene-Related Peptide Levels During Acute Migraine Predict Therapeutic Response to Rizatriptan
    Cady, Roger K.
    Vause, Carrie V.
    Ho, Tony W.
    Bigal, Marcelo E.
    Durham, Paul L.
    [J]. HEADACHE, 2009, 49 (09): : 1258 - 1266
  • [9] Migraine headache treatment with eletriptan, a second-generation serotonin receptor agonist
    Cole, P
    Rabasseda, X
    [J]. DRUGS OF TODAY, 2001, 37 (03) : 159 - 171
  • [10] ORAL SUMATRIPTAN IN PHARMACOKINETICS IN THE MIGRAINOUS STATE
    CUTLER, NR
    HUSSEY, EK
    SRAMEK, JJ
    CLEMENTS, BD
    PAULSGROVE, LA
    BUSCH, MA
    DONN, KH
    [J]. CEPHALALGIA, 1991, 11 : 222 - 223