Atıf İçin Kopyala
YILDIRIM E., ŞAHİN G., Kaltus Z., ÇOLAK E.
CLINICAL LABORATORY, cilt.65, sa.11, ss.2079-2089, 2019 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
65
Sayı:
11
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Basım Tarihi:
2019
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Doi Numarası:
10.7754/clin.lab.2019.190343
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Dergi Adı:
CLINICAL LABORATORY
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus
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Sayfa Sayıları:
ss.2079-2089
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Anahtar Kelimeler:
tacrolimus, CYP3A5, ABCB1, polymorphism, pharmacokinetics, SINGLE-NUCLEOTIDE POLYMORPHISMS, TROUGH CONCENTRATION, DOSE REQUIREMENTS, DRUG-INTERACTIONS, EARLY-STAGE, PHARMACOKINETICS, CYTOCHROME-P450, CYCLOSPORINE, METABOLISM, MDR1
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Eskişehir Osmangazi Üniversitesi Adresli:
Evet
Özet
Background: Tacrolimus (Tac) is a calcineurin inhibitor (CNI). Its therapeutic range is narrow and pharmacokinetic properties vary among patients. CYP3A5 and MDR1 single-nucleotide polymorphisms (SNPs) are the most effective polymorphisms that play an significant role in the pharmacokinetics of Tac.