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RELATIONSHIP BETWEEN TACROLIMUS ORAL DOSE AND ADULT HEART ALLOGRAFT RECIPIENT GENOTYPE

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F20%3A00073381" target="_blank" >RIV/00159816:_____/20:00073381 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.ptfarm.pl/download/?file=File%2FActa_Poloniae%2F2020%2F5%2F777.pdf" target="_blank" >https://www.ptfarm.pl/download/?file=File%2FActa_Poloniae%2F2020%2F5%2F777.pdf</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.32383/appdr/127580" target="_blank" >10.32383/appdr/127580</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    RELATIONSHIP BETWEEN TACROLIMUS ORAL DOSE AND ADULT HEART ALLOGRAFT RECIPIENT GENOTYPE

  • Original language description

    Determination patient genotype in selected ABCB, p450 CYP3A polymorphism and their potential phenotypic manifestation in measured tacrolimus level in relation oral dose. 35 adult patients after heart transplantation with itnmunosuppressant regimen containing oral tacrolimus, mycophenolate mofetil and corticosteroids were eligible. Patient weight, tacrolimus level and dose were collected retrospectively. DNA isolated from buccal smear was tested for presence of 1236C -&gt; T (rs1128503), 2677G -&gt; T/A (rs2032582), 3435C -&gt; T (rs1045642) on ABCB gene, 1508C-4T (rs1057868) on POR gene, 522-191 C-sT (rs35599367) on CYP3A4 (CYP3A4*22) and 6986 A -&gt; G (rs776746) on CYP3A5 (CYP3A5*3) gene. Statistical analysis was conducted by Chi-square test, statistical significance confirmed if p &lt;0.05. Variant allele frequency in ABCB tested polymorphisms as follows: 0.53 (3435T), 0.4(1236T) and OA (2677TA). POR 1508T, CYP3A4*22 and CYP3A5*3 variant allele frequency was 0.27, 0.07 and 0 respectively. ABCB G2677T/A hcterozygotes (83%; n = 10) required tacrolimus oral dose above 0.075 mg/kg/day more often to reach level above 15 ng/mL in comparison to wild type homozygotes (p = 0.0263). Five patients out of six with tacrolimus level above 15 ng/mL with 2677GG genotype required tacrolimus dose below 0.075 mg/kg/day in comparison to variant allele carriers, who needed tacrolirnus dose above 0.075 mg/kg/day (p = 0.0464). Wild type ABCB haplotype patients (100%; n = 3) required dose below 0.075 mg/kg/day in contrast to one patient (12.5%) with heterozygote haplotype (p = 0.0474). Patients with wild type genotype 2677GG required lower oral tacrolimus dose than recommended in comparison to variant allele carriers, who needed higher dose to achieve such level 3 months after surgery.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30104 - Pharmacology and pharmacy

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    ACTA POLONIAE PHARMACEUTICA

  • ISSN

    0001-6837

  • e-ISSN

  • Volume of the periodical

    77

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    PL - POLAND

  • Number of pages

    7

  • Pages from-to

    777-783

  • UT code for WoS article

    000597873300012

  • EID of the result in the Scopus database