Effect of Genetic Polymorphism on Calcineurin Inhibitors Levels in Egyptian Renal Transplant Patients

Sponsor
Helwan University (Other)
Overall Status
Completed
CT.gov ID
NCT03830255
Collaborator
Ain Shams University (Other)
143
1
36.9
3.9

Study Details

Study Description

Brief Summary

Renal transplantation is the treatment of choice for patients with end-stage renal disease (ESRD). Calcineurin Inhibitors tacrolimus and cyclosporine are the principle immunosuppressive agents administered to solid organ transplant recipients to prevent and treat allograft rejection.

The aim of the present study is to detect the incidence of some selected genetic polymorphism in Egyptian renal transplant population and investigate the influence of these genetic polymorphism (SNPs )on Cyclosporine and Tacrolimus blood concentration. In addition to detect the association between these genetic polymorphism variants and patients' clinical outcome after transplantation.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Tacrolimus and cyclosporine are the principle immunosuppressive agents administered to solid organ transplant recipients to prevent and treat allograft rejection.They both exert their immunosppressive action by inhibiting the calcinurein in T-lymphoctes. Subsequently,Cyclosporin and tacrolimus are both metabolic substrates for cytochrome P450 (CYP) 3A enzymes - in particular, CYP3A4 and CYP3A5 - and are transported out of cells by the P-glycoprotein (ABCB1) efflux pump. Different expression of CYP3A4, CYP3A5 and P-glycoprotein causes patient to-patient variability in the absorption, metabolism and tissue distribution of calcineurin inhibitors. This different expression is likely to be at least partially the result of mutations in the genes encoding for these enzymes and drug transporter. This may lead to variable drug concentrations within the systemic circulation and at target sites, influencing drug efficacy. Moreover, it will influence the individual's susceptibility to drug interactions and drug toxicity

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    143 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Calcineurin Inhibitors Among Egyptian Renal Transplant Patients: a Pharmacognetic Based Study.
    Actual Study Start Date :
    Mar 1, 2017
    Actual Primary Completion Date :
    Oct 1, 2019
    Actual Study Completion Date :
    Mar 29, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    Renal Transplant patients treated with cyclosporine

    Detecting the genetic polymorphism affecting cyclosporine level

    Renal Transplant patients treated with tacrolimus

    Detecting the genetic polymorphism affecting tacrolimus level

    Outcome Measures

    Primary Outcome Measures

    1. CYP enzymes genetic polymorphism and calcineurin inhibitors drug levels [3 months]

      Association of CP3A4 and CYP3A5 genetic polymorphism SNPs on Cyclosporine and Tacrolimus blood concentration

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Kidney transplant patients.

    2. Treatment with calcineurin inhibitors (CNI) either Cyclosporine (Neoral®) or Tacrolimus (Prograf®).

    3. Absence of medication known to interact with CNI

    4. Age18 years and more

    Exclusion Criteria:
    1. Patient who experience acute rejection, graft failure.

    2. Medications that interact with Calcineurin Inhibitors.

    3. Pregnant or nursing women.

    4. Patients who decline to participate

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Ain shams university specialized hospital Cairo Egypt

    Sponsors and Collaborators

    • Helwan University
    • Ain Shams University

    Investigators

    • Principal Investigator: Magdy El Sharkawy, MD, Ain Shams University
    • Study Director: Abdel hameed Ibrahim Mohamed Ebid, PhD, Helwan University
    • Study Director: Neama Lotfy, MD, Ain sham university
    • Study Director: Mohamed Adel, PhD, Helwan University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Dina Ahmed Mohamed Ali Ismail, Lecturer Assistant at Clinical Pharmacy and Pharmacy Practice department, Misr International University
    ClinicalTrials.gov Identifier:
    NCT03830255
    Other Study ID Numbers:
    • FWA000017585
    First Posted:
    Feb 5, 2019
    Last Update Posted:
    Mar 30, 2021
    Last Verified:
    Mar 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Dina Ahmed Mohamed Ali Ismail, Lecturer Assistant at Clinical Pharmacy and Pharmacy Practice department, Misr International University

    Study Results

    No Results Posted as of Mar 30, 2021