Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/5842
Title: Relation between 3435C>T multidrug resistance 1 gene polymorphism with high dose methylprednisolone treatment of childhood acute idiopathic thrombocytopenic purpura
Authors: Akin, M.
Turgut, S.
Ayada, C.
Polat, Y.
Balcı, Yasemin Işık
Erdogan, F.
Keywords: High dose methylprednisolone
Idiopathic thrombocytopenic purpura
MDR1
methylprednisolone
multidrug resistance protein 1
adolescent
article
child
clinical article
controlled study
correlation analysis
DNA polymorphism
drug megadose
exon
female
gene frequency
genotype
human
idiopathic disease
male
polymerase chain reaction
preschool child
priority journal
restriction fragment length polymorphism
school child
single nucleotide polymorphism
thrombocyte count
thrombocytopenic purpura
treatment response
Acute Disease
Alleles
Chi-Square Distribution
Child
Child, Preschool
Dose-Response Relationship, Drug
Drug Administration Schedule
Female
Gene Frequency
Genotype
Glucocorticoids
Humans
Male
Methylprednisolone
P-Glycoprotein
Platelet Count
Polymorphism, Single Nucleotide
Purpura, Thrombocytopenic, Idiopathic
Treatment Outcome
Abstract: The current study was conducted to assess 3435C>T multidrug resistance 1 gene polymorphism and the efficacy of high dose methylprednisolone (HDMP) in childhood acute idiopathic thrombocytopenic purpura patients. Methods: A total of 31 childhood acute Idiopathic thrombocytopenic purpura patients (17 females, 14 males) between the ages of 2 and 16 years of age were included in the study. High-dose methylprednisolone was given at a dose of 30 mg/kg/day for 3 days and 20 mg/kg/day for 4 days, consecutively and intravenously. Polymerase chain reaction-restriction fragment length polymorphism was used for the detection of C3435T single nucleotide polymorphism. Fragments obtained were 238 bp to T/T genotype, 172 bp and 60 bp fragments to the C/C genotype, and 238 bp, 172 bp and 60 bp to the C/T genotype. Results: The distribution of CC, CT, and TT genotypes were 19.0%, 61.3%, and 19.4%, respectively. Both allele frequencies of C and T were the same - 50%. There was no significant difference in genotype and allele distribution between the patients with ITP and the control group (? 2=0.84 p=0.65, ? 2=0.2 p=0.63, respectively). There were no significant differences in age, gender, and pre- and post-treatment platelet counts between CC, CT, and TT genotypes of the MDR gene. Response to treatment shows no significant difference between genotype and allele groups. Conclusion: In our study, there was no difference in the HDMP treatment response between MDR1 gene genotypes. However, it should be noted that this study includes a small group of patients. Our data should therefore be considered preliminary, awaiting further confirmatory studies on an expanded patient base. © 2011 Elsevier B.V.
URI: https://hdl.handle.net/11499/5842
https://doi.org/10.1016/j.gene.2011.06.019
ISSN: 0378-1119
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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