NR3C1 GENE POLYMORPHISMS IN PATIENTS WITH FOCAL SEGMENTAL GLOMERULOSCLEROSIS AND MEMBRANOUS GLOMERULONEPHRITIS

NR3C1 GENE POLYMORPHISMS IN PATIENTS WITH FOCAL SEGMENTAL GLOMERULOSCLEROSIS AND MEMBRANOUS GLOMERULONEPHRITIS


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نویسندگان: محمد رضا اردلان , سپیده زنونی واحد

عنوان کنگره / همایش: International Conference on Scientific Advances and Challenges in Biology , Azerbaijan , Baku , 2021

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نویسنده ثبت کننده مقاله سپیده زنونی واحد
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه مرکز تحقیقات کلیه
کد مقاله 77356
عنوان فارسی مقاله NR3C1 GENE POLYMORPHISMS IN PATIENTS WITH FOCAL SEGMENTAL GLOMERULOSCLEROSIS AND MEMBRANOUS GLOMERULONEPHRITIS
عنوان لاتین مقاله NR3C1 GENE POLYMORPHISMS IN PATIENTS WITH FOCAL SEGMENTAL GLOMERULOSCLEROSIS AND MEMBRANOUS GLOMERULONEPHRITIS
نوع ارائه سخنرانی
عنوان کنگره / همایش International Conference on Scientific Advances and Challenges in Biology
نوع کنگره / همایش بین المللی
کشور محل برگزاری کنگره/ همایش Azerbaijan
شهر محل برگزاری کنگره/ همایش Baku
سال انتشار/ ارائه شمسی 1400
سال انتشار/ارائه میلادی 2021
تاریخ شمسی شروع و خاتمه کنگره/همایش 1400/02/16 الی 1400/02/17
آدرس لینک مقاله/ همایش در شبکه اینترنت
آدرس علمی (Affiliation) نویسنده متقاضی Kidney Research Center, Tabriz University Of Medical Sciences, Tabriz, Iran

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نویسنده نفر چندم مقاله
محمد رضا اردلاناول
سپیده زنونی واحددوم

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عنوان متن
خلاصه مقالهGlucocorticoids (GCs) therapy is a selective treatment strategy for cases with nephrotic syndrome (NS). Due to the lack of positive response of all patients to therapy and the dependency of biological effects of GCs on its receptors (GR), here, the association of the NR3C1 gene (N363S, Bclİ, GR-9β, and ER22/23EK) polymorphisms with the response to GCs was investigated in patients with NS. İn this study, 55 patients with primary NS including 29 steroid-responder (SS) and 26 steroid-resistant (SR) and 30 healthy individuals were recruited. The polymorphisms of NR3C1 gene were studied by PCR and sequencing of the amplified fragments and the results were compared between the groups. A3669 SNP was observed in 8.7% (n=2) of patients with SRNS and 6.3% (n=2) of responders (P=0.560). İn 40.7% of steroid-responsive patients (n=11) and 21.4% of patients with SRNS (n=6), BClİ polymorphism was detected that was not statistically significant (P=0.098). The N363S and ER22/23EK polymorphisms were not detected in the studied groups. No significant differences were observed between the frequency of the studied polymorphisms between the different subtypes of NS; focal segmental glomerulosclerosis (FSGS), membranous glomerulonephritis (MGN), and control group. The NR3C1 gene N363S, Bclİ, GR-9β, and ER22/23EK polymorphisms did not affect the steroid responsiveness and the pathogenesis of NS in Azarian adult patients with primary NS. Other polymorphisms within NR3C1 gene need to be explored in large cohorts.
کلمات کلیدیNR3C1, GENE POLYMORPHISM, FOCAL SEGMENTAL GLOMERULOSCLEROSIS, MEMBRANOUS GLOMERULONEPHRITIS

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