عنوان المقالة:ارتباط التغاير الجيني في سلسلة المايوسين الثقيلة مع تطور الفشل الكلوي ASSOCIATION BETWEEN MYOSIN HEAVY CHAIN POLYMORPHISM AND PROGRESSION OF RENAL FAILURE
ثناء محمد جودة | Thana mohamed Juda | 1713
نوع النشر
مجلة علمية
المؤلفون بالعربي
ثناء محمد جودة
المؤلفون بالإنجليزي
Thana Mohammed Judah
الملخص العربي
اعتمد البحث على تحليل الانماط الجينيه المختلفة لسلسلة المايوسين الثقيلة باستخدام تقنية البلمرة المتسلسل وعلاقتها بتطور الفشل الكلوي وبينت الدراسة ان النمط الجيني TT rs4821480 يعتبر عامل خطورة وله دور في تطور المرض مقارنه بالانماط الاخرى
الملخص الانجليزي
ABSTRACT : “MYH9gene” is responsible for encoding non muscle myosin heavy chain protein that “expressed” in the “kidney, platelets and liver and in smaller amounts in the thymus, spleen, and intestine”. The expression of that protein in the podocytes which are highly specialized cell, because of capacity to ultrafilter blood and support “glomerular capillary pressures”. Unbalanced and irregular in MYH9 geneexpression, or change in its positioning, or task.these transformationcause “cytoskeleton damage, causing proteinuria:, hematuria, or “renal failure”. Renal failure is the result of a squally of different illnesses and accidents that affect directly or indirectly on the renal system. Kidney which has an vitalcharisma in regulating many body functions, so its deterioration leads to the deterioration of the whole human body, renal failure is considered incurable and need hard-hitting ways to avoid it or to compensate the function of the kidney. To evaluate the role of MYH9 SNP on developing of renal failure. The study depending on “methodology of Case-control study”, hundred subjects involved; 50 “patients”complainig renal failure who attended Marjan Medical City in Hilla,Iraq and 50 apparently healthy controls. DNA was extracted venous blood. The “MYH9 gene polymorphisms” were recognizedby applying the procedure of “polymerase chain reaction restriction fragment length polymorphism” (PCR-RFLP). Data analyses statically Statistical using SPSS. Genotype at rs4821480in patients with RF: genotyping were TT (59%), GT (34%) and GG (6.0%) and for control TT(45%)GT(40%), GG(15%). This analysis of data indicated the TT genotype homozygote at rs4821480 convenesin dependently a threating of RF than does the GT and GG genotypes. There is no significant correlation between alleles distribution and age, sex, resident, jobs, smoking habit, family history, body mass index (BMI), medical history (P>0.05). The genotyping of the MYH9 SNP rs4821480 help to identify individuals at risk of developing progression in renal function and increase the susceptibility for developing renal function deterioration.
تاريخ النشر
02/02/2019
الناشر
ثناء محمد جودة
رقم المجلد
19
رقم العدد
1
ISSN/ISBN
0972-5075
رابط DOI
DOI : 10.35124/bca.2019.19.1.881
الصفحات
881-885
رابط الملف
تحميل (56 مرات التحميل)
الكلمات المفتاحية
MYH9 SNP, renal failure, allele distribution and genotyping
رجوع