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dc.contributor.authorÇAKIRCA, MUSTAFA
dc.contributor.authorErkal, Sena Nur
dc.contributor.authorKISKAÇ, MUHARREM
dc.contributor.authorIsen, Hayati Can
dc.contributor.authorKARATOPRAK, CUMALİ
dc.contributor.authorErkoc, Reha
dc.contributor.authorCikrikcioglu, Mehmet Ali
dc.contributor.authorAintab, Emre
dc.contributor.authorToprak, Aybala Erek
dc.contributor.authorKilic, Ulkan
dc.contributor.authorGok, Ozlem
dc.contributor.authorCetin, Ayse Irem Yasin
dc.contributor.authorZORLU, MEHMET
dc.date.accessioned2021-03-03T13:58:22Z
dc.date.available2021-03-03T13:58:22Z
dc.date.issued2015
dc.identifier.citationErkoc R., Cikrikcioglu M. A. , Aintab E., Toprak A. E. , Kilic U., Gok O., Cetin A. I. Y. , ZORLU M., KISKAÇ M., ÇAKIRCA M., et al., "GAS6 intron 8 c.834+7G > A gene polymorphism in diabetic nephropathy", RENAL FAILURE, cilt.37, sa.5, ss.866-870, 2015
dc.identifier.issn0886-022X
dc.identifier.othervv_1032021
dc.identifier.otherav_3711ea91-9ac1-4b0d-a91c-3542b85b99b6
dc.identifier.urihttp://hdl.handle.net/20.500.12627/41150
dc.identifier.urihttps://doi.org/10.3109/0886022x.2015.1034606
dc.description.abstractBackground - Aim: In animal experiments, growth arrest-specific 6 (Gas6) protein plays a key role in the development of mesangial cell and glomerular hypertrophy in the early phase of diabetic nephropathy, and diabetic nephropathy is prevented by warfarin-induced inhibition of GAS6 protein. It was shown that GAS6 intron 8 c.834+7G>A polymorphism is protective against type 2 diabetes mellitus, and AA genotype is associated with higher blood levels of GAS6 protein. Our aim is to investigate whether this polymorphism is a risk factor for diabetic nephropathy in type 2 diabetes mellitus. Method: Eighty-seven patients with diabetic nephropathy were compared with 66 non-diabetic controls in terms of GAS6 intron 8 c.834+7G>A polymorphism. Patients with history of stroke, ischemic heart disease were excluded. Each patient was examined by the ophthalmologist to determine diabetic retinopathy. Results: Frequency of GG, GA and AA genotypes are similar in diabetic nephropathy and control groups according to GAS6 intron 8 c.834+7G>A polymorphism (p = 0.837). Rate of diabetic retinopathy was 54.02%. In the subgroup analysis, GA genotype was significantly more frequent than GG genotype in patients with diabetic retinopathy when compared to without diabetic retinopathy (p = 0.010). Conclusion: In our study, GAS6 intron 8 c.834+7G>A polymorphism was not associated with diabetic nephropathy in type 2 diabetes mellitus. However, heterozygous state of this polymorphism may be a risk factor for diabetic retinopathy in patients with diabetic nephropathy.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectNefroloji
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectÜROLOJİ VE NEFROLOJİ
dc.titleGAS6 intron 8 c.834+7G > A gene polymorphism in diabetic nephropathy
dc.typeMakale
dc.relation.journalRENAL FAILURE
dc.contributor.departmentBezmiâlem Vakıf Üniversitesi , ,
dc.identifier.volume37
dc.identifier.issue5
dc.identifier.startpage866
dc.identifier.endpage870
dc.contributor.firstauthorID220212


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