VEGF and eNOS variants may influence intervertebral disc degeneration     
Yazarlar (6)
Hasan Emre Aydın
Kütahya Sağlık Bilimleri Üniversitesi, Türkiye
Serbülent Yiğit
Ondokuz Mayıs Üniversitesi, Türkiye
İsmail Kaya
Uşak Üniversitesi, Türkiye
Ercan Tural
Ondokuz Mayıs Üniversitesi, Türkiye
Arş. Gör. Sadegül ŞAVKIN Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Ayşe Feyda Nursal
Hitit Üniversitesi, Türkiye
Makale Türü Özgün Makale
Makale Alt Türü SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale
Dergi Adı Nucleosides, Nucleotides & Nucleic Acids
Dergi ISSN 2022-0091
Dergi Tarandığı Indeksler SCI-Expanded
Dergi Grubu Q4
Makale Dili İngilizce
Basım Tarihi 04-2022
Cilt No 41
Sayı 10
Sayfalar 982 / 993
DOI Numarası 10.1080/15257770.2022.2093363
Makale Linki https://doi.org/10.1080/15257770.2022.2093363
Özet
Intervertebral disc degeneration (IDD) is a common and complex condition. Vascular endothelial growth factor (VEGF) is one of the key regulators of angiogenesis and vascular permeability. Nitric oxide (NO) plays a role in various physiological events. The endothelial nitric oxide synthase (eNOS) that catalyses NO generation are crucial for the regulation of NO level. This study aimed to evaluate the association between VEGF/ eNOS gene variants with IDD. Two hundred ninety-one subjects (111 IDD patients and 180 controls) were included in the present case-control study. VEGF -2549 insertion/deletion (I/D) and eNOS VNTR variants were analysed by PCR method. The results of this analysis were evaluated for statistical significance. There were no statistically significant differences in genotype and allele distribution of VEGF -2549 I/D/ eNOS VNTR variants between IDD patients and control subjects. We then evaluated the association between the allele frequencies of these variants and clinical features of IDD. Lumber IDD was more common in patients carrying VEGF I/D variant D allele (p < 0.001). Also, patients with lumbar disc herniation, cervical disc herniation, lumbar stenosis, and lumbar IDD had more 4 b allele (p = 0.005, p < 0.001, p < 0.001, and p = 0.03, respectively). In conclusion, this study demonstrates first time that some clinical characteristics of IDD have been associated with allele frequencies of VEGF -2549 I/D/ eNOS VNTR variants.
Anahtar Kelimeler
Intervertebral disc degeneration | vascular endothelial growth factor | endothelial nitric oxide synthase | variant | gene | DNA | RNA | gene regulation
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
WoS 5
VEGF and eNOS variants may influence intervertebral disc degeneration

Paylaş