Ageed Fatima Eltayb M, Tifow Fadumo Ali, Ibrahim Leylo Abdullahi, Ismael Aya B, Balcıoğlu Özlem, Özcem Barçın, Cobanogullari Havva, Yılmaz Selma, Ergören Mahmut Çerkez
Faculty of Medicine, Department of Medical Genetics, Near East University, Nicosia, 99138, Cyprus.
Faculty of Medicine, Department of Cardiovascular Surgery, Near East University, Nicosia, 99138, Cyprus.
Mol Biol Rep. 2024 Dec 16;52(1):53. doi: 10.1007/s11033-024-10153-z.
Chronic venous insufficiency (CVI) manifests as morphological and functional abnormalities in the venous system, primarily affecting the lower extremities and presenting as leg heaviness, oedema, and varicose veins. CVI is a common vascular disorder characterised by impaired blood flow in the veins, often leading to various clinical manifestations. To better understand the additional underlying mechanisms of CVI, it is essential to explore the role of Wnt proteins, which play a crucial role in regulating signalling processes. This study aimed to investigate the expression levels of the Wnt3a and Wnt5a genes using real-time PCR in patients with venous insufficiency compared to acontrol group.
68 participants were included, comprising 29 controls and 39 patients with venous insufficiency from Near East University Hospital. Real-time PCR was utilised for gene expression analysis on a segment of the great saphenous vein biopsy, encompassing all vascular layers, from each participant in both groups. With a significance threshold of p < 0.05, the analysis revealed a significant difference in Wnt3a gene expression (p ₌ 0.0007) and a nonsignificant difference in Wnt5a expression levels (p ₌ 0.5726) between patients with venous insufficiency and the healthy control group.
This study indicates fluctuations in the Wnt genes in varicose vein biopsies compared to healthy veins. Consequently, further research is essential to elucidate whether the dysregulation of the Wnt pathway induces venous insufficiency or vice versa. This may facilitate targeted interventions addressing its fundamental molecular aberrations.
慢性静脉功能不全(CVI)表现为静脉系统的形态和功能异常,主要影响下肢,表现为腿部沉重、水肿和静脉曲张。CVI是一种常见的血管疾病,其特征是静脉血流受损,常导致各种临床表现。为了更好地理解CVI的其他潜在机制,探索Wnt蛋白的作用至关重要,Wnt蛋白在调节信号传导过程中起关键作用。本研究旨在通过实时PCR检测静脉功能不全患者与对照组相比Wnt3a和Wnt5a基因的表达水平。
纳入68名参与者,包括来自近东大学医院的29名对照组和39名静脉功能不全患者。对两组中每位参与者的大隐静脉活检样本(包括所有血管层)进行实时PCR基因表达分析。以p < 0.05为显著性阈值,分析显示静脉功能不全患者与健康对照组之间Wnt3a基因表达存在显著差异(p = 0.0007),而Wnt5a表达水平无显著差异(p = 0.5726)。
本研究表明,与健康静脉相比,静脉曲张活检样本中Wnt基因存在波动。因此,进一步研究以阐明Wnt通路失调是否诱发静脉功能不全或反之亦然至关重要。这可能有助于针对其基本分子异常进行靶向干预。