Clinical and Pathological Correlations in Chronic Venous Disease

被引:5
|
作者
Serra, Raffaele [1 ,2 ]
Bracale, Umberto Marcello [3 ]
Chila, Caterina [1 ,2 ]
Renne, Maria [1 ,2 ]
Mignogna, Chiara [4 ,5 ]
Ielapi, Nicola [1 ,6 ]
Ciranni, Salvatore [1 ,2 ]
Torcia, Giuseppina [1 ,2 ]
Bevacqua, Egidio [1 ,2 ]
Di Taranto, Maria Donata [7 ]
Mastroroberto, Pasquale [8 ]
Serraino, Giuseppe Filiberto [8 ]
Provenzano, Michele [2 ]
Andreucci, Michele [9 ]
机构
[1] Magna Graecia Univ Catanzaro, Interuniv Ctr Phlebolymphol CIFL, Int Res & Educ Program Clin & Expt Biotechnol, Dept Surg & Med Sci, Viale Europa, I-88100 Catanzaro, Italy
[2] Univ Catanzaro, Dept Med & Surg Sci, Catanzaro, Italy
[3] Univ Naples Federico II, Dept Publ Hlth, Naples, Italy
[4] Univ Catanzaro, Interdipartimental Ctr Res Genom & Mol Pathol, Catanzaro, Italy
[5] Reg Hosp Pugliese Caccia, Dept Pathol, Catanzaro, Italy
[6] Sapienza Univ Rome, Dept Publ Hlth & Infect Dis, Rome, Italy
[7] Univ Naples Federico II, Dept Mol Med & Med Biotechnol, Naples, Italy
[8] Univ Catanzaro, Dept Expt & Clin Med, Catanzaro, Italy
[9] Univ Catanzaro, Dept Hlth Sci, Catanzaro, Italy
关键词
ENDOTHELIAL GROWTH-FACTOR; RECURRENT VARICOSE-VEINS; MATRIX METALLOPROTEINASES; EXTRACELLULAR-MATRIX; CEAP CLASSIFICATION; VEGF; WALL; RECEPTORS; REVISION; SURGERY;
D O I
10.1016/j.avsg.2021.06.041
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Chronic Venous Disease (CVD) has a high prevalence in the western world. Varicose veins (VVs) are the main signs of this disease that is characterized by important pathological vessel wall changes. The aim of this study is to correlate the main histopathological abnormalities with related clinical issues of CVD. Methods: A cohort of patients with VVs scheduled for open surgical treatment namely stab avulsion of VVs was recruited. Subsequently, venous tissue from stab avulsion was collected in order to evaluate the following biomarkers: Vascular-Endothelial Growth Factor (VEGF), Protein Gene Product 9.5 (PGP 9.5), Fibronectin (FN), and Matrix Metalloproteinase-9 (MMP-9). The Clinical-Etiology-Anatomy-Pathophysiology (CEAP) criteria were used to classify CVD. Results: Fourteen tissue fragments were processed for histological and immunohistochemical studies. Of these, 43% were from CEAP C2 patients, 36% from CEAP C3 patients, and 21% from CEAP C4 patients. CEAP Class C2 had few to moderate structures positive to VEGF; occasional structures positive to Fibronectin, numerous structures positive to MMP9, few to moderate structures positive to PGP 9.5. CEAP Class C3 had moderate structures positive to VEGF; few to moderate structures positive to Fibronectin; many structures positive to MMP9; few to moderate structures positive to PGP 9.5. CEAP Class C4 had numerous structures positive to VEGF; numerous structures positive to Fibronectin; abundant structures positive to MMP-9; few structures positive to PGP 9.5. Conclusions: In this study, positive VEGF, FN, and MMP-9 structures were found with increasing trends in relation to the disease staging. VEGF and FN are associated with a progressive increase from C2 to C4. The MMP-9 marker has an important positivity even at early stage of the disease, being higher in CEAP C4 patients. PGP 9.5 decreases in CEAP C4 patients and this is concordant to decreased vein wall innervation.
引用
收藏
页码:19 / 27
页数:9
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