TY - JOUR
T1 - Early rise in serum VEGF and PDGF levels predisposes patients with a normal MBL2 genotype to restenosis after eversion endarterectomy
AU - Szabó, Attila
AU - Laki, Judit
AU - Madsen, Hans O
AU - Dósa, Edit
AU - Prohászka, Zoltán
AU - Rugonfalvi-Kiss, Szabolcs
AU - Kókai, Márta
AU - Acsádi, György
AU - Karádi, István
AU - Entz, László
AU - Selmeci, László
AU - Romics, László
AU - Füst, George
AU - Garred, Peter
AU - Cervenak, László
PY - 2007/8
Y1 - 2007/8
N2 - BACKGROUND AND PURPOSE: Recently we found that the incidence of restenosis after carotid endarterectomy was significantly higher in patients homozygous for the normal genotype of mannose-binding lectin (MBL2) than in with patients with MBL2 variant genotypes. Several growth factors are also known to contribute to restenosis. Therefore, we investigated whether early postoperative changes in serum vascular endothelial growth factor (VEGF), epidermal growth factor (EGF), and platelet-derived growth factor (PDGF) concentrations and MBL2 genotypes interact in the development of restenosis.METHODS: Eighty-two patients who underwent carotid eversion endarterectomy and were followed up by carotid duplex scan sonography for 14 months were studied. Growth factors were measured preoperatively and 4 days after surgery.RESULTS: Pronounced significant increases in both VEGF and PDGF predicted restenosis but only in patients who were homozygous for the normal MBL2 genotype. In this group, the adjusted odds ratios of restenosis at 14 months in patients with high versus low early VEGF and PDGF increases were 27.73 (2.42 to 317.26) and 9.23 (1.45 to 58.70), respectively.CONCLUSIONS: These findings indicate that the development of restenosis depends on both complement activation regulated by the MBL2 gene and pathologic processes leading to enhanced production of VEGF and PDGF during the very early postoperative period.
AB - BACKGROUND AND PURPOSE: Recently we found that the incidence of restenosis after carotid endarterectomy was significantly higher in patients homozygous for the normal genotype of mannose-binding lectin (MBL2) than in with patients with MBL2 variant genotypes. Several growth factors are also known to contribute to restenosis. Therefore, we investigated whether early postoperative changes in serum vascular endothelial growth factor (VEGF), epidermal growth factor (EGF), and platelet-derived growth factor (PDGF) concentrations and MBL2 genotypes interact in the development of restenosis.METHODS: Eighty-two patients who underwent carotid eversion endarterectomy and were followed up by carotid duplex scan sonography for 14 months were studied. Growth factors were measured preoperatively and 4 days after surgery.RESULTS: Pronounced significant increases in both VEGF and PDGF predicted restenosis but only in patients who were homozygous for the normal MBL2 genotype. In this group, the adjusted odds ratios of restenosis at 14 months in patients with high versus low early VEGF and PDGF increases were 27.73 (2.42 to 317.26) and 9.23 (1.45 to 58.70), respectively.CONCLUSIONS: These findings indicate that the development of restenosis depends on both complement activation regulated by the MBL2 gene and pathologic processes leading to enhanced production of VEGF and PDGF during the very early postoperative period.
KW - Aged
KW - Carotid Arteries/pathology
KW - Carotid Stenosis/blood
KW - Complement System Proteins/metabolism
KW - DNA Mutational Analysis
KW - Endarterectomy, Carotid/statistics & numerical data
KW - Epidermal Growth Factor/blood
KW - Female
KW - Genetic Markers/physiology
KW - Genetic Predisposition to Disease/genetics
KW - Genetic Testing
KW - Genotype
KW - Graft Occlusion, Vascular/blood
KW - Humans
KW - Male
KW - Mannose-Binding Lectin/genetics
KW - Middle Aged
KW - Platelet-Derived Growth Factor/metabolism
KW - Prospective Studies
KW - Up-Regulation/physiology
KW - Vascular Endothelial Growth Factor A/blood
U2 - 10.1161/STROKEAHA.106.475954
DO - 10.1161/STROKEAHA.106.475954
M3 - Journal article
C2 - 17626901
SN - 0039-2499
VL - 38
SP - 2247
EP - 2253
JO - Stroke
JF - Stroke
IS - 8
ER -