BACKGROUND: The very high cardiovascular (CV) mortality and morbidity rates in hemodialysis (HD) patients are greatly related to atherosclerosis. CCN2 (connective tissue growth factor/CTGF) is a profibrotic factor that is secreted by endothelial cells, involved in atherogenesis, promoting fibroblast proliferation and matrix production. CCN2 protein is significantly increased in complicated fibrous plaques and enhances monocyte migration into atherosclerotic lesions. The aim of this study was to investigate a possible association between CCN2 gene polymorphism and CV morbidity and mortality in HD patients. METHODS: 98 HD patients, followed for 24 months, were genotyped for the common polymorphism on the CCN2 gene (G-945C). HD patient characteristics were: age 64 ± 13 years, males 64%, diabetes 24%, hypertension 62%, smokers 38%, dyslipidemia 28%, all undergoing standard HD three times weekly. RESULTS: All-cause mortality was not associated with CCN2 polymorphism (G-945C). In contrast, however, the GG genotype was strongly associated with CV mortality: OR 13 (1.49-155), p = 0.0048. Interestingly, the GG genotype was also greatly associated with the serious CV events of stroke and myocardial infarction in surviving HD patients: OR 13.3 (2.5-87.08), p = 0.0001. CONCLUSIONS: We demonstrate for the first time that CCN2 gene polymorphism is a prognostic risk factor for CV morbidity and mortality in HD patients. These data may have important implications for better understanding the link between accelerated atherosclerosis and increased mortality in HD population.
BACKGROUND: The very high cardiovascular (CV) mortality and morbidity rates in hemodialysis (HD) patients are greatly related to atherosclerosis. CCN2 (connective tissue growth factor/CTGF) is a profibrotic factor that is secreted by endothelial cells, involved in atherogenesis, promoting fibroblast proliferation and matrix production. CCN2 protein is significantly increased in complicated fibrous plaques and enhances monocyte migration into atherosclerotic lesions. The aim of this study was to investigate a possible association between CCN2 gene polymorphism and CV morbidity and mortality in HDpatients. METHODS: 98 HDpatients, followed for 24 months, were genotyped for the common polymorphism on the CCN2 gene (G-945C). HDpatient characteristics were: age 64 ± 13 years, males 64%, diabetes 24%, hypertension 62%, smokers 38%, dyslipidemia 28%, all undergoing standard HD three times weekly. RESULTS: All-cause mortality was not associated with CCN2 polymorphism (G-945C). In contrast, however, the GG genotype was strongly associated with CV mortality: OR 13 (1.49-155), p = 0.0048. Interestingly, the GG genotype was also greatly associated with the serious CV events of stroke and myocardial infarction in surviving HDpatients: OR 13.3 (2.5-87.08), p = 0.0001. CONCLUSIONS: We demonstrate for the first time that CCN2 gene polymorphism is a prognostic risk factor for CV morbidity and mortality in HDpatients. These data may have important implications for better understanding the link between accelerated atherosclerosis and increased mortality in HD population.
Authors: Sheila K Patel; Bryan Wai; Richard J Macisaac; Sharon Grant; Elena Velkoska; Michelle Ord; Sianna Panagiotopoulos; George Jerums; Piyush M Srivastava; Louise M Burrell Journal: Cardiovasc Diabetol Date: 2012-04-26 Impact factor: 9.951
Authors: Claire H den Hoedt; Maaike K van Gelder; Muriel P Grooteman; Menso J Nubé; Peter J Blankestijn; Roel Goldschmeding; Robbert Jan Kok; Michiel L Bots; Marinus A van den Dorpel; Karin G F Gerritsen Journal: Toxins (Basel) Date: 2019-05-13 Impact factor: 4.546
Authors: Tonia C Rothuizen; Gurbey Ocak; Jeffrey J W Verschuren; Friedo W Dekker; Ton J Rabelink; J Wouter Jukema; Joris I Rotmans Journal: PLoS One Date: 2015-11-20 Impact factor: 3.240