BACKGROUND: Two endophenotypes of arterial calcification, calcification on arterial wall and calcification in atherosclerotic plaques, are associated with different types of cardiovascular events. Mgp-deficient mice showed matrix Gla protein (MGP) is strongly associated with calcification on arterial wall without atherosclerotic plaques, and MGP variants were not significantly associated with myocardial infarction. MGP may play different roles in the 2 endophenotypes. METHODS AND RESULTS: We analyzed the associations of MGP variants rs4236, rs1800801, and rs1800802 with the 2 endophenotypes determined by multidetector computed tomography angiography. A total of 585 with calcification on coronary artery wall, 675 with calcification in coronary atherosclerotic plaques, 454 with calcification on aortic wall, and 725 controls were enrolled. After Bonferroni correction, rs4236 and rs1800801 were still associated with calcification on arterial wall, the odds ratios were 0.708 (95% confidence interval, 0.540-0.928) for rs4236 and 0.652 (95% confidence interval, 0.479-0.888) for rs1800801 in coronary artery wall calcification, and 0.699 (95% confidence interval, 0.525-0.931) for rs4236 and 0.650 (95% confidence interval, 0.467-0.905) for rs1800801 in aortic wall calcification, respectively. The variants were correlated with calcification severity by ln(CAC Agatston score+1) in coronary artery wall calcification but not in atherosclerotic plaque calcification. In accordance with their associations with calcification on arterial wall, rs4236C and rs1800801A were associated with higher MGP plasma levels, whereas rs1800802C was associated with lower MGP levels in normal controls. Because of the role of calcification in plaque vulnerability, their associations with acute myocardial infarction were also determined in 771 controls and 752 patients, no association was found. CONCLUSIONS: MGP genetic variants showed association with calcification on arterial wall but not with calcification in atherosclerotic plaques.
BACKGROUND: Two endophenotypes of arterial calcification, calcification on arterial wall and calcification in atherosclerotic plaques, are associated with different types of cardiovascular events. Mgp-deficient mice showed matrix Gla protein (MGP) is strongly associated with calcification on arterial wall without atherosclerotic plaques, and MGP variants were not significantly associated with myocardial infarction. MGP may play different roles in the 2 endophenotypes. METHODS AND RESULTS: We analyzed the associations of MGP variants rs4236, rs1800801, and rs1800802 with the 2 endophenotypes determined by multidetector computed tomography angiography. A total of 585 with calcification on coronary artery wall, 675 with calcification in coronary atherosclerotic plaques, 454 with calcification on aortic wall, and 725 controls were enrolled. After Bonferroni correction, rs4236 and rs1800801 were still associated with calcification on arterial wall, the odds ratios were 0.708 (95% confidence interval, 0.540-0.928) for rs4236 and 0.652 (95% confidence interval, 0.479-0.888) for rs1800801 in coronary artery wall calcification, and 0.699 (95% confidence interval, 0.525-0.931) for rs4236 and 0.650 (95% confidence interval, 0.467-0.905) for rs1800801 in aortic wall calcification, respectively. The variants were correlated with calcification severity by ln(CAC Agatston score+1) in coronary artery wall calcification but not in atherosclerotic plaque calcification. In accordance with their associations with calcification on arterial wall, rs4236C and rs1800801A were associated with higher MGP plasma levels, whereas rs1800802C was associated with lower MGP levels in normal controls. Because of the role of calcification in plaque vulnerability, their associations with acute myocardial infarction were also determined in 771 controls and 752 patients, no association was found. CONCLUSIONS:MGP genetic variants showed association with calcification on arterial wall but not with calcification in atherosclerotic plaques.
Authors: O Mayer; J Seidlerová; P Wohlfahrt; J Filipovský; J Vaněk; R Cífková; J Windrichová; O Topolčan; M H J Knapen; N E A Drummen; C Vermeer Journal: J Hum Hypertens Date: 2015-05-28 Impact factor: 3.012
Authors: Rajeev Malhotra; Christopher J Nicholson; Dongyu Wang; Vijeta Bhambhani; Samantha Paniagua; Charles Slocum; Haakon H Sigurslid; Christian L Lino Cardenas; Rebecca Li; Sophie L Boerboom; Yin-Ching Chen; Shih-Jen Hwang; Chen Yao; Fumito Ichinose; Donald B Bloch; Mark E Lindsay; Gregory D Lewis; Jayashri R Aragam; Udo Hoffmann; Gary F Mitchell; Naomi M Hamburg; Ramachandran S Vasan; Emelia J Benjamin; Martin G Larson; Warren M Zapol; Susan Cheng; Jason D Roh; Christopher J O'Donnell; Christopher Nguyen; Daniel Levy; Jennifer E Ho Journal: Arterioscler Thromb Vasc Biol Date: 2021-11-23 Impact factor: 8.311
Authors: Caitlin O'Rourke; Georgia Shelton; Joshua D Hutcheson; Megan F Burke; Trejeeve Martyn; Timothy E Thayer; Hannah R Shakartzi; Mary D Buswell; Robert E Tainsh; Binglan Yu; Aranya Bagchi; David K Rhee; Connie Wu; Matthias Derwall; Emmanuel S Buys; Paul B Yu; Kenneth D Bloch; Elena Aikawa; Donald B Bloch; Rajeev Malhotra Journal: J Vis Exp Date: 2016-05-31 Impact factor: 1.355