CLC number: R543.1
On-line Access: 2024-08-27
Received: 2023-10-17
Revision Accepted: 2024-05-08
Crosschecked: 2015-04-09
Cited: 6
Clicked: 4663
Zhen-kun Yang, Chen Ying, Hong-yan Zhao, Yue-hua Fang, Ying Chen, Wei-feng Shen. Mineral metabolism disturbances are associated with the presence and severity of calcific aortic valve disease[J]. Journal of Zhejiang University Science B, 2015, 16(5): 362-369.
@article{title="Mineral metabolism disturbances are associated with the presence and severity of calcific aortic valve disease",
author="Zhen-kun Yang, Chen Ying, Hong-yan Zhao, Yue-hua Fang, Ying Chen, Wei-feng Shen",
journal="Journal of Zhejiang University Science B",
volume="16",
number="5",
pages="362-369",
year="2015",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B1400292"
}
%0 Journal Article
%T Mineral metabolism disturbances are associated with the presence and severity of calcific aortic valve disease
%A Zhen-kun Yang
%A Chen Ying
%A Hong-yan Zhao
%A Yue-hua Fang
%A Ying Chen
%A Wei-feng Shen
%J Journal of Zhejiang University SCIENCE B
%V 16
%N 5
%P 362-369
%@ 1673-1581
%D 2015
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B1400292
TY - JOUR
T1 - Mineral metabolism disturbances are associated with the presence and severity of calcific aortic valve disease
A1 - Zhen-kun Yang
A1 - Chen Ying
A1 - Hong-yan Zhao
A1 - Yue-hua Fang
A1 - Ying Chen
A1 - Wei-feng Shen
J0 - Journal of Zhejiang University Science B
VL - 16
IS - 5
SP - 362
EP - 369
%@ 1673-1581
Y1 - 2015
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.B1400292
Abstract: Objective: We investigated whether disturbance of calcium and phosphate metabolism is associated with the presence and severity of calcific aortic valve disease (CAVD) in patients with normal or mildly impaired renal function. Methods: We measured serum levels of calcium, phosphate, alkaline phosphatase (AKP), intact parathyroid hormone (iPTH), 25-hydroxyvitamin D (25-OHD), and biomarkers of bone turnover in 260 consecutive patients with normal or mildly impaired renal function and aortic valve sclerosis (AVSc) (n=164) or stenosis (AVS) (n=96) and in 164 age- and gender-matched controls. Logistic regression models were used to determine the association of mineral metabolism parameters with the presence and severity of CAVD. Results: Stepwise increases were observed in serum levels of calcium, phosphate, AKP, and iPTH from the control group to patients with AVS, and with reverse changes for 25-OHD levels (all P<0.001). Similarly, osteocalcin, procollagen I N-terminal peptide, and β-isomerized type I collagen C-telopeptide breakdown products were significantly increased stepwise from the control group to patients with AVS (all P<0.001). In patients with AVS, serum levels of iPTH were positively, in contrast 25-OHD levels were negatively, related to trans-aortic peak flow velocity and mean pressure gradient. After adjusting for relevant confounding variables, increased serum levels of calcium, phosphate, AKP, and iPTH and reduced serum levels of 25-OHD were independently associated with the presence and severity of CAVD. Conclusions: This study suggests an association between mineral metabolism disturbance and the presence and severity of CAVD in patients with normal or mildly impaired renal function. Abnormal bone turnover may be a potential mechanism.
[1]ADA (American Diabetes Association), 2010. Standards of medical care in diabetes 2010. Diabetes Care, 33(Suppl. 1):S11-S61.
[2]Akat, K., Borggrefe, M., Kaden, J.J., 2009. Aortic valve calcification: basic science to clinical practice. Heart, 95(8):616-623.
[3]Akat, K., Kaden, J.J., Schmitz, F., et al., 2010. Calcium metabolism in adults with severe aortic valve stenosis and preserved renal function. Am. J. Cardiol., 105(6):862-864.
[4]Aksoy, O., Cam, A., Goel, S.S., et al., 2012. Do bisphosphonates slow the progression of aortic stenosis? J. Am. Coll. Cardiol., 59(16):1452-1459.
[5]Aksoy, Y., Yagmur, C., Tekin, G.O., et al., 2005. Aortic valve calcification: association with bone mineral density and cardiovascular risk factors. Coron. Artery Dis., 16(6):379-383.
[6]Freeman, R.V., Otto, C.M., 2005. Spectrum of calcific aortic valve disease: pathogenesis, disease progression, and treatment strategies. Circulation, 111(24):3316-3326.
[7]Hekimian, G., Boutten, A., Flamant, M., et al., 2013. Progression of aortic valve stenosis is associated with bone remodeling and secondary hyperparathyroidism in elderly patients—the COFRASA study. Eur. Heart J., 34(25):1915-1922.
[8]Innasimuthu, A.L., Katz, W.E., 2011. Effect of bisphosphonates on the progression of degenerative aortic stenosis. Echocardiography, 28(1):1-7.
[9]Iung, B., Baron, G., Butchart, E.G., et al., 2003. A prospective survey of patients with valvular heart disease in Europe: the Euro Heart Survey on valvular heart disease. Eur. Heart J., 24(13):1231-1243.
[10]Iwata, S., Hyodo, E., Yanagi, S., et al., 2013. Parathyroid hormone and systolic blood pressure accelerate the progression of aortic valve stenosis in chronic hemodialysis patients. Int. J. Cardiol., 163(3):256-259.
[11]Kume, T., Kawamoto, T., Akasaka, T., et al., 2006. Rate of progression of valvular aortic stenosis in patients undergoing dialysis. J. Am. Soc. Echocardiogr., 19(7):914-918.
[12]Linefsky, J.P., O'Brien, K.D., Katz, R., et al., 2011. Association of serum phosphate levels with aortic valve sclerosis and annular calcification: the Cardiovascular Health Study. J. Am. Coll. Cardiol., 58(3):291-297.
[13]Linhartová, K., Veselka, J., Sterbáková, G., et al., 2008. Parathyroid hormone and vitamin D levels are independently associated with calcific aortic stenosis. Circ. J., 72(2):245-250.
[14]Mills, W.R., Einstadter, D., Finkelhor, R.S., 2004. Relation of calcium-phosphorus production to the severity of aortic stenosis in patients with normal renal function. Am. J. Cardiol., 94(9):1196-1198.
[15]Nagy, E., Eriksson, P., Yousry, M., et al., 2013. Valvular osteoclasts in calcification and aortic valve stenosis severity. Int. J. Cardiol., 168(3):2264-2271.
[16]O'Neill, W.C., 2007. The fallacy of the calcium-phosphorus product. Kidney Int., 72(7):792-796.
[17]Parolari, A., Loardi, C., Mussoni, L., et al., 2009. Nonrheumatic calcific aortic stenosis: an overview from basic science to pharmacological prevention. Eur. J. Cardiothorac. Surg., 35(3):493-504.
[18]Parolari, A., Tremoli, E., Cavallotti, L., et al., 2011. Do statins improve outcomes and delay the progression of non-rheumatic calcific aortic stenosis? Heart, 97(7):523-529.
[19]Rajamannan, N.M., 2009. Calcific aortic stenosis: lessons learned from experimental and clinical studies. Arterioscler. Thromb. Vasc. Biol., 29(2):162-168.
[20]Rajamannan, N.M., Evans, F.J., Aikawa, E., et al., 2011. Calcific aortic valve disease: not simply a degenerative process: a review and agenda for research from the national heart and lung and blood institute aortic stenosis working group. Circulation, 124(16):1783-1791.
[21]Skolnick, A.H., Osranek, M., Formica, P., et al., 2009. Osteoporosis treatment and progression of aortic stenosis. Am. J. Cardiol., 104(1):122-124.
[22]Stefenelli, T., Mayr, H., Bergler-Klein, J., et al., 1993. Primary hyperparathyroidism: incidence of cardiac abnormalities and partial reversibility after successful parathyroidectomy. Am. J. Med., 95(2):197-202.
[23]Sterbakova, G., Vyskocil, V., Linhartova, K., 2010. Bisphosphonates in calcific aortic stenosis: association with slower progression in mild disease—a pilot retrospective study. Cardiology, 117(3):184-189.
[24]Strickberger, S.A., Schulman, S.P., Hutchins, G.M., 1987. Association of Paget’s disease of bone with calcific aortic valve disease. Am. J. Med., 82(5):953-956.
[25]Teo, K.K., Corsi, D.J., Tam, J.W., et al., 2011. Lipid lowering on progression of mild to moderate aortic stenosis: meta-analysis of the randomized placebo-controlled clinical trials on 2344 patients. Can. J. Cardiol., 27(6):800-808.
[26]Yetkin, E., Waltenberger, J., 2009. Molecular and cellular mechanisms of aortic stenosis. Int. J. Cardiol., 135(1):4-13.
Open peer comments: Debate/Discuss/Question/Opinion
<1>