Association of serum phosphate with vascular and valvular calcification in moderate CKD
- PMID: 19073826
- PMCID: PMC2637048
- DOI: 10.1681/ASN.2008040349
Association of serum phosphate with vascular and valvular calcification in moderate CKD
Abstract
Within the normal range, higher serum phosphate concentrations are associated with cardiovascular events and mortality in individuals with chronic kidney disease (CKD) and in those with normal kidney function. Experimental models suggest that phosphate has a direct calcifying effect on vascular smooth muscle. We examined associations of serum phosphate concentrations with vascular and valvular calcification in 439 participants from the Multi-Ethnic Study of Atherosclerosis who had moderate CKD and no clinical cardiovascular disease. Serum phosphate concentrations were within the normal range (2.5 to 4.5 mg/dl) in 95% of study participants. The prevalence of calcification in the coronary arteries, descending thoracic aorta, aortic valve, and mitral valve was 67, 49, 25, and 20%, respectively, measured by electron-beam or multi-detector row computed tomography. After adjustment for demographics and estimated GFR, each 1-mg/dl increment in serum phosphate concentration was associated with a 21% (P = 0.002), 33% (P = 0.001), 25% (P = 0.16), and 62% (P = 0.007) greater prevalence of coronary artery, thoracic, aortic valve, and mitral valve calcification, respectively. Adjustment for traditional risk factors for atherosclerosis, parathyroid hormone, or 1,25-dihydroxyvitamin D levels did not alter these associations. In conclusion, higher serum phosphate concentrations, although still within the normal range, are associated with a greater prevalence of vascular and valvular calcification in people with moderate CKD. It remains to be determined whether lowering phosphate concentrations will impact calcification risk in the setting of kidney disease.
Figures
Similar articles
-
Aortic Calcification and Arterial Stiffness Burden in a Chronic Kidney Disease Cohort with High Cardiovascular Risk: Baseline Characteristics of the Impact of Phosphate Reduction On Vascular End-Points in Chronic Kidney Disease Trial.Am J Nephrol. 2020;51(3):201-215. doi: 10.1159/000505717. Epub 2020 Feb 5. Am J Nephrol. 2020. PMID: 32023606 Clinical Trial.
-
Association of serum phosphate levels with aortic valve sclerosis and annular calcification: the cardiovascular health study.J Am Coll Cardiol. 2011 Jul 12;58(3):291-7. doi: 10.1016/j.jacc.2010.11.073. J Am Coll Cardiol. 2011. PMID: 21737022 Free PMC article.
-
A Randomized Trial on the Effect of Phosphate Reduction on Vascular End Points in CKD (IMPROVE-CKD).J Am Soc Nephrol. 2020 Nov;31(11):2653-2666. doi: 10.1681/ASN.2020040411. Epub 2020 Sep 11. J Am Soc Nephrol. 2020. PMID: 32917784 Free PMC article. Clinical Trial.
-
Vascular calcification in chronic kidney disease.J Bone Miner Metab. 2006;24(2):176-81. doi: 10.1007/s00774-005-0668-6. J Bone Miner Metab. 2006. PMID: 16502129 Review.
-
FGF23: a mature renal and cardiovascular risk factor?Blood Purif. 2013;36(1):52-7. doi: 10.1159/000351001. Epub 2013 May 25. Blood Purif. 2013. PMID: 23735695 Review.
Cited by
-
Association of circulating fibroblast growth factor-23 with renal phosphate excretion among hemodialysis patients with residual renal function.Clin J Am Soc Nephrol. 2013 Jan;8(1):116-25. doi: 10.2215/CJN.00230112. Epub 2012 Oct 18. Clin J Am Soc Nephrol. 2013. PMID: 23085728 Free PMC article.
-
Hyperphosphatemia and Cardiovascular Disease.Front Cell Dev Biol. 2021 Mar 4;9:644363. doi: 10.3389/fcell.2021.644363. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33748139 Free PMC article. Review.
-
Approach to cardiovascular disease prevention in patients with chronic kidney disease.Curr Treat Options Cardiovasc Med. 2012 Aug;14(4):391-413. doi: 10.1007/s11936-012-0189-2. Curr Treat Options Cardiovasc Med. 2012. PMID: 22660924
-
Chapter 5: Referral to specialists and models of care.Kidney Int Suppl (2011). 2013 Jan;3(1):112-119. doi: 10.1038/kisup.2012.68. Kidney Int Suppl (2011). 2013. PMID: 25599001 Free PMC article. No abstract available.
-
Predictive role of cardiac valvular calcification in all-cause mortality of Chinese initial haemodialysis patients: a follow-up study of 4 years.BMC Nephrol. 2023 Feb 16;24(1):37. doi: 10.1186/s12882-023-03076-7. BMC Nephrol. 2023. PMID: 36792978 Free PMC article.
References
-
- Dhingra R, Sullivan LM, Fox CS, Wang TJ, D'Agostino RB Sr, Gaziano JM, Vasan RS: Relations of serum phosphorus and calcium levels to the incidence of cardiovascular disease in the community. Arch Intern Med 167: 879–885, 2007 - PubMed
-
- Kestenbaum B, Sampson JN, Rudser KD, Patterson DJ, Seliger SL, Young B, Sherrard DJ, Andress DL: Serum phosphate levels and mortality risk among people with chronic kidney disease. J Am Soc Nephrol 16: 520–528, 2005 - PubMed
-
- Menon V, Greene T, Pereira AA, Wang X, Beck GJ, Kusek JW, Collins AJ, Levey AS, Sarnak MJ: Relationship of phosphorus and calcium-phosphorus product with mortality in CKD. Am J Kidney Dis 46: 455–463, 2005 - PubMed
-
- Tonelli M, Isles C, Craven T, Tonkin A, Pfeffer MA, Shepherd J, Sacks FM, Furberg C, Cobbe SM, Simes J, West M, Packard C, Curhan GC: Effect of pravastatin on rate of kidney function loss in people with or at risk for coronary disease. Circulation 112: 171–178, 2005 - PubMed
-
- Chen NX, O'Neill KD, Duan D, Moe SM: Phosphorus and uremic serum up-regulate osteopontin expression in vascular smooth muscle cells. Kidney Int 62: 1724–1731, 2002 - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- R01-HL-071739/HL/NHLBI NIH HHS/United States
- N01 HC095169/HL/NHLBI NIH HHS/United States
- N01-HC-95159/HC/NHLBI NIH HHS/United States
- N01-HC-95165/HC/NHLBI NIH HHS/United States
- N01 HC095159/HL/NHLBI NIH HHS/United States
- R01-HL-072403/HL/NHLBI NIH HHS/United States
- N01-HC-95161/HC/NHLBI NIH HHS/United States
- N01 HC095166/HL/NHLBI NIH HHS/United States
- N01-HC-95166/HC/NHLBI NIH HHS/United States
- K23 DK063274/DK/NIDDK NIH HHS/United States
- R01 HL071739/HL/NHLBI NIH HHS/United States
- N01-HC-95162/HC/NHLBI NIH HHS/United States
- R01 HL072403/HL/NHLBI NIH HHS/United States
- N01-HC-95163/HC/NHLBI NIH HHS/United States
- N01-HC-95169/HC/NHLBI NIH HHS/United States
- N01-HC-95164/HC/NHLBI NIH HHS/United States
- N01-HC-95160/HC/NHLBI NIH HHS/United States
- K23 DK63274-01/DK/NIDDK NIH HHS/United States
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases