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矿物质代谢紊乱与慢性肾脏病进展的关联

Association of disorders in mineral metabolism with progression of chronic kidney disease.

作者信息

Schwarz Stephan, Trivedi Bhairvi K, Kalantar-Zadeh Kamyar, Kovesdy Csaba P

机构信息

Department of Internal Medicine, Salem VA Medical Center, 1970 Roanoke Boulevard, Salem, VA 24153, USA.

出版信息

Clin J Am Soc Nephrol. 2006 Jul;1(4):825-31. doi: 10.2215/CJN.02101205. Epub 2006 May 17.


DOI:10.2215/CJN.02101205
PMID:17699293
Abstract

Abnormalities of mineral metabolism are associated with increased mortality in patients with ESRD, but their effects in predialysis chronic kidney disease (CKD) are less well characterized. In this study, the associations between levels of serum phosphorus, calcium, and calcium-phosphorus product and progression of CKD were examined. Historical data were collected on 985 male US veterans (age 67.4 +/- 10.9; 23.9% black) with CKD stages 1 through 5. Unadjusted and multivariable-adjusted relative risks for progressive CKD (defined as the composite of ESRD or doubling of serum creatinine) were calculated for categories of serum phosphorus, calcium, and calcium-phosphorus product using Cox proportional hazards models. Higher phosphorus was associated with a higher risk for the composite end point (adjusted hazard ratio [HR] [95% confidence interval (CI)] for phosphorus levels 3.3 to 3.8, 3.81 to 4.3, and >4.3 versus <3.3 mg/dl 0.83 [0.54 to 1.27], 1.24 [0.82 to 1.88], and 1.60 [1.06 to 2.41]; P = 0.001 for trend). A 1-mg/dl higher phosphorus level was associated with an adjusted HR (95% CI) of 1.29 (1.12 to 1.48; P < 0.001). Higher calcium-phosphorus product also was associated with higher risk for progressive CKD (adjusted HR [95% CI] for calcium-phosphorus products 30 to 35, 36 to 40, and >40 versus <30 mg2/dl2 0.58 [0.36 to 0.94], 0.87 [0.57 to 1.34], and 1.37 [0.91 to 2.07]; P = 0.002 for trend). A 10-mg2/dl2 higher calcium-phosphorus product was associated with an adjusted HR (95% CI) of 1.29 (1.11 to 1.51; P = 0.001). Lower serum calcium showed a trend toward higher risk for progressive CKD but without statistical significance. Higher serum phosphorus and higher calcium-phosphorus product are associated with progression of CKD.

摘要

矿物质代谢异常与终末期肾病(ESRD)患者死亡率增加相关,但它们在透析前慢性肾脏病(CKD)中的作用尚未得到充分描述。在本研究中,我们检测了血清磷、钙水平及钙磷乘积与CKD进展之间的关联。收集了985名美国男性退伍军人(年龄67.4±10.9岁;23.9%为黑人)CKD 1至5期的历史数据。使用Cox比例风险模型计算血清磷、钙及钙磷乘积各分类下进展性CKD(定义为ESRD或血清肌酐翻倍的复合情况)的未调整及多变量调整相对风险。较高的磷水平与复合终点风险较高相关(磷水平3.3至3.8、3.81至4.3以及>4.3mg/dl相对于<3.3mg/dl时,调整后风险比[HR][95%置信区间(CI)]分别为0.83[0.54至1.27]、1.24[0.82至1.88]以及1.60[1.06至2.41];趋势P = 0.001)。磷水平每升高1mg/dl,调整后HR(95%CI)为1.29(1.12至1.48;P<l0.001)。较高的钙磷乘积也与进展性CKD风险较高相关(钙磷乘积30至35、36至40以及>40mg²/dl²相对于<30mg²/dl²时,调整后HR[95%CI]分别为0.58[0.36至0.94]、0.87[0.57至1.34]以及1.37[0.91至2.07];趋势P = 0.002)。钙磷乘积每升高10mg²/dl²,调整后HR(95%CI)为1.29(1.11至1.51;P = 0.001)。较低的血清钙水平显示进展性CKD风险有升高趋势,但无统计学意义。较高的血清磷水平及较高的钙磷乘积与CKD进展相关。

相似文献

[1]
Association of disorders in mineral metabolism with progression of chronic kidney disease.

Clin J Am Soc Nephrol. 2006-7

[2]
Relationship of phosphorus and calcium-phosphorus product with mortality in CKD.

Am J Kidney Dis. 2005-9

[3]
Relations of serum phosphorus and calcium levels to the incidence of cardiovascular disease in the community.

Arch Intern Med. 2007-5-14

[4]
Mineral metabolism, mortality, and morbidity in maintenance hemodialysis.

J Am Soc Nephrol. 2004-8

[5]
Mortality risk for dialysis patients with different levels of serum calcium, phosphorus, and PTH: the Dialysis Outcomes and Practice Patterns Study (DOPPS).

Am J Kidney Dis. 2008-9

[6]
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Am J Med. 2009-4

[7]
Calcium and phosphorus metabolism in patients who have chronic kidney disease.

Med Clin North Am. 2005-5

[8]
Fibroblast growth factor 23 (FGF23) predicts progression of chronic kidney disease: the Mild to Moderate Kidney Disease (MMKD) Study.

J Am Soc Nephrol. 2007-9

[9]
Proteinuria, chronic kidney disease, and the effect of an angiotensin receptor blocker in addition to an angiotensin-converting enzyme inhibitor in patients with moderate to severe heart failure.

Circulation. 2009-10-20

[10]
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Nephron Clin Pract. 2009

引用本文的文献

[1]
WHEN PHYSIOLOGY MEETS THE BUILT ENVIRONMENT: THE PHOSPHORUS STORY.

Trans Am Clin Climatol Assoc. 2025

[2]
Hyperphosphatemia in Kidney Failure: Pathophysiology, Challenges, and Critical Role of Phosphorus Management.

Nutrients. 2025-5-5

[3]
Simultaneous Measurement of Calciprotein Particles with Different Assays and Clinical Outcomes in CKD.

Kidney360. 2025-4-1

[4]
The true cost of phosphate control in chronic kidney disease.

Clin Kidney J. 2025-3-13

[5]
Tight Phosphate Control in ESKD Patients Is Warranted: PRO.

Kidney360. 2024-12-13

[6]
Association of hyperphosphatemia with renal prognosis in patients with autosomal dominant polycystic kidney disease.

Clin Exp Nephrol. 2025-1

[7]
High Protein Diets and Glomerular Hyperfiltration in Athletes and Bodybuilders: Is Chronic Kidney Disease the Real Finish Line?

Sports Med. 2024-10

[8]
The Combined Effects of the Most Important Dietary Patterns on the Incidence and Prevalence of Chronic Renal Failure: Results from the US National Health and Nutrition Examination Survey and Mendelian Analyses.

Nutrients. 2024-7-12

[9]
Correlation between soluble klotho and chronic kidney disease-mineral and bone disorder in chronic kidney disease: a meta-analysis.

Sci Rep. 2024-2-23

[10]
Identifying individuals at risk of needing CKD associated medications in a European kidney disease cohort.

BMC Nephrol. 2024-2-20

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