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Estimating glomerular filtration rate in a population-based study.在一项基于人群的研究中估算肾小球滤过率。
Vasc Health Risk Manag. 2010 Aug 9;6:619-27. doi: 10.2147/vhrm.s11269.
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Impact of poverty on serum phosphate concentrations in the Third National Health and Nutrition Examination Survey.第三国家健康与营养调查中贫困对血清磷酸盐浓度的影响。
J Ren Nutr. 2011 Mar;21(2):140-8. doi: 10.1053/j.jrn.2010.03.001. Epub 2010 May 26.
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Coronary calcification in patients with chronic kidney disease and coronary artery disease.慢性肾脏病合并冠状动脉疾病患者的冠状动脉钙化。
Clin J Am Soc Nephrol. 2009 Dec;4(12):1892-900. doi: 10.2215/CJN.04320709. Epub 2009 Oct 15.
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Defining incident chronic kidney disease in the research setting: The ARIC Study.在研究背景下定义新发慢性肾脏病:动脉粥样硬化风险社区研究(ARIC研究)
Am J Epidemiol. 2009 Aug 15;170(4):414-24. doi: 10.1093/aje/kwp151. Epub 2009 Jun 17.
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Is lowering phosphate exposure the key to preventing arterial stiffening with age?降低磷酸盐暴露是预防动脉随年龄增长而硬化的关键吗?
Heart. 2009 Nov;95(21):1770-2. doi: 10.1136/hrt.2008.162594. Epub 2009 Mar 24.
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Metabolic abnormalities are present in adults with elevated serum cystatin C.血清胱抑素C升高的成年人存在代谢异常。
Kidney Int. 2009 Jul;76(1):81-8. doi: 10.1038/ki.2009.76. Epub 2009 Mar 18.
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Mechanisms of vascular calcification in chronic kidney disease.慢性肾脏病中血管钙化的机制
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A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis.人类KLOTHO基因的纯合错义突变会导致严重的肿瘤性钙化。
J Clin Invest. 2007 Sep;117(9):2684-91. doi: 10.1172/JCI31330.
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Association of disorders in mineral metabolism with progression of chronic kidney disease.矿物质代谢紊乱与慢性肾脏病进展的关联
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Phosphorus homeostasis in normal health and in chronic kidney disease patients with special emphasis on dietary phosphorus intake.正常健康状态及慢性肾脏病患者的磷稳态,特别强调膳食磷摄入量。
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血清磷预测慢性肾脏病和终末期肾病的发生。

Serum phosphorus predicts incident chronic kidney disease and end-stage renal disease.

机构信息

National Heart, Lung and Blood Institute’s Framingham Heart Study and the Center for Population Studies, Framingham, MA, USA.

出版信息

Nephrol Dial Transplant. 2011 Sep;26(9):2885-90. doi: 10.1093/ndt/gfq808. Epub 2011 Feb 3.

DOI:10.1093/ndt/gfq808
PMID:21292817
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3175050/
Abstract

BACKGROUND

Elevations in serum phosphorus are associated with renal decline in animal models and progression of established chronic kidney disease (CKD) in human observational studies. We examined whether serum phosphorus levels increase the risk of incident CKD or end-stage renal disease (ESRD) in two population-based prospective cohort studies.

METHODS

Overall, 2269 participants free of CKD [estimated glomerular filtration rate (eGFR) <60 mL/min/1.73(2)] from the Framingham Heart Study (FHS; mean age 42 years; 53% women) and 13,372 participants from the Third National Health and Nutrition Examination Survey (NHANES III; mean age 44.3 years, 52% women) contributed to the present study. In the FHS, we evaluated the relationship between baseline phosphorus category (<2.5 mg/dL, 2.5-3.49 mg/dL, 3.5-3.99 mg/dL and ≥4 mg/dL) and incident CKD (n = 267). In NHANES, we examined the relationship between phosphorus below and above 4 mg/dL in relation to incident ESRD (n = 65).

RESULTS

FHS participants in the highest phosphorus category had an increased risk of CKD [odds ratio 2.14; 95% confidence interval (CI), 1.07-4.28; P = 0.03] in multivariable-adjusted models when compared to the referent group (2.5-3.49 mg/dL). Similarly, NHANES III participants with phosphorus levels ≥4 mg/dL demonstrated an increased risk of incident ESRD compared to those <4 mg/dL (relative risk 1.90; 95% CI 1.03-3.53; P = 0.04).

CONCLUSIONS

In prospective studies of the general population, serum phosphorus levels in the upper-normal range were associated with a doubling in the risk of developing incident CKD and ESRD.

摘要

背景

血清磷升高与动物模型中的肾功能下降以及人类观察性研究中慢性肾脏病(CKD)的进展相关。我们在两项基于人群的前瞻性队列研究中,检验了血清磷水平是否会增加新发 CKD 或终末期肾病(ESRD)的风险。

方法

弗雷明汉心脏研究(FHS)中 2269 名无 CKD(估算肾小球滤过率[eGFR]<60 mL/min/1.73(2))的参与者(平均年龄 42 岁,53%为女性)和第三次全国健康和营养检查调查(NHANES III)中 13372 名参与者(平均年龄 44.3 岁,52%为女性)参与了本研究。在 FHS 中,我们评估了基线磷类别(<2.5 mg/dL、2.5-3.49 mg/dL、3.5-3.99 mg/dL 和≥4 mg/dL)与新发 CKD(n=267)之间的关系。在 NHANES 中,我们检验了磷水平<4 mg/dL 与磷水平>4 mg/dL 与新发 ESRD(n=65)之间的关系。

结果

与参考组(2.5-3.49 mg/dL)相比,FHS 中磷水平最高组的参与者发生 CKD 的风险增加(比值比 2.14;95%置信区间[CI],1.07-4.28;P=0.03)。同样,NHANES III 中磷水平≥4 mg/dL 的参与者发生新发 ESRD 的风险也高于磷水平<4 mg/dL 的参与者(相对风险 1.90;95%CI 1.03-3.53;P=0.04)。

结论

在普通人群的前瞻性研究中,血清磷水平处于正常高值范围与新发 CKD 和 ESRD 风险增加两倍相关。