Suppr超能文献

晚期慢性肾脏病矿物质代谢标志物的种族差异。

Racial differences in markers of mineral metabolism in advanced chronic kidney disease.

机构信息

Division of Renal Diseases and Hypertension, University of Colorado School of Medicine, Aurora, USA.

出版信息

Clin J Am Soc Nephrol. 2012 Apr;7(4):640-7. doi: 10.2215/CJN.07020711. Epub 2012 Mar 1.

Abstract

BACKGROUND AND OBJECTIVES

This study examined differences in the concentration of markers of mineral metabolism across race in patients with advanced CKD not requiring dialysis and ESRD.

DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Concentrations of 25-hydroxyvitamin D (25(OH)D), 1,25-dihydroxyvitamin D (1,25(OH)(2)D), intact parathyroid hormone (iPTH), and fibroblast growth factor 23 (FGF-23) were measured in stored plasma samples of 1497 patients with advanced CKD not yet on dialysis and ESRD who participated in the Homocysteine in Kidney and End Stage Renal Disease study. Linear regression models were used to examine the relationship between race and 25(OH)D, 1,25(OH)(2)D, iPTH, and FGF-23 concentrations.

RESULTS

Non-Hispanic white patients comprised 58% of the cohort, whereas non-Hispanic blacks comprised 42%. Median (interquartile range) FGF-23 concentrations were lower in blacks compared with whites with CKD (323 [181-655] versus 431 [232-1026] RU/ml; P<0.001) but not in ESRD. In adjusted linear regression models, blacks with CKD not requiring dialysis had significantly lower plasma FGF-23 concentrations (difference, -159; 95% confidence interval, -205 to -106; P<0.001) compared with whites, independent of plasma 25(OH)D, 1,25(OH)(2)D, and iPTH concentrations. This difference was not observed in the ESRD group. The magnitude of correlation for the relationships between 1,25(OH)(2)D with iPTH, FGF-23 with 1,25(OH)(2)D, and FGF-23 with iPTH were stronger among blacks than whites with CKD not requiring dialysis.

CONCLUSIONS

In advanced CKD not requiring dialysis, blacks have lower FGF-23 concentrations than whites. Blacks with CKD and ESRD have lower 25(OH)D and higher iPTH compared with whites, independent of FGF-23 concentrations.

摘要

背景和目的

本研究旨在比较不同种族的晚期慢性肾脏病(CKD)未透析和终末期肾病(ESRD)患者的矿物质代谢标志物浓度差异。

设计、地点、参与者和测量:在参加同型半胱氨酸在肾脏和终末期肾病研究的 1497 例晚期 CKD 未透析和 ESRD 患者的储存血浆样本中,测量了 25-羟维生素 D(25(OH)D)、1,25-二羟维生素 D(1,25(OH)(2)D)、完整甲状旁腺激素(iPTH)和成纤维细胞生长因子 23(FGF-23)的浓度。线性回归模型用于研究种族与 25(OH)D、1,25(OH)(2)D、iPTH 和 FGF-23 浓度之间的关系。

结果

非西班牙裔白人患者占队列的 58%,而非西班牙裔黑人患者占 42%。与 CKD 白人患者相比,黑人患者的 FGF-23 浓度中位数(四分位距)较低(323 [181-655] 与 431 [232-1026] RU/ml;P<0.001),但在 ESRD 患者中则不然。在调整后的线性回归模型中,与白人患者相比,不需要透析的 CKD 黑人患者的血浆 FGF-23 浓度显著降低(差异,-159;95%置信区间,-205 至-106;P<0.001),而与血浆 25(OH)D、1,25(OH)(2)D 和 iPTH 浓度无关。在 ESRD 组中未观察到这种差异。在不需要透析的 CKD 患者中,1,25(OH)(2)D 与 iPTH、FGF-23 与 1,25(OH)(2)D、FGF-23 与 iPTH 之间的关系,黑人的相关性强度强于白人。

结论

在不需要透析的晚期 CKD 中,黑人的 FGF-23 浓度低于白人。与白人患者相比,CKD 和 ESRD 的黑人患者的 25(OH)D 水平较低,iPTH 水平较高,而 FGF-23 浓度则不受影响。

相似文献

1
Racial differences in markers of mineral metabolism in advanced chronic kidney disease.
Clin J Am Soc Nephrol. 2012 Apr;7(4):640-7. doi: 10.2215/CJN.07020711. Epub 2012 Mar 1.
4
Effect of Cinacalcet and Vitamin D Analogs on Fibroblast Growth Factor-23 during the Treatment of Secondary Hyperparathyroidism.
Clin J Am Soc Nephrol. 2015 Jun 5;10(6):1021-30. doi: 10.2215/CJN.03270314. Epub 2015 Apr 14.
8
Differences in 25-Hydroxyvitamin D Clearance by eGFR and Race: A Pharmacokinetic Study.
J Am Soc Nephrol. 2021 Jan;32(1):188-198. doi: 10.1681/ASN.2020050625. Epub 2020 Oct 28.
9
25-Hydroxyvitamin D, parathyroid hormone, and mortality in black and white older adults: the health ABC study.
J Clin Endocrinol Metab. 2012 Nov;97(11):4156-65. doi: 10.1210/jc.2012-1551. Epub 2012 Aug 31.
10
Vitamin D metabolites and bone mineral density: The multi-ethnic study of atherosclerosis.
Bone. 2015 Sep;78:186-93. doi: 10.1016/j.bone.2015.05.008. Epub 2015 May 11.

引用本文的文献

1
Precision Renal Osteodystrophy: What's Race Got to do With It?
Curr Osteoporos Rep. 2024 Dec 2;23(1):5. doi: 10.1007/s11914-024-00894-y.
2
Estimating the global prevalence of secondary hyperparathyroidism in patients with chronic kidney disease.
Front Endocrinol (Lausanne). 2024 Jun 21;15:1400891. doi: 10.3389/fendo.2024.1400891. eCollection 2024.
3
Genetic Variants Associated With Mineral Metabolism Traits in Chronic Kidney Disease.
J Clin Endocrinol Metab. 2022 Aug 18;107(9):e3866-e3876. doi: 10.1210/clinem/dgac318.
4
Fibroblast growth factor 23-Klotho and hypertension: experimental and clinical mechanisms.
Pediatr Nephrol. 2021 Oct;36(10):3007-3022. doi: 10.1007/s00467-020-04843-6. Epub 2020 Nov 23.
5
Race and Ethnicity Predict Bone Markers and Fracture in Pediatric Patients With Chronic Kidney Disease.
J Bone Miner Res. 2021 Feb;36(2):298-304. doi: 10.1002/jbmr.4182. Epub 2020 Oct 23.
6
Pharmacological interventions for heart failure in people with chronic kidney disease.
Cochrane Database Syst Rev. 2020 Feb 27;2(2):CD012466. doi: 10.1002/14651858.CD012466.pub2.
7
Impact of Race on the Association of Mineral Metabolism With Heart Failure: the Multi-Ethnic Study of Atherosclerosis.
J Clin Endocrinol Metab. 2020 Apr 1;105(4):e1144-51. doi: 10.1210/clinem/dgz218.
10
The Role of Vitamin D in CKD Stages 3 to 4: Report of a Scientific Workshop Sponsored by the National Kidney Foundation.
Am J Kidney Dis. 2018 Dec;72(6):834-845. doi: 10.1053/j.ajkd.2018.06.031. Epub 2018 Oct 5.

本文引用的文献

1
Fibroblast growth factor 23 is elevated before parathyroid hormone and phosphate in chronic kidney disease.
Kidney Int. 2011 Jun;79(12):1370-8. doi: 10.1038/ki.2011.47. Epub 2011 Mar 9.
3
Chronic kidney disease, hypovitaminosis D, and mortality in the United States.
Kidney Int. 2009 Nov;76(9):977-83. doi: 10.1038/ki.2009.288. Epub 2009 Aug 5.
5
Fibroblast growth factor 23 and left ventricular hypertrophy in chronic kidney disease.
Circulation. 2009 May 19;119(19):2545-52. doi: 10.1161/CIRCULATIONAHA.108.844506. Epub 2009 May 4.
7
Association of serum intact parathyroid hormone with lower estimated glomerular filtration rate.
Clin J Am Soc Nephrol. 2009 Jan;4(1):186-94. doi: 10.2215/CJN.03050608. Epub 2008 Nov 19.
8
Fibroblast growth factor 23 and mortality among patients undergoing hemodialysis.
N Engl J Med. 2008 Aug 7;359(6):584-92. doi: 10.1056/NEJMoa0706130.
9
Disordered mineral metabolism in hemodialysis patients: an analysis of cumulative effects in the Hemodialysis (HEMO) Study.
Am J Kidney Dis. 2008 Sep;52(3):531-40. doi: 10.1053/j.ajkd.2008.05.020. Epub 2008 Jul 26.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验