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Safety and efficacy of ferric citrate in patients with nondialysis-dependent chronic kidney disease.柠檬酸铁对非透析依赖性慢性肾脏病患者的安全性和有效性。
PLoS One. 2017 Nov 29;12(11):e0188712. doi: 10.1371/journal.pone.0188712. eCollection 2017.
2
FGF23 and Left Ventricular Hypertrophy in Children with CKD.成纤维细胞生长因子 23 与慢性肾脏病儿童的左心室肥厚
Clin J Am Soc Nephrol. 2018 Jan 6;13(1):45-52. doi: 10.2215/CJN.02110217. Epub 2017 Oct 12.
3
Vascular calcification in CKD-MBD: Roles for phosphate, FGF23, and Klotho.慢性肾脏病-矿物质和骨异常中的血管钙化:磷酸盐、成纤维细胞生长因子23及α-klotho蛋白的作用
Bone. 2017 Jul;100:87-93. doi: 10.1016/j.bone.2016.11.012. Epub 2016 Nov 12.
4
Effects of dietary iron intake and chronic kidney disease on fibroblast growth factor 23 metabolism in wild-type and hepcidin knockout mice.膳食铁摄入量和慢性肾脏病对野生型和铁调素基因敲除小鼠成纤维细胞生长因子23代谢的影响。
Am J Physiol Renal Physiol. 2016 Dec 1;311(6):F1369-F1377. doi: 10.1152/ajprenal.00281.2016. Epub 2016 Oct 12.
5
Fibroblast Growth Factor 23 and Risk of CKD Progression in Children.成纤维细胞生长因子23与儿童慢性肾脏病进展风险
Clin J Am Soc Nephrol. 2016 Nov 7;11(11):1989-1998. doi: 10.2215/CJN.02110216. Epub 2016 Aug 25.
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Fibroblast Growth Factor 23 and Cause-Specific Mortality in the General Population: The Northern Manhattan Study.成纤维细胞生长因子23与普通人群的特定病因死亡率:北曼哈顿研究
J Clin Endocrinol Metab. 2016 Oct;101(10):3779-3786. doi: 10.1210/jc.2016-2215. Epub 2016 Aug 8.
7
Association of Fibroblast Growth Factor 23 With Atrial Fibrillation in Chronic Kidney Disease, From the Chronic Renal Insufficiency Cohort Study.成纤维细胞生长因子 23 与慢性肾脏病心房颤动的关系:来自慢性肾功能不全队列研究。
JAMA Cardiol. 2016 Aug 1;1(5):548-56. doi: 10.1001/jamacardio.2016.1445.
8
Administration of Ferric Citrate Hydrate Decreases Circulating FGF23 Levels Independently of Serum Phosphate Levels in Hemodialysis Patients with Iron Deficiency.对于缺铁的血液透析患者,给予水合柠檬酸铁可独立于血清磷酸盐水平降低循环中的成纤维细胞生长因子23(FGF23)水平。
Nephron. 2015;131(3):161-6. doi: 10.1159/000440968. Epub 2015 Nov 6.
9
Inflammation and functional iron deficiency regulate fibroblast growth factor 23 production.炎症和功能性铁缺乏调节成纤维细胞生长因子23的产生。
Kidney Int. 2016 Jan;89(1):135-46. doi: 10.1038/ki.2015.290. Epub 2016 Jan 4.
10
Novel iron-based phosphate binders in patients with chronic kidney disease.新型铁基磷酸盐结合剂用于慢性肾脏病患者
Curr Opin Nephrol Hypertens. 2015 Jul;24(4):330-5. doi: 10.1097/MNH.0000000000000128.

临床应用柠檬酸铁作为磷酸盐结合剂治疗儿科透析患者的经验。

Clinical experience with the use of ferric citrate as a phosphate binder in pediatric dialysis patients.

机构信息

Department of Pediatrics, David Geffen School of Medicine at UCLA, 10833 Le Conte Avenue, MDCC A2-383, Los Angeles, CA, 90095-1752, USA.

出版信息

Pediatr Nephrol. 2018 Nov;33(11):2137-2142. doi: 10.1007/s00467-018-3999-y. Epub 2018 Jun 28.

DOI:10.1007/s00467-018-3999-y
PMID:29956006
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6146015/
Abstract

BACKGROUND

Ferric citrate, an iron-based phosphate binder, has been shown to improve both hyperphosphatemia and iron deficiency in adult chronic kidney disease patients, but its use in the pediatric dialysis population has not been described.

METHODS

This is a retrospective analysis of 11 unselected pediatric dialysis patients who received ferric citrate as a phosphate binder between 2015 and 2017. Time-averaged laboratory values were compared pre- and post-ferric citrate initiation using the Wilcoxon signed-rank test.

RESULTS

The median age of this cohort was 13 years old (range 4-17 years old). Five patients were on hemodialysis, and six patients were on peritoneal dialysis. The median duration of ferric citrate therapy was 214 days (range 39-654 days), with a median time-averaged ferric citrate dose of 3.5 tablets per day (range 1.5-8.4 tablets per day). Compared to the pre-ferric citrate period, ferric citrate treatment was associated with decreased serum phosphate (6.5 to 5.2 mg/dl, p = 0.014), decreased phosphate age-related standard deviation score (SDS) (2.3 to 0.9, p = 0.019), increased transferrin saturation (26 to 34%, p = 0.049), increased ferritin (107 to 230 ng/ml, p = 0.074), and maintenance of hematocrit.

CONCLUSIONS

In pediatric dialysis patients, ferric citrate may be able to concurrently lower phosphate levels and treat iron deficiency. However, larger studies are needed to further evaluate safety and efficacy in the pediatric chronic kidney disease population.

摘要

背景

柠檬酸铁作为一种基于铁的磷酸盐结合剂,已被证明可改善成人慢性肾脏病患者的高磷血症和缺铁症,但尚未在儿科透析人群中描述其应用。

方法

这是一项对 2015 年至 2017 年间接受柠檬酸铁作为磷酸盐结合剂的 11 例未选择的儿科透析患者进行的回顾性分析。使用 Wilcoxon 符号秩检验比较柠檬酸铁起始前后的时间平均实验室值。

结果

该队列的中位年龄为 13 岁(范围 4-17 岁)。5 例患者接受血液透析,6 例患者接受腹膜透析。柠檬酸铁治疗的中位时间为 214 天(范围 39-654 天),中位时间平均柠檬酸铁剂量为 3.5 片/天(范围 1.5-8.4 片/天)。与柠檬酸铁治疗前相比,柠檬酸铁治疗与血清磷酸盐降低(6.5 至 5.2 mg/dl,p=0.014)、磷酸盐年龄相关标准偏差评分降低(2.3 至 0.9,p=0.019)、转铁蛋白饱和度升高(26 至 34%,p=0.049)、铁蛋白升高(107 至 230 ng/ml,p=0.074)和维持血细胞比容有关。

结论

在儿科透析患者中,柠檬酸铁可能能够同时降低磷酸盐水平并治疗缺铁症。然而,需要更大的研究进一步评估在儿科慢性肾脏病人群中的安全性和疗效。