Aydin Funda, Tezcan Gülsün, Güngör Ozgül, Cengiz Arzu Kin, Hazar Volkan, Akman Sema, Güven Ayfer Gür, Yeşilipek Akif, Akbaş Halide, Güngör Firat
Department of aNuclear Medicine, Akdeniz University School of Medicine, Antalya, Turkey.
Nucl Med Commun. 2010 Apr;31(4):301-6. doi: 10.1097/MNM.0b013e328334fc6f.
It was assessed whether cystatin C (cysC) could be used as a marker of glomerular filtration rate (GFR) by considering the technetium-99m diethylenetriamine penta-acetate (Tc-99m DTPA)-two blood sample method (GFRTc-99m DTPA) as the reference in pediatric patients under chemotherapeutic treatment.
The chemotherapy group (CG) consisted of 31 patients (21 females, 10 males median age: 8.2 years; range: 2-16 years) who had been planned to receive allogenic hematopoietic stem cell transplantation. All patients in the CG received conditioning regimen (includes chemotherapy protocol) before hematopoietic stem cell transplantation. In addition, 21 patients (14 females, seven males median age: 9.5 years; range: 4-16 years) without any chemotherapy (nonchemotherapy group: nCG) were also prospectively investigated. Serum cysC, serum creatinine, GFRTc-99m DTPA, and GFR with a cysC-based formula (GFRcysC) were analyzed. Tubular function was also assessed.
Although we found good correlation between GFRTc-99m DTPA and cysC (r = -0.78), GFRTc-99m DTPA and GFRcysC (r = 0.91), cysC and creatinine (r = 0.91) in nCG, the same correlations were poor in CG (r = -0.42, r = 0.43, r = 0.46, respectively). Tubular function was impaired after chemotherapy. Bias+/-1.96 SD values were -6+/-15.7 and -3+/-54.8 ml/min/1.73 m in nCG and CG, respectively. Precision was also better in nCG (10 ml/min/1.73 m) than in CG (27.6 ml/min/1.73 m).
Serum cysC and GFRcysC cannot reflect GFR accurately in pediatric patients under chemotherapeutic treatment. Tubular cell damage induced by chemotherapeutics could be a responsible factor through the impairment of tubular absorption and metabolism of cysC.
以锝-99m二乙三胺五乙酸(Tc-99m DTPA)双血样法(GFRTc-99m DTPA)作为参考,评估胱抑素C(cysC)是否可作为化疗患儿肾小球滤过率(GFR)的标志物。
化疗组(CG)由31例计划接受异基因造血干细胞移植的患者组成(21例女性,10例男性;中位年龄:8.2岁;范围:2 - 16岁)。CG组所有患者在造血干细胞移植前均接受预处理方案(包括化疗方案)。此外,还对21例未接受任何化疗的患者(非化疗组:nCG,14例女性,7例男性;中位年龄:9.5岁;范围:4 - 16岁)进行了前瞻性研究。分析血清cysC、血清肌酐、GFRTc-99m DTPA以及基于cysC的公式计算的GFR(GFRcysC)。同时评估肾小管功能。
虽然在nCG组中我们发现GFRTc-99m DTPA与cysC(r = -0.78)、GFRTc-99m DTPA与GFRcysC(r = 0.91)、cysC与肌酐(r = 0.91)之间具有良好的相关性,但在CG组中相同的相关性较差(分别为r = -0.42、r = 0.43、r = 0.46)。化疗后肾小管功能受损。nCG组和CG组的偏差±1.96 SD值分别为-6±15.7和-3±54.8 ml/min/1.73 m²。nCG组的精密度(10 ml/min/1.73 m²)也优于CG组(27.6 ml/min/1.73 m²)。
在接受化疗的儿科患者中,血清cysC和GFRcysC不能准确反映GFR。化疗药物诱导的肾小管细胞损伤可能是通过损害cysC的肾小管吸收和代谢而成为一个影响因素。