BACKGROUND: Unlike creatinine, Cystatin C (CysC) is believed to be independent of body composition in both adults and children. Recent findings in adults, suggesting an improved performance of CysC-based estimated glomerular filtration rate (CysC eGFR) by accounting for body mass, necessitated a careful re-evaluation of this issue in children. METHODS: We studied 240 children (median age 11.7 years, range 2-17.9 years, 107 girls), with various kidney diseases, for any change in the relationship between (99)Tc DTPA GFR and CysC eGFR after accounting for body mass. For body mass assessment, body mass index (BMI) z-score was calculated using height-adjusted age, to account for growth retardation secondary to chronic kidney disease. RESULTS: CysC eGFR did not have a significant correlation with BMI z-score (correlation coefficient = 0.06; P = 0.34). Accounting for BMI z-score did not add to the 65% variance in nuclear GFR explained by CysC eGFR. Moreover, it did not change the regression coefficient of 0.85 between CysC eGFR and nuclear GFR either. On Bland & Altman analysis, the bias of 0.05 and standard deviation of 20.39 also did not improve after accounting for BMI z-score in the revised CysC eGFR formula. CONCLUSIONS: In children, body mass exerts a minimal effect on the performance of CysC eGFR estimation.
BACKGROUND: Unlike creatinine, Cystatin C (CysC) is believed to be independent of body composition in both adults and children. Recent findings in adults, suggesting an improved performance of CysC-based estimated glomerular filtration rate (CysCeGFR) by accounting for body mass, necessitated a careful re-evaluation of this issue in children. METHODS: We studied 240 children (median age 11.7 years, range 2-17.9 years, 107 girls), with various kidney diseases, for any change in the relationship between (99)Tc DTPA GFR and CysCeGFR after accounting for body mass. For body mass assessment, body mass index (BMI) z-score was calculated using height-adjusted age, to account for growth retardation secondary to chronic kidney disease. RESULTS:CysCeGFR did not have a significant correlation with BMI z-score (correlation coefficient = 0.06; P = 0.34). Accounting for BMI z-score did not add to the 65% variance in nuclear GFR explained by CysCeGFR. Moreover, it did not change the regression coefficient of 0.85 between CysCeGFR and nuclear GFR either. On Bland & Altman analysis, the bias of 0.05 and standard deviation of 20.39 also did not improve after accounting for BMI z-score in the revised CysCeGFR formula. CONCLUSIONS: In children, body mass exerts a minimal effect on the performance of CysCeGFR estimation.
Authors: Christopher I Esezobor; Edna Iroha; Olajumoke Oladipo; Elizabeth Onifade; Oyetunji O Soriyan; Adebola O Akinsulie; Edamisan O Temiye; Chinyere Ezeaka Journal: J Int AIDS Soc Date: 2010-05-18 Impact factor: 5.396
Authors: Najila Al-Malki; Paul A Heidenheim; Guido Filler; Abeer Yasin; Robert M Lindsay Journal: Clin J Am Soc Nephrol Date: 2009-08-27 Impact factor: 8.237
Authors: Olivera Marsenic; Andrea Wierenga; Donna R Wilson; Michael Anderson; Tripti Shrivastava; Garfield A Simon; Anne M Beck; Tiffany J Swanson; Kathleen Studnicka; Dorit Elberg; Kevin Couloures; Martin A Turman Journal: Pediatr Nephrol Date: 2012-11-21 Impact factor: 3.714