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PLOS ONE  2013 

Determining Glomerular Filtration Rate in Homozygous Sickle Cell Disease: Utility of Serum Creatinine Based Estimating Equations

DOI: 10.1371/journal.pone.0069922

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Abstract:

Background Various estimating equations have been developed to estimate glomerular filtration rate (GFR) for use in clinical practice. However, the unique renal physiological and pathological processes that occur in sickle cell disease (SCD) may invalidate these estimates in this patient population. This study aims to compare GFR estimated using common existing GFR predictive equations to actual measured GFR in persons with homozygous SCD. If the existing equations perform poorly, we propose to develop a new estimating equation for use in persons with SCD. Methods 98 patients with the homozygous SS disease (55 females: 43 males; mean age 34±2.3 years) had serum measurements of creatinine, as well as had GFR measured using 99mTc-DTPA nuclear renal scan. GFR was estimated using the Modification of Diet in Renal Disease (MDRD), Cockcroft-Gault (CG), and the serum creatinine based CKD-EPI equations. The Bland-Altman limit of agreement method was used to determine agreement between measured and estimated GFR values. A SCD-specific estimating equation for GFR (JSCCS-GFR equation) was generated by means of multiple regression via backward elimination. Results The mean measured GFR±SD was 94.9±27.4 mls/min/1.73 m2 BSA, with a range of 6.4–159.0 mls/min/1.73 m2. The MDRD and CG equations both overestimated GFR, with the agreement worsening with higher GFR values. The serum creatinine based CKD-EPI equation performed relatively well, but with a systematic bias of about 45 mls/min. The new equation developed resulted in a better fit to our sickle cell disease data than the MDRD equation. Conclusion Current estimating equations, other than the CKD-EPI equation, do not perform very accurately in persons with homozygous SS disease. A fairly accurate estimating equation, suitable for persons with GFR >60 mls/min/1.73 m2 has been developed from our dataset and validated within a simulated dataset.

References

[1]  Abdu A, Emokpae MA, Uadia PO, Kuliya-Gwarzo A (2011) Proteinuria among adult sickle cell anemia patients in Nigeria. Ann Afr Med 10: 34–37.
[2]  Lopez Revuelta K, Ricard Andres MP (2011) Kidney abnormalities in sickle cell disease. Nefrologia 31: 591–601.
[3]  Powars DR, Chan LS, Hiti A, Ramicone E, Johnson C (2005) Outcome of sickle cell anemia: a 4-decade observational study of 1056 patients. Medicine (Baltimore) 84: 363–376.
[4]  Serjeant GR, Higgs DR, Hambleton IR (2007) Elderly survivors with homozygous sickle cell disease. N Engl J Med 356: 642–643.
[5]  Levey AS, Coresh J, Balk E, Kausz AT, Levin A, et al. (2003) National Kidney Foundation practice guidelines for chronic kidney disease: evaluation, classification, and stratification. Ann Intern Med 139: 137–147.
[6]  National Kidney Foundation (2002) K/DOQI clinical practice guidelines for chronic kidney disease: evaluation, classification, and stratification. Am J Kidney Dis 39: S1–266.
[7]  Stevens LA, Levey AS (2005) Measurement of kidney function. Med Clin North Am 89: 457–473.
[8]  Vassalotti JA, Stevens LA, Levey AS (2007) Testing for chronic kidney disease: a position statement from the National Kidney Foundation. Am J Kidney Dis 50: 169–180.
[9]  Levey AS, Bosch JP, Lewis JB, Greene T, Rogers N, et al. (1999) A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of Diet in Renal Disease Study Group. Ann Intern Med 130: 461–470.
[10]  Aparicio SA, Mojiminiyi S, Kay JD, Shepstone BJ, de Ceulaer K, et al. (1990) Measurement of glomerular filtration rate in homozygous sickle cell disease: a comparison of 51Cr-EDTA clearance, creatinine clearance, serum creatinine and beta 2 microglobulin. J Clin Pathol 43: 370–372.
[11]  Thompson J, Reid M, Hambleton I, Serjeant GR (2007) Albuminuria and renal function in homozygous sickle cell disease: observations from a cohort study. Arch Intern Med 167: 701–708.
[12]  Siekmann L (1985) Determination of creatinine in human serum by isotope dilution-mass spectrometry. Definitive methods in clinical chemistry, IV. J Clin Chem Clin Biochem 23: 137–144.
[13]  Poggio ED, Nef PC, Wang X, Greene T, Van Lente F, et al. (2005) Performance of the Cockcroft-Gault and modification of diet in renal disease equations in estimating GFR in ill hospitalized patients. Am J Kidney Dis 46: 242–252.
[14]  Poge U, Gerhardt T, Stoffel-Wagner B, Klehr HU, Sauerbruch T, et al. (2006) Calculation of glomerular filtration rate based on cystatin C in cirrhotic patients. Nephrol Dial Transplant 21: 660–664.
[15]  Verhave JC, Fesler P, Ribstein J, du Cailar G, Mimran A (2005) Estimation of renal function in subjects with normal serum creatinine levels: influence of age and body mass index. Am J Kidney Dis 46: 233–241.
[16]  Fontsere N, Salinas I, Bonal J, Bayes B, Riba J, et al. (2006) Are prediction equations for glomerular filtration rate useful for the long-term monitoring of type 2 diabetic patients? Nephrol Dial Transplant 21: 2152–2158.
[17]  Inker LA, Schmid CH, Tighiouart H, Eckfeldt JH, Feldman HI, et al. (2012) Estimating glomerular filtration rate from serum creatinine and cystatin C. N Engl J Med. 367: 20–29.
[18]  Levey AS, Stevens LA, Schmid CH, Zhang YL, Castro AF III, et al. (2009) A new equation to estimate glomerular filtration rate. Ann Intern Med 150: 604–612.
[19]  Bolarinwa RA, Akinlade KS, Kuti MA, Olawale OO, Akinola NO (2012) Renal disease in adult Nigerians with sickle cell anemia: a report of prevalence, clinical features and risk factors. Saudi J Kidney Dis Transpl 23: 171–175.
[20]  Guasch A, Navarrete J, Nass K, Zayas CF (2006) Glomerular involvement in adults with sickle cell hemoglobinopathies: Prevalence and clinical correlates of progressive renal failure. J Am Soc Nephrol 17: 2228–2235.
[21]  Gurkan S, Scarponi KJ, Hotchkiss H, Savage B, Drachtman R (2010) Lactate dehydrogenase as a predictor of kidney involvement in patients with sickle cell anemia. Pediatr Nephrol 25: 2123–2127.
[22]  Haymann JP, Stankovic K, Levy P, Avellino V, Tharaux PL, et al. (2010) Glomerular hyperfiltration in adult sickle cell anemia: a frequent hemolysis associated feature. Clin J Am Soc Nephrol 5: 756–761.
[23]  Marouf R, Mojiminiyi O, Abdella N, Kortom M, Al Wazzan H (2006) Comparison of renal function markers in Kuwaiti patients with sickle cell disease. J Clin Pathol 59: 345–351.
[24]  McPherson Yee M, Jabbar SF, Osunkwo I, Clement L, Lane PA, et al. (2011) Chronic kidney disease and albuminuria in children with sickle cell disease. Clin J Am Soc Nephrol 6: 2628–2633.
[25]  Silva Junior GB, Liborio AB, Vieira AP, Bem AX, Lopes Filho AS, et al. (2012) Evaluation of renal function in sickle cell disease patients in Brazil. Braz J Med Biol Res 45: 652–655.
[26]  Ware RE, Rees RC, Sarnaik SA, Iyer RV, Alvarez OA, et al.. (2010) Renal function in infants with sickle cell anemia: baseline data from the BABY HUG trial. J Pediatr 156: 66–70 e61.
[27]  Alvarez O, Miller ST, Wang WC, Luo Z, McCarville MB, et al.. (2012) Effect of hydroxyurea treatment on renal function parameters: Results from the multi-center placebo-controlled baby hug clinical trial for infants with sickle cell anemia. Pediatr Blood Cancer.
[28]  Aygun B, Mortier NA, Smeltzer MP, Hankins JS, Ware RE (2011) Glomerular hyperfiltration and albuminuria in children with sickle cell anemia. Pediatr Nephrol 26: 1285–1290.

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