Comparison of 24-hour urinary creatinine clearance and estimated glomerular filtration rate based on a panel of filtration markers in patients with chronic kidney disease

被引:2
作者
Iversen, Esben [1 ,2 ]
Boesby, Lene [3 ,4 ]
Hansen, Ditte [3 ,5 ]
Houlind, Morten Baltzer [1 ,6 ,7 ]
机构
[1] Copenhagen Univ Hosp Amager & Hvidovre, Dept Clin Res, Hvidovre, Denmark
[2] Icahn Sch Med Mt Sinai, New York, NY 10029 USA
[3] Copenhagen Univ Hosp Herley & Gentofte, Dept Nephrol, Copenhagen, Denmark
[4] Zealand Univ Hosp Roskilde, Dept Internal Med, Roskilde, Denmark
[5] Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark
[6] Capital Reg Pharm, Herlev, Denmark
[7] Univ Copenhagen, Dept Drug Design & Pharmacol, Copenhagen, Denmark
关键词
beta-2; microglobulin; beta-trace protein; chronic kidney disease; creatinine; cystatin C; estimated glomerular filtration rate; panel equation; SERUM CYSTATIN-C; RENAL-FUNCTION; GFR; PROTEIN;
D O I
10.1002/prp2.1002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Diagnosis and management of chronic kidney disease (CKD) requires accurate assessment of glomerular filtration rate (GFR). In practice, GFR is typically estimated by equations based on creatinine concentration in blood, but creatinine is affected by non-GFR factors such as age and sex. Alternative filtration markers such as cystatin C, beta-trace protein (BTP), and beta-2 microglobulin (B2M) may be less dependent on age and sex, but equations combining these markers have not been investigated in patients with chronic kidney disease (CKD). In this cross-sectional study of 50 patients with CKD stage 3-4, we compared kidney function estimates based on creatinine, cystatin C, BTP, B2M, or a combination of markers. Compared to the creatinine/cystatin C combination equation, the panel equation yielded a mean difference of only 2.8 ml/min/1.73 m(2), indicating that switching to the panel equation would be unlikely to affect management.
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页数:5
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