Estimated glomerular filtration rate based on creatinine, cystatin C, β-trace protein and β2 microglobulin in patients undergoing nontraumatic lower extremity amputation
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Estimated glomerular filtration rate based on creatinine, cystatin C, β-trace protein and β2 microglobulin in patients undergoing nontraumatic lower extremity amputation. / Iversen, Esben; Walls, Anne Byriel; Petersen, Annamarie; Jensen, Pia Søe; Kallemose, Thomas; Andersen, Aino; Nielsen, Rikke Lundsgaard; Bengaard, Anne Kathrine; Juul-Larsen, Helle Gybel; Bornæs, Olivia; Damgaard, Morten; Andersen, Ove; Tavenier, Juliette; Houlind, Morten Baltzer.
In: British Journal of Clinical Pharmacology, Vol. 89, No. 6, 2023, p. 1789-1798.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Estimated glomerular filtration rate based on creatinine, cystatin C, β-trace protein and β2 microglobulin in patients undergoing nontraumatic lower extremity amputation
AU - Iversen, Esben
AU - Walls, Anne Byriel
AU - Petersen, Annamarie
AU - Jensen, Pia Søe
AU - Kallemose, Thomas
AU - Andersen, Aino
AU - Nielsen, Rikke Lundsgaard
AU - Bengaard, Anne Kathrine
AU - Juul-Larsen, Helle Gybel
AU - Bornæs, Olivia
AU - Damgaard, Morten
AU - Andersen, Ove
AU - Tavenier, Juliette
AU - Houlind, Morten Baltzer
N1 - Funding Information: This study was performed as part of the Clinical Academic Group (ACUTE‐CAG) for Recovery Capacity nominated by the Greater Copenhagen Health Science Partners (GCHSP). The study was conducted at the Department of Clinical Research, Copenhagen University Hospital Amager & Hvidovre, Hvidovre, Denmark. M.B.H. was supported by a postdoctoral fellowship from The Capital Region's Research Foundation for Health Research and the BRIDGE Translational Excellence Program (grant NNF20SA0064340). We thank all patients and staff involved in the Time to Eat study and OptiNAM trial. Publisher Copyright: © 2022 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.
PY - 2023
Y1 - 2023
N2 - Aims: The study's aim is to compare current and new equations for estimating glomerular filtration rate (GFR) based on creatinine, cystatin C, β-trace protein (BTP) and β2 microglobulin (B2M) among patients undergoing major amputation. Methods: This is a secondary analysis of data from a prospective cohort study investigating patients undergoing nontraumatic lower extremity amputation. Estimated GFR (eGFR) was calculated using equations based on creatinine (eGFRcre[2009] and eGFRcre[2021]), cystatin C (eGFRcys), the combination of creatinine and cystatin C (eGFRcomb[2012] and eGFRcomb[2021]) or a panel of all 4 filtration markers (eGFRpanel). Primary outcome was changed in eGFR across amputation according to each equation. Two case studies of prior amputation with GFR measured by 99mTc-DTPA clearance are described to illustrate the relative accuracies of each eGFR equation. Results: Analysis of the primary outcome included 29 patients (median age 75 years, 31% female). Amputation was associated with a significant decrease in creatinine concentration (−0.09 mg/dL, P = 0.004), corresponding to a significant increase in eGFRcre[2009] (+6.1 mL/min, P = 0.006) and eGFRcre[2021] (+6.3 mL/min, P = 0.006). Change across amputation was not significant for cystatin C, BTP, B2M or equations incorporating these markers (all P > 0.05). In both case studies, eGFRcre[2021] yielded the largest positive bias, eGFRcys yielded the largest negative bias and eGFRcomb[2012] and eGFRcomb[2021] yielded the smallest absolute bias. Conclusion: Creatinine-based estimates were substantially higher than cystatin C-based estimates before amputation and significantly increased across amputation. Estimates combining creatinine and cystatin were stable across amputation, while the addition of BTP and B2M is unlikely to be clinically relevant.
AB - Aims: The study's aim is to compare current and new equations for estimating glomerular filtration rate (GFR) based on creatinine, cystatin C, β-trace protein (BTP) and β2 microglobulin (B2M) among patients undergoing major amputation. Methods: This is a secondary analysis of data from a prospective cohort study investigating patients undergoing nontraumatic lower extremity amputation. Estimated GFR (eGFR) was calculated using equations based on creatinine (eGFRcre[2009] and eGFRcre[2021]), cystatin C (eGFRcys), the combination of creatinine and cystatin C (eGFRcomb[2012] and eGFRcomb[2021]) or a panel of all 4 filtration markers (eGFRpanel). Primary outcome was changed in eGFR across amputation according to each equation. Two case studies of prior amputation with GFR measured by 99mTc-DTPA clearance are described to illustrate the relative accuracies of each eGFR equation. Results: Analysis of the primary outcome included 29 patients (median age 75 years, 31% female). Amputation was associated with a significant decrease in creatinine concentration (−0.09 mg/dL, P = 0.004), corresponding to a significant increase in eGFRcre[2009] (+6.1 mL/min, P = 0.006) and eGFRcre[2021] (+6.3 mL/min, P = 0.006). Change across amputation was not significant for cystatin C, BTP, B2M or equations incorporating these markers (all P > 0.05). In both case studies, eGFRcre[2021] yielded the largest positive bias, eGFRcys yielded the largest negative bias and eGFRcomb[2012] and eGFRcomb[2021] yielded the smallest absolute bias. Conclusion: Creatinine-based estimates were substantially higher than cystatin C-based estimates before amputation and significantly increased across amputation. Estimates combining creatinine and cystatin were stable across amputation, while the addition of BTP and B2M is unlikely to be clinically relevant.
KW - creatinine
KW - cystatin C
KW - estimated glomerular filtration rate
KW - nontraumatic lower extremity amputation
KW - optimized prescribing
KW - β-trace protein
KW - β2 microglobulin
U2 - 10.1111/bcp.15639
DO - 10.1111/bcp.15639
M3 - Journal article
C2 - 36511684
AN - SCOPUS:85145855513
VL - 89
SP - 1789
EP - 1798
JO - British Journal of Clinical Pharmacology, Supplement
JF - British Journal of Clinical Pharmacology, Supplement
SN - 0264-3774
IS - 6
ER -
ID: 334646940