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Original ArticleDiabetes and the Kidney
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Association between TNF Receptors and KIM-1 with Kidney Outcomes in Early-Stage Diabetic Kidney Disease

Simke W. Waijer, Taha Sen, Clare Arnott, Bruce Neal, Jos G.W. Kosterink, Kenneth W. Mahaffey, Chirag R. Parikh, Dick de Zeeuw, Vlado Perkovic, Brendon L. Neuen, Steven G. Coca, Michael K. Hansen, Ron T. Gansevoort and Hiddo J.L. Heerspink
CJASN February 2022, 17 (2) 251-259; DOI: https://doi.org/10.2215/CJN.08780621
Simke W. Waijer
1Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands
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Taha Sen
1Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands
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Clare Arnott
2The George Institute for Global Health, University of New South Wales Sydney, Sydney, New South Wales, Australia
3Department of Cardiology, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia
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Bruce Neal
2The George Institute for Global Health, University of New South Wales Sydney, Sydney, New South Wales, Australia
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Jos G.W. Kosterink
1Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands
4Department of PharmacoTherapy, Epidemiology and Economics, University of Groningen, Groningen, The Netherlands
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Kenneth W. Mahaffey
5Stanford Center for Clinical Research, Department of Medicine, Stanford University School of Medicine, Stanford, California
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Chirag R. Parikh
6Department of Internal Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland
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Dick de Zeeuw
1Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands
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Vlado Perkovic
2The George Institute for Global Health, University of New South Wales Sydney, Sydney, New South Wales, Australia
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Brendon L. Neuen
2The George Institute for Global Health, University of New South Wales Sydney, Sydney, New South Wales, Australia
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Steven G. Coca
7Department of Internal Medicine, Icahn School of Medicine at Mount Sinai, New York, New York
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Michael K. Hansen
8Janssen Research & Development, LLC, Spring House, Pennsylvania
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Ron T. Gansevoort
9Department of Internal Medicine, Division of Nephrology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands
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Hiddo J.L. Heerspink
1Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands
2The George Institute for Global Health, University of New South Wales Sydney, Sydney, New South Wales, Australia
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Abstract

Background and objectives Clinical trials in nephrology are enriched for patients with micro- or macroalbuminuria to enroll patients at risk of kidney failure. However, patients with normoalbuminuria can also progress to kidney failure. TNF receptor-1, TNF receptor-2, and kidney injury marker-1 (KIM-1) are known to be associated with kidney disease progression in patients with micro- or macroalbuminuria. We assessed the value of TNF receptor-1, TNF receptor-2, and KIM-1 as prognostic biomarkers for CKD progression in patients with type 2 diabetes and normoalbuminuria.

Design, setting, participants, & measurements TNF receptor-1, TNF receptor-2, and KIM-1 were measured using immunoassays in plasma samples from patients with type 2 diabetes at high cardiovascular risk participating in the Canagliflozin Cardiovascular Assessment Study trial. We used multivariable adjusted Cox proportional hazards analyses to estimate hazard ratios per doubling of each biomarker for the kidney outcome, stratified the population by the fourth quartile of each biomarker distribution, and assessed the number of events and event rates.

Results In patients with normoalbuminuria (n=2553), 51 kidney outcomes were recorded during a median follow-up of 6.1 (interquartile range, 5.8–6.4) years (event rate, 3.5; 95% confidence interval, 2.6 to 4.6 per 1000 patient-years). Each doubling of baseline TNF receptor-1 (hazard ratio, 4.2; 95% confidence interval, 1.8 to 9.6) and TNF receptor-2 (hazard ratio, 2.3; 95% confidence interval, 1.5 to 3.6) was associated with a higher risk for the kidney outcome. Baseline KIM-1, urinary albumin-creatinine ratio, and eGFR were not associated with kidney outcomes. The event rates in the highest quartile of TNF receptor-1 (≥2992 ng/ml) and TNF receptor-2 (≥11,394 ng/ml) were 5.6 and 7.0 events per 1000 patient-years, respectively, compared with 2.8 and 2.3, respectively, in the lower three quartiles.

Conclusions TNF receptor-1 and TNF receptor-2 are associated with kidney outcomes in patients with type 2 diabetes and normoalbuminuria.

Clinical Trial registry name and registration number: CANagliflozin cardioVascular Assessment Study (CANVAS), NCT01032629

  • TNFR-1
  • TNFR-2
  • KIM-1
  • biomarkers
  • clinical trial design
  • risk prediction
  • normoalbuminuria
  • kidney outcomes
  • prognosis
  • hepatitis a virus cellular receptor 1
  • Received June 25, 2021.
  • Accepted November 29, 2021.
  • Copyright © 2022 by the American Society of Nephrology
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Clinical Journal of the American Society of Nephrology: 17 (2)
Clinical Journal of the American Society of Nephrology
Vol. 17, Issue 2
February 2022
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Association between TNF Receptors and KIM-1 with Kidney Outcomes in Early-Stage Diabetic Kidney Disease
Simke W. Waijer, Taha Sen, Clare Arnott, Bruce Neal, Jos G.W. Kosterink, Kenneth W. Mahaffey, Chirag R. Parikh, Dick de Zeeuw, Vlado Perkovic, Brendon L. Neuen, Steven G. Coca, Michael K. Hansen, Ron T. Gansevoort, Hiddo J.L. Heerspink
CJASN Feb 2022, 17 (2) 251-259; DOI: 10.2215/CJN.08780621

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Association between TNF Receptors and KIM-1 with Kidney Outcomes in Early-Stage Diabetic Kidney Disease
Simke W. Waijer, Taha Sen, Clare Arnott, Bruce Neal, Jos G.W. Kosterink, Kenneth W. Mahaffey, Chirag R. Parikh, Dick de Zeeuw, Vlado Perkovic, Brendon L. Neuen, Steven G. Coca, Michael K. Hansen, Ron T. Gansevoort, Hiddo J.L. Heerspink
CJASN Feb 2022, 17 (2) 251-259; DOI: 10.2215/CJN.08780621
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Original Article

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Keywords

  • TNFR-1
  • TNFR-2
  • KIM-1
  • biomarkers
  • clinical trial design
  • risk prediction
  • normoalbuminuria
  • kidney outcomes
  • prognosis
  • hepatitis a virus cellular receptor 1

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