CKD therapy to improve outcomes of immune-mediated glomerular diseases

Author:

Anders Hans-Joachim1,Fernandez-Juarez Gema M2,Vaglio Augusto3,Romagnani Paola34,Floege Jürgen5

Affiliation:

1. Division of Nephrology, Department of Internal Medicine IV, Hospital of the Ludwig-Maximilians-University , Munich , Germany

2. Department of Nephrology, Hospital Universitario La Paz , IdiPaz, Madrid , Spain

3. Nephrology Unit, Anna Meyer Children's Hospital , Florence , Italy

4. Department of Clinical and Experimental Biomedical Sciences “Mario Serio”, University of Florence , Florence , Italy

5. Division of Nephrology and Clinical Immunology, RWTH Aachen University Hospital , Aachen , Germany

Abstract

ABSTRACT The management of immunoglobulin A nephropathy, membranous nephropathy, lupus nephritis, anti-neutrophil cytoplasmic antibody–associated vasculitis, C3 glomerulonephritis, autoimmune podocytopathies and other immune-mediated glomerular disorders is focused on two major treatment goals, preventing overall mortality and the loss of kidney function. Since minimizing irreversible kidney damage best serves both goals, the management of immune-mediated kidney disorders must focus on the two central pathomechanisms of kidney function decline, i.e., controlling the underlying immune disease process (e.g. with immunotherapies) and controlling the non-immune mechanisms of chronic kidney disease (CKD) progression. Here we review the pathophysiology of these non-immune mechanisms of CKD progression and discuss non-drug and drug interventions to attenuate CKD progression in immune-mediated kidney disorders. Non-pharmacological interventions include reducing salt intake, normalizing body weight, avoiding superimposed kidney injuries, smoking cessation and regular physical activity. Approved drug interventions include inhibitors of the renin–angiotensin–aldosterone system and sodium–glucose cotransporter-2. Numerous additional drugs to improve CKD care are currently being tested in clinical trials. Here we discuss how and when to use these drugs in the different clinical scenarios of immune-mediated kidney diseases.

Funder

Deutsche Forschungsgemeinschaft

Instituto de Salud Carlos II

RICORS

ERK-NET

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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5. SGLT2 inhibition requires reconsideration of fundamental paradigms in chronic kidney disease, ‘diabetic nephropathy’, IgA nephropathy and podocytopathies with FSGS lesions;Anders;Nephrol. Dial. Transplant,2022

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