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The DOI matches its Crossref record; 136 of the 136 references it cites were found in a registry or an index.

Diabetic Nephropathy: Update on Pillars of Therapy Slowing Progression

Open access
Naaman, Sandra C., Bakris, George L.·2023·Diabetes Care

Abstract

Management of diabetic kidney disease (DKD) has evolved in parallel with our growing understanding of the multiple interrelated pathophysiological mechanisms that involve hemodynamic, metabolic, and inflammatory pathways. These pathways and others play a vital role in the initiation and progression of DKD. Since its initial discovery, the blockade of the renin-angiotensin system has remained a cornerstone of DKD management, leaving a large component of residual risk to be dealt with. The advent of sodium–glucose cotransporter 2 inhibitors followed by nonsteroidal mineralocorticoid receptor antagonists and, to some extent, glucagon-like peptide 1 receptor agonists (GLP-1 RAs) has ushered in a resounding paradigm shift that supports a pillared approach in maximizing treatment to reduce outcomes. This pillared approach is like that derived from the approach to heart failure treatment. The approach mandates that all agents that have been shown in clinical trials to reduce cardiovascular outcomes and/or mortality to a greater extent than a single drug class alone should be used in combination. In this way, each drug class focuses on a specific aspect of the disease's pathophysiology. Thus, in heart failure, β-blockers, sacubitril/valsartan, a mineralocorticoid receptor antagonist, and a diuretic are used together. In this article, we review the evolution of the pillar concept of therapy as it applies to DKD and discuss how it should be used based on the outcome evidence. We also discuss the exciting possibility that GLP-1 RAs may be an additional pillar in the quest to further slow kidney disease progression in diabetes.

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Research works printed but not linked: 4

  1. Bakris, 1991, Arginine vasopressin stimulates human mesangial cell production of endothelin, J Clin Invest, 87, 1158, 10.1172/JCI115113 · doi:10.1172/jci115113
  2. Hostetter, 2003, Hyperfiltration and glomerulosclerosis, Semin Nephrol, 23, 194, 10.1053/snep.2003.50017 · doi:10.1053/snep.2003.50017
  3. Tsimihodimos, 2017, Renoprotective effects of SGLT2 inhibitors: beyond glucose reabsorption inhibition, Curr Vasc Pharmacol, 15, 96, 10.2174/1570161114666161007163426 · doi:10.2174/1570161114666161007163426
  4. Tostes, 2002, Contribution of endothelin-1 to renal activator protein-1 activation and macrophage infiltration in aldosterone-induced hypertension, Clin Sci (Lond), 103, 25S, 10.1042/CS103S025S · doi:10.1042/cs103s025s

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Metadata

Authors
Naaman, S. C., & Bakris, G. L.
Venue
Diabetes Care
Published
2023-08-25
Volume
46
Issue
9
Pages
1574-1586
ISSN
  • 0149-5992 (ISSN-L)
  • 1935-5548
OpenAlex
W4386156942
Cited by
292
References
136
FWCI
47.90
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Diabetic Nephropathy: Update on Pillars of Therapy Slowing Progression. https://app.cochat.ai/papers/10.2337/dci23-0030
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Naaman, S. C., & Bakris, G. L. (2023). Diabetic Nephropathy: Update on Pillars of Therapy Slowing Progression. Diabetes Care. https://doi.org/10.2337/dci23-0030

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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