Affiliation:
1. Nephrology, Dresden University Hospital, Dresden, Germany
2. Biotechnology Center, Technische Universität Dresden, Dresden,
Germany
Abstract
AbstractDiabetic nephropathy is the most common condition that requires a chronic renal
replacement therapy, such as hemodialysis, peritoneal dialysis, kidney
transplantation, or simultaneous kidney-pancreas transplantation. Chronic kidney
disease progression, that is the loss of nephrons, which causes the continuous
decline of the eGFR, underlies the pathogenesis of diabetic nephropathy. During
the COVID-19 pandemic, it became clear that diabetic nephropathy is amongst the
independent risk factors that predicts unfavourable outcome upon SARS-CoV2
infection. While we still lack conclusive mechanistic insights into how nephrons
are rapidly lost upon SARS-CoV2 infection and why patients with diabetic
nephropathy are more susceptible to severe outcomes upon SARS-CoV2 infection,
here, we discuss several aspects of the interface of COVID-19 with diabetic
nephropathy. We identify the shortage of reliable rodent models of diabetic
nephropathy, limited treatment options for human diabetic nephropathy and the
lack of knowledge about virus-induced signalling pathways of regulated necrosis,
such as necroptosis, as key factors that explain our failure to understand this
system. Finally, we focus on immunosuppressed patients and discuss vaccination
efficacy in these and diabetic patients. We conclude that more basic science and
mechanistic understanding will be required both in diabetic nephropathy as well
as in host immune responses to the SARS-CoV2 virus if novel therapeutic
strategies are desired.
Subject
Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,General Medicine,Endocrinology, Diabetes and Metabolism
Cited by
5 articles.
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