Multicenter Clinicopathologic Correlation of Kidney Biopsies Performed in COVID-19 Patients Presenting With Acute Kidney Injury or Proteinuria.

Coronavirus disease 2019 (COVID-19) acute kidney injury (AKI) allograft biopsy antibody-mediated rejection (AMR) case series collapsing glomerulopathy kidney biopsy renal complications of COVID-19 renal pathology severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) thrombotic microangiopathy

Journal

American journal of kidney diseases : the official journal of the National Kidney Foundation
ISSN: 1523-6838
Titre abrégé: Am J Kidney Dis
Pays: United States
ID NLM: 8110075

Informations de publication

Date de publication:
01 2021
Historique:
received: 21 07 2020
accepted: 04 10 2020
pubmed: 13 10 2020
medline: 29 12 2020
entrez: 12 10 2020
Statut: ppublish

Résumé

Kidney biopsy data inform us about pathologic processes associated with infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). We conducted a multicenter evaluation of kidney biopsy findings in living patients to identify various kidney disease pathology findings in patients with coronavirus disease 2019 (COVID-19) and their association with SARS-CoV-2 infection. Case series. We identified 14 native and 3 transplant kidney biopsies performed for cause in patients with documented recent or concurrent SARS-CoV-2 infection treated at 7 large hospital systems in the United States. Men and women were equally represented in this case series, with a higher proportion of Black (n=8) and Hispanic (n=5) patients. All 17 patients had SARS-CoV-2 infection confirmed by reverse transcriptase-polymerase chain reaction, but only 3 presented with severe COVID-19 symptoms. Acute kidney injury (n=15) and proteinuria (n=11) were the most common indications for biopsy and these symptoms developed concurrently or within 1 week of COVID-19 symptoms in all patients. Acute tubular injury (n=14), collapsing glomerulopathy (n=7), and endothelial injury/thrombotic microangiopathy (n=6) were the most common histologic findings. 2 of the 3 transplant recipients developed active antibody-mediated rejection weeks after COVID-19. 8 patients required dialysis, but others improved with conservative management. Small study size and short clinical follow-up. Cases of even symptomatically mild COVID-19 were accompanied by acute kidney injury and/or heavy proteinuria that prompted a diagnostic kidney biopsy. Although acute tubular injury was seen among most of them, uncommon pathology such as collapsing glomerulopathy and acute endothelial injury were detected, and most of these patients progressed to irreversible kidney injury and dialysis.

Identifiants

pubmed: 33045255
pii: S0272-6386(20)31014-3
doi: 10.1053/j.ajkd.2020.10.001
pmc: PMC7546949
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

82-93.e1

Subventions

Organisme : NCATS NIH HHS
ID : KL2 TR001882
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK017047
Pays : United States

Informations de copyright

Copyright © 2020 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.

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Auteurs

Shreeram Akilesh (S)

Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA. Electronic address: shreeram@uw.edu.

Cynthia C Nast (CC)

Department of Pathology, Cedars-Sinai Medical Center, Los Angeles, CA.

Michifumi Yamashita (M)

Department of Pathology, Cedars-Sinai Medical Center, Los Angeles, CA.

Kammi Henriksen (K)

Department of Pathology, University of Chicago, Chicago, IL.

Vivek Charu (V)

Department of Pathology, Stanford University, Stanford, CA.

Megan L Troxell (ML)

Department of Pathology, Stanford University, Stanford, CA.

Neeraja Kambham (N)

Department of Pathology, Stanford University, Stanford, CA.

Erika Bracamonte (E)

Department of Pathology, University of Arizona, Tucson, AZ.

Donald Houghton (D)

Department of Pathology, Oregon Health & Science University, Portland, OR.

Naila I Ahmed (NI)

Northeast Nephrology Consultants, Joliet, IL.

Chyi Chyi Chong (CC)

Division of Nephrology, Department of Medicine, University of Arizona, Tucson, AZ.

Bijin Thajudeen (B)

Division of Nephrology, Department of Medicine, University of Arizona, Tucson, AZ.

Shehzad Rehman (S)

Division of Nephrology Department of Medicine, Oregon Health & Science University, Portland, OR.

Firas Khoury (F)

Oregon Kidney & Hypertension Clinic, Portland, OR.

Jonathan E Zuckerman (JE)

Department of Pathology and Laboratory Medicine, University of California Los Angeles, Los Angeles, CA.

Jeremy Gitomer (J)

Providence Alaska Medical Center, Anchorage, AK.

Parthassarathy C Raguram (PC)

CHI Franciscan Nephrology Associates, Tacoma, WA.

Shanza Mujeeb (S)

CHI Franciscan Nephrology Associates, Tacoma, WA.

Ulrike Schwarze (U)

Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA.

M Brendan Shannon (MB)

Division of Nephrology, Department of Medicine, University of Washington, Seattle, WA.

Iris De Castro (I)

Division of Nephrology, Department of Medicine, University of Washington, Seattle, WA.

Charles E Alpers (CE)

Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA.

Behzad Najafian (B)

Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA.

Roberto F Nicosia (RF)

Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA.

Nicole K Andeen (NK)

Department of Pathology, Oregon Health & Science University, Portland, OR. Electronic address: andeen@ohsu.edu.

Kelly D Smith (KD)

Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA. Electronic address: kelsmith@uw.edu.

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Classifications MeSH