Cited by 11Acute Kidney Injury ResearchRenal Diseases and GlomerulopathiesNephrotoxicity and Medicinal Plants

The spectrum of biopsy-proven kidney diseases, causes, and renal outcomes in acute kidney injury patients

Open access
Abuduwupuer, Zulihumaer, Lei, Qunjuan, Liang, Shaoshan, Xu, Feng, Liang, Dandan, Yang, Xue, Liu, Xumeng, Zeng, Caihong·2023·Nephron

Abstract

Introduction: Acute kidney injury (AKI) is a group of highly heterogeneous, complicated clinical syndromes. Although kidney biopsy plays an irreplaceable role in evaluating complex AKI, a few studies have focused on the clinicopathology of AKI biopsies. This study analyzed the pathological disease spectrum, causes, and renal outcomes of biopsied AKI patients. Methods: We retrospectively included 2,027 AKI patients who underwent kidney biopsies at a national clinical research center of kidney diseases from 2013 through 2018. To compare the biopsied AKI cases without and with coexisting glomerulopathy, patients were classified into acute tubular/tubulointerstitial nephropathy-associated AKI (ATIN-AKI) and glomerular disease-associated AKI (GD-AKI) groups. Results: Of 2,027 biopsied AKI patients, 65.1% were male, with a median age of 43 years. A total of 1,590 (78.4%) patients had coexisting GD, while only 437 (21.6%) patients had ATIN alone. The AKI patients with GD mainly (53.5%) manifested as stage 1 AKI, while most ATIN-AKI patients (74.8%) had stage 3 AKI. In the ATIN-AKI group, 256 (58.6%) patients had acute interstitial nephritis (AIN), and 77 (17.6%) had acute tubular injury (ATI). ATIN-AKI was mainly caused by drugs in 85.5% of AIN and 63.6% of ATI cases, respectively. In AKI patients with coexisting GD, the leading pathological diagnoses in over 80% of patients were IgA nephropathy (IgAN, 22.5%), minimal change disease (MCD, 17.5%), focal segmental glomerulosclerosis (FSGS, 15.3%), lupus nephritis (LN, 11.9%), membranous nephropathy (MN, 10.2%), and ANCA-associated vasculitis (AAV, 4.7%). A total of 775 patients were followed up within 3 months after renal biopsy; ATIN-AKI patients achieved statistically higher complete renal recovery than the GD-AKI patients (83.5% vs. 70.5%, p < 0.001). Conclusions: Most biopsied AKI patients have coexisting GD, while ATIN alone is seen less frequently. ATIN-AKI is mainly caused by drugs. In GD-AKI patients, IgAN, MCD, FSGS, LN, MN, and AAV are the leading diagnoses. Compared to AKI patients without GD, patients with GD suffer from worse renal function recovery.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1159/000530615

Cites

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • The disparity in recovery rates might be attributable to the direct reversibility of drug effects upon cessation compared to the often-progressive nature of autoimmune or infectious etiologies.

    “The disparity in recovery rates might be attributable to the direct reversibility of drug effects upon cessation compared to the often-progressive nature of autoimmune or infectious etiologies.”

    From Clinicopathological Characteristics and Kidney Outcomes in Biopsy-Confirmed Acute Interstitial Nephritis (2024) · cites this paper as [2]

    The Results section (Causes of ATI in AKI patients; page unavailable) reports higher complete recovery in ATIN-AKI than in glomerular disease-associated AKI, and identifies drugs as a common cause of ATIN-AKI. It does not attribute that disparity to recovery after stopping drugs or describe autoimmune or infectious etiologies as often progressive. (LLM, conf=0.84)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

The citation lists haven’t been fetched yet

References 31 · Cited by 11

Research works printed but not linked: 2

  1. [16]16. Kidney Disease: Improving Global Outcomes (KDIGO) Acute Kidney Injury Work Group. KDIGO clinical practice guideline for acute kidney injury. Kidney Int Suppl. 2012; 2:1-138.
  2. [30]30. Hida M, Saitoh H, Satoh T. Autopsy findings in postoperative acute renal failure patients, collected from the annuals of pathological autopsy cases in Japan. Tokai J Exp Clin Med. 1984;9(5-6):349-355.

Authors
Abuduwupuer, Z., Lei, Q., Liang, S., Xu, F., Liang, D., Yang, X., Liu, X., & Zeng, C.
Affiliations
Nanjing General Hospital of Nanjing Military Command (CN)
Corresponding author
Zeng, Caihong
Venue
Nephron
Publisher
S. Karger AG
Published
2023
Volume
147
Issue
9
Pages
541-549
ISSN
  • 1660-8151 (ISSN-L)
  • 2235-3186
OpenAlex
W4366815959
Cited by
11
References
31
Citations by year
2026: 1 · 2025: 4 · 2024: 6
FWCI
2.13
Type
journal article
Language
en
Open access
Locations
  • The Nephron journals/Nephron journals (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Natural Science Foundation of China (82070793)
  • Government of Jiangsu Province
Topics
  • Health Sciences › Medicine › Nephrology › Acute Kidney Injury Research
  • Health Sciences › Medicine › Nephrology › Renal Diseases and Glomerulopathies
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Nephrotoxicity and Medicinal Plants
Keywords
acute kidney injury, renal biopsy, glomerular disease, acute interstitial nephritis, acute tubular injury, drug-induced nephrotoxicity, IgA nephropathy, minimal change disease, focal segmental glomerulosclerosis, lupus nephritis, membranous nephropathy, ANCA-associated vasculitis, renal function recovery
MeSH terms
Adult, Biopsy, Female, Glomerulonephritis, IGA, Glomerulosclerosis, Focal Segmental, Humans, Kidney, Kidney Diseases, Male, Nephritis, Interstitial, Retrospective Studies, Acute Kidney Injury

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review