Evidence map›Paper›PMID 33305127›Full record

ArticleKidney international reports2020

Low-Level Proteinuria in Systemic Lupus Erythematosus.

Alice Chedid, Giovanni M Rossi, Francesco Peyronel, Steven Menez, Mohamed G Atta, Serena M Bagnasco, Lois J Arend, Avi Z Rosenberg, Derek M Fine

Open access · goldAbstract read
In one paragraph

Article in Kidney international reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
6.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 46 citations in OpenAlex.

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  10. Predictive Value of Laboratory Assays Toward Autoimmune Diseases.Journal of clinical laboratory analysis · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Alice ChedidDivision of Nephrology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Giovanni M RossiUO Nefrologia, Azienda Ospedaliero-Universitaria di Parma, Parma, Italy.
Francesco PeyronelUO Nefrologia, Azienda Ospedaliero-Universitaria di Parma, Parma, Italy.
Steven MenezDivision of Nephrology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Mohamed G AttaDivision of Nephrology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Serena M BagnascoDepartment of Pathology, Johns Hopkins University and Johns Hopkins Hospital, Baltimore, Maryland, USA.
Lois J ArendDepartment of Pathology, Johns Hopkins University and Johns Hopkins Hospital, Baltimore, Maryland, USA.
Avi Z RosenbergDepartment of Pathology, Johns Hopkins University and Johns Hopkins Hospital, Baltimore, Maryland, USA.
Derek M FineDivision of Nephrology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Johns Hopkins University · USUniversity of Parma · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionIn patients with systemic lupus erythematosus (SLE) without concurrent active urinary sediment or unexplained acute kidney injury (AKI), current guidelines recommend performing a kidney biopsy in those with at least 500 mg/24-hour (European League Against Rheumatism/European Renal Association-European Dialysis and Transplant Association [EULAR/ERA-EDTA]) or 1000 mg/24-hour (American College of Rheumatology [ACR]) proteinuria. To evaluate the relevance of these indications, we studied histopathologic findings in patients with SLE with proteinuria below these cutoffs.

methodsWe retrospectively reviewed the clinical, laboratory and histological characteristics of patients with SLE with <1000 mg/24-hour proteinuria (or mg/g urinary protein-to-creatinine ratio [UPCR]) who underwent their first kidney biopsy between 2003 and 2018.

resultsWe identified 87 patients with SLE with proteinuria less than 1000 mg/24-hour (or mg/g UPCR); 52 of 87 (60%) with isolated proteinuria, that is, without AKI or active urinary sediment (hematuria). Histologic evidence of lupus nephritis (LN) was present in 40 of 52 (76%). Of the 40 patients with LN, 12 had class I or II, 14 had class III or IV, 8 had class V, 6 had a combined proliferative and membranous LN. Non-lupus diagnoses included focal segmental glomerulosclerosis, acute interstitial nephritis, and others. Patient's age, low C3, low C4, and positivity for anti-double-stranded DNA (anti-dsDNA) antibodies predicted the histological diagnosis of LN on univariate logistic regression; however, a multivariate model including these parameters as independent covariates failed to predict LN.

conclusionsPatients with SLE with low-level proteinuria may have significant lupus- or non-lupus-related kidney disease with management implications. There was a significant burden of severe forms of LN. The presence of LN was not predicted by laboratory abnormalities. Based on our findings, we suggest current guidelines be revised to expand kidney biopsy indications to include isolated proteinuria of any grade.

Indexed as

acute kidney injuryhematuriahistologylupus nephritisproteinuria

Identifiers

PMID33305127
PMCPMC7710831
OpenAlexW3087382977

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.