Evidence map›Paper›PMID 37868666›Full record

ArticleJournal of community hospital internal medicine perspectives2023

Lupus Podocytopathy: A Rare Cause of Nephrotic Syndrome in Patients with Systemic Lupus Erythematosus.

Omair Khan, Fatemeh Mohammadrezaei, Sadia Aslam, Mohammad H Khan, Rita D M Wilches, Sehajpreet Singh, Joshua Scheers-Masters

Abstract readCase Reports
In one paragraph

Article in Journal of community hospital internal medicine perspectives, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. [Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
    Article
  3. Article
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

7 authors.

Omair KhanMaimonides Medical Center, USA.
Fatemeh MohammadrezaeiMaimonides Medical Center, USA.
Sadia AslamMaimonides Medical Center, USA.
Mohammad H KhanShifa College of Medicine, Islamabad, Pakistan.
Rita D M WilchesMaimonides Medical Center, USA.
Sehajpreet SinghMaimonides Medical Center, USA.
Joshua Scheers-MastersMaimonides Medical Center, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lupus podocytopathy, a unique form of lupus nephritis, mimics minimal change disease (MCD) or primary focal segmental glomerulosclerosis (FSGS) and represents approximately 1% of lupus nephritis biopsies. Lupus podocytopathy is characterized by diffuse epithelial cell foot process effacement without immune complex deposition or with only mesangial immune complex deposition. We present the case of a young woman with systemic lupus erythematosus (SLE) who presented with nephrotic syndrome and acute kidney injury (AKI) and was subsequently diagnosed with lupus podocytopathy.

Indexed as

Lupus nephritisLupus podocytopathyMinimal change diseaseNephrotic syndromeSLE

Identifiers

PMID37868666
PMCPMC10589041

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.