Evidence map›Paper›PMID 37563703›Full record

Observational studyBMC nephrology2023

Clinical covariates influencing clinical outcomes in primary membranous nephropathy.

Lukas Westermann, Felix A Rottmann, Martin J Hug, Dawid L Staudacher, Rika Wobser, Frederic Arnold, Thomas Welte

Erratum issuedOpen access · goldAbstract readObservational Study
In one paragraph

Observational study in BMC nephrology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Observational
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Lukas WestermannDepartment of Medicine IV, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Felix A RottmannDepartment of Medicine IV, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Martin J HugPharmacy, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Dawid L StaudacherInterdisciplinary Medical Intensive Care (IMIT), Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Rika WobserDepartment of Medicine IV, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Frederic Arnold *Department of Medicine IV, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany. frederic.arnold@uniklinik-freiburg.de.
Thomas Welte *Department of Medicine IV, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany. thomas.welte@uniklinik-freiburg.de.
University of Freiburg · DEUniversity Medical Center Freiburg · DEInstitute of Medical Microbiology and Hygiene · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrimary membranous nephropathy (PMN) frequently causes nephrotic syndrome and declining kidney function. Disease progression is likely modulated by patient-specific and therapy-associated factors awaiting characterization. These cofactors may facilitate identification of risk groups and could result in more individualized therapy recommendations.

methodsIn this single-center retrospective observational study, we analyze the effect of patient-specific and therapy-associated covariates on proteinuria, hypoalbuminemia, and estimated glomerular filtration rate (eGFR) in 74 patients diagnosed with antibody positive PMN and nephrotic-range proteinuria (urine-protein-creatinine-ratio [UPCR] ≥ 3.5 g/g), treated at the University of Freiburg Medical Center between January 2000 - November 2022. The primary endpoint was defined as time to proteinuria / serum-albumin response (UPCR ≤ 0.5 g/g or serum-albumin ≥ 3.5 g/dl), the secondary endpoint as time to permanent eGFR decline (≥ 40% relative to baseline).

resultsThe primary endpoint was reached after 167 days. The secondary endpoint was reached after 2413 days. Multivariate time-to-event analyses showed significantly faster proteinuria / serum-albumin response for higher serum-albumin levels (HR 2.7 [95% CI: 1.5 - 4.8]) and cyclophosphamide treatment (HR 3.6 [95% CI: 1.3 - 10.3]). eGFR decline was significantly faster in subjects with old age at baseline (HR 1.04 [95% CI: 1 - 1.1]).

conclusionHigh serum-albumin levels, and treatment with cyclophosphamide are associated with faster proteinuria reduction and/or serum-albumin normalization. Old age constitutes a risk factor for eGFR decline in subjects with PMN.

Indexed as

Glomerulonephritis, MembranousNephrotic SyndromeCyclophosphamideHumansProteinuriaSerum AlbuminCyclophosphamideSerum AlbuminChronic kidney diseaseImmunosuppressionNephrotic syndromePLA2-RPrimary membranous nephropathyRituximabTHSD7A

Identifiers

PMID37563703
PMCPMC10413503
OpenAlexW4385722885

What OpenQuestion holds

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LicenceCC BY
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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.