Evidence map›Paper›PMID 31080631›Full record

ArticleLupus science & medicine2019

Outcome of participants with nephrotic syndrome in combined clinical trials of lupus nephritis.

Liliana Michelle Gomez Mendez, Matthew D Cascino, Tamiko R Katsumoto, Paul Brakeman, Paul Brunetta, David Jayne, Maria Dall'Era, Brad Rovin, Jay Garg

Open access · goldAbstract read
In one paragraph

Article in Lupus science & medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

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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 3 institutions in 2 countries.

Liliana Michelle Gomez MendezDepartment of Pediatric Nephrology, University of California San Francisco, San Francisco, California, USA.
Matthew D CascinoProduct Development Clinical Science, Genentech Inc, South San Francisco, California, USA.
Tamiko R KatsumotoProduct Development Clinical Science, Genentech Inc, South San Francisco, California, USA.
Paul BrakemanDepartment of Pediatric Nephrology, University of California San Francisco, San Francisco, California, USA.
Paul BrunettaProduct Development Clinical Science, Genentech Inc, South San Francisco, California, USA.
David JayneDepartment of Medicine, University of Cambridge School of Clinical Medicine, Cambridge, UK.
Maria Dall'EraDepartment of Rheumatology, University of California San Francisco, San Francisco, CA, United States.
Brad RovinDepartment of Internal Medicine/Nephrology, Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
Jay GargProduct Development Clinical Science, Genentech Inc, South San Francisco, California, USA.
University of California, San Francisco · USThe Ohio State University Wexner Medical Center · USUniversity of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe outcome of participants with nephrotic syndrome in clinical trials of lupus nephritis has not been studied in detail.

methodsCollated data from two randomised controlled trials in lupus nephritis, Lupus Nephritis Assessment of Rituximab (LUNAR) and A Study to Evaluate Ocrelizumab in Patients With Nephritis due to Systemic Lupus Erythematosus (BELONG) were analysed. Nephrotic syndrome was defined as albumin <3 g/dL and urine protein/creatinine ratio ≥3.5 g/g at start of trial. Renal response was defined as a first morning urine protein/creatinine ratio ≤0.5 g/g in addition to ≤25% increase in creatinine from trial entry assessed at week 48. Logistic regression was used to evaluate the association of nephrotic syndrome with renal response while adjusting for treatment received and ACE inhibitor or angiotensin receptor blocker use.

results28 (26%) participants with nephrotic syndrome achieved renal response as compared with 130 (52.5%) of those without (p<0.001). Having nephrotic syndrome at baseline significantly lowered the likelihood of achieving renal response (OR 0.32, 95 % CI 0.19 to 0.54, p<0.001). 125 (80%) participants achieved resolution of their nephrotic syndrome in a median time of 16 weeks.

conclusionsNephrotic syndrome at baseline decreases the likelihood of renal response at 1 year. Longer clinical trials or better short-term predictors of long-term outcomes may better assess the effect of novel therapeutic approaches on subjects with nephrotic syndrome.

Indexed as

biologicslupus nephritisoutcomes researchsystemic lupus erythematosus

Identifiers

PMID31080631
PMCPMC6485211
OpenAlexW2913712442

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Registered trials

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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.