Evidence map›Paper›PMID 28717937›Full record

ArticlePediatric nephrology (Berlin, Germany)2017

Clinical presentation and outcomes of childhood-onset membranous lupus nephritis.

Maria Pereira, Eyal Muscal, Karen Eldin, M John Hicks, Anna Carmela P Sagcal-Gironella, Marietta DeGuzman, Scott E Wenderfer

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Article in Pediatric nephrology (Berlin, Germany), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 19% 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, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

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  5. Advances in proteomic profiling of pediatric kidney diseases.Pediatric nephrology (Berlin, Germany) · 2022
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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

7 authors at 1 institution in 1 country.

Maria PereiraDepartment of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Eyal MuscalDepartment of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Karen EldinDepartment of Pathology and Immunology, Baylor College of Medicine-Texas Children's Hospital, Houston, TX, USA.
M John HicksDepartment of Pathology and Immunology, Baylor College of Medicine-Texas Children's Hospital, Houston, TX, USA.
Anna Carmela P Sagcal-GironellaDepartment of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Marietta DeGuzmanDepartment of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Scott E WenderferDepartment of Pediatrics, Baylor College of Medicine, Houston, TX, USA. wenderfe@bcm.edu.ORCID http://orcid.org/0000-0002-8991-8277
Baylor College of Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBest practices for managing childhood-onset membranous lupus nephritis (MLN) are not yet established. Most studies involve primarily or exclusively adult cohorts or pediatric cohorts with combinations of pure or mixed membranous and proliferative nephritis.

methodsWe performed a single-center cohort study of consecutively diagnosed children with pure MLN from 1990 and 2016. Patients received care in Houston, Texas, one of the most diverse metropolitan areas in North America. Renal outcomes were obtained using consensus definitions from the Childhood Arthritis and Rheumatology Research Alliance (CARRA). Logistic regression was used to detect predictors of complete renal response.

resultsA total of 56 children with MLN were identified (82% females, 44% black, 35% Hispanic) with a median follow-up time of 4.1 years. The mean age of MLN onset was 13.7 ± 3.4 years. On initial presentation 69% had nephrotic syndrome and 11% had acute kidney injury. Glucocorticoids were prescribed in 96% of patients and anti-malarials in 88%. Mycophenolate mofetil was the most common non-steroid immunosuppressive agent (69%), followed by rituximab (25%), cyclophosphamide (18%), and azathioprine (9%). Renin-angiotensin aldosterone system blocking agents were prescribed in 78% of patients. Of 37 patients with ≥2 years of follow-up, 74% achieved complete renal response at 24 months. No predictor variable of complete renal response was identified in this small cohort. Renal flares occurred in 48% of patients (86% proteinuric, 14% nephritic). On subsequent renal biopsy, 13% patients had developed proliferative nephritis.

conclusionsThis single-center cohort of childhood-onset MLN showed favorable outcomes. Utilizing pediatric renal outcomes definitions, we found that response rates were high, as were rates of renal flare.

Indexed as

AdolescentChildCohort StudiesFemaleFollow-Up StudiesGlomerulonephritis, MembranousGlucocorticoidsHumansImmunosuppressive AgentsKidneyLogistic ModelsLupus NephritisMaleRetrospective StudiesTexasTreatment OutcomeGlucocorticoidsImmunosuppressive AgentsChildrenLupus nephritisMembranous glomerulonephritisOutcomePediatric nephrology

Identifiers

PMID28717937
OpenAlexW2735866017

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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.