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1108 Repeat kidney biopsy for lupus nephritis after induction: histologic and clinical responses in childhood-onset SLE

2022· article· en· W4313533193 on OpenAlexaff
Scott E. Wenderfer, Bianca Saenz, Maria M. Pereira, M John Hicks

Bibliographic record

Venuenot available
Typearticle
Languageen
FieldMedicine
TopicSystemic Lupus Erythematosus Research
Canadian institutionsBC Children's HospitalUniversity of British Columbia
Fundersnot available
KeywordsLupus nephritisMedicineBiopsyInternal medicineRenal biopsySystemic lupus erythematosusCohortRetrospective cohort studyGastroenterologyPathologyDisease

Abstract

fetched live from OpenAlex

Background In children with proliferative lupus nephritis, response to induction treatment is based on clinical parameters. The added benefit of repeat kidney biopsy in defining therapy response remains unclear. Emerging adult data suggests a discordancy between clinical and histological outcomes. In children, we hypothesize that histologic reassessment after induction therapy correlates better with clinical remission. Methods A single-center retrospective observational cohort study was conducted in childhood-onset proliferative lupus nephritis with a repeat biopsy after 5-9 months of induction therapy from 2007 to 2019. LN response was determined clinically. Histologic activity and damage were calculated using National Institutes of Health activity and chronicity indices. Lupus nephritis class transformation and changes in the degree of immune complex deposition were determined. Descriptive statistics and comparison tests were used before and after induction treatment. Results A total of 44 patients were identified. Complete clinical response was achieved in 43% (19/44) after induction and 69% (29/42) at one year. None of the complete responders after induction had histologic activity index of > 2 on repeat biopsy (figure 1). Activity index after induction in complete responders (median 1, range 0-2) was lower than in partial or non-responders (median 2, range 0-10) (p-value < 0.005). Complete clinical response was associated with transformation to a non-proliferative class in 79% (15/19) and a reduction in immune complex deposition in 68% (13/19) on repeat biopsy. Conclusions Unlike adult-onset lupus nephritis, clinical and histologic remission are more congruent after induction therapy in childhood-onset disease. There was good correlation between clinical response and activity index. Lay Summary Lupus nephritis can cause kidney failure. The need to balance risks and benefits of immunosuppression requires stringent monitoring. In adults with lupus, available diagnostics are insufficient to gauge response to initial ”induction” therapy and repeat biopsy studies are necessary to rigorously test novel biomarkers. Here we show that repeat biopsy in children performed 1/2 year into therapy correlates well with clinical response, but there is a subset of children with sub-clinical scarring that would be missed without repeat biopsy - this subset may be at risk long-term for kidney failure.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.004
Threshold uncertainty score0.008

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.040
GPT teacher head0.345
Teacher spread0.305 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2022
Admission routes1
Has abstractyes

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