Evidence map›Paper›PMID 29435367›Full record

ArticleAutoimmune diseases2017

Anti-Myeloperoxidase Antibodies Associate with Future Proliferative Lupus Nephritis.

S W Olson, J J Lee, M Poirier, D J Little, L K Prince, T P Baker, J D Edison, K C Abbott

Open access · goldAbstract read
In one paragraph

Article in Autoimmune diseases, 2017. 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
0.4field-weighted citation impact, top 37% 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, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Detection of PLA2R Autoantibodies before the Diagnosis of Membranous Nephropathy.Journal of the American Society of Nephrology : JASN · 2020
    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

8 authors at 4 institutions in 1 country.

S W OlsonWalter Reed National Military Medical Center, 8901 Wisconsin Avenue, Bethesda, MD 20889, USA.ORCID 0000-0002-1567-6201
J J LeeNaval Medical Center San Diego, 34800 Bob Wilson Drive, San Diego, CA 92134, USA.
M PoirierSan Antonio Military Medical Center, 3551 Roger Brooke Dr., Fort Sam Houston, TX 78234, USA.
D J LittleWalter Reed National Military Medical Center, 8901 Wisconsin Avenue, Bethesda, MD 20889, USA.
L K PrinceWalter Reed National Military Medical Center, 8901 Wisconsin Avenue, Bethesda, MD 20889, USA.
T P BakerWalter Reed National Military Medical Center, 8901 Wisconsin Avenue, Bethesda, MD 20889, USA.
J D EdisonWalter Reed National Military Medical Center, 8901 Wisconsin Avenue, Bethesda, MD 20889, USA.
K C AbbottThe National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), NIH, 6707 Democracy Blvd, Bethesda, MD 20892, USA.
Walter Reed National Military Medical Center · USBrooke Army Medical Center · USNational Institute of Diabetes and Digestive and Kidney Diseases · USNaval Medical Center San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe subclinical pathophysiology of proliferative lupus nephritis (PLN) has not been fully elucidated. Myeloperoxidase anti-neutrophil cytoplasmic antibody (MPO-ANCA) is associated with PLN, but prediagnostic levels have not been reported.

methodsWe performed a retrospective case-control Department of Defense Serum Repository (DoDSR) study comparing MPO-ANCA levels in longitudinal prediagnostic serum samples for 23 biopsy confirmed proliferative lupus nephritis (PLN) patients to DoDSR identified age, sex, race, and age of serum matched healthy and SLE without LN disease controls. We also compared the temporal relationship of MPO-ANCA to anti-double stranded DNA antibodies (dsDNAab).

resultsA greater proportion of PLN patients had prediagnostic MPO-ANCA levels above ≥3 U/mL and ≥6 U/mL compared to SLE without LN (91% versus 43%,

conclusionsSubclinical MPO-ANCA levels could distinguish future PLN from SLE without LN. MPO-ANCA manifests prior to clinical disease and subclinical dsDNAab to suggest that it may contribute directly to PLN pathogenicity.

Identifiers

PMID29435367
PMCPMC5757094
OpenAlexW2776402174

What OpenQuestion holds

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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.