Evidence map›Paper›PMID 33585954›Full record

ArticleRheumatology international2021

Antibody subtypes and titers predict clinical outcomes in ANCA-associated vasculitis.

Muhammad Aljuhani, Devan Makati, Abigail Hoff, Jesse Thompson, Bethany Pellegrino, Khaled Shawwa, Rebecca Schmidt, Dinesh Kannabhiran

Abstract read
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In one paragraph

Article in Rheumatology international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
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  3. Observational
  4. Review
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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

8 authors at 1 institution in 1 country.

Muhammad AljuhaniDepartment of Nephrology, University of Minnesota, Minneapolis, MN, USA.
Devan MakatiSection of Nephrology, Department of Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.
Abigail HoffDepartment of Pharmacy, West Virginia University School of Pharmacy, Morgantown, WV, USA.ORCID http://orcid.org/0000-0002-8497-451X
Jesse ThompsonDepartment of Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.
Bethany PellegrinoSection of Nephrology, Department of Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.ORCID http://orcid.org/0000-0003-3688-9377
Khaled ShawwaSection of Nephrology, Department of Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.ORCID http://orcid.org/0000-0001-8849-5244
Rebecca SchmidtSection of Nephrology, Department of Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.ORCID http://orcid.org/0000-0001-5232-5083
Dinesh KannabhiranSection of Nephrology, Department of Medicine, West Virginia University School of Medicine, Morgantown, WV, USA. dk0053@hsc.wvu.edu.ORCID http://orcid.org/0000-0003-1686-827X
West Virginia University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of this study is to evaluate the association between antineutrophil cytoplasmic autoantibody (ANCA) subtype and ANCA titers on clinical outcomes and disease activity among a cohort of patients from Central Appalachia diagnosed with ANCA-associated vasculitis (AAV) over a 3-decade period. This is a retrospective chart review of all patients diagnosed with AAV. ANCA subtypes (myeloperoxidase (MPO) and proteinase 3 (PR3)) and titers at the time of diagnosis and at the time of relapse or last follow-up were evaluated along with patient outcomes. Outcomes of interest included relapse, development of end-stage renal disease (ESRD) and mortality. Sensitivity analysis and multivariable analysis were performed. Of the 202 patients, 111 patients were MPO-ANCA positive and 91 patients were PR3-ANCA positive. Relapse was more frequent among patients with PR3-ANCA compared to MPO-ANCA (35% vs 12%, p < 0.001). In both ANCA subgroups, the strongest predictor of relapse was an increase in titers prior to relapse, HR 8.1 (95% CI 1.6-40), p 0.009. Patients who achieved serological remission had a lower risk of ESRD [sub-HR 0.31 (95% CI 0.11-0.89)] and mortality [HR (95% CI) 0.24 (0.07-0.7)]. PR3-ANCA was associated with higher risk of ESRD [sub-HR 3.1 (95% CI 1.1-8.5)]. There was no difference in mortality between patients with MPO-ANCA and PR3-ANCA. Our study supports the use of both ANCA subtypes and titer levels for predicting clinical outcomes in patients receiving treatment for AAV. Monitoring of ANCA antibody titers may be useful since both serological remission and increase in titers provide prognostic information.

Indexed as

AdultAgedAntibodies, Antineutrophil CytoplasmicAnti-Neutrophil Cytoplasmic Antibody-Associated VasculitisBiomarkersDisease ProgressionFemaleHumansKidney Failure, ChronicMaleMiddle AgedMyeloblastinPeroxidaseRecurrenceRetrospective StudiesAntibodies, Antineutrophil CytoplasmicBiomarkersMPO protein, humanMyeloblastinPeroxidaseANCA-associated vasculitisANCA subtypesANCA titersClinical outcomesEnd-stage renal diseaseMortalityRelapseSerological remission

Identifiers

PMID33585954
OpenAlexW3131355547

What OpenQuestion holds

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Read underepoch 390

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.