Evidence map›Paper›PMID 32691878›Full record

SynthesisClinical and experimental immunology2020

The alternative complement pathway in ANCA-associated vasculitis: further evidence and a meta-analysis.

S Moiseev, J M Lee, A Zykova, N Bulanov, P Novikov, E Gitel, M Bulanova, E Safonova, J I Shin, A Kronbichler and 1 more

Open access · bronzeAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Clinical and experimental immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 4% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 63 citations in OpenAlex.

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  12. Making use of avacopan in clinical practice.Clinical kidney journal · 2026
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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

11 authors at 6 institutions in 4 countries.

S Moiseev *Tareev Clinic of Internal Diseases, Sechenov First Moscow State Medical University, Moscow, Russia.ORCID 0000-0002-7232-4640
J M Lee *Department of Pediatrics, Chungnam National University Hospital and College of Medicine, Daejeon, Korea.ORCID 0000-0003-3932-614X
A ZykovaTareev Clinic of Internal Diseases, Sechenov First Moscow State Medical University, Moscow, Russia.ORCID 0000-0002-7674-8643
N BulanovTareev Clinic of Internal Diseases, Sechenov First Moscow State Medical University, Moscow, Russia.ORCID 0000-0002-3989-2590
P NovikovTareev Clinic of Internal Diseases, Sechenov First Moscow State Medical University, Moscow, Russia.ORCID 0000-0003-0148-5655
E GitelCentral Laboratory, Sechenov First Moscow State Medical University, Moscow, Russia.ORCID 0000-0001-5089-0249
M BulanovaVladimir Regional Clinical Hospital, Vladimir, Russia.
E SafonovaLomonosov Moscow State University, Moscow, Russia.
J I ShinDepartment of Pediatrics, Yonsei University College of Medicine, Seoul, South Korea.ORCID 0000-0003-2326-1820
A KronbichlerDepartment of Internal Medicine IV (Nephrology and Hypertension), Medical University Innsbruck, Innsbruck, Austria.ORCID 0000-0002-2945-2946
D R W JayneDepartment of Medicine, University of Cambridge, Cambridge, UK.
Sechenov University · RUChungnam National University Hospital · KRInnsbruck Medical University · ATLomonosov Moscow State University · RUUniversity of Cambridge · GBYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We compared the common pathway components C3a, C5a and membrane attack complex (MAC), also known as C5b-9, and the alternative pathway components factor B and properdin in patients with ANCA-associated vasculitis (AAV) and healthy controls, and conducted a meta-analysis of the available clinical evidence for the role of complement activation in the pathogenesis of AAV. Complement components were evaluated in 59 patients with newly diagnosed or relapsing granulomatosis with polyangiitis or microscopic polyangiitis and 36 healthy volunteers. In 28 patients, testing was repeated in remission. Next, we performed a meta-analysis by searching databases to identify studies comparing complement levels in AAV patients and controls. A random-effects model was used for statistical analyses. The median concentrations of MAC, C5a, C3a and factor B were higher in active AAV patients (P < 0·001). Achievement of remission was associated with reductions in C3a (P = 0·005), C5a (P = 0·035) and factor B levels (P = 0·045), whereas MAC and properdin levels did not change. In active AAV, there were no effects of ANCA specificity, disease phenotype, previous immunosuppression or disease severity on complement levels. A total of 1122 articles were screened, and five studies, including this report, were entered into the meta-analysis. Plasma MAC, C5a and factor B in patients with active AAV were increased compared to patients in remission (excluding factor B) and controls. Changes in C3a were of borderline significance. Our findings and the results of the meta-analysis support activation of the complement system predominantly via the alternative pathway in AAV patients.

Indexed as

Anti-Neutrophil Cytoplasmic Antibody-Associated VasculitisComplement Pathway, AlternativeComplement System ProteinsHumansComplement System ProteinsANCAbiomarkercomplementmeta-analysisvasculitis

Identifiers

PMID32691878
PMCPMC7670131
OpenAlexW3045184294

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.