Evidence map›Paper›PMID 36227113›Full record

ArticleRheumatology (Oxford, England)2023

Antiphospholipid antibody positivity in early systemic lupus erythematosus is associated with subsequent vascular events.

Nicola Farina, Ruya Abdulsalam, Thomas McDonnell, Charis Pericleous, Amrita D'Souza, Vera M Ripoll, Jemma Webster, David A Isenberg, Ian Giles, Anisur Rahman

Open access · bronzeAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

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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

10 authors at 2 institutions in 2 countries.

Nicola FarinaCentre for Rheumatology Research, Division of Medicine, University College London, London, UK.
Ruya AbdulsalamCentre for Rheumatology Research, Division of Medicine, University College London, London, UK.
Thomas McDonnellCentre for Rheumatology Research, Division of Medicine, University College London, London, UK.
Charis PericleousCentre for Rheumatology Research, Division of Medicine, University College London, London, UK.
Amrita D'SouzaCentre for Rheumatology Research, Division of Medicine, University College London, London, UK.
Vera M RipollCentre for Rheumatology Research, Division of Medicine, University College London, London, UK.
Jemma WebsterCentre for Rheumatology Research, Division of Medicine, University College London, London, UK.
David A IsenbergCentre for Rheumatology Research, Division of Medicine, University College London, London, UK.ORCID 0000-0001-9514-2455
Ian GilesCentre for Rheumatology Research, Division of Medicine, University College London, London, UK.
Anisur RahmanCentre for Rheumatology Research, Division of Medicine, University College London, London, UK.ORCID 0000-0003-2346-4484
University College London · GBVita-Salute San Raffaele University · IT

Funding

Arthritis Research UK 19423Department of HealthVersus Arthritis 19423Versus Arthritis 21223
6 · The paper itself

Abstract

objectiveaPL are found in the blood of 20-30% of patients with SLE. Although aPL cause vascular thrombosis in the antiphospholipid syndrome, it is not clear whether positive aPL levels in early SLE increase risk of subsequent vascular events (VE). In a previous analysis of 276 patients with SLE, we found that early positivity for ≥2 of IgG anti-cardiolipin (anti-CL), IgG anti-β2-glycoprotein I (anti-β2GPI) and anti-domain I of β2-glycoprotein I (anti-DI) showed a possible association with VE. Here we have extended that analysis.

methodsSerum samples taken from 501 patients with SLE early in their disease had been tested for IgG anti-CL, anti-β2GPI and anti-DI by ELISA. Complete VE history was available for 423 patients of whom 23 were excluded because VE occurred before the diagnosis of SLE. For the remaining 400 patients we carried out Kaplan-Meier survival analysis to define groups at higher risk of VE.

resultsOf 400 patients, 154 (38.5%) were positive for one or more aPL, 27 (6.8%) were double/triple-positive and 127 (31.8%) were single-positive. There were 91 VE in 77 patients, of whom 42 were aPL-positive in early disease. VE were significantly increased in aPL-positive vs aPL-negative patients (P = 0.041) and in double/triple-positive vs single-positive vs aPL-negative patients (P = 0.0057). Omission of the IgG anti-DI assay would have missed 14 double/triple-positive patients of whom six had VE.

conclusionDouble/triple-positivity for IgG anti-CL, anti-β2GPI and anti-DI in early SLE identifies a population at higher risk of subsequent VE.

Indexed as

Antiphospholipid SyndromeLupus Erythematosus, SystemicAntibodies, Antiphospholipidbeta 2-Glycoprotein ICardiolipinsHumansImmunoglobulin GAntibodies, Antiphospholipidbeta 2-Glycoprotein ICardiolipinsImmunoglobulin GAPScardiovascularSLE

Identifiers

PMID36227113
PMCPMC10234200
OpenAlexW4304990504

What OpenQuestion holds

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LicenceCC BY-NC
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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.