Evidence map›Paper›PMID 39192704›Full record

ArticleClinical and experimental immunology2024

Antibody profiles in the mosaic of 'seronegative' APS syndrome.

Simona Truglia, Gloria Riitano, Silvia Mancuso, Serena Recalchi, Luca Rapino, Cristina Garufi, Valeria Manganelli, Tina Garofalo, Roberta Misasi, Cristiano Alessandri and 4 more

Abstract read
In one paragraph

Article in Clinical and experimental immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

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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

14 authors.

Simona TrugliaReumatologia, Dipartimento di Scienze Cliniche Internistiche, Anestesiologiche Cardiovascolari, Sapienza University, Rome, Italy.
Gloria RiitanoDipartimento di Medicina Sperimentale, Sapienza University, Rome, Italy.
Silvia MancusoReumatologia, Dipartimento di Scienze Cliniche Internistiche, Anestesiologiche Cardiovascolari, Sapienza University, Rome, Italy.
Serena RecalchiDipartimento di Medicina Sperimentale, Sapienza University, Rome, Italy.
Luca RapinoReumatologia, Dipartimento di Scienze Cliniche Internistiche, Anestesiologiche Cardiovascolari, Sapienza University, Rome, Italy.
Cristina GarufiReumatologia, Dipartimento di Scienze Cliniche Internistiche, Anestesiologiche Cardiovascolari, Sapienza University, Rome, Italy.
Valeria ManganelliDipartimento di Medicina Sperimentale, Sapienza University, Rome, Italy.
Tina GarofaloDipartimento di Medicina Sperimentale, Sapienza University, Rome, Italy.
Roberta MisasiDipartimento di Medicina Sperimentale, Sapienza University, Rome, Italy.
Cristiano AlessandriReumatologia, Dipartimento di Scienze Cliniche Internistiche, Anestesiologiche Cardiovascolari, Sapienza University, Rome, Italy.ORCID 0000-0003-4149-5321
Maurizio SoriceDipartimento di Medicina Sperimentale, Sapienza University, Rome, Italy.ORCID 0000-0003-3534-1502
Agostina LongoDipartimento di Medicina Sperimentale, Sapienza University, Rome, Italy.
Fabrizio ContiReumatologia, Dipartimento di Scienze Cliniche Internistiche, Anestesiologiche Cardiovascolari, Sapienza University, Rome, Italy.
Antonella CapozziDipartimento di Medicina Sperimentale, Sapienza University, Rome, Italy.

Funding

Sapienza University of Rome Rome_Tech_Spoke_1_DMS
6 · The paper itself

Abstract

Clinical manifestations, as distinct from thrombotic and obstetric morbidity, were recently included in the update of classification criteria of the antiphospholipid syndrome (APS). However, the existence of several patients with clinical manifestations suggestive of APS, but negative for criteria antiphospholipid antibodies (aPLs) [anti-cardiolipin antibodies (aCL), anti-β2-glycoprotein I antibodies (aβ2-GPI), and lupus anticoagulant] may suggest an update of diagnostic criteria. In this study, we analysed the prevalence of six non-criteria aPLs in a large monocentric cohort of patients with seronegative APS (SN-APS), to investigate their possible diagnostic role. aCL IgA, aβ2-GPI IgA, and aβ2-GPI Domain 1 antibodies were detected by chemiluminescence, anti-phosphatidylserine/prothrombin (aPS/PT) IgG, anti-vimentin/cardiolipin (aVim/CL) IgG, and anti-carbamylated-β2-glycoprotein I (aCarb-β2-GPI) IgG by ELISA in sera from 144 SN-APS patients. In SN-APS patients, aCL IgA was detected in 4/144 (2.77%), aβ2-GPI IgA in 2/144 (1.39%), aβ2-GPI-Domain 1 in 1/144 (0.69%), aPS/PT in 16/144 (11.11%), aVim/CL in 37/144 (25.69%), and aCarb-β2-GPI in 43/144 patients (29.86%). Patients negative for all non-criteria aPL assays were 77/144 (53.47%). Notably, the Venn diagram showed that aCarb-β2-GPI together with aVim/CL represented the prevalent combination of positive antibodies. In SN-APS patients, aCL IgA were associated with recurrent thrombosis (OR 11.48; P = 0.03); in obstetric SN-APS patients, aPS/PT were significantly associated with foetal deaths (OR 4.84; P = 0.01), aVim/CL with spontaneous abortions (OR 2.71; P = 0.016). This study indicates that aPS/PT, aVim/CL and aCarb-β2-GPI antibodies may represent useful tools to identify 'seronegative' APS patients, who are negative for criteria aPLs, supporting the need to make testing for non-criteria aPLs more accessible in patients with SN-APS.

Indexed as

Antibodies, AnticardiolipinAntibodies, AntiphospholipidAntiphospholipid Syndromebeta 2-Glycoprotein IAdultAgedAutoantibodiesFemaleHumansImmunoglobulin AImmunoglobulin GMaleMiddle AgedPregnancyAntibodies, AnticardiolipinAntibodies, AntiphospholipidAutoantibodiesbeta 2-Glycoprotein IImmunoglobulin AImmunoglobulin Ganti-phosphatidylserine/prothrombinantiphospholipid syndromeanti-vimentin/cardiolipinanti-β2-GPIcarbamylationseronegative APS

Identifiers

PMID39192704
PMCPMC11557137

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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.