Evidence map›Paper›PMID 35018582›Full record

ArticleClinical rheumatology2022

Cardiac manifestations in primary antiphospholipid syndrome and their association to antiphospholipid antibodies' types and titers-cross-sectional study of Serbian cohort.

Aleksandra Djokovic, Ljudmila Stojanovich, Natasa Stanisavljevic, Sandra Djokic, Branka Filipovic, Predrag Matic, Milomir Milanovic, Svetlana Apostolovic, Jovica Saponjski

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Article in Clinical rheumatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors at 5 institutions in 1 country.

Aleksandra DjokovicDepartment of Cardiology, Division of Interventional Cardiology, University Hospital Medical Center Bezanijska Kosa, Belgrade, Serbia. drsaska@yahoo.com.ORCID http://orcid.org/0000-0002-6094-7306
Ljudmila StojanovichDepartment of Rheumatology, University Hospital Medical Center Bezanijska Kosa, Belgrade, Serbia.
Natasa StanisavljevicDepartment of Hematology, University Hospital Medical Center Bezanijska Kosa, Belgrade, Serbia.
Sandra DjokicClinical Center of Serbia, Pulmonology Clinic, Belgrade, Serbia.
Branka FilipovicFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Predrag MaticFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Milomir MilanovicClinic for Infectious and Tropical Diseases, Military Medical Academy, Belgrade, Serbia.
Svetlana ApostolovicDepartment of Professional and Scientific Training, Cardiology Clinic, Clinical Center of Nis, Nis, Serbia.
Jovica SaponjskiFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
University of Belgrade · RSUniversity Hospital Medical Center Bezanijska kosa · RSCentar za Promociju Nauke · RSMilitary Medical Academy · RSUniversity of Nis · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAntiphospholipid syndrome (APS) is multisystem autoimmune coagulopathy with antiphospholipid antibodies (aPL) in its ground, manifested as a primary disease (PAPS) or in the setting of other conditions, most commonly systemic lupus erythematosus. The objective of this cross-sectional study was to investigate various cardiac manifestations and their possible relation to aPL type and titer in a Serbian cohort of PAPS patients.

methodsA total of 360 PAPS patients were analyzed and aPL analysis included detection of anticardiolipin antibodies (aCL: IgG/IgM), anti-ß2glycoprotein I (ß2GPI: IgG/IgM), and lupus anticoagulant (LA). Cardiac manifestations investigated were valvular lesions (comprehending valvular thickening and dysfunction not related to age and pseudoinfective endocarditis), coronary artery disease (CAD) with specific insight for myocardial infarction (MI), chronic cardiomyopathy (CMP), and acute decompensated heart failure (ADHF) as well as pulmonary hypertension (PH) and intracardiac thrombus presence.

resultsThe prevalence of cardiac manifestations overall was 19.6%. There was a strong association between age and the majority of cardiac manifestations, as well as standard atherosclerotic risk factors. aCL IgG-positive patients had a higher prevalence of valvular lesions (p = 0.042). LA presence was significantly related to MI (p = 0.031) and PH (p = 0.044). CMP and ADHF were significantly related to higher titers of aCl IgG (p = 0.033, p = 0.025 respectively). Age and smoking were independent risk predictors for MI in PAPS with meaningful risk for LA positivity (OR 2.567 CI 0.671-9.820 p = 0.168).

conclusionsCertain cardiac manifestations in PAPS were related to certain aPL type and/or titer levels, imposing confirmation in prospective studies. Preventive actions, comprehending proper anticoagulant/antithrombotic therapy, and intense action against standard atherosclerotic risk factors are of utmost importance in this group of patients. Key Points • In Serbian patients with primary antiphospholipid syndrome (PAPS), prevalence of non-criteria cardiac manifestations was 19.6% and they were significantly related to certain antiphospholipid antibodies and titers. • Lupus anticoagulant was a meaningful predictor of myocardial infarction, enabling possible risk stratification and proper preventive and therapeutical strategies in this subgroup of PAPS patients. • Patients with high titers of aCL IgG are more prone to acute decompensated heart failure occurence, imposing careful follow-up of these patients • Based on the analysis of the Serbian PAPS cohort, even being non-criterial, cardiology manifestations are significantly present and inclusion of cardiologists in treatment and follow-up of these patients should be implied from the diagnosis establishment.

Indexed as

Antiphospholipid SyndromeHeart FailureHypertension, PulmonaryMyocardial InfarctionAntibodies, AnticardiolipinAntibodies, AntiphospholipidCross-Sectional StudiesHumansImmunoglobulin GImmunoglobulin MLupus Coagulation InhibitorProspective StudiesSerbiaAntibodies, AnticardiolipinAntibodies, AntiphospholipidImmunoglobulin GImmunoglobulin MLupus Coagulation InhibitorAntiphospholipid antibodiesAntiphospholipid syndromeCardiac manifestationsNational cohort study

Identifiers

PMID35018582
OpenAlexW4206630004

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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.