Evidence map›Paper›PMID 41377428›Full record

ReviewAnnals of medicine and surgery (2012)2025

Acute myocardial infarction and antiphospholipid syndrome: an updated systematic review and meta-analysis.

Arash Ghani Dehkordi, Ryan Koh, Prashasthi Devaiah, Aleena Anna Alexander, Dilisa Rajamanoharan, Mekha Mohan, Pranav Mohandas, Nino Akubardia

Abstract readReview
In one paragraph

Review in Annals of medicine and surgery (2012), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Arash Ghani DehkordiDepartment of Molecular and Clinical Medicine, University of Dundee, Dundee, Scotland.ORCID https://orcid.org/0009-0002-1754-2271
Ryan KohDepartment of Molecular and Clinical Medicine, University of Dundee, Dundee, Scotland.ORCID https://orcid.org/0009-0005-6241-5812
Prashasthi DevaiahDepartment of Molecular and Clinical Medicine, University of Dundee, Dundee, Scotland.ORCID https://orcid.org/0009-0002-5456-2327
Aleena Anna AlexanderDepartment of Cardiovascular Diseases, Tbilisi State Medical University, Tbilisi, Georgia.ORCID https://orcid.org/0009-0003-3404-3703
Dilisa RajamanoharanDepartment of Cardiovascular Diseases, Tbilisi State Medical University, Tbilisi, Georgia.ORCID https://orcid.org/0009-0005-7161-3351
Mekha MohanDepartment of Cardiovascular Diseases, Tbilisi State Medical University, Tbilisi, Georgia.ORCID https://orcid.org/0009-0009-5675-9140
Pranav MohandasDepartment of Cardiovascular Diseases, Tbilisi State Medical University, Tbilisi, Georgia.ORCID https://orcid.org/0009-0007-1664-8724
Nino AkubardiaDepartment of Molecular and Clinical Medicine, University of Dundee, Dundee, Scotland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Antiphospholipid syndrome (APS) is an autoimmune condition associated with an increased risk of thrombosis, myocardial infarction, strokes, recurrent miscarriages, and other cardiovascular events. Acute myocardial infarction (AMI) is a severe, potentially fatal, but yet uncommon complication of APS. This comprehensive systematic review, the largest to date, aims to explore the occurrence, clinical presentations, and outcomes of AMI in individuals with APS from inception to March 2025, highlighting the evolution of management and outcomes over time. Methods: We searched through PubMed, Scopus, Web of Science, and Cochrane Central Register from inception to March 2025 in order to find case studies, series, and reports of AMI in individuals diagnosed with APS. Data were analysed quantitatively with continuous variables presented as means ± standard deviations and categorical data as frequencies or percentages. Results: Our review included 108 cases of AMI complicating APS, with 47 cases of primary APS, and 60 cases to secondary APS due to systemic lupus erythematosus. The average age at diagnosis was 36.37 ± 13.95 years. Among subjects, 36 had no history of thromboembolic events (challenging the assumption that previous thrombosis predicts cardiac complications), 34 had deep vein thrombosis, and 10 experienced cardiac-related thromboembolic events. The most common presentation of AMI in subjects with APS was ST-elevation in 90 subjects (83% of cases). The median activated partial thromboplastin time was 54 s (interquartile range: 42-84 s). Thrombocytopenia was observed in 23 cases, while 11 cases had thrombocytosis. Positive results for antiphospholipid antibodies included anticardiolipin antibody in 75 cases, lupus anticoagulant in 60 cases, and anti-β2 glycoprotein I in 25 cases. The overall prognosis was favourable, with a survival rate of 93.5% (101 individuals survived), 7 deaths, and 15 recurrent AMI episodes (13.8% of cases). Conclusion: This comprehensive systematic review calls attention to the importance of considering APS as a potential risk factor for AMI, particularly in younger adults without typical cardiovascular risk factors, yet it carries a more favourable prognosis than previously thought. The findings highlight the high prevalence of thrombotic events, emphasise the importance of considering APS in young individuals with AMI, and suggest favourable outcomes in APS-associated AMI.

Indexed as

acute myocardial infarctionantiphospholipid syndromemeta-analysissystemic lupus erythematosus

Identifiers

PMID41377428
PMCPMC12688783

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.