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Updated: Jul 11, 2026

Pipeline for Multi-Scale Three-Dimensional Anatomic Study of the Human Heart
Published on: June 28, 2024
The Heart and APS
1Instituto Nacional de Cardiología Ignacio Chávez, Universidad Nacional Autónoma de México, Juan Badiano # 1 Tlalpan, Mexico City 14080, Mexico. marycarmenamigo@gmail.com
Insights
Antiphospholipid syndrome (APS) frequently affects the heart, particularly heart valves, leading to characteristic thickening. Standard treatments are ineffective for valvular lesions, and surgery carries high risks in APS patients.
Area of Science:
- Cardiology
- Rheumatology
- Immunology
Background:
- Antiphospholipid syndrome (APS) is an autoimmune disorder.
- The heart is a known target organ in APS, with various cardiovascular manifestations.
- Understanding these cardiac impacts is crucial for patient management.
Observation:
- Valvular involvement is the most common cardiac manifestation in APS, affecting 82% of patients.
- Characteristic findings include symmetrical, nodular thickening of the mitral and/or aortic valves.
- Other cardiac issues include endocardial disease, intracardiac thrombosis, and pulmonary hypertension.
Findings:
- Anticoagulant and antiplatelet therapies do not reverse valvular lesions in APS.
- Intracardiac thrombosis is a rare but serious complication, potentially causing emboli.
- Cardiac valve replacement may be necessary but is associated with increased perioperative risks.
Implications:
- Current treatments are insufficient for managing APS-related valvular heart disease.
- Increased perioperative morbidity and mortality highlight the challenges of surgical interventions in APS patients.
- Further research is needed to explore effective therapeutic strategies and improve surgical outcomes for APS patients with cardiac involvement.
Abstract:
The heart is a target organ in antiphospholipid syndrome (APS). Endocardial disease, intracardiac thrombosis, myocardial involvement including coronary heart disease and microvascular thrombosis, as well as pulmonary hypertension have all been described in APS patients. Valvular involvement is the most common manifestation with a prevalence of 82% detected by transesophageal echocardiography. Symmetrical, nodular thickening of the mitral and/or aortic valves is characteristic. Anticoagulant/antiplatelet treatment is ineffective in terms of valvular lesion regression. Some patients require cardiac valve replacement. However, patients with APS have shown an increased perioperative morbidity and mortality. Intracardiac thrombosis, although a rare complication, can cause pulmonary and systemic emboli. Differential diagnosis with myxoma may be very difficult.
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