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Closure of a Patent Foramen Ovale PFO: An Intervention Sequence
Published on: December 23, 2022
Factors associated with patent foramen ovale-related stroke: SAFAS study
T Pommier1, A Lafont2, R Didier1
1Cardiology Department, University Hospital, 14, rue Paul-Gaffarel, 21079 Dijon cedex, France; Pathophysiology and Epidemiology of Cerebro-Cardiovascular diseases (EA 7460), Faculty of Health Sciences, université de Bourgogne, université de Bourgogne Franche-Comté, Dijon, France.
Insights
Persistent foramen ovale (PFO) is linked to cryptogenic stroke. Low levels of galectin-3 and osteoprotegerin may help identify patients with PFO-related strokes, suggesting a specific clinical and biological profile.
Area of Science:
- Cardiology
- Neurology
- Biomarker Research
Background:
- Persistent foramen ovale (PFO) is a known contributor to cryptogenic stroke and stroke recurrence.
- The precise mechanisms linking PFO to ischemic events remain unclear.
- Limited data exists on the diagnostic value of biomarkers for PFO-related strokes.
Purpose of the Study:
- To investigate the association between PFO-related stroke and specific biomarkers.
- To identify potential biomarkers for diagnosing PFO-related strokes.
- To characterize the clinical and biological phenotype of patients with PFO-related cryptogenic stroke.
Main Methods:
- Prospective single-center study of ischemic stroke patients without a history of atrial fibrillation.
- Systematic PFO screening using transthoracic echocardiography with CLOSE trial criteria.
- Multivariate logistic regression analysis to assess the association of PFO-related stroke with biomarkers of cardiac fibrosis and inflammation (galectin-3, GDF-15, ST-2, osteoprotegerin, NT-proBNP).
Main Results:
- 10% of patients (23/229) had PFO-related stroke.
- PFO-related stroke patients were younger, had less hypertension, and more cerebellar involvement.
- Low galectin-3 (<9.5ng/mL) and osteoprotegerin (<1133pg/L) levels were independently associated with PFO-related stroke (OR 3.4 and 5.0, respectively).
Conclusions:
- Patients with cryptogenic stroke attributed to PFO exhibit a distinct clinical and biological profile.
- Low serum levels of galectin-3 and osteoprotegerin may serve as indicators for PFO-related strokes.
- These findings aid in identifying patients who may benefit from PFO evaluation.
Background:
Persistent foramen ovale (PFO) contributes to cryptogenic stroke and is associated with stroke recurrence, although the exact mechanism of ischemic events is not fully understood. Several biomarkers have been developed for the prediction of atrial fibrillation after stroke, but there are currently only limited data on their potential value for the diagnosis of PFO-related stroke.
Methods:
This study was a prospective single-center study that included all patients hospitalized between March 31, 2018, and January 18, 2020, in the stroke department of the Dijon University Hospital for ischemic stroke without obvious cause and without a history of atrial fibrillation. PFO was systematically screened by transthoracic echocardiography and images were reviewed by an independent cardiologist blinded from clinical data. PFO was defined according to the CLOSE trial criteria: PFO associated with interatrial septal aneurysm or significant interatrial shunt (> 30 microbubbles in the left atrium within three cardiac cycles after right atrial opacification). The potential association of PFO-related stroke with biomarkers of cardiac fibrosis and inflammation such as galectin-3, GDF-15, ST-2, osteoprotegerin and NT-proBNP was tested using multivariate backward stepwise logistic regression.
Results:
Of the 240 patients included in the SAFAS study, 229 had complete echocardiographic data, and 23 (10%) had PFO-related stroke. Patients with PFO-related stroke were significantly younger (58±14 vs. 69±14, P<0.001), had less frequent previous arterial hypertension (30 vs. 60%, P=0.008), and more frequent cerebellar territory involvement (26 vs. 9%, P=0.014) compared to the other patients. In addition, they had less frequently left atrial dilatation (left atrial index volume>34mL/m2 [9 vs. 35%, P=0.009]). After ROC curve analysis for definition of thresholds, PFO-related stroke patients more often had galectin-3<9.5ng/mL (59 vs. 27%, P=0.002), ST2<13380pg/ml (23 vs. 50%, P=0.007), GDF-15<1200ng/mL (59 vs. 27%, P=0.002), osteoprotegerin<1133pg/mL (82 vs. 58%, P=0.033) and NT-proBNP<300pg/mL (88 vs. 55%, P=0.009). After multivariate analysis, only galectin-3<9.5ng/mL (OR [95% CI] 3.4 [1.18; 9.8], P=0.024) and osteoprotegerin<1133pg/L (OR [95% CI] 5.0 [1.1; 22.9], P=0.038) were independently associated with PFO-related stroke.
Conclusion:
Patients in whom cryptogenic stroke is attributed to a significant PFO have a specific clinical and biological phenotype. Low levels of galectin-3 and osteoprotegerin may help identify patients with PFO-related strokes.
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