Abstract 4147535: Cryptogenic stroke and Patent Foramen Ovale: Elevated Lipoprotein (a), a factor in the equation

Background: Despite the association between cryptogenic stroke and patent foramen ovale (PFO), data on the efficacy of PFO closure for secondary prevention remains limited. Guidelines recommend PFO closure only for patients with a prior stroke. As recent studies indicate a correlation between elevated Lipoprotein(a) levels and stroke, its measure could be relevant in evaluating the need for PFO closure. Aims/Hypothesis: This study aims to determine if elevated Lipoprotein (a) levels in patients with PFO increase the likelihood of stroke or transient ischemic attack (TIA). We hypothesize that elevated Lp(a) levels, given their known association with cryptogenic stroke, should be considered when evaluating patients for PFO closure. Methods: Case-control study on patients with PFO between January 2018 to April 2024. Patients with previous TIA or evidence of a prior stroke on CT/MRI were classified as “Stroke Group”. An Lp(a) level ≤ 30mg/dL was considered normal. Multivariate logistic regression was used to analyze the impact of age, gender, hypertension, diabetes, smoking status, coronary artery disease, hypothyroidism, dyslipidemia, and LP(a) levels on developing stroke or TIA. Results: A total of 96 patients were included (Stroke group=55; Control group=45). Significant differences were found between groups in age [46.38±11.06 vs 44.42±13.01; p=0.02], BMI [27.75(4.8) vs 25.34(4.8); p=0.02], hypertension [43.6% vs 17.1%; p<0.01], and migraine [27.3% vs 7.3%; p<0.01]. Elevated Lp(a)was more prevalent in the Stroke Group [60% vs 39.02%; p=0.04]. No significant differences were observed in LDL [94.80±33.95 vs 108.84±28.92; p=0.669], HDL (54.77±13.63 vs 63.89±15.16; p=0.205), Non-HDL (132.35±47.88 vs 156.23±38.86; p=0.651), and HbA1c [5.5%(0.35) vs 5.3%(0.30); p=0.143]. The logistic regression model revealed that besides the difference in baseline characteristics, only dyslipidemia (OR=4.02, 95% CI:1.145–14.125, p<0.002), migraine (OR=4.02, 95% CI:1.145–14.13, p<0.03), and elevated Lp(a) (OR=8.68, 95% CI: 2.15–35.02, p<0.002) were significantly associated with increased odds of TIA/Stroke. Conclusion: In patients with PFO, elevated LP(a) increases the odds of developing cerebrovascular events. Measure of Lp(a) should be included in the evaluation for PFO closure.

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Journal
Circulation
Published
2024-11-12
DOI
https://doi.org/10.1161/circ.150.suppl_1.4147535
Primary Topic
Cardiovascular and Diving-Related Complications
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article

Abstract 4147535: Cryptogenic stroke and Patent Foramen Ovale: Elevated Lipoprotein (a), a factor in the equation

D. Herrera, Ana Paula Ureña Neme, Javier E. Santiago, Jorge Tarafa et al.
Circulation
Cardiovascular and Diving-Related Complications
article

Abstract 4147535: Cryptogenic stroke and Patent Foramen Ovale: Elevated Lipoprotein (a), a factor in the equation

D. Herrera, Ana Paula Ureña Neme, Javier E. Santiago, Jorge Tarafa, Juan David Bravo Acosta, Patricia Velásquez, Joan Rodriguez‐Taveras, Claudia Suero, Renal Amel Peralta, Alejandro Araujo, Guilherme Campelo da Cruz, Claudia Olvera Guzmán, Karla Herrera Baez, Beatriz Díaz, Ernesto Perez Colome
article en

Abstract

Background: Despite the association between cryptogenic stroke and patent foramen ovale (PFO), data on the efficacy of PFO closure for secondary prevention remains limited. Guidelines recommend PFO closure only for patients with a prior stroke. As recent studies indicate a correlation between elevated Lipoprotein(a) levels and stroke, its measure could be relevant in evaluating the need for PFO closure. Aims/Hypothesis: This study aims to determine if elevated Lipoprotein (a) levels in patients with PFO increase the likelihood of stroke or transient ischemic attack (TIA). We hypothesize that elevated Lp(a) levels, given their known association with cryptogenic stroke, should be considered when evaluating patients for PFO closure. Methods: Case-control study on patients with PFO between January 2018 to April 2024. Patients with previous TIA or evidence of a prior stroke on CT/MRI were classified as “Stroke Group”. An Lp(a) level ≤ 30mg/dL was considered normal. Multivariate logistic regression was used to analyze the impact of age, gender, hypertension, diabetes, smoking status, coronary artery disease, hypothyroidism, dyslipidemia, and LP(a) levels on developing stroke or TIA. Results: A total of 96 patients were included (Stroke group=55; Control group=45). Significant differences were found between groups in age [46.38±11.06 vs 44.42±13.01; p=0.02], BMI [27.75(4.8) vs 25.34(4.8); p=0.02], hypertension [43.6% vs 17.1%; p<0.01], and migraine [27.3% vs 7.3%; p<0.01]. Elevated Lp(a)was more prevalent in the Stroke Group [60% vs 39.02%; p=0.04]. No significant differences were observed in LDL [94.80±33.95 vs 108.84±28.92; p=0.669], HDL (54.77±13.63 vs 63.89±15.16; p=0.205), Non-HDL (132.35±47.88 vs 156.23±38.86; p=0.651), and HbA1c [5.5%(0.35) vs 5.3%(0.30); p=0.143]. The logistic regression model revealed that besides the difference in baseline characteristics, only dyslipidemia (OR=4.02, 95% CI:1.145–14.125, p<0.002), migraine (OR=4.02, 95% CI:1.145–14.13, p<0.03), and elevated Lp(a) (OR=8.68, 95% CI: 2.15–35.02, p<0.002) were significantly associated with increased odds of TIA/Stroke. Conclusion: In patients with PFO, elevated LP(a) increases the odds of developing cerebrovascular events. Measure of Lp(a) should be included in the evaluation for PFO closure.

CirculationVol. 150(Suppl_1)
Rutgers, The State University of New Jersey (US), Boston University (US), New York City Health and Hospitals Corporation (US), Boston Medical Center (US), Morristown Medical Center (US), Instituto Tecnológico de Santo Domingo (DO), Trinitas Regional Medical Center (US), Montefiore Health System (US), Atlantic Health System (US)
Good health and well-being
Openalex Percentile: Top 61%
Cardiovascular and Diving-Related Complications
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