Clinical and infarction patterns of PFO-related cryptogenic strokes and a prediction model

Ann Clin Transl Neurol. 2018 Sep 24;5(11):1323-1337. doi: 10.1002/acn3.647. eCollection 2018 Nov.

Abstract

Objectives: The higher than expected PFO rate in CS patients has raised concerns that paradoxical embolism maybe the pathophysiologic mechanism for strokes. However, only a small proportion of pathogenic PFOs cause CS. Therefore, accurate recognition of patients with pathogenic PFOs among all CS patients could guide clinical decision making in selecting the most appropriate treatment. The aim of this study was to devise a new algorithm to stratify cryptogenic stroke (CS) patients into pathogenic patent foramen ovale (p-PFO)- and non-p-PFO-related patients.

Methods: A total of 1201 patients with acute ischemic stroke were recruited from two different medical centers, and 253 CS patients were identified. Of the 253 patients, 111 were diagnosed with PFO using contrast transcranial Doppler. Data on medical histories, neuroimaging and laboratory tests were compared in CS patients with or without PFO.

Results: Compared with PFO-negative CS patients, PFO-positive CS patients showed younger onset age, lower incidence of hypertension and dyslipidemia, characteristic infarction pattern in magnetic resonance imaging and specifically altered platelet activity and coagulation function. Based on the above information, we constructed a PFO judgment formula (Hr-PFOJ) by means of feature weight estimation and predictive performance evaluation to predict pathogenic PFO in CS patients with a sensitivity of 76.3% and a specificity of 66.5%.

Interpretations: Hr-PFOJ judgment formula is a useful screening tool for identification of patients with pathogenic PFO who may benefit from PFO-related treatment.

Grants and funding

This work was funded by Natural Science Foundation of China grants 81301126, 81471200, 81000521, and 81771341; Science and technology program of Guangzhou grant 201803010067; Fundamental Research Funds for the Central Universities grant 2017KFYXJJ111; Clinical Research Physician Program of Tongji Medical College grant ; HUST grant ; Natural Science foundation of Hubei Province grant 2015CFB572; Project of Health and Family Planning Commission of Hubei Province grant WJ2015 MB056; Guangdong Provincial Key Laboratory for Diagnosis and Treatment of Major Neurological Diseases grant 2014B030301035; The Southern China International Cooperation Base for Early Intervention and Functional Rehabilitation of Neurological Diseases grant 2015B050501003; Guangzhou Clinical Research and Translational Center for Major Neurological Diseases grant 201604020010; Guangdong Provincial Engineering Center for Major Neurological Disease Treatment grant .