Why the study?
Does testing for PITX2 and ZFHX3 gene mutations correlate with the detection of occult paroxysmal atrial fibrillation by implantable long-term ECG monitoring in patients with cryptogenic stroke or TIA?
Does testing for PITX2 and ZFHX3 gene mutations correlate with the detection of occult paroxysmal atrial fibrillation by implantable long-term ECG monitoring in patients with cryptogenic stroke or TIA?
This study protocol outlines a prospective matched cohort study to investigate the correlation between PITX2 and ZFHX3 gene mutations and the detection of occult paroxysmal atrial fibrillation using implantable loop recorders in patients with cryptogenic stroke or TIA.
May identify genetic predictors of occult AF in cryptogenic stroke; leaves open whether PITX2/ZFHX3 testing improves detection or outcomes.
BACKGROUND: Cardio-embolic etiology is the most frequently predicted cause of cryptogenic stroke/TIA. Detection of occult paroxysmal atrial fibrillation is crucial for selection of appropriate medication. METHODS: Enrolment of eligible cryptogenic stroke and TIA patients began in 2014 and will continue until 2018. The patients undergo long-term (12 months) ECG monitoring (implantable loop recorder) and testing for PITX2 (chromosome 4q25) and ZFHX3 (chromosome 16q22) gene mutations. There will be an appropriate control group of age- and sex-matched healthy volunteers. To analyse the results descriptive statistics, statistical tests for group differences, and correlation analyses will be used. DISCUSSION: In our study we are focusing on a possible correlation between detection of atrial fibrillation by an implantable ECG recorder, and PITX2 and/or ZFHX3 gene mutations in cryptogenic stroke/TIA patients. A correlation could lead to implementation of this genomic approach to cryptogenic stroke/TIA diagnostics and management. The results will be published in 2018. TRIAL REGISTRATION: ClinicalTrials.gov: NCT02216370 .
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Petrovičová et al. (2015) studied this question.
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