Stroke Clinical Trial
— METHYSTROKEOfficial title:
Identification of Epigenetic Risk Factors for Ischemic Complication During the TAVR Procedure in the Elderly
Over the past ten years, the number of endovascular procedures has increased by 5% per year in Europe with the development of interventional cardiology, such as percutaneous coronary angioplasty, aortic valve replacements (TAVR), and vascular endoprosthesis. The neurological lesions detected on cerebral MRI caused by these endovascular procedures are frequent with an incidence of about 30-70%. These events, although subclinical, have an impact on morbidity and mortality and especially on long-term cognitive decline. TAVR is the reference treatment for symptomatic elderly patients with stenosis of the aortic valve, considered by a multidisciplinary "Heart Team" as at high surgical risk due to comorbidities, age and high perioperative risk scores ( Euroscore 2 and STS scores). Despite the net clinical benefit, an increase of silent neurological events was detected on post-procedural cerebral MRI with an incidence of approximately 70%. The epigenetic involvement in the occurrence of ischemic cerebral lesions is still largely unknown. Epigenetic mechanisms, such as DNA methylation, can be associated with aging processes and modulate the risk of developing cerebrovascular pathologies. They are likely to provide new biomarkers that predict the risk of brain damage. Hypomethylation of leukocyte DNA is directly related to atherosclerosis in humans. This hypomethylation of DNA would represent an easily measurable marker reflecting the presence and progression of atherosclerosis. Because atherosclerotic lesions often precede the clinical manifestation of ischemic cardiovascular disease, such as ischemic heart disease and stroke, DNA hypomethylation could be used to identify individuals at risk for cerebrovascular events. The investigator hypothesize that hypomethylation of leukocyte DNA can predict the risk of developing new ischemic brain lesions especially after a TAVI procedure.
Status | Recruiting |
Enrollment | 542 |
Est. completion date | February 2024 |
Est. primary completion date | February 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 70 Years and older |
Eligibility | Inclusion Criteria: - Patients over 70 years with severe aortic stenosis requiring percutaneous aortic valve replacement (TAVI) Exclusion Criteria: - Patient contraindicated for the TAVI procedure - Patient with a pace-maker - Patient with contra-indication for cerebral MRI - Ongoing cancer - Patient already involved in therapeutic research - Major persons under protection of justice. |
Country | Name | City | State |
---|---|---|---|
France | Hôpital cardiologie, CHRU | Lille |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Lille |
France,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pre-operative leukocyte DNA methylation rate | This rate will be measured by the LUMA method in patients treated with TAVI according to the presence of at least one new cerebral ischemic lesion and/or microbleeds cerebral lesion appearing on post-procedural MRI | Within one week after the procedure | |
Secondary | Variation of the leukocyte DNA methylation rate during the TAVI procedure | This rate will be measured by the LINE-1 method in all patients | At time between the pre (day-1) and postprocedural (day 1) samples | |
Secondary | Pre-operative leukocyte DNA methylation rate (stroke/TIA) | This rate will be measured by the LUMA method in patients treated with TAVI according to the presence of a neurological deficit (stroke, transient ischemic attack) | One day before the procedure and within one week after the procedure | |
Secondary | Mortality | The mortality in patients treated with TAVI according to the presence of at least one new micro-ischemic cerebral lesion and/or one new microbleeds cerebral lesion detected on postoperative cerebral MRI and / or postprocedural ischemic stroke / TIA | At 1 year after procedure | |
Secondary | MMSE score variation | The MMSE score variation is compared according to the presence or not of at least one new micro-ischemic cerebral lesion and/or one new microbleeds cerebral lesion | At day-1 before TAVI procedure, at 6 months and at 1 year after procedure | |
Secondary | Change of EQ-5D questionnaire | The evolution of quality of life is compared to the occurrence of new cerebral events one new micro-ischemic cerebral lesion and/or one new microbleeds cerebral lesion | At day-1 before TAVI procedure, at 6 months and at 1 year after procedure | |
Secondary | Change of modified Rankin Scale (mRS) | The MRS (measure degree of disability- troke) is compared to the occurrence of new cerebral events one new micro-ischemic cerebral lesion and/or one new microbleeds cerebral lesion | At day-1 before TAVI procedure, at 6 months and at 1 year after procedure | |
Secondary | Change of National Institutes of Health Stroke Scale (NIHSS) | TheNIHSS (quantify the impairment caused by a stroke) is compared to the occurrence of new cerebral events one new micro-ischemic cerebral lesion and/or one new microbleeds cerebral lesion | At day-1 before TAVI procedure, at 6 months and at 1 year after procedure | |
Secondary | Clinical and Biological predictors of new cerebral events | The clinical (measured before the procedure) and biological characteristics of the patients (measured before the procedure and after the procedure) and of the peri-procedural parameters associated with the occurrence of new events detected on post-procedural MRI (new ischemic and/or new microbleeds cerebral lesion appearing on post-procedural MRI) | At day-1 before TAVI procedure, at 6 months and at 1 year after procedure | |
Secondary | Hemostasis predictors of new cerebral events | Hemostasis parameters (measured before the procedure and after the procedure) including Willebrand factor parameters associated with the occurrence of new events detected on postoperative MRI (new ischemic and/or new microbleeds cerebral lesion) | At day-1 before TAVI procedure, at 6 months and at 1 year after procedure | |
Secondary | Number of complications in peri-procedural according to VARC-2 criteria | Evaluation of multi criteria according to the Valve academic Research Consortium (VARC-2) | Within one week after the procedure |
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