| Literature DB >> 30354977 |
Anne-Sophie Pulcrano-Nicolas1,2, Carole Proust1,2, Frédéric Clarençon3,4, Alice Jacquens5,6, Claire Perret1,2, Maguelonne Roux1,2, Eimad Shotar3,4, Florian Thibord1,2, Louis Puybasset5,6, Sophie Garnier1,2, Vincent Degos5,6, David-Alexandre Trégouët1,2.
Abstract
Background and Purpose- Arterial vasospasm is a well-known delayed complication of aneurysmal subarachnoid hemorrhage (aSAH). However, no validated biomarker exists to help clinicians discriminating patients with aSAH who will develop vasospasm (VSP+) and identifying those who then deserve aggressive preventive therapy. We hypothesized that whole-blood miRNAs could be a source of candidate biomarkers for vasospasm. Methods- Using a next-generation sequencing approach, we performed whole-blood miRNA profiling between VSP+patients with aSAH and patients who did not develop vasospasm (VSP-) in a prospective cohort of 32 patients. Profiling was performed on the admission day and 3 days before vasospasm. Results- Four hundred forty-two miRNAs were highly expressed in whole blood of patients with aSAH. Among them, hsa-miR-3177-3p demonstrated significant ( P=5.9×10-5; PBonferroni corrected=0.03) lower levels in VSP- compared with VSP+ patients. Looking for whole-blood mRNA correlates of hsa-miR-3177-3p, we observed some evidence that the decrease in hsa-miR-3177-3p levels after aSAH was associated with an increase in LDHA mRNA levels in VSP- ( P<10-3) but not in VSP+ ( P=0.66) patients. Conclusions- Whole-blood miRNA levels of hsa-miR-3177-3p could serve as a biomarker for vasospasm. Clinical Trial Registration- URL: https://www.clinicaltrials.gov . Unique identifier: NCT01779713.Entities:
Keywords: biomarkers; humans; microRNAs; prospective studies; vasospasm, intracranial
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Year: 2018 PMID: 30354977 DOI: 10.1161/STROKEAHA.118.021101
Source DB: PubMed Journal: Stroke ISSN: 0039-2499 Impact factor: 7.914