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An Integrative Study of Aortic mRNA/miRNA Longitudinal Changes in Long-Term LVAD Support

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    0550594 - BTÚ 2022 RIV CH eng J - Journal Article
    Dlouhá, D. - Ivák, P. - Netuka, I. - Benešová, Šárka - Tucanova, Z. - Hubáček, J. A.
    An Integrative Study of Aortic mRNA/miRNA Longitudinal Changes in Long-Term LVAD Support.
    International Journal of Molecular Sciences. Roč. 22, č. 14 (2021), č. článku 7414. E-ISSN 1422-0067
    Institutional support: RVO:86652036
    Keywords : ventricular assist device * micrornas * stiffness * inflammation * transplant * pathology
    OECD category: Biochemistry and molecular biology
    Impact factor: 6.208, year: 2021
    Method of publishing: Open access
    https://www.mdpi.com/1422-0067/22/14/7414

    Studying the long-term impact of continuous-flow left ventricular assist device (CF-LVAD) offers an opportunity for a complex understanding of the pathophysiology of vascular changes in aortic tissue in response to a nonphysiological blood flow pattern. Our study aimed to analyze aortic mRNA/miRNA expression changes in response to long-term LVAD support. Paired aortic samples obtained at the time of LVAD implantation and at the time of heart transplantation were examined for mRNA/miRNA profiling. The number of differentially expressed genes (Pcorr < 0.05) shared between samples before and after LVAD support was 277. The whole miRNome profile revealed 69 differentially expressed miRNAs (Pcorr < 0.05). Gene ontology (GO) analysis identified that LVAD predominantly influenced genes involved in the extracellular matrix and collagen fibril organization. Integrated mRNA/miRNA analysis revealed that potential targets of miRNAs dysregulated in explanted samples are mainly involved in GO biological process terms related to dendritic spine organization, neuron projection organization, and cell junction assembly and organization. We found differentially expressed genes participating in vascular tissue engineering as a consequence of LVAD duration. Changes in aortic miRNA levels demonstrated an effect on molecular processes involved in angiogenesis.
    Permanent Link: http://hdl.handle.net/11104/0327763

     
     
Number of the records: 1  

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