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Transcriptomal Insights of Heart Failure from Normality to Recovery.
Quttainah, Mohammed; Raveendran, Vineesh Vimala; Saleh, Soad; Parhar, Ranjit; Aljoufan, Mansour; Moorjani, Narain; Al-Halees, Zohair Y; AlShahid, Maie; Collison, Kate S; Westaby, Stephen; Al-Mohanna, Futwan.
Afiliação
  • Quttainah M; Department of Cell Biology, King Faisal Specialist Hospital & Research Centre, Riyadh 11211, Saudi Arabia.
  • Raveendran VV; Department of Cell Biology, King Faisal Specialist Hospital & Research Centre, Riyadh 11211, Saudi Arabia.
  • Saleh S; Department of Cell Biology, King Faisal Specialist Hospital & Research Centre, Riyadh 11211, Saudi Arabia.
  • Parhar R; Department of Cell Biology, King Faisal Specialist Hospital & Research Centre, Riyadh 11211, Saudi Arabia.
  • Aljoufan M; Heart Centre, King Faisal Specialist Hospital & Research Centre, Riyadh 11211, Saudi Arabia.
  • Moorjani N; Department of Cardiothoracic Surgery, Papworth Hospital, University of Cambridge, Cambridge CB23 3RE, UK.
  • Al-Halees ZY; Heart Centre, King Faisal Specialist Hospital & Research Centre, Riyadh 11211, Saudi Arabia.
  • AlShahid M; Heart Centre, King Faisal Specialist Hospital & Research Centre, Riyadh 11211, Saudi Arabia.
  • Collison KS; Department of Cell Biology, King Faisal Specialist Hospital & Research Centre, Riyadh 11211, Saudi Arabia.
  • Westaby S; Oxford Heart Centre, John Radcliffe Hospital, Oxford OX9 3DU, UK.
  • Al-Mohanna F; Department of Cell Biology, King Faisal Specialist Hospital & Research Centre, Riyadh 11211, Saudi Arabia.
Biomolecules ; 12(5)2022 05 23.
Article em En | MEDLINE | ID: mdl-35625658
ABSTRACT
Current management of heart failure (HF) is centred on modulating the progression of symptoms and severity of left ventricular dysfunction. However, specific understandings of genetic and molecular targets are needed for more precise treatments. To attain a clearer picture of this, we studied transcriptome changes in a chronic progressive HF model. Fifteen sheep (Ovis aries) underwent supracoronary aortic banding using an inflatable cuff. Controlled and progressive induction of pressure overload in the LV was monitored by echocardiography. Endomyocardial biopsies were collected throughout the development of LV failure (LVF) and during the stage of recovery. RNA-seq data were analysed using the PANTHER database, Metascape, and DisGeNET to annotate the gene expression for functional ontologies. Echocardiography revealed distinct clinical differences between the progressive stages of hypertrophy, dilatation, and failure. A unique set of transcript expressions in each stage was identified, despite an overlap of gene expression. The removal of pressure overload allowed the LV to recover functionally. Compared to the control stage, there were a total of 256 genes significantly changed in their expression in failure, 210 genes in hypertrophy, and 73 genes in dilatation. Gene expression in the recovery stage was comparable with the control stage with a well-noted improvement in LV function. RNA-seq revealed the expression of genes in each stage that are not reported in cardiovascular pathology. We identified genes that may be potentially involved in the aetiology of progressive stages of HF, and that may provide future targets for its management.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Disfunção Ventricular Esquerda / Insuficiência Cardíaca Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Disfunção Ventricular Esquerda / Insuficiência Cardíaca Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article