首页> 美国卫生研究院文献>Journal of Cardiovascular Magnetic Resonance >Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study
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Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study

机译:HIF1α的遗传变异与法洛患者四联症修复后的右心室纤维化负荷有关:一项心血管磁共振研究

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摘要

BackgroundStudies suggest that right ventricular (RV) fibrosis is associated with RV remodeling and long-term outcomes in patients with tetralogy of Fallot (TOF). Pre-operative hypoxia may increase expression of hypoxia inducible factor-1-alpha (HIF1α) and promote transforming growth factor β1 (TGFβ1)-mediated fibrosis. We hypothesized that there would be associations between: (1) RV fibrosis and RV function, (2) HIF1α variants and RV fibrosis, and (3) HIF1α variants and RV function among post-surgical TOF cases.
机译:背景研究表明,在患有法洛四联症(TOF)的患者中,右心室(RV)纤维化与RV重塑和长期预后相关。术前缺氧可能增加缺氧诱导因子-1-α(HIF1α)的表达并促进转化生长因子β1(TGFβ1)介导的纤维化。我们假设在以下情况之间存在关联:(1)术后TOF病例中RV纤维化与RV功能,(2)HIF1α变异体与RV纤维化以及(3)HIF1α变异体与RV功能之间存在关联。

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