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Can intestinal rnicrobiota and circulating microbial products contribute to pulmonary arterial hypertension?

机译:肠道rnicrobiota和循环微生物产品可以促进肺动脉高压吗?

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摘要

Pulmonary arterial hypertension (PAH) is a fatal disease with a median survival of only 5-7 yr. PAH is characterized by remodeling of the pulmonary vasculature causing reduced pulmonary arterial compliance (PAC) and increased pulmonary vascular resistance (PVR), ultimately resulting in right ventricular failure and death. Better therapies for PAH will require a paradigm shift in our understanding of the early pathophysiology. PAC decreases before there is an increase in the PVR. Unfortunately, present treatment has little effect on PAC. The loss of compliance correlates with extracellular matrix remodeling and fibrosis in the pulmonary vessels, which have been linked to chronic peri vascular inflammation and immune dysregulau'on. However, what initiates the perivascular inflammation and immune dysregulation in PAH is unclear. Alteration of the gut microbiota composition and function underlies the level of immuno-pathogenic involvement in several diseases, including atherosclerosis, obesity, diabetes mellitus, and depression, among others. In this review, we discuss evidence that raises the possibility of an etiologic role for changes in the gut and circulating microbiome in the initiation of perivascular inflammation in the early pathogenesis of PAH.
机译:肺动脉高压(PAH)是一种致命的疾病,中位数仅为5-7 YR。 PAH的特征在于改造肺动脉抑制(PAC)和肺血管抗性(PVR)降低的肺脉管系统,最终导致右心室失效和死亡。更好的PAH疗法将需要在我们对早期病理生理学的理解方面进行范式转变。 PAC在PVR增加之前减少。不幸的是,目前的治疗对PAC几乎没有影响。顺应性丧失与肺部血管中的细胞外基质重塑和纤维化相关,这与慢性Peri血管炎症和免疫Dysregulau'on相关联。然而,在PAH中引发血管外炎症和免疫失调的原因尚不清楚。肠道微生物群组成和功能的改变是免疫致病程度的影响,包括动脉粥样硬化,肥胖,糖尿病和抑郁症等。在这篇综述中,我们讨论了在PAH的早期发病机制中启动血管外炎症中的肠道和循环微生物的变化的病因作用的可能性。

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