Metabolic syndrome, neurohumoral modulation, and pulmonary arterial hypertension

被引:24
|
作者
Maron, Bradley A. [1 ,2 ]
Leopold, Jane A. [1 ,2 ]
Hemnes, Anna R. [3 ]
机构
[1] Brigham & Womens Hosp, Dept Med, Div Cardiovasc Med, 75 Francis St, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Vanderbilt Univ, Med Ctr, Dept Med, Div Allergy Pulm & Crit Care Med, T1218 Med Ctr North,1161 21st Ave South, Nashville, TN 37232 USA
关键词
ANGIOTENSIN-CONVERTING ENZYME; RIGHT-VENTRICULAR LIPOTOXICITY; ACTIVATED PROTEIN-KINASE; HEART-FAILURE; CONCISE GUIDE; INSULIN-RESISTANCE; ENDOTHELIAL-CELLS; BARIATRIC SURGERY; POTENTIAL ROLE; UP-REGULATION;
D O I
10.1111/bph.14968
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Pulmonary vascular disease, including pulmonary arterial hypertension (PAH), is increasingly recognized to be affected by systemic alterations including up-regulation of the renin-angiotensin-aldosterone system and perturbations to metabolic pathways, particularly glucose and fat metabolism. There is increasing preclinical and clinical data that each of these pathways can promote pulmonary vascular disease and right heart failure and are not simply disease markers. More recently, trials of therapeutics aimed at neurohormonal activation or metabolic dysfunction are beginning to shed light on how interventions in these pathways may affect patients with PAH. This review will focus on underlying mechanistic data that supports neurohormonal activation and metabolic dysfunction in the pathogenesis of PAH and right heart failure as well as discussing early translational data in patients with PAH.
引用
收藏
页码:1457 / 1471
页数:15
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