Assad Tufik R, Hemnes Anna R, Larkin Emma K, Glazer Andrew M, Xu Meng, Wells Quinn S, Farber-Eger Eric H, Sheng Quanhu, Shyr Yu, Harrell Frank E, Newman John H, Brittain Evan L
Division of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee.
Division of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee.
J Am Coll Cardiol. 2016 Dec 13;68(23):2525-2536. doi: 10.1016/j.jacc.2016.09.942.
Pulmonary hypertension (PH) is a common and morbid complication of left heart disease with 2 subtypes: isolated post-capillary pulmonary hypertension (Ipc-PH) and combined post-capillary and pre-capillary pulmonary hypertension (Cpc-PH). Little is known about the clinical or physiological characteristics that distinguish these 2 subphenotypes or if Cpc-PH shares molecular similarities to pulmonary arterial hypertension (PAH).
The goal of this study was to test the hypothesis that the hemodynamic and genetic profile of Cpc-PH would more closely resemble PAH than Ipc-PH.
Vanderbilt University's electronic medical record linked to a DNA biorepository was used to extract demographic characteristics, clinical data, invasive hemodynamic data, echocardiography, and vital status for all patients referred for right heart catheterization between 1998 and 2014. Shared genetic variants between PAH and Cpc-PH compared with Ipc-PH were identified by using pre-existing single-nucleotide polymorphism data.
A total of 2,817 patients with PH (13% Cpc-PH, 52% Ipc-PH, and 20% PAH) were identified. Patients with Cpc-PH were on average 6 years younger, with more severe pulmonary vascular disease than patients with Ipc-PH, despite similar comorbidities and prevalence, severity, and chronicity of left heart disease. After adjusting for relevant covariates, the risk of death was similar between the Cpc-PH and Ipc-PH groups (hazard ratio: 1.14; 95% confidence interval: 0.96 to 1.35; p = 0.15) when defined according to diastolic pressure gradient. We identified 75 shared exonic single-nucleotide polymorphisms between Cpc-PH and PAH enriched in pathways involving cell structure, extracellular matrix, and immune function. These genes are expressed, on average, 32% higher in lungs relative to other tissues.
Patients with Cpc-PH develop pulmonary vascular disease similar to patients with PAH, despite younger age and similar prevalence of obesity, diabetes mellitus, and left heart disease compared with patients with Ipc-PH. An exploratory genetic analysis in Cpc-PH identified genes and biological pathways in the lung known to contribute to PAH pathophysiology, suggesting that Cpc-PH may be a distinct and highly morbid PH subphenotype.
肺动脉高压(PH)是左心疾病常见且严重的并发症,有两种亚型:孤立性毛细血管后肺动脉高压(Ipc-PH)和毛细血管后与毛细血管前联合性肺动脉高压(Cpc-PH)。对于区分这两种亚表型的临床或生理特征,或者Cpc-PH是否与肺动脉高压(PAH)存在分子相似性,我们知之甚少。
本研究的目的是检验以下假设:与Ipc-PH相比,Cpc-PH的血流动力学和基因特征与PAH更为相似。
利用范德比尔特大学与DNA生物样本库相链接的电子病历,提取1998年至2014年间所有接受右心导管检查患者的人口统计学特征、临床数据、有创血流动力学数据、超声心动图以及生命状态。通过使用现有的单核苷酸多态性数据,确定PAH与Cpc-PH之间相对于Ipc-PH的共享基因变异。
共识别出2817例PH患者(13%为Cpc-PH,52%为Ipc-PH,20%为PAH)。Cpc-PH患者平均比Ipc-PH患者年轻6岁,尽管合并症以及左心疾病的患病率、严重程度和病程相似,但Cpc-PH患者的肺血管疾病更为严重。在根据舒张压梯度进行定义并调整相关协变量后,Cpc-PH组和Ipc-PH组的死亡风险相似(风险比:1.14;95%置信区间:0.96至1.35;p = 0.15)。我们在Cpc-PH和PAH之间识别出75个共享的外显子单核苷酸多态性,这些多态性在涉及细胞结构、细胞外基质和免疫功能的通路中富集。相对于其他组织,这些基因在肺中的平均表达水平高32%。
尽管与Ipc-PH患者相比,Cpc-PH患者年龄更小,肥胖、糖尿病和左心疾病的患病率相似,但Cpc-PH患者所患的肺血管疾病与PAH患者相似。对Cpc-PH进行的探索性基因分析确定了肺中已知与PAH病理生理学相关的基因和生物学通路,这表明Cpc-PH可能是一种独特且严重的PH亚表型。