Connective Tissue Disease, Interstitial Lung Disease, and Pulmonary Hypertension (CTD PH-ILD): A Distinct Entity and Potential Opportunity

D. Sese, K. Highland
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Abstract

Connective tissue diseases are a multisystem disorder that can cause impairments in quality of life, shorten life expectancy, and increase the risk of mortality at a younger age. These patients have an increased risk for the development of pulmonary hypertension through several mechanisms including pulmonary arterial hypertension and pulmonary hypertension associated with interstitial lung disease. This review aims to discuss the various presentations of connective tissue disease associated with pulmonary hypertension associated with interstitial lung disease, demographics, and survival. It gives an overview of accepted mechanisms of disease pathogenesis, discusses advances in diagnostics, and treatment options. Despite a deeper understanding of disease pathogenesis, treatment for this remains limited to prevention of disease progression. The identification of the primary disease driver requires careful evaluation of the disease phenotype and is a potential target for treatment and prevention of death.
结缔组织疾病、间质性肺病和肺动脉高压(CTD PH-ILD):一个独特的实体和潜在的机会
结缔组织疾病是一种多系统疾病,可导致生活质量下降,缩短预期寿命,并增加年轻时的死亡率。通过多种机制,包括肺动脉高压和与间质性肺病相关的肺动脉高压,这些患者发展为肺动脉高压的风险增加。这篇综述旨在讨论结缔组织疾病与肺动脉高压相关的各种表现与间质性肺病、人口统计学和生存率。它概述了公认的疾病发病机制,讨论了诊断和治疗选择的进展。尽管对疾病的发病机制有了更深入的了解,但治疗仍然局限于预防疾病进展。确定主要疾病驱动因素需要仔细评估疾病表型,是治疗和预防死亡的潜在目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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