Grygiel-Górniak Bogna, Lucki Mateusz, Daroszewski Przemysław, Lucka Ewa
Department of Rheumatology, Rehabilitation and Internal Diseases, Poznan University of Medical Sciences, 61-701 Poznań, Poland.
Department and Clinic of Cardiology, University of Medical Sciences, 60-545 Poznań, Poland.
J Clin Med. 2025 Jul 4;14(13):4742. doi: 10.3390/jcm14134742.
Pulmonary arterial hypertension (PAH) is a severe complication associated with connective tissue diseases (CTDs), which is characterized by a significant influence on the patient's prognosis and mortality. The prevalence of PAH varies depending on the type of CTD. Still, it is highly prevalent in patients with systemic sclerosis (SSc), systemic lupus erythematosus (SLE), mixed connective tissue disease (MCTD), and primary Sjögren's syndrome (pSS). Identifying rheumatic disease-specific risk factors is crucial for early diagnosis and intervention. Risk factors for PAH development include specific sociological factors (related to race, gender, and age), clinical features (particularly severe Raynaud's phenomenon and multiple telangiectasias), cardiological factors (pericarditis and left heart disease), biochemical factors (elevated NT-proBNP and decreased HDL-cholesterol), serological factors (presence of ANA, e.g., anti-U1-RNP or SSA, and antiphospholipid antibodies), and pulmonary factors (interstitial lung disease and decreased DLCO or DLCO/alveolar volume ratio < 70%, FVC/DLCO > 1.6). The analysis of risk factors can be the most useful during the selection of patients at high risk of PAH development. The initial diagnosis of PAH is usually based on transthoracic echocardiography (TTE) and is finally confirmed by right heart catheterization (RHC). Targeted therapies can improve outcomes and include endothelin receptor antagonists, prostacyclin analogs, phosphodiesterase inhibitors, and tailored immunosuppressive treatments. Effective management strategies require a multidisciplinary approach involving rheumatologists, cardiologists, and pulmonologists. The risk stratification and individualized treatment strategies can enhance survival and quality of life in patients with PAH-CTD.
肺动脉高压(PAH)是一种与结缔组织病(CTD)相关的严重并发症,其特点是对患者的预后和死亡率有重大影响。PAH的患病率因CTD类型而异,但在系统性硬化症(SSc)、系统性红斑狼疮(SLE)、混合性结缔组织病(MCTD)和原发性干燥综合征(pSS)患者中非常普遍。识别风湿性疾病特异性危险因素对于早期诊断和干预至关重要。PAH发生的危险因素包括特定的社会学因素(与种族、性别和年龄有关)、临床特征(特别是严重的雷诺现象和多发性毛细血管扩张)、心脏病学因素(心包炎和左心疾病)、生化因素(NT-proBNP升高和高密度脂蛋白胆固醇降低)、血清学因素(抗核抗体如抗U1-RNP或抗SSA的存在以及抗磷脂抗体)和肺部因素(间质性肺疾病以及一氧化碳弥散量降低或一氧化碳弥散量/肺泡容积比<70%,用力肺活量/一氧化碳弥散量>1.6)。在选择有PAH发生高风险的患者时,对危险因素的分析可能最有用。PAH的初步诊断通常基于经胸超声心动图(TTE),最终通过右心导管检查(RHC)确诊。靶向治疗可以改善预后,包括内皮素受体拮抗剂、前列环素类似物、磷酸二酯酶抑制剂和定制的免疫抑制治疗。有效的管理策略需要多学科方法,涉及风湿病学家、心脏病学家和肺科医生。风险分层和个体化治疗策略可以提高PAH-CTD患者的生存率和生活质量。