Tang Heng, Lu Fengyun, Huang Yingheng, Wang Qiang, Sun Xiaoxuan, Zhang Miaojia, Zhou Lei
Department of Cardiology, First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Department of Rheumatology, First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Healthcare (Basel). 2024 Aug 16;12(16):1633. doi: 10.3390/healthcare12161633.
Group-based trajectory modeling (GBTM) allows the trajectory analyses of repeated N-terminal pro-brain natriuretic peptide (NT-proBNP) measurements during follow-up visits of pulmonary artery hypertension associated with connective tissue disease (CTD-PAH) patients. This study aimed to (1) identify trajectories of NT-proBNP changing over time, (2) explore the association between NT-proBNP trajectories and prognosis, and (3) explore the effects of baseline clinical characteristics on NT-proBNP trajectories. A retrospective, single-centred, observational study was performed on 52 CTD-PAH patients who had undergone at least three follow-up visits within 1 year from baseline. Four NT-proBNP trajectories were identified using GBTM: low stability ( = 15, 28.85%), early remission (remission within 3 months) ( = 20, 38.46%), delayed remission (remission after 6 or 9 months) ( = 11, 21.15%), and high stability ( = 6, 11.54%). The low-stability and early-remission trajectories were related to a similar positive prognosis, while the delayed-remission and high-stability trajectories were associated with a gradually worsening prognosis ( = 0.000). Intensive CTD immunotherapy (corticosteroids plus immunosuppressants) was the only factor that remained significant after least absolute shrinkage and selection operator regression and multivariate logistic regression, and was independently associated with a lower risk NT-proBNP trajectory ( = 0.048, odds ratio = 0.027, 95% confidence interval: 0.001-0.963), which preliminarily indicated a benefit of CTD-PAH patients undergoing intensive CTD immunotherapy.
基于群组的轨迹建模(GBTM)可对结缔组织病相关肺动脉高压(CTD-PAH)患者随访期间重复测量的N末端脑钠肽前体(NT-proBNP)进行轨迹分析。本研究旨在:(1)确定NT-proBNP随时间变化的轨迹;(2)探索NT-proBNP轨迹与预后之间的关联;(3)探索基线临床特征对NT-proBNP轨迹的影响。对52例CTD-PAH患者进行了一项回顾性、单中心观察性研究,这些患者自基线起1年内至少接受了3次随访。使用GBTM确定了4种NT-proBNP轨迹:低稳定性(n = 15,28.85%)、早期缓解(3个月内缓解)(n = 20,38.46%)、延迟缓解(6或9个月后缓解)(n = 11,21.15%)和高稳定性(n = 6,11.54%)。低稳定性和早期缓解轨迹与相似的良好预后相关,而延迟缓解和高稳定性轨迹与逐渐恶化的预后相关(P = 0.000)。强化CTD免疫治疗(皮质类固醇加免疫抑制剂)是在最小绝对收缩和选择算子回归及多变量逻辑回归后仍具有显著意义的唯一因素,且与较低风险的NT-proBNP轨迹独立相关(P = 0.048,比值比 = 0.027,95%置信区间:0.001 - 0.963),这初步表明CTD-PAH患者接受强化CTD免疫治疗有益。