结节性支气管扩张(NB)型非结核分枝杆菌肺病患者的疾病进展:空腔NB和可溶性程序性死亡蛋白-1的作用

Sheng Wei Pan, Wei Juin Su, Yu Jiun Chan, Mei Lin Ho, Jia Yih Feng, Chin Chung Shu, Jann Yuan Wang, Hao Chien Wang, Chong Jen Yu, Yuh Min Chen
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引用次数: 5

摘要

背景:在结节性支气管扩张(NB)非结核性分枝杆菌肺病(NTM-LD)患者中,疾病进展的危险因素尚未明确调查。空腔NB和可溶性程序性死亡蛋白-1(一种免疫相关生物标志物)在NB - NTM-LD疾病过程中的作用尚不清楚。方法:选取2014-2020年2个医疗中心NB - NTM-LD患者。我们确定了空腔NB,测量了sPD-1水平,并分析了与空腔NB相关的因素和NB NTM-LD疾病进展的预测因素。结果:120例NB - NTM-LD中,87例(72.5%)由鸟分枝杆菌复合体引起。13例(10.8%)空腔NB患者的sPD-1水平低于非空腔NB患者(P = 0.020)。在1.41±1.43年的随访中,腔室组12例(92.3%),非腔室组66例(61.7%)出现疾病进展(P = 0.032)。在多变量分析中,体重指数(BMI [kg/m2];校正风险比[aHR], 0.895[95%可信区间,0.811 - 0.988]),痰涂片分级(aHR, 1.247[1.014-1.534]),腔内NB (aHR, 2.008 [1.052-3.834]), sPD-1(每10 pg/mL升高;aHR(.889[.816-.967])预测疾病进展。值得注意的是,sPD-1与疾病进展呈剂量依赖性关联(sPD-1≤23.5 pg/mL;aHR, 3.306 [1.664-6.567];sPD-1: 23.6-53.7 pg/mL;aHR为2.496[1.390-4.483]),与参比(sPD-1 >53.7 pg/mL)比较。结论:NB - NTM-LD合并低sPD-1、低BMI、高涂片分级和空腔NB的患者有较高的疾病进展风险。在空腔NB表型患者中sPD-1较低,且与疾病进展呈剂量反应性相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Disease Progression in Patients With Nontuberculous Mycobacterial Lung Disease of Nodular Bronchiectatic (NB) Pattern: The Roles of Cavitary NB and Soluble Programmed Death Protein-1.

Background: In patients with nodular bronchiectatic (NB) nontuberculous mycobacterial lung disease (NTM-LD), risk factors for disease progression have not been clearly investigated. The roles of cavitary NB and soluble programmed death protein-1 (sPD-1), an immune-related biomarker, in the disease course of NB NTM-LD remain unknown.

Methods: Patients with NB NTM-LD were enrolled from 2 medical centers in 2014-2020. We identified cavitary NB, measured sPD-1 levels, and analyzed factors associated with cavitary NB and predictors for disease progression of NB NTM-LD.

Results: Of 120 cases of NB NTM-LD, 87 (72.5%) were caused by Mycobacterium avium complex. sPD-1 levels were lower in 13 (10.8%) patients with cavitary NB than in noncavitary patients (P = .020). Over 1.41 ± 1.43 years of follow-up, 12 (92.3%) patients in the cavitary and 66 (61.7%) in the noncavitary group developed disease progression (P = .032). In multivariable analysis, body mass index (BMI [kg/m2]; adjusted hazard ratio [aHR], .895 [95% confidence interval, .811-.988]), sputum smear grade (aHR, 1.247 [1.014-1.534]), cavitary NB (aHR, 2.008 [1.052-3.834]), and sPD-1 (per 10-pg/mL increase; aHR, .889 [.816-.967]) were predictive for disease progression. Notably, sPD-1 showed a dose-dependent association with disease progression (sPD-1 ≤23.5 pg/mL; aHR, 3.306 [1.664-6.567]; sPD-1: 23.6-53.7 pg/mL; aHR, 2.496 [1.390-4.483]) compared with the reference (sPD-1 >53.7 pg/mL).

Conclusions: Patients with NB NTM-LD and low sPD-1, low BMI, high smear grade, and cavitary NB were at high risk for disease progression. sPD-1 was low in patients with cavitary NB phenotype and dose-responsively associated with disease progression.

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