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治疗后淋巴细胞减少与分枝杆菌复合群肺病患者发生非结核性肺病再发的风险增加相关。

Posttreatment Lymphopenia Is Associated With an Increased Risk of Redeveloping Nontuberculous Lung Disease in Patients With Mycobacterium avium Complex Lung Disease.

机构信息

Respiratory Disease Center, Fukujuji Hospital, Japan Anti-Tuberculosis Association, Tokyo, Japan.

Department of Pathophysiology and Host Defense, the Research Institute of Tuberculosis, Japan Anti-Tuberculosis Association, Tokyo, Japan.

出版信息

Clin Infect Dis. 2021 Jul 1;73(1):e152-e157. doi: 10.1093/cid/ciaa729.

Abstract

BACKGROUND

Lymphopenia has been reported as a risk factor for poor prognosis in various infectious diseases, including Mycobacterium avium complex lung disease (MAC-LD), and recurrence in several infectious diseases. However, the association between lymphopenia and the risk of redeveloping nontuberculous lung disease (NTM-LD) after completed treatment for MAC-LD is unknown.

METHODS

We performed a retrospective cohort study with 147 patients with MAC-LD who successfully completed guideline-based therapy. Lymphopenia was defined as an absolute lymphocyte count (ALC) <1000 cells/μL based on commonly accepted reference values.

RESULTS

During the median follow-up period of 41.9 months after treatment completion, 59 (40.1%) patients redeveloped NTM-LD. Patients with NTM-LD redevelopment had significantly lower posttreatment ALCs (median, 1260 vs 1420 cells/μL) than those without, and the univariate Cox proportional hazard analysis identified posttreatment ALC as a predictive factor for redevelopment (hazard ratio, .94 [95% confidence interval, .89-.99] for every increase of 100 cells/μL; P = .04). In the multivariate analysis, posttreatment ALC and the extent of bronchiectasis were independently associated with NTM-LD redevelopment. The cumulative rate of NTM-LD redevelopment was significantly higher in patients with posttreatment lymphopenia than in those without (P = .008).

CONCLUSIONS

Posttreatment lymphopenia could predict an increased risk of NTM-LD redevelopment after completed treatment for MAC-LD.

摘要

背景

淋巴细胞减少已被报道为包括鸟分枝杆菌复合体肺病(MAC-LD)在内的各种传染病以及某些传染病复发的不良预后的危险因素。然而,淋巴细胞减少与 MAC-LD 治疗完成后发生非结核分枝杆菌肺病(NTM-LD)的风险之间的关联尚不清楚。

方法

我们进行了一项回顾性队列研究,纳入了 147 例成功完成基于指南治疗的 MAC-LD 患者。淋巴细胞减少定义为根据公认的参考值,绝对淋巴细胞计数(ALC)<1000 个/μL。

结果

在治疗完成后 41.9 个月的中位随访期间,有 59 例(40.1%)患者重新发生了 NTM-LD。与未重新发生 NTM-LD 的患者相比,重新发生 NTM-LD 的患者治疗后 ALC 明显更低(中位数分别为 1260 与 1420 个/μL),单变量 Cox 比例风险分析确定治疗后 ALC 是重新发生的预测因素(每增加 100 个/μL,比值比为.94[95%置信区间为.89-.99];P =.04)。在多变量分析中,治疗后 ALC 和支气管扩张程度与 NTM-LD 重新发生独立相关。与无治疗后淋巴细胞减少的患者相比,治疗后淋巴细胞减少的患者 NTM-LD 重新发生的累积率明显更高(P =.008)。

结论

治疗后淋巴细胞减少可能预测 MAC-LD 治疗完成后 NTM-LD 重新发生的风险增加。

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