北京大学学报(医学版) ›› 2021, Vol. 53 ›› Issue (6): 1055-1060. doi: 10.19723/j.issn.1671-167X.2021.06.008
张朴丽1,2,杨红霞1,2,张立宁1,2,葛勇鹏1,彭清林1,王国春1,卢昕1,△()
ZHANG Pu-li1,2,YANG Hong-xia1,2,ZHANG Li-ning1,2,GE Yong-peng1,PENG Qing-lin1,WANG Guo-chun1,LU Xin1,△()
摘要:
目的:研究血清及支气管肺泡灌洗液(bronchoalveolar lavage fluid, BALF)中YKL-40(chitinase-3-like-1 protein)在抗黑色素瘤分化相关基因5(anti-melanoma differentiation-associated gene 5, MDA5)阳性皮肌炎(dermatomyositis, DM)合并严重肺损伤中的价值,严重肺损伤包括快速进展间质性肺病(rapidly progressive interstitial lung disease, RP-ILD)和肺部感染。方法:选择2013—2018年中日友好医院风湿免疫科住院的抗MDA5阳性DM患者的病例资料进行回顾性分析,收集患者的人口学信息,临床、实验室及影像学检查资料,应用酶联免疫吸附法检测患者血清和BALF中YKL-40水平。绘制受试者工作特征(receiver operating characteristic, ROC)曲线,计算曲线下面积(area under the curve, AUC),评估血清YKL-40对肺损伤的诊断效能。间质性肺病(interstitial lung disease, ILD)由胸部高分辨率CT(high-resolution CT, HRCT)证实。RP-ILD定义为呼吸道症状在3个月内进行性加重,出现呼吸困难和低氧血症,或胸部HRCT显示ILD较之前加重或出现新的ILD。肺部感染经痰、血液、BALF、肺穿刺活检样本检验出病原体确诊。结果:共收集到168例抗MDA5阳性DM患者病例,其中154例合并ILD,66例(39.3%)表现为RP-ILD。经病原学依据证实合并肺部感染患者70例。合并RP-ILD患者中39例(59.1%)合并肺部感染,而非RP-ILD患者仅31例(30.4%)合并肺部感染。RP-ILD合并肺部感染的发生率高于非RP-ILD合并肺部感染者(P<0.001)。血清YKL-40水平在RP-ILD合并肺部感染组高于RP-ILD未合并肺部感染组、非RP-ILD合并肺部感染组和非RP-ILD未合并肺部感染组[83(42~142) vs. 42(21~91) vs. 43(24~79) vs. 38(22~69), P<0.01]。血清YKL-40诊断抗MDA5阳性DM患者RP-ILD合并肺部感染的敏感性、特异性及AUC分别为75%、67%、0.72,其诊断同时存在RP-ILD和肺部感染的抗MDA5阳性DM患者的AUC较诊断仅有RP-ILD和仅有肺部感染者的AUC高,且差异有统计学意义(0.72 vs. 0.54和0.55, Z=2.10和2.11, P<0.05)。结论:抗MDA5阳性DM患者合并RP-ILD和肺部感染预后差,血清YKL-40水平对这类患者同时合并RP-ILD和肺部感染有一定的诊断价值。
中图分类号:
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