北京大学学报(医学版) ›› 2018, Vol. 50 ›› Issue (3): 501-506. doi: 10.3969/j.issn.1671-167X.2018.03.018

• 论著 • 上一篇    下一篇

甲周毛细血管异常与系统性硬化相关肺间质纤维化的关系

季兰岚1,王鹤2,张晓慧1,张卓莉1△   

  1. (北京大学第一医院1.风湿免疫科,2.影像科, 北京100034)
  • 出版日期:2018-06-18 发布日期:2018-06-18
  • 通讯作者: 张卓莉 E-mail: zhuoli.zhang@126.com
  • 基金资助:
    北京大学第一医院院级青年基金(2017QN06)资助

Correlation between nailfold capillaroscopic findings and presence of interstitial lung disease in systemic sclerosis patients

JI Lan-lan1, WANG He2, ZHANG Xiao-hui1, ZHANG Zhuo-li1△   

  1. (1. Department of Rheumatology and Immunology, 2. Department of Radiology, Peking University First Hospital, Beijing 100034, China)
  • Online:2018-06-18 Published:2018-06-18
  • Contact: ZHANG Zhuo-li E-mail: zhuoli.zhang@126.com
  • Supported by:
    Supported by Youth Research Project of Peking University First Hospital(2017QN06)

摘要:  目的: 评估甲周毛细血管异常与系统性硬化(systemic sclerosis,SSc)患者发生肺间质病(interstitial lung disease,ILD)的关系。方法:共纳入71例SSc患者,其中合并ILD患者45例、无ILD患者26例,对所有入选患者均进行了甲周毛细血管显微镜(nailfold capillaroscopy,NC)检查,并对显微镜下的异常表现包括毛细血管扩张、巨大毛细血管、微出血、毛细血管数量减少、无血管区、分叉/绒毛样毛细血管以及毛细血管分布紊乱进行了半定量评分。进一步将这些患者的甲周毛细血管显微镜改变与患者的性别、年龄、病程、有/无雷诺现象等临床表现、血清学指标、有/无ILD、ILD患者的肺CT评分以及肺功能参数进行相关分析。结果:71例患者中女性占91.5%,平均年龄(52.59±12.77)岁,平均病程(3.00±6.00)年。90.1%的患者甲周毛细血管呈硬皮病样改变,71例患者中45例(63.3%)合并ILD。与无ILD的患者相比,合并ILD患者的NC中毛细血管数量减少[0.50(1.03) vs. 0.00(0.43),P=0.003]、无血管区评分[0.75(1.24) vs. 0.25(0.83),P=0.006]和分叉/绒毛样毛细血管评分[0.33(0.88) vs. 0.13(0.25),P=0.006]均显著升高,而其他NC评分在合并ILD和无ILD患者间差异均无统计学意义。Logistic分析发现,分叉/绒毛样毛细血管评分与弥漫型SSc同为预测ILD发生的独立危险因素。ILD受累更严重的患者巨大毛细血管评分更低,轻度ILD和严重ILD组分别为0.25(0.94)和0.00(0.28)(P=0.019)。结论:SSc中甲周毛细血管的缺失及严重畸形与ILD的发生存在相关性,其中严重畸形毛细血管评分是预测ILD发生的独立危险因素,巨大毛细血管的减少与ILD的严重程度相关,提示NC表现在SSc相关ILD中可能具有一定的临床意义。

关键词:  , 硬皮病, 系统性, 肺疾病, 间质性, 毛细血管显微镜

Abstract: Objective: To evaluate the correlation between nailfold capillaroscopic (NC) findings and the presence of interstitial lung disease (ILD) in systemic sclerosis (SSc) patients. Methods: We retrospectively involved 71 SSc patients, 45 patients with ILD. NC was performed in all the patients according to the standard method. The NC findings were semi-quantitatively scored, including enlarged and giant capillaries, hemorrhages, loss of capillaries, avascular areas, ramified/bushy capillaries and disorganization of the vascular array. The demographic and clinical data collected were gender, age, presence/absence of Raynaud phenomenon (RP), duration of RP, serological acute phase reactants and antibodies, presence of ILD (also evaluated the CT score for ILD) and pulmonary function parameters. Results: Among the 71 patients, the frequency of the women was 91.5%, the mean age was (52.59±12.77) years, and disease duration was (3.00±6.00) years. NC changes of the scleroderma pattern were observed in 90.1% patients. There were 45 patients with ILD and 26 patients without ILD. The patients with ILD had significantly higher loss of capillaries score [0.50 (1.03) vs. 0.00 (0.43), P=0.003], avascular area score [0.75 (1.24) vs. 0.25 (0.83), P=0.006] and ramified/bushy capillaries score [0.33 (0.88) vs. 0.13 (0.25), P=0.006] compared with those without ILD. Moreover, ramified/bushy capillaries score together with diffused SSc were independent risk factors for the presence of ILD. And the score of giant capillaries were significantly lower in the patients with more severe ILD group [0.25 (0.94) vs. 0.00 (0.28), for the mild and severe ILD groups respectively, P=0.019]. There was no statistically significant difference between the two groups with respect to the scores of enlarged capillaries, hemorrhages, or disorganization of the vascular array. Conclusion: Capillary deletion and severe deformity in NC were associated with the presence of ILD in SSc patients. And patients with less giant capillaries had more severe ILD involvement. These indicated that NC maybe a useful tool to evaluate ILD in SSc.

Key words: Scleroderma, systemic, Lung diseases, interstitial, Capillaroscopy

中图分类号: 

  • R593.25
[1] 左蒙, 张文楼, 陈柏锜, 赵晨, 陈亚红, 何建辉, 郭新彪, 邓芙蓉. 环境温度个体暴露与慢性阻塞性肺疾病患者睡眠期间血氧饱和度的关联[J]. 北京大学学报(医学版), 2026, 58(3): 592-599.
[2] 赵豆豆, 齐晅, 黄博, 高伟波, 裴源源, 金月波, 邵苗, 何菁. 感染性肺炎与免疫相关间质性肺病中淋巴细胞亚群的表达[J]. 北京大学学报(医学版), 2026, 58(3): 624-630.
[3] 马豆豆, 马晓彩, 常天静, 王丽芳, 丁艳, 石连杰. 临床表现似系统性红斑狼疮的大B细胞淋巴瘤骨髓受累1例[J]. 北京大学学报(医学版), 2026, 58(3): 666-669.
[4] 汤晓菲, 丁秋玲, 张阳, 王育梅, 田美伊, 孙卓, 王荣荣, 陈妍, 刘坚. 阿伐曲泊帕治疗难治性系统性红斑狼疮相关血小板减少1例[J]. 北京大学学报(医学版), 2026, 58(2): 405-409.
[5] 李欣艺, 赵金霞, 穆荣. 阿司匹林对系统性红斑狼疮妊娠者结局的影响[J]. 北京大学学报(医学版), 2025, 57(6): 1074-1080.
[6] 王晓林, 郭邵逸, 陈大召, 温锡杰, 华勇, 张亮, 张秦. 全髋关节置换术治疗系统性红斑狼疮继发股骨头缺血性坏死的随访研究[J]. 北京大学学报(医学版), 2025, 57(6): 1081-1088.
[7] 兰静雯, 陈哲, 程永静, 赵丽珂. 老年结缔组织病相关间质性肺病临床特征及抗纤维化治疗的疗效和安全性[J]. 北京大学学报(医学版), 2025, 57(6): 1101-1106.
[8] 卫春, 杨月, 赵新菊, 刘栩, 贾园. 系统性红斑狼疮合并自身免疫性郎飞结病1例[J]. 北京大学学报(医学版), 2025, 57(6): 1174-1179.
[9] 梁景原, 张霞, 姚海红. 误诊为系统性硬化症的POEMS综合征1例[J]. 北京大学学报(医学版), 2025, 57(6): 1184-1187.
[10] 赵凯, 鲁芙爱, 王永福. 中枢神经系统感染模拟神经精神狼疮1例[J]. 北京大学学报(医学版), 2025, 57(6): 1188-1192.
[11] 王小梦, 曾晓君, 李娟. 黎族与汉族系统性红斑狼疮患者的主要临床特征[J]. 北京大学学报(医学版), 2025, 57(6): 1213-1218.
[12] 曹沛, 栾庆先. 牙周炎与全身系统性疾病的思考与探索[J]. 北京大学学报(医学版), 2025, 57(5): 852-858.
[13] 袁显墩, 李照华, 徐丹, 李婷, 方丹, 穆荣. 丝氨酸蛋白酶23在系统性硬化病皮肤纤维化中的作用和机制[J]. 北京大学学报(医学版), 2025, 57(5): 903-910.
[14] 张烁, 兰勇兵, 孙点剑一, 裴培, 杜怀东, 陈君石, 陈铮鸣, 吕筠, 李立明, 余灿清, (代表中国慢性病前瞻性研究项目协作组). 慢性阻塞性肺疾病患者体力活动与死亡风险的前瞻性关联[J]. 北京大学学报(医学版), 2025, 57(3): 537-544.
[15] 王文琼, 侯玉珂, 李春, 张学武. 系统性红斑狼疮患者不良妊娠结局的预测因素[J]. 北京大学学报(医学版), 2025, 57(3): 599-603.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!