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抗拓扑异构酶I是否为系统性硬化症肺部受累的血清标志物?

Is anti-topoisomerase I a serum marker of pulmonary involvement in systemic sclerosis?

作者信息

Diot E, Giraudeau B, Diot P, Degenne D, Ritz L, Guilmot J L, Lemarié E

机构信息

Groupe de Recherche Epithélium Respiratoire et Inflammation, Service de Médecine Interne B, CHU Bretonneau, Tours, France.

出版信息

Chest. 1999 Sep;116(3):715-20. doi: 10.1378/chest.116.3.715.

DOI:10.1378/chest.116.3.715
PMID:10492277
Abstract

STUDY OBJECTIVE

To determine the value of the level of anti-topoisomerase I (anti-topo I) to evaluate lung involvement defined by abnormal high-resolution computed tomography (HRCT) score and pulmonary function tests (PFTs) in systemic sclerosis (SS).

PATIENTS

Forty-eight patients with SS, 20 with lung involvement and 28 with no lung involvement.

DESIGN

PFT measurement, HRCT scoring of lung involvement, and anti-topo I assay by enzyme-linked immunosorbent assay. Normal anti-topo I level was defined as < 30.

RESULTS

There was a significant association between cutaneous extent and anti-topo I level (6.5% of patients with limited cutaneous scleroderma had abnormal anti-topo I levels vs 70.6% of patients with diffuse cutaneous scleroderma, p = 0.0001). In patients with diffuse cutaneous scleroderma, pulmonary involvement was associated with a higher percentage of abnormal anti-topo I level: 91.7% vs 20% (p = 0.010). In patients with diffuse cutaneous scleroderma, a significant association was found between the class of anti-topoII level and total lung capacity (median, 69 in patients with abnormal anti-topo I level vs 87 in patients with normal anti-topo I level, p = 0.010), between the class of anti-topo I level and HRCT score (median, 12 in patients with abnormal anti-topo I level vs 5 in patients with normal anti-topo I level, p = 0.05).

CONCLUSION

Anti-topo I can be considered as a marker of lung involvement in patients with diffuse cutaneous scleroderma.

摘要

研究目的

确定抗拓扑异构酶I(抗拓扑异构酶I)水平在评估系统性硬化症(SS)中由异常高分辨率计算机断层扫描(HRCT)评分和肺功能测试(PFT)定义的肺部受累情况时的价值。

患者

48例SS患者,其中20例有肺部受累,28例无肺部受累。

设计

进行PFT测量、对肺部受累情况进行HRCT评分,并通过酶联免疫吸附测定法检测抗拓扑异构酶I。正常抗拓扑异构酶I水平定义为<30。

结果

皮肤受累范围与抗拓扑异构酶I水平之间存在显著关联(局限性皮肤硬皮病患者中有6.5%抗拓扑异构酶I水平异常,而弥漫性皮肤硬皮病患者中有70.6%,p = 0.0001)。在弥漫性皮肤硬皮病患者中,肺部受累与抗拓扑异构酶I水平异常的比例较高相关:91.7% 对20%(p = 0.010)。在弥漫性皮肤硬皮病患者中,发现抗拓扑异构酶II水平类别与肺总量之间存在显著关联(抗拓扑异构酶I水平异常的患者中位数为69,抗拓扑异构酶I水平正常的患者中位数为87,p = 0.010),抗拓扑异构酶I水平类别与HRCT评分之间也存在显著关联(抗拓扑异构酶I水平异常的患者中位数为12,抗拓扑异构酶I水平正常的患者中位数为5,p = 0.05)。

结论

抗拓扑异构酶I可被视为弥漫性皮肤硬皮病患者肺部受累的标志物。

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