Comparative study of serum surfactant protein-D and KL-6 concentrations in patients with systemic sclerosis as markers for monitoring the activity of pulmonary fibrosis

被引:2
作者
Yanaba, K
Hasegawa, M
Takehara, K
Sato, S
机构
[1] Kanazawa Univ, Grad Sch Med Sci, Dept Dermatol, Kanazawa, Ishikawa 9208641, Japan
[2] Jikei Univ, Sch Med, Dept Dermatol, Tokyo, Japan
关键词
systemic sclerosis; surfactant protein-D; KL-6; pulmonary fibrosis; disease activity;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To clarify the clinical significance of surfactant protein-D (SP-D) and KL-6 in the diagnosis and monitoring of pulmonary fibrosis (PF) in patients with systemic sclerosis (SSc), and to evaluate the differences between SP-D and KL-6. Methods. Serum SP-D and KL-6 concentrations were determined by ELISA in 42 SSc patients. In a retrospective longitudinal study, 83 serum samples from 6 SSc patients were analyzed during a followup, period of 0.6-6.3 years. Results. SP-D and KL-6 concentrations at the first visit were higher in patients with SSc, especially those with PF, compared with healthy controls. Increased concentrations of SP-D were associated with decreased DLCO and decreased vital capacity in SSc patients more strongly than those of KL-6. The sensitivity and specificity for PF were 91% and 88% for SP-D and 39% and 100% for KL-6, respectively. In the longitudinal study, both SP-D and KL-6 concentrations were associated with activity of PF in patients with SSc. SP-D concentrations changed more rapidly than KL-6 concentrations, in parallel with the PF activity. Conclusion. SP-D was a more sensitive marker for PF than KL-6. By contrast, KL-6 showed higher specificity than SP-D. Combined use of these 2 serum markers would be more helpful to diagnose and monitor the PF activity in patients with SSc than single use of each marker.
引用
收藏
页码:1112 / 1120
页数:9
相关论文
共 37 条
[1]   PRELIMINARY CRITERIA FOR THE CLASSIFICATION OF SYSTEMIC-SCLEROSIS (SCLERODERMA) [J].
不详 .
ARTHRITIS AND RHEUMATISM, 1980, 23 (05) :581-590
[2]  
Asano Y, 2001, ARTHRITIS RHEUM-US, V44, P1363, DOI 10.1002/1529-0131(200106)44:6<1363::AID-ART229>3.0.CO
[3]  
2-5
[4]  
CLEMENTS PJ, 1993, J RHEUMATOL, V20, P1892
[6]   PULMONARY DISEASE OF VASCULAR ORIGIN [J].
DINES, DE .
DISEASES OF THE CHEST, 1968, 54 (01) :3-+
[7]  
Giacomelli R, 2002, J RHEUMATOL, V29, P731
[8]   Serum surfactant proteins-A and -D as biomarkers in idiopathic pulmonary fibrosis [J].
Greene, KE ;
King, TE ;
Kuroki, Y ;
Bucher-Bartelson, B ;
Hunninghake, GW ;
Newman, LS ;
Nagae, H ;
Mason, RJ .
EUROPEAN RESPIRATORY JOURNAL, 2002, 19 (03) :439-446
[9]   MONITORING OF SERUM KL-6 ANTIGEN IN A PATIENT WITH RADIATION PNEUMONIA [J].
HAMADA, H ;
KOHNO, N ;
AKIYAMA, M ;
HIWADA, K .
CHEST, 1992, 101 (03) :858-860
[10]   Lung epithelium-specific proteins - Characteristics and potential applications as markers [J].
Hermans, C ;
Bernard, A .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 159 (02) :646-678