TY - JOUR
T1 - Usefulness of serum Krebs von den Lungen-6 for the management of myositis-associated interstitial lung disease
AU - Takanashi, Satoshi
AU - Nishina, Naoshi
AU - Nakazawa, Maho
AU - Kaneko, Yuko
AU - Takeuchi, Tsutomu
N1 - Funding Information:
Disclosure statement: Y.K. has received grants or speaking fees from AbbVie, Astellas, Ayumi, Bristol-Myers Squibb, Chugai, Eisai, Eli Lilly, Hisamitsu, Jansen, Kissei, Pfizer, Sanofi, Takeda, Tanabe-Mitsubishi, and UCB. T.T. has received research grants or speaking fees from Astellas Pharma Inc, Bristol Myers K.K., Chugai Pharmaceutical Co., Ltd, Daiichi Sankyo Co., Ltd, Takeda Pharmaceutical Co., Ltd, Teijin Pharma Ltd, AbbVie GK, Asahikasei Pharma Corp., Mitsubishi Tanabe Pharma, Astra Zeneca K.K., Eli Lilly Japan K.K., Novartis Pharma K.K., Abbivie GK, Nipponkayaku Co. Ltd, Janssen, Pharmaceutical K.K., Taiho Pharmaceutical Co., Ltd And Pfizer Japan Inc. The other authors have declared no conflicts of interest.
Publisher Copyright:
© The Author(s) 2019.
PY - 2019/6/1
Y1 - 2019/6/1
N2 - Objective. To identify biomarkers for assessing myositis-associated interstitial lung disease (ILD). Methods. We reviewed consecutive patients from our institution who had been newly diagnosed with PM, DM, or clinically amyopathic DM during the years 20022017. The patients were divided into two groups according to the presence of ILD, and the ILD group was further subdivided into three groups according to the clinical courses of induction failure, relapse and non-relapse. Baseline and time-course changes in the parameters were compared between groups. Results. Among 110 patients enrolled, 75 (68%) had ILD. Baseline serum Krebs von den Lungen-6 (KL-6) was significantly higher in the ILD group than in the non-ILD group (1120 vs 236 U/ml; P < 0.001). In the ILD group consisting of the induction failure cases (n = 3), the relapse group (n = 24) and the non-relapse group (n = 48), baseline serum KL-6 was significantly different between the three groups [1971 vs 1870 vs 935 U/ml, respectively; P = 0.003 (relapse group vs non-relapse group)]. The time-course changes in serum KL-6 revealed that KL-6 significantly increased along with relapse, with the increase of 625 U/ml relevant to relapse. Conclusion. Serum KL-6 is a useful biomarker for assessing the disease activity of myositis-associated ILD.
AB - Objective. To identify biomarkers for assessing myositis-associated interstitial lung disease (ILD). Methods. We reviewed consecutive patients from our institution who had been newly diagnosed with PM, DM, or clinically amyopathic DM during the years 20022017. The patients were divided into two groups according to the presence of ILD, and the ILD group was further subdivided into three groups according to the clinical courses of induction failure, relapse and non-relapse. Baseline and time-course changes in the parameters were compared between groups. Results. Among 110 patients enrolled, 75 (68%) had ILD. Baseline serum Krebs von den Lungen-6 (KL-6) was significantly higher in the ILD group than in the non-ILD group (1120 vs 236 U/ml; P < 0.001). In the ILD group consisting of the induction failure cases (n = 3), the relapse group (n = 24) and the non-relapse group (n = 48), baseline serum KL-6 was significantly different between the three groups [1971 vs 1870 vs 935 U/ml, respectively; P = 0.003 (relapse group vs non-relapse group)]. The time-course changes in serum KL-6 revealed that KL-6 significantly increased along with relapse, with the increase of 625 U/ml relevant to relapse. Conclusion. Serum KL-6 is a useful biomarker for assessing the disease activity of myositis-associated ILD.
KW - Biomarker
KW - Clinically amyopathic DM
KW - DM
KW - Interstitial lung disease
KW - Krebs von den lungen-6
KW - Myositis
KW - PM
KW - Relapse
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U2 - 10.1093/rheumatology/key420
DO - 10.1093/rheumatology/key420
M3 - Article
C2 - 30624752
AN - SCOPUS:85066496367
SN - 1462-0324
VL - 58
SP - 1034
EP - 1039
JO - Rheumatology and Rehabilitation
JF - Rheumatology and Rehabilitation
IS - 6
ER -