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DOI 10.1016/j.resinv.2020.07.003

Медицинская библиотека · Respiratory investigation · 2020

Plasma matrix metalloproteinase 7, CC-chemokine ligand 18, and periostin as markers for pulmonary sarcoidosis.

Isshiki Takuma, Matsuyama Hisayo, Yamaguchi Tetsuo, Morita Toshisuke, Ono Junya, Nunomura Satoshi, Izuhara Kenji, Sakamoto Susumu, Homma Sakae, Kishi Kazuma

СтатьяПеревод пока не подготовлен

Аннотация

BACKGROUND

Some patients with sarcoidosis experience worsening of pulmonary lesions. However, no biomarker has been identified that reflects pulmonary disease status in sarcoidosis. We investigated the usefulness of potential markers of pulmonary fibrosis in patients with sarcoidosis.

METHODS

Plasma matrix metalloproteinase 7 (MMP-7), CC-chemokine ligand 18 (CCL-18), and periostin levels were evaluated in 60 patients with sarcoidosis and 30 healthy controls; bronchoalveolar lavage fluid levels were analyzed in 22 patients with sarcoidosis. To determine the usefulness of these markers, we explored potential correlations between these markers and sarcoidosis clinical characteristics.

RESULTS

Plasma MMP-7, CCL-18, and periostin concentrations were significantly higher in patients with sarcoidosis than those in healthy controls. MMP-7 concentrations in plasma and bronchoalveolar lavage fluid were higher in patients with sarcoidosis with parenchymal infiltration than in those without lung lesions. Moreover, MMP-7 concentration was negatively correlated with pulmonary function.

CONCLUSION

Among these novel biomarkers, MMP-7 most precisely reflected pulmonary sarcoidosis disease status and thus, might be useful for diagnosing and evaluating sarcoidosis, particularly in patients with pulmonary parenchymal lesions.

Для цитирования: Isshiki Takuma, Matsuyama Hisayo, Yamaguchi Tetsuo, Morita Toshisuke, Ono Junya, Nunomura Satoshi, Izuhara Kenji, Sakamoto Susumu, Homma Sakae, Kishi Kazuma. Plasma matrix metalloproteinase 7, CC-chemokine ligand 18, and periostin as markers for pulmonary sarcoidosis.. Respiratory investigation. 2020. DOI: 10.1016/j.resinv.2020.07.003.

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