摘要
Background: Serum levels of tissue inhibitor ofmetalloproteinases (TIMPs) have been reported to be elevated in patients with various connective tissue diseases. However, there has been no report that evaluates TIMPs in patients with eosinophilic fasciitis (EF). Objectives: To determine serum TIMP-1 and TIMP-2 levels in patients with EF and to investigate their clinical significance. Methods: Immunohistochemical stainings were performed in normal and EF skin samples. Serum TIMP-1 and TIMP-2 levels of 11 patients with EF and 12 healthy individuals were also measured with specific enzyme-linked immunosorbent assays. Results: The fascia of EF patients was stained only by TIMP-1. Serum TIMP-1 levels (mean ±SD) were significantly higher in EF patients than in healthy individuals (206.3 ±65.4 vs. 145.2 ±36.2 ng mL-1, P < 0.01). Serum TIMP-1 levels in EF patients were significantly correlated with serum γ-globulin and IgG levels (r = 0.86, P < 0.05; r = 0.83, P < 0.005, respectively). Conclusions: These results suggest that TIMP-1 is involved in the pathogenesis of EF, and that TIMP-1 may be a useful marker for the disease activity as well as serum γ-globulin or IgG levels.
Background: Serum levels of tissue inhibitor ofmetalloproteinases (TIMPs) have been reported to be elevated in patients with various connective tissue diseases. However, there has been no report that evaluates TIMPs in patients with eosinophilic fasciitis (EF). Objectives: To determine serum TIMP-1 and TIMP-2 levels in patients with EF and to investigate their clinical significance. Methods: Immunohistochemical stainings were performed in normal and EF skin samples. Serum TIMP-1 and TIMP-2 levels of 11 patients with EF and 12 healthy individuals were also measured with specific enzyme-linked immunosorbent assays. Results: The fascia of EF patients was stained only by TIMP-1. Serum TIMP-1 levels (mean ±SD) were significantly higher in EF patients than in healthy individuals (206.3 ±65.4 vs. 145.2 ±36.2 ng mL-1, P < 0.01). Serum TIMP-1 levels in EF patients were significantly correlated with serum γ-globulin and IgG levels (r = 0.86, P < 0.05; r = 0.83, P < 0.005, respectively). Conclusions: These results suggest that TIMP-1 is involved in the pathogenesis of EF, and that TIMP-1 may be a useful marker for the disease activity as well as serum γ-globulin or IgG levels.
