Elevated Serum Amyloid a Levels Are not Specific for Sarcoidosis but Associate with a Fibrotic Pulmonary Phenotype
Autor: | Jan C. Grutters, Claudia Roodenburg-Benschop, Bob Meek, Marcel Veltkamp, Milou C. Schimmelpennink, Els Beijer |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
Adult
Male 0301 basic medicine medicine.medical_specialty animal diseases Gene Expression Gastroenterology Article Cohort Studies Pathogenesis 03 medical and health sciences Idiopathic pulmonary fibrosis 0302 clinical medicine Fibrosis Internal medicine hemic and lymphatic diseases Eosinophilic medicine Humans Serum amyloid A sarcoidosis lcsh:QH301-705.5 Aged Serum Amyloid A Protein business.industry fibrosis Granulomatosis with Polyangiitis General Medicine Middle Aged medicine.disease Idiopathic Pulmonary Fibrosis Infliximab SAA stomatognathic diseases C-Reactive Protein Methotrexate 030104 developmental biology lcsh:Biology (General) 030228 respiratory system Case-Control Studies Prednisone Female Sarcoidosis business Granulomatosis with polyangiitis Immunosuppressive Agents Hypersensitivity pneumonitis Alveolitis Extrinsic Allergic |
Zdroj: | Cells Volume 10 Issue 3 Cells, Vol 10, Iss 585, p 585 (2021) |
ISSN: | 2073-4409 |
DOI: | 10.3390/cells10030585 |
Popis: | Elevated Serum Amyloid A (SAA) levels have been found in several inflammatory diseases, including sarcoidosis. SAA is suggested to be involved in sarcoidosis pathogenesis by involvement in granuloma formation and maintenance. We hypothesized that SAA serum levels would be higher in sarcoidosis compared to other non-infectious granulomatous and non-granulomatous diseases. SAA levels were measured in serum from sarcoidosis, Hypersensitivity pneumonitis (HP), and (eosinophilic) granulomatosis with polyangiitis ((E)GPA) patients. Idiopathic pulmonary fibrosis (IPF) patients were included as non-granulomatous disease group. SAA levels of patients with sarcoidosis (31.0 µg/mL), HP (23.4 µg/mL), (E)GPA (36.9 µg/mL), and IPF (22.1 µg/mL) were all higher than SAA levels of healthy controls (10.1 µg/mL). SAA levels did not differ between the diagnostic groups. When SAA serum levels were analyzed in sarcoidosis subgroups, fibrotic sarcoidosis patients showed higher SAA levels than sarcoidosis patients without fibrosis (47.8 µg/mL vs. 29.4 µg/mL, p = 0.005). To conclude, the observation that fibrotic sarcoidosis patients have higher SAA levels, together with our finding that SAA levels were also increased in IPF patients, suggests that SAA may next to granulomatous processes also reflect the process of fibrogenesis. Further studies should clarify the exact role of SAA in fibrosis and the underlying mechanisms involved. |
Databáze: | OpenAIRE |
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