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Serum 20S proteasome levels are associated with disease activity in MPO-ANCA-associated microscopic polyangiitis

BACKGROUND: Proteasomes are found in both the cell nucleus and cytoplasm and play a major role in the ubiquitin-dependent and -independent non-lysosomal pathways of intracellular protein degradation. Proteasomes are also involved in the turnover of various regulatory proteins, antigen processing, ce...

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Autores principales: Maruyama, Hiroshi, Hirayama, Kouichi, Yamashita, Marina, Ohgi, Kentaro, Tsujimoto, Ryuji, Takayasu, Mamiko, Shimohata, Homare, Kobayashi, Masaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7447580/
https://www.ncbi.nlm.nih.gov/pubmed/32864569
http://dx.doi.org/10.1186/s41927-020-00137-4
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author Maruyama, Hiroshi
Hirayama, Kouichi
Yamashita, Marina
Ohgi, Kentaro
Tsujimoto, Ryuji
Takayasu, Mamiko
Shimohata, Homare
Kobayashi, Masaki
author_facet Maruyama, Hiroshi
Hirayama, Kouichi
Yamashita, Marina
Ohgi, Kentaro
Tsujimoto, Ryuji
Takayasu, Mamiko
Shimohata, Homare
Kobayashi, Masaki
author_sort Maruyama, Hiroshi
collection PubMed
description BACKGROUND: Proteasomes are found in both the cell nucleus and cytoplasm and play a major role in the ubiquitin-dependent and -independent non-lysosomal pathways of intracellular protein degradation. Proteasomes are also involved in the turnover of various regulatory proteins, antigen processing, cell differentiation, and apoptosis. To determine the diagnostic value of serum proteasome in antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), we investigated patients with AAV at various stages of the disease. METHODS: Serum 20S-proteasome was measured by ELISA in 44 patients with MPO-ANCA-associated microscopic polyangiitis (MPA) and renal involvement. Thirty of the patients provided serum samples before the initial treatment, and 30 provided samples during remission; 16 provided samples at both time points. RESULTS: The mean serum 20S-proteasome level was significantly higher in the active-vasculitis patients (3414.6 ± 2738.9 ng/mL; n = 30) compared to the inactive-vasculitis patients (366.4 ± 128.4 ng/mL; n = 30; p <  0.0001) and 40 controls (234.9 ± 90.1 ng/mL; p <  0.0001). There were significant positive correlations between the serum 20S-proteasome level and the Birmingham Vasculitis Activity Score (BVAS) (r = 0.581, p <  0.0001), the ANCA titer (r = 0.384, p <  0.0001), the white blood cell (WBC) count (r = 0.284, p = 0.0042), the platelet count (r = 0.369, p = 0.0002), and the serum C-reactive protein (CRP) level (r = 0.550, p < 0.0001). There were significant negative correlations between the serum 20S-proteasome level and both the hemoglobin concentration (r = − 0.351, p = 0.0003) and the serum albumin level (r = − 0.460, p < 0.0001). In a multiple regression analysis, there was a significant positive correlation between the serum 20S-proteasome level and only the BVAS results (β = 0.851, p = 0.0009). In a receiver operating curve analysis, the area under the curve for the serum 20S-proteasome level was 0.996, which is higher than those of the WBC count (0.738) and the serum CRP level (0.963). CONCLUSION: The serum level of 20S-proteasome may be a useful marker for disease activity in AAV.
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spelling pubmed-74475802020-08-27 Serum 20S proteasome levels are associated with disease activity in MPO-ANCA-associated microscopic polyangiitis Maruyama, Hiroshi Hirayama, Kouichi Yamashita, Marina Ohgi, Kentaro Tsujimoto, Ryuji Takayasu, Mamiko Shimohata, Homare Kobayashi, Masaki BMC Rheumatol Research Article BACKGROUND: Proteasomes are found in both the cell nucleus and cytoplasm and play a major role in the ubiquitin-dependent and -independent non-lysosomal pathways of intracellular protein degradation. Proteasomes are also involved in the turnover of various regulatory proteins, antigen processing, cell differentiation, and apoptosis. To determine the diagnostic value of serum proteasome in antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), we investigated patients with AAV at various stages of the disease. METHODS: Serum 20S-proteasome was measured by ELISA in 44 patients with MPO-ANCA-associated microscopic polyangiitis (MPA) and renal involvement. Thirty of the patients provided serum samples before the initial treatment, and 30 provided samples during remission; 16 provided samples at both time points. RESULTS: The mean serum 20S-proteasome level was significantly higher in the active-vasculitis patients (3414.6 ± 2738.9 ng/mL; n = 30) compared to the inactive-vasculitis patients (366.4 ± 128.4 ng/mL; n = 30; p <  0.0001) and 40 controls (234.9 ± 90.1 ng/mL; p <  0.0001). There were significant positive correlations between the serum 20S-proteasome level and the Birmingham Vasculitis Activity Score (BVAS) (r = 0.581, p <  0.0001), the ANCA titer (r = 0.384, p <  0.0001), the white blood cell (WBC) count (r = 0.284, p = 0.0042), the platelet count (r = 0.369, p = 0.0002), and the serum C-reactive protein (CRP) level (r = 0.550, p < 0.0001). There were significant negative correlations between the serum 20S-proteasome level and both the hemoglobin concentration (r = − 0.351, p = 0.0003) and the serum albumin level (r = − 0.460, p < 0.0001). In a multiple regression analysis, there was a significant positive correlation between the serum 20S-proteasome level and only the BVAS results (β = 0.851, p = 0.0009). In a receiver operating curve analysis, the area under the curve for the serum 20S-proteasome level was 0.996, which is higher than those of the WBC count (0.738) and the serum CRP level (0.963). CONCLUSION: The serum level of 20S-proteasome may be a useful marker for disease activity in AAV. BioMed Central 2020-08-25 /pmc/articles/PMC7447580/ /pubmed/32864569 http://dx.doi.org/10.1186/s41927-020-00137-4 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Maruyama, Hiroshi
Hirayama, Kouichi
Yamashita, Marina
Ohgi, Kentaro
Tsujimoto, Ryuji
Takayasu, Mamiko
Shimohata, Homare
Kobayashi, Masaki
Serum 20S proteasome levels are associated with disease activity in MPO-ANCA-associated microscopic polyangiitis
title Serum 20S proteasome levels are associated with disease activity in MPO-ANCA-associated microscopic polyangiitis
title_full Serum 20S proteasome levels are associated with disease activity in MPO-ANCA-associated microscopic polyangiitis
title_fullStr Serum 20S proteasome levels are associated with disease activity in MPO-ANCA-associated microscopic polyangiitis
title_full_unstemmed Serum 20S proteasome levels are associated with disease activity in MPO-ANCA-associated microscopic polyangiitis
title_short Serum 20S proteasome levels are associated with disease activity in MPO-ANCA-associated microscopic polyangiitis
title_sort serum 20s proteasome levels are associated with disease activity in mpo-anca-associated microscopic polyangiitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7447580/
https://www.ncbi.nlm.nih.gov/pubmed/32864569
http://dx.doi.org/10.1186/s41927-020-00137-4
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