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Relationship between ceruloplasmin and oxidative biomarkers including ferritin among healthy Japanese
Serum ceruloplasmin (CP), a marker relevant to copper metabolism, is one of famous inflammation markers with a reduction in Wilson’s disease, whereas serum ferritin is a marker relevant to iron metabolism. Recently, ferritin is pointed out to be related with oxidative stress. However, there is still...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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the Society for Free Radical Research Japan
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3593134/ https://www.ncbi.nlm.nih.gov/pubmed/23524455 http://dx.doi.org/10.3164/jcbn.12-122 |
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author | Inoue, Kiyomi Sakano, Noriko Ogino, Keiki Sato, Yoshie Wang, Da-Hong Kubo, Masayuki Takahashi, Hidekazu Kanbara, Sakiko Miyatake, Nobuyuki |
author_facet | Inoue, Kiyomi Sakano, Noriko Ogino, Keiki Sato, Yoshie Wang, Da-Hong Kubo, Masayuki Takahashi, Hidekazu Kanbara, Sakiko Miyatake, Nobuyuki |
author_sort | Inoue, Kiyomi |
collection | PubMed |
description | Serum ceruloplasmin (CP), a marker relevant to copper metabolism, is one of famous inflammation markers with a reduction in Wilson’s disease, whereas serum ferritin is a marker relevant to iron metabolism. Recently, ferritin is pointed out to be related with oxidative stress. However, there is still no population research which showed the relation of CP and ferritin. Therefore, we investigated the relationship between CP and ferritin including oxidative stress biomarkers among healthy Japanese (n = 389). We measured serum CP, ferritin, Fe, high-sensitivity C-reactive protein (hs-CRP), and urinary oxidative stress biomarkers [H(2)O(2), 8-hydroxy-2’-deoxyguanosine (8-OHdG), 8-isoprostane] and so on. Subjects showed that age; 41.7 ± 10.0 (year), CP; 31.9 ± 6.8 (mg/dl), ferritin; 123.5 ± 121.0 (ng/ml), hs-CRP; 0.89 ± 2.53 (mg/l), 8-OHdG; 10.2 ± 4.4 [ng/mg creatinine (Cre)] and H(2)O(2); 6.5 ± 10.9 (µM/g Cre), (All data mentioned above were expressed as mean ± SD). CP was significantly and positively correlated with hs-CRP and inversely correlated with ferritin, Fe and 8-OHdG. By a multiple logistic regression analysis, odds ratio of CP according to quartiles of hs-CRP was 4.86, and according to quartiles of 8-OHdG was 0.39 after adjusting for age and other confounding factors. In conclusion, our findings suggest that CP was an antioxidative biomarker which controls oxidative stress, whereas ferritin was a marker which may participate in the generation of oxidative stress. |
format | Online Article Text |
id | pubmed-3593134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-35931342013-03-22 Relationship between ceruloplasmin and oxidative biomarkers including ferritin among healthy Japanese Inoue, Kiyomi Sakano, Noriko Ogino, Keiki Sato, Yoshie Wang, Da-Hong Kubo, Masayuki Takahashi, Hidekazu Kanbara, Sakiko Miyatake, Nobuyuki J Clin Biochem Nutr Original Article Serum ceruloplasmin (CP), a marker relevant to copper metabolism, is one of famous inflammation markers with a reduction in Wilson’s disease, whereas serum ferritin is a marker relevant to iron metabolism. Recently, ferritin is pointed out to be related with oxidative stress. However, there is still no population research which showed the relation of CP and ferritin. Therefore, we investigated the relationship between CP and ferritin including oxidative stress biomarkers among healthy Japanese (n = 389). We measured serum CP, ferritin, Fe, high-sensitivity C-reactive protein (hs-CRP), and urinary oxidative stress biomarkers [H(2)O(2), 8-hydroxy-2’-deoxyguanosine (8-OHdG), 8-isoprostane] and so on. Subjects showed that age; 41.7 ± 10.0 (year), CP; 31.9 ± 6.8 (mg/dl), ferritin; 123.5 ± 121.0 (ng/ml), hs-CRP; 0.89 ± 2.53 (mg/l), 8-OHdG; 10.2 ± 4.4 [ng/mg creatinine (Cre)] and H(2)O(2); 6.5 ± 10.9 (µM/g Cre), (All data mentioned above were expressed as mean ± SD). CP was significantly and positively correlated with hs-CRP and inversely correlated with ferritin, Fe and 8-OHdG. By a multiple logistic regression analysis, odds ratio of CP according to quartiles of hs-CRP was 4.86, and according to quartiles of 8-OHdG was 0.39 after adjusting for age and other confounding factors. In conclusion, our findings suggest that CP was an antioxidative biomarker which controls oxidative stress, whereas ferritin was a marker which may participate in the generation of oxidative stress. the Society for Free Radical Research Japan 2013-03 2013-03-01 /pmc/articles/PMC3593134/ /pubmed/23524455 http://dx.doi.org/10.3164/jcbn.12-122 Text en Copyright © 2013 JCBN This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Inoue, Kiyomi Sakano, Noriko Ogino, Keiki Sato, Yoshie Wang, Da-Hong Kubo, Masayuki Takahashi, Hidekazu Kanbara, Sakiko Miyatake, Nobuyuki Relationship between ceruloplasmin and oxidative biomarkers including ferritin among healthy Japanese |
title | Relationship between ceruloplasmin and oxidative biomarkers including ferritin among healthy Japanese |
title_full | Relationship between ceruloplasmin and oxidative biomarkers including ferritin among healthy Japanese |
title_fullStr | Relationship between ceruloplasmin and oxidative biomarkers including ferritin among healthy Japanese |
title_full_unstemmed | Relationship between ceruloplasmin and oxidative biomarkers including ferritin among healthy Japanese |
title_short | Relationship between ceruloplasmin and oxidative biomarkers including ferritin among healthy Japanese |
title_sort | relationship between ceruloplasmin and oxidative biomarkers including ferritin among healthy japanese |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3593134/ https://www.ncbi.nlm.nih.gov/pubmed/23524455 http://dx.doi.org/10.3164/jcbn.12-122 |
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