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Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders
http://hdl.handle.net/2297/26279
http://hdl.handle.net/2297/26279719fcd2f-c711-44f3-8df9-a2c20ab361cc
| 名前 / ファイル | ライセンス | アクション |
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| Item type | 学術雑誌論文 / Journal Article(1) | |||||
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| 公開日 | 2017-10-03 | |||||
| タイトル | ||||||
| タイトル | Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders | |||||
| 言語 | ||||||
| 言語 | eng | |||||
| 資源タイプ | ||||||
| 資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
| 資源タイプ | journal article | |||||
| 著者 |
Kaneko, Yoshibumi
× Kaneko, Yoshibumi× Miyajima, Hiroaki× Piperno, Alberto× Tomosugi, Naohisa× Hayashi, Hisao× Morotomi, Natsuko× Tsuchida, Ken-ichi× Ikeda, Takaaki× Ishikawa, Akihisa× Ota, Yusuke× Wakusawa, Shinya× Yoshioka, Kentaro× Kono, Satoshi× Pelucchi, Sara× Hattori, Ai× Tatsumi, Yasuaki× Okada, Toshihide× Yamagishi, Masakazu |
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| 提供者所属 | ||||||
| 内容記述タイプ | Other | |||||
| 内容記述 | 石川県立中央病院 | |||||
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| 内容記述タイプ | Other | |||||
| 内容記述 | 金沢大学医薬保健研究域医学系 | |||||
| 書誌情報 |
Journal of Gastroenterology 巻 45, 号 11, p. 1163-1171, 発行日 2010-11-01 |
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| 収録物識別子タイプ | ISSN | |||||
| 収録物識別子 | 0944-1174 | |||||
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| 収録物識別子タイプ | NCID | |||||
| 収録物識別子 | AA10988015 | |||||
| DOI | ||||||
| 関連タイプ | isVersionOf | |||||
| 識別子タイプ | DOI | |||||
| 関連識別子 | 10.1007/s00535-010-0259-8 | |||||
| 出版者 | ||||||
| 出版者 | Springer | |||||
| 抄録 | ||||||
| 内容記述タイプ | Abstract | |||||
| 内容記述 | Iron overload syndromes include a wide spectrum of genetic and acquired conditions. Recent studies suggest suppressed hepcidin synthesis in the liver to be the molecular basis of hemochromatosis. However, a liver with acquired iron overload synthesizes an adequate amount of hepcidin. Thus, hepcidin could function as a biochemical marker for differential diagnosis of iron overload syndromes. Methods We measured serum iron parameters and hepcidin- 25 levels followed by sequencing HFE, HJV, HAMP, TFR2, and SLC40A1 genes in 13 Japanese patients with iron overload syndromes. In addition, we performed direct measurement of serum hepcidin-25 levels using liquid chromatography-tandem mass spectrometry in 3 Japanese patients with aceruloplasminemia and 4 Italians with HFE hemochromatosis. Results One patient with HJV hemochromatosis, 2 with TFR2 hemochromatosis, and 3 with ferroportin disease were found among the 13 Japanese patients. The remaining 7 Japanese patients showed no evidence for genetic basis of iron overload syndrome. As far as the serum hepcidin-25 was concerned, seven patients with hemochromatosis and 3 with aceruloplasminemia showed markedly decreased serum hepcidin-25 levels. In contrast, 3 patients with ferroportin disease and 7 with secondary iron overload syndromes showed serum hepcidin levels parallel to their hyperferritinemia. Patients with iron overload syndromes were divided into 2 phenotypes presenting as low and high hepcidinemia. These were then associated with their genotypes. Conclusion Determining serum hepcidin-25 levels may aid differential diagnosis of iron overload syndromes prior to genetic analysis. © Springer 2010. | |||||
| 著者版フラグ | ||||||
| 出版タイプ | AM | |||||
| 出版タイプResource | http://purl.org/coar/version/c_ab4af688f83e57aa | |||||