Literature DB >> 25659646

Hepcidin levels in hyperprolactinemic women monitored by nanopore thin film based assay: correlation with pregnancy-associated hormone prolactin.

Jing Wang1, Gang Liu2, Zi Xu3, Jiwei Dai4, Ping Song4, Jian Shi2, Ye Hu5, Zhongbo Hu6, Guangjun Nie7, Yan-Zhong Chang8, Yuliang Zhao9.   

Abstract

Hepcidin is a central regulator in human iron metabolism. Although it is often regarded as a promising indicator of iron status, the lack of effective quantification method has impeded the comprehensive assessment of its physiological and clinical significance. Herein we applied a newly established, nanopore film enrichment based hepcidin assay to examine the correlation between hepcidin and prolactin, the hormone with an important role during pregnancy and lactation. Women with pathologically elevated prolactin secretion (hyperprolactinemia) were found to have lower serum hepcidin compared to those with normal prolactin levels, without showing significant difference in other hepcidin-regulating factors. Moreover, prolactin-reducing drug bromocriptine mesylate resulted in elevated expression of the hepcidin in hyperprolactinemia patients. These findings suggest a possible role of prolactin in regulation of hepcidin, and may render hepcidin a useful biomarker for progress monitoring and treatment of iron-related diseases under hyperprolactinemic conditions. FROM THE CLINICAL EDITOR: The level of hepcidin has been shown to reflect the underlying iron status of the patient. Nonentheless, there is an urgent need of reliable, fast and easy-to-do hepcidin assay in the clinical setting. In this paper, the authors described a further modification of their previously described nanopore silica film-based enrichment approach for quantification of hepcidin and found correlation between hepcidin and prolactin. This new knowledge may add to current understanding of iron homeostasis during pregnancy.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Biomarker; Hepcidin; Hyperprolactinemia; MALDI-TOF MS; Nanopore silica film; Prolactin

Mesh:

Substances:

Year:  2015        PMID: 25659646     DOI: 10.1016/j.nano.2015.01.008

Source DB:  PubMed          Journal:  Nanomedicine        ISSN: 1549-9634            Impact factor:   5.307


  4 in total

1.  The Role of Insulin Therapy in Correcting Hepcidin Levels in Patients with Type 2 Diabetes Mellitus.

Authors:  Driton Vela; Jovica Leshoski; Elizabeta S Gjorgievska; Nikola Hadzi-Petrushev; Muharrem Jakupaj; Ramadan B Sopi; Mitko Mladenov
Journal:  Oman Med J       Date:  2017-05

2.  Iron Homeostasis and Hepcidin Concentration in Patients With Acromegaly.

Authors:  Aleksandra Krygier; Ewelina Szczepanek-Parulska; Maja Cieślewicz; Elżbieta Wrotkowska; Justyna Chanaj-Kaczmarek; Marek Ruchała
Journal:  Front Endocrinol (Lausanne)       Date:  2022-02-08       Impact factor: 5.555

3.  Astrocyte-derived hepcidin controls iron traffic at the blood-brain-barrier via regulating ferroportin 1 of microvascular endothelial cells.

Authors:  Linhao You; Pan-Pan Yu; Tianyu Dong; Wenhuan Guo; Shiyang Chang; Bingjie Zheng; Yunzhe Ci; Fudi Wang; Peng Yu; Guofen Gao; Yan-Zhong Chang
Journal:  Cell Death Dis       Date:  2022-08-01       Impact factor: 9.685

4.  Correlation of serum hepcidin levels with disease progression in hepatitis B virus-related disease assessed by nanopore film based assay.

Authors:  Jing Wang; Ailian Dong; Gang Liu; Gregory J Anderson; Tony Y Hu; Jian Shi; Yulin Hu; Guangjun Nie
Journal:  Sci Rep       Date:  2016-10-03       Impact factor: 4.379

  4 in total

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