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Hepcidin: An emerging biomarker for iron disorders,inflammatory diseases, and infections

机译:肝素:用于铁障碍,炎症性疾病和感染的新兴生物标志物

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The peptide hormone hepcidin, has emerged as the master regulator of iron homeostasis. Dysregulation of hepcidin is a principal or contributing factor in most genetic and acquired systemic iron disorders, including anemia of inflammation (anemia of chronic disease). Hepcidin maintains healthy blood iron levels by regulating dietary iron absorption and transport from body iron stores to plasma. High serum hepcidin levels observed in chronic and acute inflammatory conditions can cause anemia by limiting plasma iron available for erythropoiesis. Chronically low serum hepcidin levels cause iron-overload and ultimately, accumulation of iron in liver and heart. We recently validated the first immunoassay for serum hepcidin and established the normal ranges in adults. Hepcidin has excellent potential as a biomarker and has a known mechanism of action, good stability, and rapid response to iron stores, inflammatory stimuli, and bacterial infections. Hepcidin can be measured in blood, urine, and saliva, and is generally not measurable in iron deficient/anemic patients and highly elevated in inflammatory diseases and infections. Intrinsic LifeSciences (ILS) is developing second generation hepcidin immunoassays and lateral-flow POC devices for hepcidin, a well characterized multi-purpose biomarker with applications in global health security.
机译:所述肽激素铁调素,已经成为铁稳态的主要调节剂。铁调素的失调是在大多数遗传性和获得全身性铁病症,包括炎症(慢性疾病的贫血)的贫血的主要或促进因素。铁调素通过调节从体内铁储存食物铁的吸收和运输血浆维持健康的血液铁含量。在慢性和急性炎性病症观察到高血清铁调素水平可通过限制可用于红细胞生成等离子体铁导致贫血。长期低血清铁调素水平会导致铁过载,并最终在肝脏和心脏铁的积累。我们最近证实血清铁调素的第一免疫,并建立成人正常范围。铁调素具有优异的潜力作为生物标志物,具有行动的已知机制,稳定性好,并储存铁,炎症刺激,和细菌感染的快速响应。铁调素可在血液,尿液,和唾液来测量,并且一般不缺铁/贫血患者可测量和炎性疾病和感染高度升高。固有生命科学(ILS)正在开发第二代的hepcidin免疫测定法和横流POC设备铁调素,与在全球卫生安全应用充分表征多用途生物标志物。

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