Department of Clinical Biochemistry, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Clin Chem. 2012 Jan;58(1):83-91. doi: 10.1373/clinchem.2011.165696. Epub 2011 Nov 29.
Plasma cardiac natriuretic peptides and peptide fragments from their molecular precursors are markers of heart disease. Clinical studies have defined the current diagnostic utility of these markers, whereas biochemical elucidation of peptide structure and posttranslational processing has revealed new plasma peptide forms of potential clinical use.
Natriuretic propeptide structures undergo variable degrees of endo- and exoproteolytic cleavages as well as amino acid modifications, which leave the plasma phase of the peptides highly heterogeneous and dependent on cardiac pathophysiology and capacity. An ongoing characterization of the molecular heterogeneity may not only help us to appreciate the biosynthetic capacity of the endocrine heart but may also lead to the discovery of new and more disease-specific targets for future molecular diagnosis.
Peptides derived from pro-atrial natriuretic peptide and pro-B-type natriuretic peptide are useful plasma markers in heart failure. New data have defined cardiac myocytes as competent endocrine cells in posttranslational processing and cellular secretion.
血浆心钠肽及其前体分子中的肽片段是心脏病的标志物。临床研究已经确定了这些标志物的当前诊断效用,而对肽结构和翻译后加工的生化阐明揭示了具有潜在临床应用的新的血浆肽形式。
钠尿肽原结构经历不同程度的内切和外切裂解以及氨基酸修饰,这使得肽的血浆相高度异质,并取决于心脏病理生理学和能力。对分子异质性的持续特征分析不仅有助于我们了解内分泌心脏的生物合成能力,而且可能导致发现新的、更具疾病特异性的未来分子诊断目标。
源自心钠肽原和脑钠肽原的肽是心力衰竭的有用血浆标志物。新数据定义了心肌细胞在后翻译加工和细胞分泌中作为有能力的内分泌细胞。