@article{MAKHILLRJMS20082411636,
    title = {Low Serum Fetuin A Levels and Cardiovascular Events in End-Stage Renal Disease (ESRD) Patients},
    journal = {Research Journal of Medical Sciences},
    volume = {2},
    number = {4},
    pages = {200-202},
    year = {2008},
    issn = {1815-9346},
    doi = {rjmsci.2008.200.202},
    url = {https://makhillpublications.co/view-article.php?issn=1815-9346&doi=rjmsci.2008.200.202},
    author = {Giulia Bivona,Chiara Bellia,Antonietta Caruso,Daniela Butera,Bruna Lo Sasso,Patrizia Altavilla,Rosa C. Carollo,Gaia Chiarello and},
    keywords = {Fetuin-A,ESRD,inflammation,vascular calcification,CVD},
    abstract = {The atherosclerotic Cardiovascular Disease (CVD) is frequently observed in End-Stage Renal Disease (ESRD) patients; according to the hypothesis of non-traditional risk factors for CVD, accelerated atherogenesis in these patients could be linked to both vascular calcification and inflammation.  2-Heremans-Schmid Glycoprotein (AHSG) also known as Fetuin-A, is considered a negative marker of inflammation and represents one of the <I>in vivo</I> circulating calcification modulators; these molecules are proteins working as endogenous inhibitors of Ca×PO<SUB>4</SUB> precipitation and are probably involved in the pathogenesis vascular calcification. Aim of this study is to evaluate the differences in serum Fetuin-A levels between 2 Haemodialysis (HD) patient groups distinguished on the basis of history of cardio and/or cerebrovascular events. All patients took part in clinical data collection and 2 patient groups were identified as no cardiovascular and cardiovascular on the basis of history of cardio and/or cerebrovascular events. Serum Fetuin-A levels were determined using sandwich immunoenzymatic assay, ELISA (Epitope Diagnostics Inc., San Diego, CA, USA). Serum Fetuin-A levels were significantly lower in cardiovascular HD patients than in those without cardiovascular event. The role of Fetuin A in the context of the different pathogenetic moments of atherosclerosis remains unclearly assessed; it would be of some interest to investigate the hypothesis, almost unexplored, of a relationship between low Fetuin A levels and endothelial dysfunction.}
    }