Assessment of serum uric acid as risk factor for tauopathies

被引:0
作者
Tommaso Schirinzi
Giulia Di Lazzaro
Vito Luigi Colona
Paola Imbriani
Mohammad Alwardat
Giulia Maria Sancesario
Alessandro Martorana
Antonio Pisani
机构
[1] University of Roma Tor Vergata,Neurology Unit, Department of Systems Medicine
[2] Bambino Gesù Children Hospital,Department of Neurosciences
[3] University of Roma Tor Vergata,Department of Neuroscience
[4] University of Roma Tor Vergata,Department of Experimental Medicine and Surgery
来源
Journal of Neural Transmission | 2017年 / 124卷
关键词
Tauopathies; Urate; Uric acid; Progressive supranuclear palsy; Alzheimer’s disease; Frontotemporal dementia;
D O I
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中图分类号
学科分类号
摘要
Low levels of serum uric acid (UA) are a risk factor for many neurodegenerative diseases but the role of UA in tauopathies has not been yet fully evaluated. In this study, we assessed the risk associated with serum UA levels in a large group of patients with tauopathies, either primary or secondary. The mean serum UA concentrations of 111 patients with tauopathies (TAU), including 41 with progressive supranuclear palsy (PSP), 45 with Alzheimer’s disease (AD) and 25 with frontotemporal dementia (FTD) were compared to that of 130 controls (CTL). The association between serum UA and TAU condition, PSP, AD and FTD was calculated as odd ratio (OR) adjusted for age and gender. A cut-off value of serum UA was finally obtained to predict subjects at risk for TAU. The serum UA levels in TAU and PSP, AD and FTD subgroups were similar, and significantly lower than CTL. Linear regression revealed inverse relationships between UA and TAU (OR = 0.610), PSP (OR = 0.626), AD (OR = 0.685) and FTD (OR = 0.577). The cut-off value of 4.35 mg/dl (AUC = 0.655) discriminates TAU from CTL, although with poor specificity and sensitivity. Low concentrations of serum UA represent a common risk factor for different tauopathies (PSP, FTD and AD). These findings may represent a starting point for preventive strategies or novel therapeutic approaches in this group of severe neurodegenerative diseases.
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页码:1105 / 1108
页数:3
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