Serum Cholinesterase Activities Distinguish between Stroke Patients and Controls and Predict 12-Month Mortality

被引:89
作者
Ben Assayag, Einor [3 ,4 ]
Shenhar-Tsarfaty, Shani [3 ,4 ,5 ]
Ofek, Keren [1 ,2 ]
Soreq, Lilach [6 ]
Bova, Irena [3 ,4 ]
Shopin, Ludmila [3 ,4 ]
Berg, Ronan M. G. [7 ]
Berliner, Shlomo [3 ,4 ,5 ]
Shapira, Itzhak [3 ,4 ,5 ]
Bornstein, Natan M. [3 ,4 ,5 ]
Soreq, Hermona [1 ,2 ]
机构
[1] Hebrew Univ Jerusalem, Inst Life Sci, IL-91904 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Interdisciplinary Ctr Neuronal Computat, IL-91904 Jerusalem, Israel
[3] Tel Aviv Univ, Tel Aviv Sourasky Med Ctr, Dept Neurol, IL-69978 Tel Aviv, Israel
[4] Tel Aviv Univ, Tel Aviv Sourasky Med Ctr, Dept Internal Med D, IL-69978 Tel Aviv, Israel
[5] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel
[6] Hebrew Univ Jerusalem, Hadassah Med Sch, IMRIC, Dept Med Neurobiol Physiol, IL-91904 Jerusalem, Israel
[7] Rigshosp, Dept Infect Dis, Univ Hosp, Ctr Inflammat & Metab, DK-2100 Copenhagen, Denmark
基金
以色列科学基金会;
关键词
BUTYRYLCHOLINESTERASE-K-VARIANT; ISCHEMIC-STROKE; PROINFLAMMATORY CYTOKINES; INFLAMMATION; SENSITIVITY; NERVE; RISK;
D O I
10.2119/molmed.2010.00015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To date there is no diagnostic biomarker for mild stroke, although elevation of inflammatory biomarkers has been reported at early stages. Previous studies implicated acetylcholinesterase (AChE) involvement in stroke, and circulating AChE activity reflects inflammatory response, since acetylcholine suppresses inflammation. Therefore, carriers of polymorphisms that modify cholinergic activity should be particularly susceptible to inflammatory damage. Our study sought diagnostic values of AChE and Cholinergic Status (CS, the total capacity for acetylcholine hydrolysis) in suspected stroke patients. For this purpose, serum cholinesterase activities, butyrylcholinesterase-K genotype and inflammatory biomarkers were determined in 264 ischemic stroke patients and matched controls during the acute phase. AChE activities were lower (P < 0.001), and butyrylcholinesterase activities were higher in patients than in controls (P = 0.004). When normalized to sampling time from stroke occurrence, both cholinergic parameters were correlated with multiple inflammatory biomarkers, including fibrinogen, interleukin-6 and C-reactive protein (r = 0.713, r = 0.607; r = 0.421, r = 0.341: r = 0.276, r = 0.255: respectively: all P values < 0.001). Furthermore, very low AChE activities predicted subsequent nonsurvival (P = 0.036). Also, carriers of the unstable butyrylcholinesterase-K variant were more abundant among patients than controls, and showed reduced activity (P < 0.001). Importantly, a cholinergic score combining the two cholinesterase activities discriminated between 94.3% matched pairs of patients and controls, compared with only 75% for inflammatory measures. Our findings present the power of circulation cholinesterase measurements as useful early diagnostic tools for the occurrence of stroke. Importantly, these were considerably more distinctive than the inflammatory biomarkers, albeit closely associated with them, which may open new venues for stroke diagnosis and treatment. (C) 2010 The Feinstein Institute for Medical Research, www.feinsteininstitute.org
引用
收藏
页码:278 / 286
页数:9
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