Sarfo Fred S, Owusu Dorcas, Adamu Sheila, Awuah Dominic, Appiah Lambert, Amamoo Mansa, Loglo Aloysius, Owolabi Mayowa, Ovbiagele Bruce
Kwame Nkrumah University of Science & Technology, Kumasi, Ghana; Komfo Anokye Teaching Hospital, Kumasi, Ghana.
Komfo Anokye Teaching Hospital, Kumasi, Ghana.
J Stroke Cerebrovasc Dis. 2018 Mar;27(3):633-644. doi: 10.1016/j.jstrokecerebrovasdis.2017.09.035. Epub 2017 Oct 23.
Measurement of plasma molecular markers among stroke patients has been proposed as an avenue for improving the accuracy of stroke diagnosis. There is paucity of data on the potential role of these markers in resource-limited settings, where the burden of stroke is greatest.
To assess the potential diagnostic and prognostic performance of 3 proposed biomarkers for stroke in a resource-constrained setting.
Consecutive stroke subjects presenting at a tertiary medical center in Kumasi, Ghana, with radiologically confirmed diagnosis and etiologic subtype information available were recruited along with age- and gender-matched controls in a 2:1 ratio. Plasma concentrations of glial fibrillary acidic protein (GFAP), copeptin, and matrix metalloproteinase-9 (MMP-9) among stroke patients and stroke-free controls were measured in duplicates using enzyme linked immunoassays. Diagnostic and prognostic correlates were assessed using area-under-the-curve (AUC) measures of receiver operator curves and logistic regression analysis, respectively.
There were 156 stroke subjects with a mean age of 61.3 years of which 47.4% were females and 74 age- and gender-matched stroke-free controls. Median (interquartile range) time from symptom onset to hospital presentation for care was 7 days (5-11). Diagnostic accuracy of a single measurement of the 3 biomarkers for stroke using AUC (95% confidence interval) plots were as follows: .84 (.77-0.91), P < .0001, for GFAP; .85 (.79-0.92), P < .0001, for copeptin; and .65 (.56-0.73), P = .0003, for MMP-9. None of the biomarkers was associated with stroke severity or mortality.
Plasma concentrations of GFAP and copeptin demonstrated stronger associations with stroke occurrence in this West African cohort compared with controls.
测量中风患者的血浆分子标志物被认为是提高中风诊断准确性的一种途径。在中风负担最重的资源有限环境中,关于这些标志物潜在作用的数据很少。
在资源受限的环境中评估3种提议的中风生物标志物的潜在诊断和预后性能。
在加纳库马西的一家三级医疗中心,招募连续就诊的中风患者,这些患者经放射学确诊且有病因亚型信息,同时按2:1的比例招募年龄和性别匹配的对照。使用酶联免疫吸附测定法对中风患者和无中风对照者的血浆胶质纤维酸性蛋白(GFAP)、 copeptin和基质金属蛋白酶-9(MMP-9)浓度进行双份测量。分别使用受试者操作曲线的曲线下面积(AUC)测量和逻辑回归分析来评估诊断和预后相关性。
有156名中风患者,平均年龄61.3岁,其中47.4%为女性,以及74名年龄和性别匹配的无中风对照者。从症状发作到就医的中位(四分位间距)时间为7天(5 - 11天)。使用AUC(95%置信区间)图对3种中风生物标志物单次测量的诊断准确性如下:GFAP为0.84(0.77 - 0.91),P < 0.0001;copeptin为0.85(0.79 - 0.92),P < 0.0001;MMP-9为0.65(0.56 - 0.73),P = 0.0003。没有一种生物标志物与中风严重程度或死亡率相关。
与对照组相比,在这个西非队列中,GFAP和copeptin的血浆浓度与中风发生的关联更强。