Department of Neurology, University Medical Center Hamburg-Eppendorf, Martinistraße 52, 20246, Hamburg, Germany.
Department of Medical Biometry and Epidemiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Neurol Sci. 2020 Jan;41(1):149-153. doi: 10.1007/s10072-019-04058-0. Epub 2019 Sep 3.
Guanidino compounds, including asymmetric dimethylarginine (ADMA), symmetric dimethylarginine (SDMA), and L-homoarginine (hArg), have been associated with cardio- and cerebrovascular events and risk. We aimed to study if low hArg/ADMA and hArg/SDMA ratios are associated with mortality and outcome after stroke.
In two prospective cohorts of acute stroke patients from Germany and the UK, we analyzed hArg, ADMA, and SDMA to determine hArg/ADMA and hArg/SDMA ratios. The guanidino compound levels were associated with mortality, adverse events, and neurological impairment, i.e., National Institutes of Health Stroke Scale (NIHSS) and modified Rankin Scale (mRS).
During 7.4 years, high hArg/ADMA and hArg/SDMA ratios were both associated with a reduction in all-cause mortality in patients with ischemic stroke in a UK stroke cohort (hArg/ADMA: hazard ratio (HR) 0.75 [95% confidence interval (CI) 0.62-0.92]; n = 394; P = 0.006; hArg/SDMA: HR 0.68 [0.54-0.85]; n = 394; P = 0.001). In a German stroke cohort, patients with high hArg/SDMA ratio experienced fewer adverse events compared with those with low hArg/SDMA ratios within 30 days after stroke (HR 0.73 [0.57-0.92]; n = 135; P = 0.009), whereas hArg/ADMA was not predictive. Furthermore, hArg/SDMA ratios inversely correlated with the degree of neurological impairment (NIHSS) (r = - 0.27; P = 0.001; n = 138). Lower hArg/SDMA ratios were also found in dependent (mRS 3-6) compared with independent patients (mRS < 3; P = 0.007; n = 138), whereas hArg/ADMA did not.
These results from two prospective stroke studies reveal that hArg/SDMA ratio could prove a valuable blood-based biomarker to discriminate patients with poor short- and long-term outcome, increased neurological impairment, and severe disability after stroke.
胍基化合物,包括不对称二甲基精氨酸(ADMA)、对称二甲基精氨酸(SDMA)和 L-同型精氨酸(hArg),与心脑血管事件和风险有关。我们旨在研究低 hArg/ADMA 和 hArg/SDMA 比值是否与卒中后死亡率和结局有关。
在来自德国和英国的急性卒中患者的两个前瞻性队列中,我们分析了 hArg、ADMA 和 SDMA,以确定 hArg/ADMA 和 hArg/SDMA 比值。胍基化合物水平与死亡率、不良事件和神经功能缺损(即国立卫生研究院卒中量表(NIHSS)和改良 Rankin 量表(mRS))相关。
在 7.4 年的时间里,高 hArg/ADMA 和 hArg/SDMA 比值均与英国卒中队列中缺血性卒中患者的全因死亡率降低相关(hArg/ADMA:风险比(HR)0.75 [95%置信区间(CI)0.62-0.92];n=394;P=0.006;hArg/SDMA:HR 0.68 [0.54-0.85];n=394;P=0.001)。在德国卒中队列中,与低 hArg/SDMA 比值的患者相比,高 hArg/SDMA 比值的患者在卒中后 30 天内发生不良事件的风险更低(HR 0.73 [0.57-0.92];n=135;P=0.009),而 hArg/ADMA 则无预测价值。此外,hArg/SDMA 比值与神经功能缺损程度(NIHSS)呈负相关(r=-0.27;P=0.001;n=138)。与独立患者(mRS<3)相比,依赖患者(mRS 3-6)的 hArg/SDMA 比值更低(P=0.007;n=138),而 hArg/ADMA 则不然。
这两项前瞻性卒中研究的结果表明,hArg/SDMA 比值可能是一种有价值的基于血液的生物标志物,可用于区分短期和长期预后不良、神经功能缺损加重以及卒中后严重残疾的患者。