Department of Anaesthesiology and Intensive Care Medicine, HELIOS Kliniken, Rudolf Virchow Str. 2, 04552 Borna, Germany.
Neurocrit Care. 2011 Dec;15(3):410-5. doi: 10.1007/s12028-011-9542-7.
Cerebral vasospasm is one of the most serious complications after subarachnoid hemorrhage (SAH). The cerebral artery diameter is regulated by complex physiological mechanisms. Among them the regulation of intracellular calcium homeostasis seems to play a crucial role. Recent data suggest that ryanodine receptors (RYRs) are involved in regulating the luminal calcium concentration in vascular smooth muscle cells. In this gene association investigation, we studied the question as to whether variants in the gene for the ryanodine receptors subtype 1 (RYR1) are associated with symptomatic cerebral vasospasm following SAH.
After informed consent genomic DNA analysis was performed from a whole blood sample in 46 patients suffering from aneurysmal SAH. 16 Patients were affected by symptomatic vasospasm. The RYR1 gene was screened for possible genetic variants by means of direct sequencing. The association of these variants was correlated to the development of symptomatic vasospasm, which was confirmed by clinical examination combined with cerebral angiography, transcranial doppler sonography, or CT scan.
Three different genetic RYR1 variants (c.5360C>T, c.6178G>T, and c.7244G>A) were identified in the study. The G/T genotype of RYR1 c.6178G>T was associated with an increased risk for development of symptomatic vasospasm (odds ratio 6.4; 95% CI 1.1-37.8; P = 0.04).
Our pilot study suggests that RYRs are involved in the complex pathophysiology of vasospasm development following SAH. The potential role of RYR1 as a biomarker for prediction of cerebral vasospasm after SAH has to be confirmed in a larger clinical trial.
脑血管痉挛是蛛网膜下腔出血(SAH)后最严重的并发症之一。脑动脉直径受复杂的生理机制调节。其中,细胞内钙稳态的调节似乎起着至关重要的作用。最近的数据表明,ryanodine 受体(RYR)参与调节血管平滑肌细胞内腔钙浓度。在这项基因关联研究中,我们研究了 RYR1 基因的变体是否与 SAH 后症状性脑血管痉挛有关。
在知情同意的情况下,从 46 名患有动脉瘤性 SAH 的患者的全血样本中进行了基因组 DNA 分析。16 名患者出现症状性血管痉挛。通过直接测序对 RYR1 基因进行了可能的遗传变异筛选。这些变体的相关性与症状性血管痉挛的发展相关,这通过临床检查结合脑血管造影、经颅多普勒超声或 CT 扫描得到证实。
在研究中发现了三种不同的 RYR1 基因遗传变异(c.5360C>T、c.6178G>T 和 c.7244G>A)。RYR1 c.6178G>T 的 G/T 基因型与症状性血管痉挛发展的风险增加相关(比值比 6.4;95%置信区间 1.1-37.8;P=0.04)。
我们的初步研究表明,RYR 参与了 SAH 后血管痉挛发展的复杂病理生理学过程。RYR1 作为 SAH 后脑血管痉挛预测的生物标志物的潜在作用需要在更大的临床试验中得到证实。