Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing 100050, China.
J Neurol Sci. 2011 Mar 15;302(1-2):63-7. doi: 10.1016/j.jns.2010.11.024. Epub 2010 Dec 24.
Tumor-related seizures are a well-known presenting symptom of primary brain tumors, particularly low-grade gliomas (LGGs). The objective of the present study was to investigate the possible correlation between tumor-related seizures and molecular genetic profile in Chinese patients with LGGs. A series of 103 LGGs, including 27 oligodendrogliomas, 41 oligoastrocytomas and 35 astrocytomas, was analyzed by denaturing high-performance liquid chromatography (DHPLC) for 1p and 19q status, with particular emphasis on correlations with tumor-related seizures. Most oligodendrogliomas and oligoastrocytomas had LOH 1p and LOH 19q, which were rarely seen in combination in astrocytomas (p<0.001). LOH 1p and LOH 19q were also closely associated (p=0.022). The majority of patients with LGGs presented with seizures at disease onset (68.9% of all patients). The most common seizure type was secondary generalized seizures (81.7% of patients with seizures). Patients without LOH 19q were more likely to present with seizures (p=0.033), particularly secondary generalized seizures (p=0.005), than those with this alteration. The current study presented an update on studies on tumor-related seizures and molecular genetic profile, and brought forward putative candidate genes for secondary generalized seizures on chromosome 19q, based on the assumption that common molecular genetic pathways may exist for glioma development and tumor-related seizures.
肿瘤相关性发作是原发性脑肿瘤,特别是低级别胶质瘤(LGG)的一种常见表现症状。本研究的目的是探讨中国 LGG 患者肿瘤相关性发作与分子遗传学特征之间可能存在的相关性。通过变性高效液相色谱(DHPLC)分析了一系列 103 例 LGG,包括 27 例少突胶质细胞瘤、41 例少突星形细胞瘤和 35 例星形细胞瘤,以研究 1p 和 19q 状态与肿瘤相关性发作的相关性。大多数少突胶质细胞瘤和少突星形细胞瘤存在 1p 和 19q 的杂合性缺失(LOH),而星形细胞瘤中很少同时存在这两种缺失(p<0.001)。1p 和 19q 的 LOH 也密切相关(p=0.022)。大多数 LGG 患者在发病时出现发作(所有患者的 68.9%)。最常见的发作类型是继发性全身性发作(有发作的患者中 81.7%)。无 19q LOH 的患者更可能出现发作(p=0.033),尤其是继发性全身性发作(p=0.005)。本研究更新了关于肿瘤相关性发作和分子遗传学特征的研究,并提出了 19q 染色体上可能与继发性全身性发作相关的候选基因,假设胶质瘤发生和肿瘤相关性发作可能存在共同的分子遗传途径。