Pruthi Nupur, Chandramouli B A, Kuttappa Thelma B, Rao Shobini L, Subbakrishna D K, Abraham Mariamma Philips, Mahadevan Anita, Shankar S K
Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bangalore, India.
Neurol India. 2010 Mar-Apr;58(2):264-9. doi: 10.4103/0028-3886.63810.
The nature and extent of recovery after traumatic brain injury (TBI) is heterogeneous. Apolipoprotein E (APOE) plays a major role in repair of cell membrane and growth of neurites following injury to cells. Studies done on the western population have shown that the APOE e4 genotype is associated with poor survival following neurotrauma.
To explore the association of APOE polymorphism and outcome following TBI in a patient population from a tertiary care hospital exclusive for neurological diseases in south India.
Ninety eight patients who sustained mild to moderate TBI (computed tomography (CT) scan brain showing traumatic parenchymal contusions) were the subjects of the study and the study period was from November 2003 to December 2008. APOE polymorphism status was determined by PCR technique using venous blood. Patients were assessed on follow-up with a battery of four neuropsychological tests as well as Glasgow outcome scale.
Of the 98 patients, 20 (20%) patients had at least one APOE e4 allele. A follow-up of minimum six months was available for 73 patients. None of the 12 patients who had at least one APOE e4 allele had a poor outcome at six-month follow-up whereas 11(18%) patients without an APOE e4 allele had a poor outcome (Fisher's Exact test, P=0.192). On the neuropsychological tests, performance of patients with APOE e4 allele did not differ significantly from those without these alleles.
This study does not support the current contention that the presence of APOE e4 allele should have a significant negative effect on the outcome after TBI.
创伤性脑损伤(TBI)后的恢复性质和程度具有异质性。载脂蛋白E(APOE)在细胞损伤后细胞膜修复和神经突生长中起主要作用。对西方人群的研究表明,APOE e4基因型与神经创伤后生存率低有关。
在印度南部一家专门治疗神经系统疾病的三级医院的患者群体中,探讨APOE基因多态性与TBI后结局的关联。
98例轻度至中度TBI患者(脑部计算机断层扫描(CT)显示创伤性实质挫伤)为研究对象,研究时间为2003年11月至2008年12月。采用静脉血通过PCR技术确定APOE基因多态性状态。通过一系列四项神经心理学测试以及格拉斯哥结局量表对患者进行随访评估。
98例患者中,20例(20%)患者至少有一个APOE e4等位基因。73例患者获得了至少六个月的随访。12例至少有一个APOE e4等位基因的患者在六个月随访时均未出现不良结局,而11例(18%)无APOE e4等位基因的患者出现了不良结局(Fisher精确检验,P = 0.192)。在神经心理学测试中,有APOE e4等位基因的患者表现与无这些等位基因的患者无显著差异。
本研究不支持目前关于APOE e4等位基因的存在应在TBI后结局上产生显著负面影响的观点。