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载脂蛋白Eε4等位基因与腔隙性脑梗死患者的白质病变体积相关。

Apolipoprotein E epsilon4 allele is associated with the volume of white matter changes in patients with lacunar infarcts.

作者信息

Wen H M, Baum L, Cheung W S, Mok V, Lam W W M, Tomlinson B, Wong K S, Ng H K

机构信息

Department of Rehabilitation, the third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.

出版信息

Eur J Neurol. 2006 Nov;13(11):1216-20. doi: 10.1111/j.1468-1331.2006.01436.x.

Abstract

The relationship between the apolipoprotein E (APOE) exon 4 polymorphism and white matter changes (WMC) in elderly subjects or patients with Alzheimer's disease is controversial. To investigate this polymorphism in relation to WMC in patients with lacunar infarcts, we prospectively observed 67 patients with acute lacunar infarct and 134 age- and sex-matched controls. Genotypes were determined using a nested polymerase chain reaction. WMC were measured quantitatively and were divided into two groups, severe and mild, with the mean volume of WMC as the cut point. Twenty-two patients (33%) had severe WMC. There was a significant difference in the distribution of APOE epsilon2, epsilon3, and epsilon4 alleles between severe and mild WMC groups (P = 0.002). The frequency of epsilon4 alleles was higher in patients with severe WMC than in those with mild WMC (25% vs. 7%, P = 0.003). These results suggest that APOE epsilon4 may exacerbate WMC in patients with lacunar infarcts. Further studies are required to confirm this finding.

摘要

载脂蛋白E(APOE)外显子4多态性与老年受试者或阿尔茨海默病患者的白质改变(WMC)之间的关系存在争议。为了研究腔隙性脑梗死患者中这种多态性与WMC的关系,我们前瞻性地观察了67例急性腔隙性脑梗死患者和134例年龄及性别匹配的对照者。使用巢式聚合酶链反应确定基因型。对WMC进行定量测量,并根据WMC的平均体积作为切点将其分为重度和轻度两组。22例患者(33%)有重度WMC。重度和轻度WMC组之间APOE ε2、ε3和ε4等位基因的分布存在显著差异(P = 0.002)。重度WMC患者中ε4等位基因的频率高于轻度WMC患者(25%对7%,P = 0.00)。这些结果表明,APOE ε4可能会加重腔隙性脑梗死患者的WMC。需要进一步研究来证实这一发现。

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