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载脂蛋白(a)缺失表型与阿尔茨海默病发病年龄延迟有关。

Apolipoprotein(a) null phenotype is related to a delayed age at onset of Alzheimer's disease.

作者信息

Emanuele Enzo, Peros Emmanouil, Tomaino Carmine, Feudatari Enrica, Bernardi Livia, Binetti Giuliano, Maletta Raffaele, D'Angelo Angela, Montagna Lorenza, Bruni Amalia C, Geroldi Diego

机构信息

Molecular Medicine Laboratory, IRCCS Policlinico San Matteo, Piazzale Golgi 2, University of Pavia, 27100 Pavia, Italy.

出版信息

Neurosci Lett. 2004 Feb 26;357(1):45-8. doi: 10.1016/j.neulet.2003.12.043.

Abstract

Apolipoprotein(a) [apo(a)] is a highly polymorphic glycoprotein which has been suggested to play a role in Alzheimer's disease (AD). Plasma lipoprotein(a) [Lp(a)] levels and the differential expression of apo(a) isoforms were analyzed in 73 sporadic AD patients compared with 73 age- and gender-matched healthy controls. The distribution of apo(a) isoforms and Lp(a) concentrations were similar in the two groups. However, we observed that AD patients with no apo(a) isoform from immunoblots (subjects with the 'null phenotype') had a mean age at onset of 76.8+/-8.8 versus 66.9+/-9.6 years of those who expressed at least one apo(a) band (P = 0.010). Multivariate analysis showed that this effect was independent of apolipoproteinE epsilon4 allele. We conclude that the expression of at least one apo(a) isoform may interact with other pathogenic mechanisms involved in controlling the age at onset of AD.

摘要

载脂蛋白(a)[apo(a)]是一种高度多态性的糖蛋白,有人认为它在阿尔茨海默病(AD)中起作用。对73例散发性AD患者和73例年龄及性别匹配的健康对照者的血浆脂蛋白(a)[Lp(a)]水平及apo(a)异构体的差异表达进行了分析。两组apo(a)异构体的分布和Lp(a)浓度相似。然而,我们观察到,免疫印迹中无apo(a)异构体的AD患者(“无效表型”受试者)的平均发病年龄为76.8±8.8岁,而至少表达一条apo(a)条带的患者为66.9±9.6岁(P = 0.010)。多变量分析表明,这种效应独立于载脂蛋白E ε4等位基因。我们得出结论,至少一种apo(a)异构体的表达可能与控制AD发病年龄的其他致病机制相互作用。

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