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谷胱甘肽S-转移酶P1和T1基因多态性可预测阿尔茨海默病的病程进展及发病年龄。

Glutathione S-transferase P1 and T1 gene polymorphisms predict longitudinal course and age at onset of Alzheimer disease.

作者信息

Spalletta Gianfranco, Bernardini Sergio, Bellincampi Lorenza, Federici Giorgio, Trequattrini Alberto, Ciappi Fabrizio, Bria Pietro, Caltagirone Carlo, Bossù Paola

机构信息

Istituto di Ricovero e Cura a Carattere Scientifico Santa Lucia Foundation, Rome, Italy.

出版信息

Am J Geriatr Psychiatry. 2007 Oct;15(10):879-87. doi: 10.1097/JGP.0b013e3180547076.

Abstract

OBJECTIVE

Oxidative stress has been suggested as a contributor of Alzheimer disease (AD) neurodegeneration, particularly in those patients with late-onset AD (LOAD). Therefore, the authors studied the effect of glutathione S-transferase (GST) P1-M1-T1 gene polymorphisms and their interactions with the apolipoprotein E (ApoE) epsilon4 allelic variant on the three-year longitudinal course of AD.

METHODS

Global cognitive level as measured by the Mini-Mental State Exam, basic activities of daily living (BADLs) as measured by the Physical Self-Maintenance Scale, and behavior as measured by the Neuropsychiatric Inventory, were assessed at baseline and after 1, 2, and 3 years in a sample of 99 LOAD patients. These subjects were drug naive and had undergone the first clinical examination for the diagnosis of AD.

RESULTS

A multiple regression analysis indicated that the presence of ApoE epsilon4 allelic variant or GSTT1 null phenotype predicted the faster age at onset of the illness (F = 5.76, df = 2, 96, p = 0.0043). Carriers of GSTP1 *C allelic variant had a faster decline in cognitive functions (repeated measures analysis of variance [ANOVA]: F = 4.00, df = 3, 285, p = 0.008) and in BADLs (repeated measures ANOVA: F = 5.27, df = 3, 285, p = 0.001). This faster decline was independent from ApoE epsilon4 allele possession. No effect of GST P1-M1-T1 polymorphisms was found on behavioral symptom severity.

CONCLUSION

These data are in line with the hypotheses that oxidative damage is a prominent feature in the clinical progression and the age at onset of LOAD.

摘要

目的

氧化应激被认为是阿尔茨海默病(AD)神经退行性变的一个促成因素,尤其是在晚发性AD(LOAD)患者中。因此,作者研究了谷胱甘肽S-转移酶(GST)P1-M1-T1基因多态性及其与载脂蛋白E(ApoE)ε4等位基因变异对AD三年纵向病程的影响。

方法

在99例LOAD患者样本中,于基线时以及1年、2年和3年后,通过简易精神状态检查评估整体认知水平,通过身体自我维持量表评估日常生活基本活动能力(BADLs),通过神经精神科问卷评估行为。这些受试者未服用过药物,且已接受首次临床检查以诊断AD。

结果

多元回归分析表明,ApoE ε4等位基因变异或GSTT1无效表型的存在预示着发病年龄更快(F = 5.76,自由度 = 2, 96,p = 0.0043)。GSTP1 *C等位基因变异携带者的认知功能下降更快(重复测量方差分析[ANOVA]:F = 4.00,自由度 = 3, 285,p = 0.008),BADLs下降也更快(重复测量ANOVA:F = 5.27,自由度 = 3, 285,p = 0.001)。这种更快的下降与是否拥有ApoE ε4等位基因无关。未发现GST P1-M1-T1多态性对行为症状严重程度有影响。

结论

这些数据符合氧化损伤是LOAD临床进展和发病年龄的一个突出特征这一假设。

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