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转钴胺素II基因776C→G多态性与阿尔茨海默型痴呆的关联:依赖于5,10-亚甲基四氢叶酸还原酶1298A→C多态性基因型。

Association of the transcobalamin II gene 776C → G polymorphism with Alzheimer's type dementia: dependence on the 5, 10-methylenetetrahydrofolate reductase 1298A → C polymorphism genotype.

作者信息

Cascalheira José F, Gonçalves Mónica, Barroso Madalena, Castro Rita, Palmeira Manuela, Serpa André, Dias-Cabral Ana C, Domingues Fernanda C, Almeida Sofia

机构信息

CICS-UBI - Health Sciences Research Centre, University of Beira Interior, Covilhã, Portugal

CICS-UBI - Health Sciences Research Centre, University of Beira Interior, Covilhã, Portugal.

出版信息

Ann Clin Biochem. 2015 Jul;52(Pt 4):448-55. doi: 10.1177/0004563214561770. Epub 2014 Nov 13.

Abstract

BACKGROUND

Decreased serum concentrations of vitamin B12 are associated with Alzheimer's type dementia. The transcobalamin II gene (TCN2) 776C → G polymorphism affects transcobalamin II function as a carrier of vitamin B12 and might modify its availability. The association of the TCN2 776C → G polymorphism with Alzheimer's type dementia is unclear and was investigated in the present study.

METHODS

Case-control study including 27 individuals diagnosed with Alzheimer's type dementia and 28 healthy controls. Serum concentrations of vitamin B12, homocysteine and other analytes were determined and the presence of TCN2 776C → G and 5, 10-methylenetetrahydrofolate reductase 1298A → C polymorphisms genotypes was ascertained by polymerase chain reaction-restriction fragment length polymorphism.

RESULTS

Serum concentrations of vitamin B12 were lower while those of homocysteine were higher in patients than in controls (P < 0.05). The frequency of individuals carrying at least one 5, 10-methylenetetrahydrofolate reductase 1298C allele was higher (59% versus 32%) while frequency of individuals harbouring at least one TCN2 776G allele was lower (58% versus 86%) in patients than in controls (P < 0.05). Univariate logistic regression showed negative association of TCN2 776CG genotype with Alzheimer's type dementia (OR = 0.17 versus CC genotype, P < 0.02). Multivariate logistic regression identified TCN2 776C → G polymorphism as independent predictor of Alzheimer's type dementia together with higher concentrations of homocysteine, cholesterol and uric acid and lower concentrations of oestradiol. Association of TCN2 776C → G polymorphism with Alzheimer's type dementia was observed for individuals carrying the 5,10-methylenetetrahydrofolate reductase 1298AA genotype but not the AC or CC genotypes, indicating interaction between the two polymorphisms.

CONCLUSIONS

The TCN2 776C → G polymorphism is negatively associated with Alzheimer's type dementia, suggesting a protective role against the disease in subjects with the 5, 10-methylenetetrahydrofolate reductase 1298AA genotype.

摘要

背景

血清维生素B12浓度降低与阿尔茨海默病型痴呆有关。转钴胺素II基因(TCN2)776C→G多态性影响转钴胺素II作为维生素B12载体的功能,并可能改变其可用性。TCN2 776C→G多态性与阿尔茨海默病型痴呆的关联尚不清楚,本研究对此进行了调查。

方法

病例对照研究,包括27例被诊断为阿尔茨海默病型痴呆的个体和28例健康对照。测定血清维生素B12、同型半胱氨酸和其他分析物的浓度,并通过聚合酶链反应-限制性片段长度多态性确定TCN2 776C→G和5,10-亚甲基四氢叶酸还原酶1298A→C多态性基因型的存在。

结果

患者血清维生素B12浓度低于对照组,而同型半胱氨酸浓度高于对照组(P<0.05)。携带至少一个5,10-亚甲基四氢叶酸还原酶1298C等位基因的个体频率在患者中高于对照组(59%对32%),而携带至少一个TCN2 776G等位基因的个体频率在患者中低于对照组(58%对86%)(P<0.05)。单因素逻辑回归显示TCN2 776CG基因型与阿尔茨海默病型痴呆呈负相关(与CC基因型相比,OR=0.17,P<0.02)。多因素逻辑回归确定TCN2 776C→G多态性与同型半胱氨酸、胆固醇和尿酸浓度升高以及雌二醇浓度降低一起,是阿尔茨海默病型痴呆的独立预测因素。在携带5,10-亚甲基四氢叶酸还原酶1298AA基因型而非AC或CC基因型的个体中观察到TCN2 776C→G多态性与阿尔茨海默病型痴呆的关联,表明这两种多态性之间存在相互作用。

结论

TCN2 776C→G多态性与阿尔茨海默病型痴呆呈负相关,提示在携带5,10-亚甲基四氢叶酸还原酶1298AA基因型的个体中对该病具有保护作用。

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