MTHFR (677 and 1298) and IL-6-174 G/C genes in pathogenesis of Alzheimer's and vascular dementia and their epistatic interaction

被引:60
作者
Mansoori, Nasim [1 ]
Tripathi, Manjari [2 ]
Luthra, Kalpana
Alam, Rizwan [1 ,5 ]
Lakshmy, Ramakrishnan [3 ]
Sharma, Subhadra [1 ]
Arulselvi, Subramanyam [4 ]
Parveen, Shama [5 ]
Mukhopadhyay, Asok K. [1 ]
机构
[1] All India Inst Med Sci, Dept Lab Med, New Delhi 110029, India
[2] All India Inst Med Sci, Dept Neurol, New Delhi 110029, India
[3] All India Inst Med Sci, Dept Cardiacbiochem, New Delhi 110029, India
[4] All India Inst Med Sci, JPN Apex Trauma Ctr, New Delhi 110029, India
[5] Jamia Millia Islamia, Ctr Interdisciplinary Res Basic Sci, New Delhi 110025, India
关键词
Alzheimer's disease; Vascular dementia; Homocysteine; Epistasis; MTHFR; Interleukin-6; Polymorphism; Indian population; METHYLENETETRAHYDROFOLATE REDUCTASE GENE; ENDOPLASMIC-RETICULUM STRESS; MILD COGNITIVE IMPAIRMENT; PLASMA HOMOCYSTEINE; COMMON MUTATION; INCREASED RISK; DISEASE; POLYMORPHISMS; FOLATE; C677T;
D O I
10.1016/j.neurobiolaging.2011.09.018
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Genetic risk factors play an important role in the pathogenesis of Alzheimer disease (AD) and vascular dementia (VaD). In this case-control study, we examined C677T and A1298C (rs1801133 and rs1801131) polymorphism in the methylenetetrahydrofolate reductase (MTHFR) genes and their correlation with plasma levels of homocysteine (Hcy) in AD and VaD cases and evaluated the gene-gene interaction (epistasis) with IL-6-174 G/C (rs1800795). CC genotype was associated with elevated levels of plasma homocysteine (p = 0.004) as compared with genotype AA of rs1801131. In AD, we observed a significant (p = 0.04) association with C alleles of rs1801131. Regression analysis revealed that the presence of both rs1801133 T and rs1800795 C alleles increased the odds of developing AD by 2.5 and VaD by 3.7-fold. While rs1800795 (CC or GC) genotypes alone increased the odds of developing VaD by 2.2-fold, the presence of CC genotype of rs1801131 nullified this effect. The findings support the hypothesis that multiple genes are involved to alter the odds of developing AD and VaD. (C) 2012 Elsevier Inc. All rights reserved.
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页码:1003.e1 / 1003.e8
页数:8
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