Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The presence of MPO-G/G and A2M-Val/Val genotypes synergistically increased the risk of AD (OR, 25.5; 95% CI, 4.65-139.75).
|
15023809 |
2004 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The deletion polymorphism and Val1000Ile in alpha-2-macroglobulin and Alzheimer disease in Caribbean Hispanics.
|
10688047 |
2000 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Our findings do not support the fact that the previously reported positive association between A2M deletion polymorphism and AD modifies the disease risk in the studied population.Am.J. Med.Genet.(Neuropsychiatr.Genet.)96:775-777, 2000.
|
11121179 |
2000 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
These results indicated that A2M-D allele was probably a weak AD protective factor, and there was a possible interaction of APOE-epsilon 4 and A2M-G alleles to increase AD risk in Mainland Han Chinese.
|
14675603 |
2004 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The results from this study indicate that polymorphisms in LRP and A2M are not associated with increased risk for AD in Northern Ireland.
|
11496365 |
2001 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Our results failed to demonstrate an association between this polymorphism and Japanese sporadic AD, and the A2M I1000V mutation does not seem to be a risk factor per se for sporadic AD.
|
10936700 |
2000 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
On the lack of a clear-cut association between alpha-2-macroglobulin deletion and the risk of Alzheimer disease in Poland.
|
25574746 |
2014 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
In conclusion, our data suggests that the A2M D allele is a modest risk factor for late-onset sporadic AD in Koreans, and the AD risk conferred by the A2M D allele increases in APOE epsilon4 negative subjects.
|
11231028 |
2001 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The coexistence of at least one allele Val (A2M-Val+) and one allele C (LRP1-C+) increased up two times the risk of AD (OR 2.32; 95% CI 1.23-4.35; p<0.009).
|
20637261 |
2010 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Earlier identified regions on chromosomes 10 and 12, nor the effect of the alpha-2-macroglobulin (A2M) I/D polymorphism on Alzheimer's disease could be confirmed in our study.
|
15130954 |
2004 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Analysis of alpha-2-macroglobulin-2 allele as a risk factor in Alzheimer's disease.
|
11455130 |
2001 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
LHGDN |
Interaction of CTSD and A2M polymorphisms in the risk for Alzheimer's disease.
|
16784755 |
2006 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Therefore, we conclude that in our samples, the A2M I/V genotype might be a susceptibility variant, even with minor effect, for both sporadic AD and PD.
|
12133586 |
2002 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
LHGDN |
These results indicated that A2M-D allele was probably a weak AD protective factor, and there was a possible interaction of APOE-epsilon 4 and A2M-G alleles to increase AD risk in Mainland Han Chinese.
|
14675603 |
2004 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Substantial linkage disequilibrium was detected across the gene as a whole, and haplotype analysis also showed significant association between AD and groups of A2M polymorphisms.
|
12966032 |
2003 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
There was no significant difference in the severity of CAA between individuals with the A2M deletion allele and those without in the AD, non-AD, or total cases.
|
10548657 |
1999 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Thus, our studies do not support the A2M polymorphisms as a risk factor for Alzheimer disease.
|
12116268 |
2002 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The meta-analysis suggests that there is no enough evidence for associations of A2M gene polymorphisms (5 bp I/D, Ile1000Val) with AD risk at present, even after stratification by ethnicity and APOE ε4 with genotypes of polymorphism sites.
|
24756728 |
2014 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Through combination-analysis of the data about the A2M-I/D and the A2M-Ile1000Val variants, the A2M gene was suggested to be associated with Alzheimer's disease.
|
15931081 |
2005 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Drug response from pharmacogenetic viewpoint after 3-year follow-up of AD patients and Clinical Dementia Rating (CDR) analysis demonstrated that AD patients carrying bigenic genotype IL-6 CC-A2M AG (ΔCDR = 4.5) and male patients with IL-6 CC genotype (ΔCDR = 3.83) provided the best response and the A2M GG genotype (ΔCDR = 7.97) and bigenic genotype IL-6 GG-A2M GG (ΔCDR = 8.5) conferred the worst response to the rivastigmine, suggesting likely involvement of genotype-specific response to rivastigmine therapy in AD patients.
|
26289409 |
2016 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Recent reports have suggested that genetic polymorphisms in the alpha-2 macroglobulin (A2M) gene are associated with an increased risk for Alzheimer's disease.
|
11058789 |
2000 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Angiotensin-converting enzyme and alpha-2-macroglobulin gene polymorphisms are not associated with Alzheimer's disease in Colombian patients.
|
14759632 |
2004 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
To evaluate the genetic factors for AD among a Chinese population in Taiwan, we studied the polymorphisms of six candidate genes of Alzheimer's disease (AD), including the regulatory region of apolipoprotein E (Apo-E, G-186T), the promoter of apolipoprotein E (Apo-E, A-491T), the bleomycin hydrolase gene (BH, A1450G), a mutation of alpha(2)-macroglobulin gene (A2M G2998A), low-density lipoprotein receptor-related protein gene (LRP, C766T), and alpha(1)-antichymotrypsin gene (ACT, -15Ala/Thr) in AD patients and non-affected elder individuals among Taiwanese Chinese.
|
11099722 |
2000 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease.
|
10203250 |
1999 |
Alzheimer's Disease
|
0.500 |
GeneticVariation
|
disease |
LHGDN |
Genetic association of alpha2-macroglobulin polymorphisms with AD in southern Italy.
|
12221172 |
2002 |