Association between genetic and environmental factors and the risk of Alzheimer's disease

被引:0
|
作者
Styczynska, Maria [1 ]
Strosznajder, Joanna B. [2 ]
Religa, Dorota [1 ,5 ]
Chodakowska-Zebrowska, Malgorzata [3 ]
Pfeffer, Anna [1 ]
Gabryelewicz, Tomasz [1 ]
Czapski, Grzegorz A. [2 ]
Kobrys, Malgorzata [1 ]
Karciauskas, Gytis [4 ]
Barcikowska, Maria [1 ]
机构
[1] Polish Acad Sci, Mossakowski Med Res Ctr, Dept Neurodegenerat Disorders, PL-02106 Warsaw, Poland
[2] Polish Acad Sci, Mossakowski Med Res Ctr, Dept Cellular Signalling, PL-02106 Warsaw, Poland
[3] MSWiA Hosp, Dept Neurol, Warsaw, Poland
[4] Polish Acad Sci, Inst Fundamental Technol Res, PL-02106 Warsaw, Poland
[5] Karolinska Univ Hosp, Dept Geriatr, Stockholm, Sweden
关键词
Alzheimer's disease; APOE; NOS3; MTHFR; homocysteine;
D O I
暂无
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The only well confirmed genetic risk factor for sporadic Alzheimer's disease (AD) is the possession of apolipoprotein E (APOE) epsilon 4 allele. As it contributes to 40-70% of AD cases, a large proportion of genetic variance may be determined by additional loci. Our aim was to estimate how reported genetic factors (APOE, NOS3, MTHFR) interact to increase the risk for AD and combine them with environmental factors (homocysteine, vitamin B-12, cholesterol). Genotyping was performed in 154 AD patients and 176 healthy controls, Levels of homocysteine, vitamin B-12 and cholesterol were assessed in subgroups of 100 AD patients and 100 controls. We found a difference in APOE epsilon 4 and NOS3 GIG distribution between groups (p<0.005). Plasma total homocysteine was increased and vitamin B-12 decreased in AD patients (p<0.001). The influence of APOE epsilon 4 and NOS3 G alleles on the risk of AD was independent of homocysteine, vitamin B-12 levels and MTHFR status.
引用
收藏
页码:249 / 254
页数:6
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