Exploring an interaction of adenosine A2A receptor variability with coffee and tea intake in Parkinson's disease

被引:16
作者
Tan, E. K.
Lu, Z. Y.
Fook-Chong, S. M. C.
Tan, E.
Shen, H.
Chua, E.
Yih, Y.
Teo, Y. Y.
Zhao, Y.
机构
[1] Singapore Gen Hosp, Dept Neurol, Singapore 169608, Singapore
[2] Singapore Gen Hosp, Dept Clin Res, Singapore 169608, Singapore
[3] Singapore Gen Hosp, Dept Hlth Screening, Singapore 169608, Singapore
[4] Singapore Gen Hosp, Dept Natl Neurosci Inst, Singapore 169608, Singapore
[5] Singapore Gen Hosp, Dept SingHlth, Singapore 169608, Singapore
[6] Singapore Gen Hosp, Dept Natl Univ Singapore, Singapore 169608, Singapore
关键词
polymorphism; caffeine; A2A adenosine receptor; Parkinson's disease;
D O I
10.1002/ajmg.b.30359
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Caffeine is an adenosine receptor A1 and A2A receptor antagonist and a putative functional genetic variant of the A2A receptor (2592C > Tins) mediates caffeine-induced anxiety. Here we investigated the potential interaction of this A2A genetic variant with the quantity of coffee and tea intake and their relationship with the risk of PD. A total of 441 subjects consisting of 222 PD and 219 race, gender and age matched controls were included. A multivariate analysis of the variables including the 2592C > Tins A2A genotypes, age of onset, gender, and the quantity of tea and coffee intake, interaction of the A2A genotypes with coffee intake, interaction of A(2)A genotypes with tea intake demonstrated the quantity of coffee intake to be significantly associated with PD (P < 0.0005, OR = 0.922, 95% CI: 0.881, 0.964). However, there was no significant interaction of the A2A genotypes with the quantity of coffee and tea intake in modulating the risk of PD. The dose dependent protective effect of coffee intake in PD was independent of the 2592C > Tins A2A genotype suggesting that the pharmacogenetic action of caffeine in PD may be mediated differently from other caffeine-induced neurologic syndromes. (c) 2006 Wiley-Liss, Inc.
引用
收藏
页码:634 / 636
页数:3
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