Institute of Cardiology, Center of Excellence on Aging, "G. d’Annunzio" University, Chieti, Italy.
Am J Clin Nutr. 2012 Jan;95(1):241-8. doi: 10.3945/ajcn.111.018267. Epub 2011 Dec 14.
The widely observed between-subject variability in cardiovascular responses to coffee may have a genetic basis.
We evaluated acute blood pressure (BP) responses to caffeine and explored whether they are influenced by candidate gene variants affecting caffeine metabolism (for cytochrome P450 1A2), adenosine metabolism (for adenosine receptor and AMP deaminase), or catecholamine receptors.
We recruited 110 healthy male habitual moderate coffee drinkers who refrained from drinking coffee on the day preceding the study. Each subject underwent ambulatory BP monitoring at 6-min intervals for 2 h. Each participant was administered, in a double-blind design, 40 mL of either a decaffeinated coffee preparation plus 3 mg caffeine/kg (caf) or the corresponding vehicle (decaf). The protocol was repeated 24 h later with the alternative preparation. Blood samples were collected for genetic and plasma caffeine and catecholamine evaluations.
Compared with decaf, caf was associated with a mean (± SD) significant increase in systolic BP of 4 ± 12 mm Hg and in diastolic BP of 3 ± 10 mm Hg (P < 0.001 for both). Plasma caffeine and adrenaline increased after caf, but not after decaf. Of 11 gene polymorphisms analyzed, a relation was observed between the ADORA2A TT variant and the change in SBP peak and between the ADRA2B I variant and the changes in both SBP mean and peak; mean peak change in SBP; these variants were associated with increased SBP responses to caf.
Variability in the acute BP response to coffee may be partly explained by genetic polymorphisms of the adenosine A2A receptors and α(2)-adrenergic receptors. This trial is registered at clinicaltrials.gov as NCT01330680.
喝咖啡后心血管反应的个体间差异很大,这种差异可能有遗传基础。
我们评估了咖啡因对急性血压(BP)的影响,并探讨了候选基因变异是否影响咖啡因代谢(细胞色素 P4501A2)、腺苷代谢(腺苷受体和 AMP 脱氨酶)或儿茶酚胺受体对急性血压的影响。
我们招募了 110 名健康的男性习惯性适量饮用咖啡者,他们在研究前一天避免饮用咖啡。每位受试者在 2 小时内每 6 分钟进行一次动态血压监测。每位参与者以双盲设计分别服用 40 毫升去咖啡因咖啡制剂加 3 毫克咖啡因/公斤(caf)或相应的载体(去咖啡因)。24 小时后,用替代制剂重复该方案。采集血样进行基因和血浆咖啡因及儿茶酚胺评估。
与去咖啡因相比, caf 与收缩压平均(± SD)升高 4 ± 12 mmHg 和舒张压升高 3 ± 10 mmHg 相关(均 P < 0.001)。服用 caf 后血浆咖啡因和肾上腺素增加,但服用去咖啡因后没有增加。在分析的 11 种基因多态性中,ADORA2A TT 变异与收缩压峰值的变化以及 ADRA2B I 变异与收缩压均值和峰值的变化之间存在相关性;收缩压峰值的平均变化;这些变异与 caf 引起的收缩压反应增加有关。
咖啡引起的急性血压反应的个体差异可能部分由腺苷 A2A 受体和 α2-肾上腺素能受体的遗传多态性解释。本试验在 clinicaltrials.gov 上注册为 NCT01330680。