Department of Epidemiology, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana 70112, USA.
J Hypertens. 2011 Sep;29(9):1719-30. doi: 10.1097/HJH.0b013e32834a4d1f.
Observational epidemiologic studies and clinical trials have documented that dietary potassium intake lowers blood pressure (BP). We examined the association between genetic variants in the renin-angiotensin-aldosterone system and BP responses to potassium intervention.
A 7-day high-sodium followed by a 7-day high-sodium plus 60 mmol/day potassium-supplementation feeding study was conducted among 1906 participants from rural northern China. Nine BP measurements were obtained at each intervention phase using a random-zero sphygmomanometer and 181 single-nucleotide polymorphisms (SNPs) in 11 candidate genes of the renin-angiotensin-aldosterone system were used for analyses.
Several SNPs in nuclear receptor subfamily 3, group C, member 2 (NR3C2), angiotensin II type 1 receptor (AGTR1), hydroxysteroid (11-beta) dehydrogenase 1 (HSD11B1), and hydroxysteroid (11-beta) dehydrogenase 2 (HSD11B2) genes were significantly associated with BP responses to potassium intervention. For example, the number of G alleles of the N554S missense mutation (rs5527) of NR3C2 was significantly associated with greater SBP responses to potassium intervention; mean [95% confidence interval (CI)] responses (mmHg) were -3.33 (-3.65 to -3.02) for genotype A/A and -5.47 (-6.64 to -4.29) for A/G, respectively (P value = 0.0004). In addition, the number of C alleles of the A1166C variant (rs5186) in AGTR1 was significantly and inversely associated with SBP responses to potassium intervention; mean (95% CI) responses were -3.55 (-3.87 to -3.24) for genotype A/A, -2.45 (-3.27 to -1.62) for A/C, and 3.25 (-5.73 to 12.23) for CC (P value = 0.003).
These novel findings indicated that genetic variants in the renin-angiotensin-aldosterone system may play an important role in determining an individual's BP responses to dietary potassium intake.
观察性流行病学研究和临床试验已经证实,膳食钾的摄入可降低血压(BP)。我们研究了肾素-血管紧张素-醛固酮系统中的遗传变异与钾干预后 BP 反应之间的关系。
在中国北方农村地区的 1906 名参与者中进行了为期 7 天的高钠饮食加 7 天高钠饮食加 60mmol/天补钾喂养研究。在每个干预阶段使用随机零式血压计进行 9 次 BP 测量,并使用肾素-血管紧张素-醛固酮系统中 11 个候选基因的 181 个单核苷酸多态性(SNP)进行分析。
核受体亚家族 3、C 组、成员 2(NR3C2)、血管紧张素 II 型 1 受体(AGTR1)、羟甾类 11-β 脱氢酶 1(HSD11B1)和羟甾类 11-β 脱氢酶 2(HSD11B2)基因中的几个 SNP 与钾干预后 BP 反应显著相关。例如,NR3C2 的 N554S 错义突变(rs5527)的 G 等位基因数量与钾干预后 SBP 反应的增加显著相关;基因型 A/A 的平均(95%置信区间[CI])反应(mmHg)为-3.33(-3.65 至-3.02),A/G 分别为-5.47(-6.64 至-4.29)(P 值=0.0004)。此外,AGTR1 中的 A1166C 变体(rs5186)的 C 等位基因数量与钾干预后的 SBP 反应呈显著负相关;基因型 A/A 的平均(95%CI)反应为-3.55(-3.87 至-3.24),A/C 为-2.45(-3.27 至-1.62),CC 为 3.25(-5.73 至 12.23)(P 值=0.003)。
这些新发现表明,肾素-血管紧张素-醛固酮系统中的遗传变异可能在决定个体对膳食钾摄入的 BP 反应方面发挥重要作用。