Di Zhang, Qi-Fang Huang, Chang-Sheng Sheng, Yan Li, Ji-Guang Wang
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Analysis of covariance and multiple regression analyses were performed to study the associations between serum uric acid changes and the achieved clinic and ambulatory blood pressure during follow-up.</p><p><strong>Results: </strong>At baseline, 67 (16.0%) of the 418 patients had hyperuricaemia. Antihypertensive treatment reduced clinic and 24-h daytime and night-time systolic/diastolic blood pressure by a mean (±standard error [SE]) change of -17.4 ± 0.6/-8.6 ± 0.4 mm Hg and -13.7 ± 0.5/-8.3 ± 0.3 mm Hg, -13.8 ± 0.6/-8.4 ± 0.4 mm Hg, and -12.7 ± 0.7/-8.0 ± 0.4 mm Hg, respectively. Antihypertensive treatment reduced serum uric acid by a mean (±SE) change of -9.3 ± 2.8 μmol/L. The serum uric acid changes differed according to the achieved clinic and ambulatory blood pressure, and were statistically significant (mean ± SE -20.6 ± 6.6 to -10.7 ± 2.9 μmol/L, <i>p</i> ≤ 0.04) at the systolic/diastolic ranges of 130-139/≥90 mm Hg in clinic pressure, and <130/75-84 mm Hg, <145/80-84 mm Hg and <120/65-69 mm Hg in 24-h, daytime and night-time ambulatory pressure.</p><p><strong>Conclusion: </strong>Our study showed that antihypertensive therapy with a dihydropyridine calcium channel blocker was associated with reduced serum uric acid, especially when 24-h ambulatory systolic blood pressure was controlled.</p>","PeriodicalId":9000,"journal":{"name":"Blood Pressure","volume":" ","pages":"395-402"},"PeriodicalIF":1.8000,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Serum uric acid change in relation to antihypertensive therapy with the dihydropyridine calcium channel blockers.\",\"authors\":\"Di Zhang, Qi-Fang Huang, Chang-Sheng Sheng, Yan Li, Ji-Guang Wang\",\"doi\":\"10.1080/08037051.2021.1996220\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>We investigated serum uric acid changes in relation to the achieved clinic and ambulatory blood pressure after 8 weeks of antihypertensive therapy with two dihydropyridine calcium channel blockers.</p><p><strong>Materials and methods: </strong>The study participants were patients with clinic and ambulatory hypertension, enrolled in a randomised controlled trial that compared amlodipine (5-10 mg, <i>n</i> = 215) and nifedipine gastrointestinal therapeutic system (GITS, 30-60 mg, <i>n</i> = 203). Hyperuricaemia was defined as a serum uric acid concentration of ≥420 µmol/L in men and ≥360 µmol/L in women. Analysis of covariance and multiple regression analyses were performed to study the associations between serum uric acid changes and the achieved clinic and ambulatory blood pressure during follow-up.</p><p><strong>Results: </strong>At baseline, 67 (16.0%) of the 418 patients had hyperuricaemia. Antihypertensive treatment reduced clinic and 24-h daytime and night-time systolic/diastolic blood pressure by a mean (±standard error [SE]) change of -17.4 ± 0.6/-8.6 ± 0.4 mm Hg and -13.7 ± 0.5/-8.3 ± 0.3 mm Hg, -13.8 ± 0.6/-8.4 ± 0.4 mm Hg, and -12.7 ± 0.7/-8.0 ± 0.4 mm Hg, respectively. Antihypertensive treatment reduced serum uric acid by a mean (±SE) change of -9.3 ± 2.8 μmol/L. 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引用次数: 5
摘要
目的:研究两种二氢吡啶钙通道阻滞剂抗高血压治疗8周后血清尿酸变化与临床和动态血压的关系。材料和方法:研究对象为临床和动态高血压患者,纳入随机对照试验,比较氨氯地平(5-10 mg, n = 215)和硝苯地平胃肠道治疗系统(GITS, 30-60 mg, n = 203)。高尿酸血症定义为男性血清尿酸浓度≥420µmol/L,女性血清尿酸浓度≥360µmol/L。采用协方差分析和多元回归分析研究随访期间血清尿酸变化与临床及动态血压的相关性。结果:在基线时,418例患者中有67例(16.0%)患有高尿酸血症。降压治疗使临床和24小时白天和夜间收缩压/舒张压的平均(±标准误差[SE])变化分别为-17.4±0.6/-8.6±0.4 mm Hg、-13.7±0.5/-8.3±0.3 mm Hg、-13.8±0.6/-8.4±0.4 mm Hg和-12.7±0.7/-8.0±0.4 mm Hg。降压治疗降低血清尿酸的平均(±SE)变化为-9.3±2.8 μmol/L。在130 ~ 139/≥90 mm Hg收缩压/舒张压范围内,血清尿酸的变化随临床和动态血压的不同而不同,且具有统计学意义(平均值±SE -20.6±6.6 ~ -10.7±2.9 μmol/L, p≤0.04)。结论:本研究表明,应用二氢吡啶钙通道阻滞剂降压可降低血清尿酸,特别是在控制24 h动态收缩压的情况下。
Serum uric acid change in relation to antihypertensive therapy with the dihydropyridine calcium channel blockers.
Purpose: We investigated serum uric acid changes in relation to the achieved clinic and ambulatory blood pressure after 8 weeks of antihypertensive therapy with two dihydropyridine calcium channel blockers.
Materials and methods: The study participants were patients with clinic and ambulatory hypertension, enrolled in a randomised controlled trial that compared amlodipine (5-10 mg, n = 215) and nifedipine gastrointestinal therapeutic system (GITS, 30-60 mg, n = 203). Hyperuricaemia was defined as a serum uric acid concentration of ≥420 µmol/L in men and ≥360 µmol/L in women. Analysis of covariance and multiple regression analyses were performed to study the associations between serum uric acid changes and the achieved clinic and ambulatory blood pressure during follow-up.
Results: At baseline, 67 (16.0%) of the 418 patients had hyperuricaemia. Antihypertensive treatment reduced clinic and 24-h daytime and night-time systolic/diastolic blood pressure by a mean (±standard error [SE]) change of -17.4 ± 0.6/-8.6 ± 0.4 mm Hg and -13.7 ± 0.5/-8.3 ± 0.3 mm Hg, -13.8 ± 0.6/-8.4 ± 0.4 mm Hg, and -12.7 ± 0.7/-8.0 ± 0.4 mm Hg, respectively. Antihypertensive treatment reduced serum uric acid by a mean (±SE) change of -9.3 ± 2.8 μmol/L. The serum uric acid changes differed according to the achieved clinic and ambulatory blood pressure, and were statistically significant (mean ± SE -20.6 ± 6.6 to -10.7 ± 2.9 μmol/L, p ≤ 0.04) at the systolic/diastolic ranges of 130-139/≥90 mm Hg in clinic pressure, and <130/75-84 mm Hg, <145/80-84 mm Hg and <120/65-69 mm Hg in 24-h, daytime and night-time ambulatory pressure.
Conclusion: Our study showed that antihypertensive therapy with a dihydropyridine calcium channel blocker was associated with reduced serum uric acid, especially when 24-h ambulatory systolic blood pressure was controlled.
Blood PressureMedicine-Cardiology and Cardiovascular Medicine
CiteScore
3.20
自引率
5.60%
发文量
41
期刊介绍:
For outstanding coverage of the latest advances in hypertension research, turn to Blood Pressure, a primary source for authoritative and timely information on all aspects of hypertension research and management.
Features include:
• Physiology and pathophysiology of blood pressure regulation
• Primary and secondary hypertension
• Cerebrovascular and cardiovascular complications of hypertension
• Detection, treatment and follow-up of hypertension
• Non pharmacological and pharmacological management
• Large outcome trials in hypertension.