Juraschek Stephen P, Simpson Lara M, Davis Barry R, Shmerling Robert H, Beach Jennifer L, Ishak Anthony, Mukamal Kenneth J
Beth Israel Deaconess Medical Center, Department of Medicine, Harvard Medical School, Boston, Massachusetts.
Department of Biostatistics, Health Science Center at Houston, University of Texas, Houston, Texas.
J Hypertens. 2020 May;38(5):954-960. doi: 10.1097/HJH.0000000000002359.
Gout is a common complication of blood pressure management and a frequently cited cause of medication nonadherence. Little trial evidence exists to inform antihypertensive selection with regard to gout risk.
The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT) was a randomized clinical trial on the effects of first-step hypertension therapy with amlodipine, chlorthalidone, or lisinopril on fatal coronary heart disease or nonfatal myocardial infarction (1994-2002). Trial participants were linked to CMS and VA gout claims (ICD9 274.XX). We determined the effect of drug assignment on gout with Cox regression models. We also determined the adjusted association of self-reported atenolol use (ascertained at the 1-month visit for indications other than hypertension) with gout.
Claims were linked to 23 964 participants (mean age 69.8 ± 6.8 years, 45% women, 31% black). Atenolol use was reported by 928 participants at the 1-month visit. Over a mean follow-up of 4.9 years, we documented 597 gout claims. Amlodipine reduced the risk of gout by 37% (hazard ratio 0.63; 95% CI 0.51--0.78) compared with chlorthalidone and by 26% (hazard ratio 0.74; 95% CI 0.58--0.94) compared with lisinopril. Lisinopril nonsignificantly lowered gout risk compared with chlorthalidone (hazard ratio 0.85; 95% CI 0.70--1.03). Atenolol use was not associated with gout risk (adjusted hazard ratio 1.18; 95% CI 0.78--1.80). Gout risk reduction was primarily observed after 1 year of follow-up.
Amlodipine lowered long-term gout risk compared with lisinopril or chlorthalidone. This finding may be useful in cases where gout risk is a principal concern among patients being treated for hypertension.This trial is registered at clinicaltrials.gov, number: NCT00000542.
痛风是血压管理的常见并发症,也是药物治疗依从性差的常见原因。关于痛风风险,几乎没有试验证据可用于指导抗高血压药物的选择。
抗高血压和降脂治疗预防心脏病发作试验(ALLHAT)是一项随机临床试验,研究氨氯地平、氯噻酮或赖诺普利进行第一步高血压治疗对致命性冠心病或非致命性心肌梗死的影响(1994 - 2002年)。试验参与者与医疗保险和医疗补助服务中心(CMS)以及退伍军人事务部(VA)的痛风索赔记录(国际疾病分类第九版,ICD9 274.XX)相关联。我们使用Cox回归模型确定药物分配对痛风的影响。我们还确定了自我报告的阿替洛尔使用情况(在1个月随访时确定,用于除高血压以外的适应症)与痛风之间的校正关联。
索赔记录与23964名参与者相关联(平均年龄69.8±6.8岁,45%为女性,31%为黑人)。在1个月随访时,有928名参与者报告使用了阿替洛尔。在平均4.9年的随访期内,我们记录了597例痛风索赔。与氯噻酮相比,氨氯地平使痛风风险降低了37%(风险比0.63;95%置信区间0.51 - 0.78),与赖诺普利相比降低了26%(风险比0.74;95%置信区间0.58 - 0.94)。与氯噻酮相比,赖诺普利降低痛风风险的差异无统计学意义(风险比0.85;95%置信区间0.70 - 1.03)。使用阿替洛尔与痛风风险无关(校正风险比1.18;95%置信区间0.78 - 1.80)。痛风风险降低主要在随访1年后观察到。
与赖诺普利或氯噻酮相比,氨氯地平降低了长期痛风风险。这一发现可能有助于那些痛风风险是高血压治疗患者主要关注点的情况。本试验已在clinicaltrials.gov注册,编号:NCT00000542。