Universitätsklinikum des Saarlandes, Saarland University, Department of Internal Medicine III, Homburg.
Statistical Consultant, Ingelheim, Germany.
J Hypertens. 2021 Apr 1;39(4):766-774. doi: 10.1097/HJH.0000000000002697.
Diabetes and hypertension are risk factors for renal and cardiovascular outcomes. Data on the association of achieved blood pressure (BP) with renal outcomes in patients with and without diabetes are sparse. We investigated the association of achieved SBP, DBP with renal outcomes and urinary albumin excretion (UAE) in people with vascular disease.
In this pooled analysis, we assessed renal outcome data from high-risk patients aged 55 years or older with a history of cardiovascular disease, 70% of whom had hypertension, randomized to The Ongoing Telmisartan Alone and in Combination with Ramipril Global Endpoint Trial and to Telmisartan Randomized Assessment Study in ACE Intolerant Subjects with Cardiovascular Disease trials investigating telmisartan, ramipril and their combination with a median follow-up of 56 months. Standardized office BP was measured every 6 months, estimated glomerular filtration rate (eGFR) and UAE at baseline, 2 years and study end. Associations of mean achieved BP on treatment were investigated on major renal outcomes including end-stage renal disease (ESRD), decline of eGFR by at least 40%, doubling of creatinine and the composites thereof and on UAE. Analyses were by Cox regression analysis, analysis of variance and Chi2-test. Of 30 937 patients with complete data, 19 450 patients without and 11 487 with diabetes were enrolled between 1 December 2001 and 31 July 2003 and followed until 31 July 2008. Data were pooled as the outcomes for telmisartan 80 mg/day (n = 2903) or placebo (n = 2907) for Telmisartan Randomized Assessment Study in ACE Intolerant Subjects with Cardiovascular Disease and ramipril 10 mg/day (n = 8407), telmisartan 80 mg/day (n = 8386) or the combination of both (n = 8334) were similar.
For both those with and without diabetes, the hazard ratios for the composites ESRD or doubling of serum creatinine (707 events overall) and ESRD or 40% eGFR loss (2371 events overall) reached a nadir at achieved SBP of 120 to less than 140 mmHg, and increased with higher and lower SBP with similar relative risk with or without diabetes. For example, risk for the former composite reached a hazard ratios 3.06 (confidence interval 1.90-4.92) with a mean achieved SBP more than 160 mmHg compared with 120 to less than 130 mmHg with diabetes and hazard ratios 2.14 (1.09-4.26) without diabetes. In contrast, the development of new microalbuminuria and macroalbuminuria (3002 and 846 events overall) associated linearly over the whole range of achieved SBP (apart from a slight increase in risk at SBP less than 120 mmHg only in those without diabetes). Absolute risks for the composite and albuminuria outcomes were consistently greater in those with diabetes as compared with without diabetes with high event rates over the whole SBP spectrum. The increased renal risk at low SBP was not related to a meaningful reduction of mandated study drugs or open label renin-angiotensin-aldosterone system inhibition.
In patients at high cardiovascular risk, SBP levels more than 140 mmHg and less than 120 are associated with increased risk for renal outcomes. Renal risk was greater in diabetes across the whole range of achieved SBP and DBP. These data suggest similar target BP range in patients with and without diabetes to prevent renal outcomes, a frequent complication in high-risk vascular patients.
Clinical Trial registration: http://clinicaltrials.gov.Unique identifier: NCT00153101.
糖尿病和高血压是肾脏和心血管结局的危险因素。关于已达到的血压(BP)与患有和不患有糖尿病的患者的肾脏结局之间的关联的数据很少。我们研究了在患有血管疾病的人群中,收缩压(SBP)和舒张压(DBP)与肾脏结局和尿白蛋白排泄(UAE)的关系。
在这项汇总分析中,我们评估了高危、年龄在 55 岁或以上、有心血管疾病史的患者的肾脏结局数据,其中 70%患有高血压,随机分为替米沙坦单独治疗和替米沙坦与雷米普利联合治疗的全球终点试验,以及替米沙坦在不耐受血管紧张素转换酶的心血管疾病患者中的评估研究。这些试验研究了替米沙坦、雷米普利及其组合,中位随访时间为 56 个月。每 6 个月测量一次标准诊室血压,在基线、2 年和研究结束时测量估算肾小球滤过率(eGFR)和 UAE。研究了治疗期间平均达到的 BP 与主要肾脏结局(包括终末期肾病(ESRD)、eGFR 至少下降 40%、肌酐加倍和这些复合结局)以及 UAE 的关系。分析采用 Cox 回归分析、方差分析和 Chi2 检验。在 30937 名有完整数据的患者中,19450 名无糖尿病和 11487 名有糖尿病的患者分别于 2001 年 12 月 1 日至 2003 年 7 月 31 日登记,并随访至 2008 年 7 月 31 日。作为替米沙坦 80mg/天(n=2903)或安慰剂(n=2907)的替米沙坦在不耐受血管紧张素转换酶的心血管疾病患者中的评估研究的结局,以及雷米普利 10mg/天(n=8407)、替米沙坦 80mg/天(n=8386)或两者的组合(n=8334)的数据进行了汇总,结果相似。
对于有和没有糖尿病的患者,复合终点 ESRD 或肌酐加倍(总共有 707 例事件)和 ESRD 或 eGFR 下降 40%(总共有 2371 例事件)的危险比在达到的 SBP 为 120 至小于 140mmHg 时达到最低点,并且随着 SBP 的升高和降低而增加,无论是否有糖尿病,相对风险相似。例如,与 SBP 为 120 至小于 130mmHg 相比,前者的复合终点的风险比达到 3.06(置信区间 1.90-4.92),而 SBP 大于 160mmHg 时的风险比为 2.14(1.09-4.26),无论是否有糖尿病。相比之下,新的微量白蛋白尿和大量白蛋白尿(总共有 3002 和 846 例事件)在整个达到的 SBP 范围内呈线性相关(仅在没有糖尿病的患者中,SBP 小于 120mmHg 时风险略有增加)。与没有糖尿病的患者相比,糖尿病患者的整个 SBP 谱中,肾脏复合终点和白蛋白尿的绝对风险始终更高,且整个 SBP 谱中事件发生率很高。低 SBP 时的肾脏风险增加与规定研究药物或开放标签肾素-血管紧张素-醛固酮系统抑制的明显减少无关。
在心血管风险较高的患者中,SBP 水平大于 140mmHg 和小于 120mmHg 与肾脏结局风险增加相关。在整个达到的 SBP 和 DBP 范围内,糖尿病患者的肾脏风险更大。这些数据表明,在有和没有糖尿病的患者中,预防肾脏结局的目标 BP 范围相似,这是高危血管患者的常见并发症。