Department of Psychiatry and Behavioral Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Department of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Lancet Neurol. 2020 Nov;19(11):899-907. doi: 10.1016/S1474-4422(20)30319-7.
Results from the Systolic Blood Pressure Intervention Trial (SPRINT) showed that intensive control of systolic blood pressure significantly reduced the occurrence of mild cognitive impairment, but not probable dementia. We investigated the effects of intensive lowering of systolic blood pressure on specific cognitive functions in a preplanned substudy of participants from SPRINT.
SPRINT was an open-label, multicentre, randomised controlled trial undertaken at 102 sites, including academic medical centres, Veterans Affairs medical centres, hospitals, and independent clinics, in the USA and Puerto Rico. Participants were adults aged 50 years or older with systolic blood pressure higher than 130 mm Hg, but without diabetes, history of stroke, or dementia. Participants were randomly assigned (1:1) to a systolic blood pressure goal of less than 120 mm Hg (intensive treatment) versus less than 140 mm Hg (standard treatment). All major classes of antihypertensive agents were included. A subgroup of randomly assigned participants including, but not limited to, participants enrolled in an MRI substudy was then selected for a concurrent substudy of cognitive function (target 2800 participants). Each individual was assessed with a screening cognitive test battery and an extended cognitive test battery at baseline and biennially during the planned 4-year follow-up. The primary outcomes for this substudy were standardised composite scores for memory (Logical Memory I and II, Modified Rey-Osterrieth Complex Figure [immediate recall], and Hopkins Verbal Learning Test-Revised [delayed recall]) and processing speed (Trail Making Test and Digit Symbol Coding). SPRINT was registered with ClinicalTrials.gov, NCT01206062.
From Nov 23, 2010, to Dec 28, 2012, 2921 participants (mean age 68·4 years [SD 8·6], 1080 [37%] women) who had been randomly assigned in SPRINT were enrolled in the substudy (1448 received intensive treatment and 1473 received standard treatment). SPRINT was terminated early due to benefit observed in the primary outcome (composite of cardiovascular events). After a median follow-up of 4·1 years (IQR 3·7-5·8), there was no between-group difference in memory, with an annual decline in mean standardised domain score of -0·005 (95% CI -0·010 to 0·001) in the intensive treatment group and -0·001 (-0·006 to 0·005) in the standard treatment group (between-group difference -0·004, 95% CI -0·012 to 0·004; p=0·33). Mean standardised processing speed domain scores declined more in the intensive treatment group (between-group difference -0·010, 95% CI -0·017 to -0·002; p=0·02), with an annual decline of -0·025 (-0·030 to -0·019) for the intensive treatment group and -0·015 (-0·021 to 0·009) for the standard treatment group.
Intensive treatment to lower systolic blood pressure did not result in a clinically relevant difference compared with standard treatment in memory or processing speed in a subgroup of participants from SPRINT. The effect of blood pressure lowering might not be evident in specific domains of cognitive function, but instead distributed across multiple domains.
National Heart, Lung, and Blood Institute, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute on Aging, National Institute of Neurological Disorders and Stroke, and the Alzheimer's Association.
收缩压干预试验(SPRINT)的结果表明,强化控制收缩压显著降低了轻度认知障碍的发生,但不能预防痴呆。我们在 SPRINT 的一项预先计划的亚研究中,调查了强化降低收缩压对特定认知功能的影响。
SPRINT 是一项在美国和波多黎各的 102 个地点进行的开放标签、多中心、随机对照试验,包括学术医疗中心、退伍军人事务医疗中心、医院和独立诊所。参与者为年龄在 50 岁或以上、收缩压高于 130mmHg 但无糖尿病、中风或痴呆病史的成年人。参与者被随机分配(1:1)接受收缩压目标低于 120mmHg(强化治疗)或低于 140mmHg(标准治疗)。所有主要类别的抗高血压药物均被包括在内。然后,从随机分配的参与者中选择了一个亚组,包括但不限于参加 MRI 亚研究的参与者,进行认知功能的平行亚研究(目标参与者 2800 名)。每位个体在基线和计划的 4 年随访期间每两年接受一次标准的认知测试和扩展的认知测试。该亚研究的主要结局是记忆(逻辑记忆 I 和 II、改良 Rey-Osterrieth 复杂图形[即时回忆]和 Hopkins 言语学习测试-修订[延迟回忆])和处理速度(Trail 制作测试和数字符号编码)的标准化综合评分。SPRINT 在 ClinicalTrials.gov 上注册,编号为 NCT01206062。
从 2010 年 11 月 23 日至 2012 年 12 月 28 日,2921 名(平均年龄 68.4 岁[标准差 8.6],1080 名[37%]女性)随机分配在 SPRINT 中的参与者被纳入亚研究(1448 名接受强化治疗,1473 名接受标准治疗)。SPRINT 因主要结局(心血管事件的综合结果)观察到的益处而提前终止。中位随访 4.1 年后(IQR 3.7-5.8),两组间记忆无差异,强化治疗组平均标准域评分每年下降 0.005(95%CI -0.010 至 0.001),标准治疗组每年下降 0.001(95%CI -0.006 至 0.005)(组间差异 -0.004,95%CI -0.012 至 0.004;p=0.33)。强化治疗组处理速度的平均标准域评分下降更多(组间差异 -0.010,95%CI -0.017 至 -0.002;p=0.02),强化治疗组每年下降 0.025(95%CI -0.030 至 -0.019),标准治疗组每年下降 0.015(95%CI -0.021 至 0.009)。
与标准治疗相比,在 SPRINT 的一个亚组参与者中,强化治疗降低收缩压并没有导致记忆或处理速度出现临床相关差异。降压的效果可能不会在认知功能的特定领域显现,而是分布在多个领域。
美国国立心肺血液研究所、美国国立糖尿病、消化和肾脏疾病研究所、美国国立老龄问题研究所、美国国立神经病学和中风研究所和阿尔茨海默病协会。