Department of Radiology, University of Pennsylvania, Philadelphia.
Department of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, North Carolina.
JAMA Neurol. 2021 May 1;78(5):568-577. doi: 10.1001/jamaneurol.2021.0178.
Meta-analyses of randomized clinical trials have indicated that improved hypertension control reduces the risk for cognitive impairment and dementia. However, it is unclear to what extent pathways reflective of Alzheimer disease (AD) pathology are affected by hypertension control.
To evaluate the association of intensive blood pressure control on AD-related brain biomarkers.
DESIGN, SETTING, AND PARTICIPANTS: This is a substudy of the Systolic Blood Pressure Intervention Trial (SPRINT MIND), a multicenter randomized clinical trial that compared the efficacy of 2 different blood pressure-lowering strategies. Potential participants (n = 1267) 50 years or older with hypertension and without a history of diabetes or stroke were approached for a brain magnetic resonance imaging (MRI) study. Of these, 205 participants were deemed ineligible and 269 did not agree to participate; 673 and 454 participants completed brain MRI at baseline and at 4-year follow-up, respectively; the final follow-up date was July 1, 2016. Analysis began September 2019 and ended November 2020.
Participants were randomized to either a systolic blood pressure goal of less than 120 mm Hg (intensive treatment: n = 356) or less than 140 mm Hg (standard treatment: n = 317).
Changes in hippocampal volume, measures of AD regional atrophy, posterior cingulate cerebral blood flow, and mean fractional anisotropy in the cingulum bundle.
Among 673 recruited patients who had baseline MRI (mean [SD] age, 67.3 [8.2] years; 271 women [40.3%]), 454 completed the follow-up MRI at a median (interquartile range) of 3.98 (3.7-4.1) years after randomization. In the intensive treatment group, mean hippocampal volume decreased from 7.45 cm3 to 7.39 cm3 (difference, -0.06 cm3; 95% CI, -0.08 to -0.04) vs a decrease from 7.48 cm3 to 7.46 cm3 (difference, -0.02 cm3; 95% CI, -0.05 to -0.003) in the standard treatment group (between-group difference in change, -0.033 cm3; 95% CI, -0.062 to -0.003; P = .03). There were no significant treatment group differences for measures of AD regional atrophy, cerebral blood flow, or mean fractional anisotropy.
Intensive treatment was associated with a small but statistically significant greater decrease in hippocampal volume compared with standard treatment, consistent with the observation that intensive treatment is associated with greater decreases in total brain volume. However, intensive treatment was not associated with changes in any of the other MRI biomarkers of AD compared with standard treatment.
ClinicalTrials.gov Identifier: NCT01206062.
随机临床试验的荟萃分析表明,改善高血压控制可降低认知障碍和痴呆的风险。然而,目前尚不清楚反映阿尔茨海默病(AD)病理的途径在多大程度上受到高血压控制的影响。
评估强化血压控制对 AD 相关脑生物标志物的影响。
设计、地点和参与者:这是一项名为收缩压干预试验(SPRINT MIND)的子研究,该试验是一项多中心随机临床试验,比较了两种不同降压策略的疗效。潜在参与者(n=1267)年龄在 50 岁或以上,患有高血压且无糖尿病或中风病史,被要求进行脑磁共振成像(MRI)研究。其中,205 名参与者被认为不符合条件,269 名参与者不同意参与;673 名和 454 名参与者分别在基线和 4 年随访时完成了脑 MRI;最终随访日期为 2016 年 7 月 1 日。分析于 2019 年 9 月开始,2020 年 11 月结束。
参与者被随机分配到收缩压目标低于 120 mmHg(强化治疗:n=356)或低于 140 mmHg(标准治疗:n=317)。
海马体积变化、AD 区域萎缩、后扣带回脑血流和扣带束平均各向异性分数的变化。
在招募的 673 名基线有 MRI 的患者中(平均[标准差]年龄为 67.3[8.2]岁,271 名女性[40.3%]),454 名患者在随机分组后中位数(四分位距)3.98(3.7-4.1)年完成了随访 MRI。在强化治疗组中,海马体积从 7.45 cm3 下降到 7.39 cm3(差异,-0.06 cm3;95%CI,-0.08 至 -0.04),而标准治疗组从 7.48 cm3 下降到 7.46 cm3(差异,-0.02 cm3;95%CI,-0.05 至 -0.003)(组间差异,-0.033 cm3;95%CI,-0.062 至 -0.003;P=0.03)。强化治疗组和标准治疗组在 AD 区域萎缩、脑血流或平均各向异性分数等其他 MRI 生物标志物方面均无显著的治疗组差异。
与标准治疗相比,强化治疗与海马体积的小但具有统计学意义的更大下降相关,这与强化治疗与总脑体积更大下降的观察结果一致。然而,与标准治疗相比,强化治疗与 AD 的任何其他 MRI 生物标志物的变化均无相关性。
ClinicalTrials.gov 标识符:NCT01206062。