Geriatric Research and Education Clinical Center, Palo Alto VA Health Care System, Palo Alto, CA; Division of Nephrology, Stanford University School of Medicine, Palo Alto, CA.
Departments of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, NC.
Am J Kidney Dis. 2022 May;79(5):677-687.e1. doi: 10.1053/j.ajkd.2021.07.024. Epub 2021 Sep 17.
RATIONALE & OBJECTIVE: The safety of intensive blood pressure (BP) targets is controversial for persons with chronic kidney disease (CKD). We studied the effects of hypertension treatment on cerebral perfusion and structure in individuals with and without CKD.
Neuroimaging substudy of a randomized trial.
SETTING & PARTICIPANTS: A subset of participants in the Systolic Blood Pressure Intervention Trial (SPRINT) who underwent brain magnetic resonance imaging studies. Presence of baseline CKD was assessed by estimated glomerular filtration rate (eGFR) and urinary albumin-creatinine ratio (UACR).
Participants were randomly assigned to intensive (systolic BP <120 mm Hg) versus standard (systolic BP <140 mm Hg) BP lowering.
The magnetic resonance imaging outcome measures were the 4-year change in global cerebral blood flow (CBF), white matter lesion (WML) volume, and total brain volume (TBV).
A total of 716 randomized participants with a mean age of 68 years were enrolled; follow-up imaging occurred after a median 3.9 years. Among participants with eGFR <60 mL/min/1.73 m (n = 234), the effects of intensive versus standard BP treatment on change in global CBF, WMLs, and TBV were 3.38 (95% CI, 0.32 to 6.44) mL/100 g/min, -0.06 (95% CI, -0.16 to 0.04) cm (inverse hyperbolic sine-transformed), and -3.8 (95% CI, -8.3 to 0.7) cm, respectively. Among participants with UACR >30 mg/g (n = 151), the effects of intensive versus standard BP treatment on change in global CBF, WMLs, and TBV were 1.91 (95% CI, -3.01 to 6.82) mL/100 g/min, 0.003 (95% CI, -0.13 to 0.13) cm (inverse hyperbolic sine-transformed), and -7.0 (95% CI, -13.3 to -0.3) cm, respectively. The overall treatment effects on CBF and TBV were not modified by baseline eGFR or UACR; however, the effect on WMLs was attenuated in participants with albuminuria (P = 0.04 for interaction).
Measurement variability due to multisite design.
Among adults with hypertension who have primarily early kidney disease, intensive versus standard BP treatment did not appear to have a detrimental effect on brain perfusion or structure. The findings support the safety of intensive BP treatment targets on brain health in persons with early kidney disease.
SPRINT was funded by the National Institutes of Health (including the National Heart, Lung, and Blood Institute; the National Institute of Diabetes and Digestive and Kidney Diseases; the National Institute on Aging; and the National Institute of Neurological Disorders and Stroke), and this substudy was funded by the National Institutes of Diabetes and Digestive and Kidney Diseases.
SPRINT was registered at ClinicalTrials.gov with study number NCT01206062.
对于慢性肾脏病(CKD)患者,强化血压(BP)目标的安全性存在争议。我们研究了高血压治疗对伴有和不伴有 CKD 的个体脑灌注和结构的影响。
一项随机试验的神经影像学亚研究。
SPRINT 试验中接受脑磁共振成像研究的参与者的亚组。基线 CKD 的存在通过估计肾小球滤过率(eGFR)和尿白蛋白-肌酐比(UACR)进行评估。
参与者被随机分配接受强化(收缩压 <120mmHg)与标准(收缩压 <140mmHg)降压治疗。
磁共振成像的转归指标为全脑血流(CBF)、脑白质病变(WML)体积和总脑体积(TBV)的 4 年变化。
共纳入了 716 名平均年龄为 68 岁的随机参与者;中位随访时间为 3.9 年后进行了影像学随访。在 eGFR<60mL/min/1.73m(n=234)的参与者中,强化与标准 BP 治疗对全脑 CBF、WML 和 TBV 变化的影响分别为 3.38(95%CI,0.32 至 6.44)mL/100g/min、-0.06(95%CI,-0.16 至 0.14)cm(双曲正弦逆变换)和-3.8(95%CI,-8.3 至 0.7)cm。在 UACR>30mg/g(n=151)的参与者中,强化与标准 BP 治疗对全脑 CBF、WML 和 TBV 变化的影响分别为 1.91(95%CI,-3.01 至 6.82)mL/100g/min、0.003(95%CI,-0.13 至 0.13)cm(双曲正弦逆变换)和-7.0(95%CI,-13.3 至-0.3)cm。全脑 CBF 和 TBV 的总体治疗效果不受基线 eGFR 或 UACR 的影响;然而,WML 的治疗效果在白蛋白尿患者中减弱(交互作用 P=0.04)。
由于多中心设计导致的测量变异性。
在主要为早期肾脏疾病的高血压成年人中,与标准 BP 治疗相比,强化 BP 治疗似乎对脑灌注或结构没有不良影响。这些发现支持在早期肾脏疾病患者中强化 BP 治疗目标对脑健康的安全性。
SPRINT 由美国国立卫生研究院(包括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、美国国立衰老研究所和美国国立神经病学和中风研究所)资助,本亚研究由美国国立糖尿病、消化和肾脏疾病研究所资助。
SPRINT 在 ClinicalTrials.gov 上注册,注册号为 NCT01206062。