Hypertension Center of People's Hospital of Xinjiang Uygur Autonomous Region, Xinjiang Hypertension Institute, National Health Committee Key Laboratory of Hypertension Clinical Research, Key Laboratory of Xinjiang Uygur Autonomous Region "Hypertension Research Laboratory", Xinjiang Clinical Medical Research Center for Hypertension (Cardio-Cerebrovascular) Diseases, Urumqi, China.
Xinjiang Medical University, Urumqi, China.
Front Endocrinol (Lausanne). 2021 Nov 18;12:753074. doi: 10.3389/fendo.2021.753074. eCollection 2021.
White matter lesions (WMLs) are imaging changes in MRI of cerebral small vessel disease associated with vascular risk factors, increasing the risk of dementia, depression, and stroke. Aldosterone (ALD) or activation of mineralocorticoid receptor (MR) causes cerebrovascular injury in a mouse model. We aimed to analyze the relationship between ALD and WMLs in a population with hypertension.
We conducted a retrospective review of all patients screened for causes of secondary hypertension. We enrolled 547 patients with WMLs and matched these to controls without WMLs at a 1:1 ratio. White matter lesion load was assessed by using a modified Scheltens' scale.
Among the analytic sample (N = 1,094) with ages ranging from 30 to 64 years, 62.2% were male. We divided plasma ALD concentration (PAC), plasma renin activity (PRA), and ALD-renin ratio (ARR) into the third tertile (Q3), second tertile (Q2), and first tertile (Q1). We also analyzed them simultaneously as continuous variables. Multivariate logistic regression analysis showed that participants in Q3 (>17.26 ng/dl) of PAC (OR 1.59, 95% CI 1.15, 2.19), Q3 (<0.80 ng/dl) of PRA (OR 2.50, 95% CI 1.81, 3.44), and Q3 (>18.59 ng/dl per ng/ml*h) of ARR (OR 2.90, 95% CI 2.10, 4.01) had a significantly higher risk of WMLs than those in Q1 (<12.48) of PAC, Q1 (>2.19) of PRA, and Q1 (<6.96) of ARR. In linear regression analysis, we separately analyzed the correlation between the modified Scheltens' scale score and log(PAC) (β = 2.36; 95% CI 1.30, 3.41; < 0.001), log(PRA) (β = -1.76; 95% CI -2.09, -1.43; < 0.001), and log(ARR) (β = 1.86; 95% CI 1.55, 2.17; < 0.001), which were all significantly correlated with white matter lesion load, after adjusting for confounding factors. Simple mediation analyses showed that systolic blood pressure (SBP) or diastolic blood pressure (DBP) mediated -3.83% or -2.66% of the association between PAC and white matter lesion load, respectively. In stratified analyses, there was no evidence of subgroup heterogeneity concerning the change in the risk of WMLs ( > 0.05 for interaction for all).
Higher PAC, especially in PAC >17.26 ng/dl, increased the risk of WMLs. PAC was positively associated with white matter lesion load independent of SBP or DBP.
脑小血管疾病相关的血管危险因素所致的磁共振成像(MRI)脑白质病变(WMLs)是一种影像学改变,会增加痴呆、抑郁和中风的风险。醛固酮(ALD)或矿物质皮质激素受体(MR)的激活会导致小鼠模型中的脑血管损伤。我们旨在分析高血压人群中 ALD 与 WMLs 之间的关系。
我们对所有筛查继发性高血压病因的患者进行了回顾性审查。我们纳入了 547 例有 WMLs 的患者,并按照 1:1 的比例与没有 WMLs 的对照组进行匹配。采用改良 Scheltens 量表评估脑白质病变负荷。
在分析样本(N=1094)中,年龄在 30 至 64 岁之间,其中 62.2%为男性。我们将血浆 ALD 浓度(PAC)、血浆肾素活性(PRA)和 ALD-肾素比值(ARR)分为第三三分位数(Q3)、第二三分位数(Q2)和第一三分位数(Q1)。我们还同时将其作为连续变量进行分析。多变量逻辑回归分析显示,PAC 的 Q3(>17.26ng/dl)(OR 1.59,95%CI 1.15,2.19)、PRA 的 Q3(<0.80ng/dl)(OR 2.50,95%CI 1.81,3.44)和 ARR 的 Q3(>18.59ng/dl/ng/ml*h)(OR 2.90,95%CI 2.10,4.01)的患者发生 WMLs 的风险明显高于 PAC 的 Q1(<12.48)、PRA 的 Q1(>2.19)和 ARR 的 Q1(<6.96)。在线性回归分析中,我们分别分析了改良 Scheltens 量表评分与 log(PAC)(β=2.36;95%CI 1.30,3.41;<0.001)、log(PRA)(β=-1.76;95%CI -2.09,-1.43;<0.001)和 log(ARR)(β=1.86;95%CI 1.55,2.17;<0.001)之间的相关性,这些都与经混杂因素调整后的脑白质病变负荷呈显著相关。简单中介分析显示,收缩压(SBP)或舒张压(DBP)分别介导了 PAC 与脑白质病变负荷之间关联的-3.83%或-2.66%。分层分析中,PAC 与 WMLs 风险变化之间无亚组异质性证据(所有交互作用的 P 值均>0.05)。
较高的 PAC,特别是 PAC>17.26ng/dl,增加了 WMLs 的风险。PAC 与 SBP 或 DBP 无关,与脑白质病变负荷呈正相关。