Department of Internal Medicine, Maastricht University Medical Centre.
Cardiovascular Research Institute Maastricht (CARIM).
J Hypertens. 2018 Feb;36(2):259-267. doi: 10.1097/HJH.0000000000001543.
The mechanisms associating (pre)diabetes and cardiovascular disease (CVD) are incompletely understood. We hypothesize that greater blood pressure variability (BPV) may underlie this association, due to its association with (incident) CVD. Therefore, we investigated the association between (pre)diabetes and very short-term to mid-term BPV, that is within-visit, 24-h and 7-day BPV.
Cross-sectional data from The Maastricht Study [normal glucose metabolism (NGM), n = 1924; prediabetes, n = 511; type 2 diabetes mellitus (T2DM), n = 975; 51% men, aged 60 ± 8 years]. We determined SD for within-visit BPV (n = 3244), average real variability for 24-h BPV (n = 2699) day (0900-2100 h) and night (0100-0600 h) separately, and SD for 7-day BPV (n = 2259). Differences in BPV as compared with NGM were assessed by multiple linear regressions with adjustment for potential confounders.
In T2DM, the average systolic/diastolic values of within-visit, 24-h and 7-day BPV were 4.8/2.6, 10.5/7.3 and 10.4/6.5 mmHg, respectively, and in prediabetes 4.9/2.6, 10.3/7.0 and 9.4/5.9 mmHg, respectively. T2DM was associated with greater nocturnal systolic BPV [0.42 mmHg (95% confidence interval: 0.05-0.80)], and greater 7-day systolic [0.76 mmHg (0.32-1.19)] and diastolic BPV [0.65 mmHg (0.29-1.01)], whereas prediabetes was associated with greater within-visit systolic BPV only [0.35 mmHg (0.06-0.65)], as compared with NGM.
Both T2DM and prediabetes are associated with slightly greater very short-term to mid-term BPV, which may, according to previous literature, explain a small part of the increased CVD risk seen in (pre)diabetes. Nevertheless, these findings do not detract from the fact that very short-term to mid-term BPV is substantial and important in individuals with and without (pre)diabetes.
目前尚不完全清楚(前)糖尿病与心血管疾病(CVD)之间的关联机制。我们假设,由于血压变异性(BPV)与(新发)CVD 相关,因此更大的血压变异性可能是这种关联的基础。因此,我们研究了(前)糖尿病与非常短期到中期 BPV 之间的关系,即访间、24 小时和 7 天 BPV。
横断面数据来自马斯特里赫特研究[正常葡萄糖代谢(NGM),n=1924;糖尿病前期,n=511;2 型糖尿病(T2DM),n=975;51%男性,年龄 60±8 岁]。我们确定了访间 BPV 的标准差(n=3244)、24 小时 BPV 的平均真实变异性(n=2699)、日间(0900-2100 小时)和夜间(0100-0600 小时)分别和 7 天 BPV 的标准差(n=2259)。通过多元线性回归分析评估与 NGM 相比 BPV 的差异,并调整潜在混杂因素。
在 T2DM 中,访间、24 小时和 7 天 BPV 的平均收缩压/舒张压值分别为 4.8/2.6、10.5/7.3 和 10.4/6.5mmHg,而在糖尿病前期分别为 4.9/2.6、10.3/7.0 和 9.4/5.9mmHg。T2DM 与夜间收缩压 BPV 增加有关[0.42mmHg(95%置信区间:0.05-0.80)],与 7 天收缩压[0.76mmHg(0.32-1.19)]和舒张压[0.65mmHg(0.29-1.01)]BPV 增加有关,而糖尿病前期仅与访间收缩压 BPV 增加有关[0.35mmHg(0.06-0.65)],与 NGM 相比。
T2DM 和糖尿病前期均与较短时间到中期 BPV 略有增加相关,根据以往文献,这可能解释了(前)糖尿病患者 CVD 风险增加的一小部分原因。然而,这些发现并不能否定在(前)糖尿病患者和无(前)糖尿病患者中,短期到中期 BPV 非常大且重要的事实。