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Blood pressure variability in Binswanger's disease and isolated lacunar infarction
J Martí-Fàbregas1, C Valencia, J López-Contreras
1Department of Neurology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain. jmarti@hsp.santpau.es
Insights
Blood pressure variability is not significantly higher in patients with Binswanger
Area of Science:
- Neurology
- Cardiology
- Geriatrics
Background:
- Binswanger's disease (BD) is a form of small-vessel disease.
- Hypertension is a common comorbidity in BD.
- The relationship between BP variability and BD requires further investigation.
Purpose of the Study:
- To investigate whether blood pressure (BP) variability is increased in hypertensive patients with Binswanger's disease (BD).
Main Methods:
- Two groups of treated hypertensive patients were studied: 11 with BD and 16 with lacunar infarction without cognitive impairment.
- Averaged baseline office BP was recorded for 3 weeks.
- Ambulatory BP monitoring was used to measure BP variability, defined as the standard deviation of consecutive BP values.
Main Results:
- Diurnal systolic BP (SBP) variability was initially higher in the BD group (p = 0.04).
- After adjusting for age and baseline office BP, this difference was no longer statistically significant (p = 0.17 and p = 0.09).
- Increased BP variability in BD patients appears related to older age and higher baseline BP.
Conclusions:
- Increased BP variability in Binswanger's disease patients is likely attributable to older age and elevated baseline blood pressure.
- While increased BP variability may be a risk factor for small-vessel disease, it is not directly linked to cognitive impairment in this context.
Unlabelled:
To determine whether blood pressure (BP) variability is increased in hypertensive patients with Binswanger's disease (BD), we studied two samples of consecutive treated hypertensive patients: (1) 11 with BD (mean age 71.3 +/- 5.2 years); (2) 16 with lacunar infarction (mean age 65.2 +/- 8.3 years) without cognitive impairment. An averaged baseline office BP was obtained for 3 consecutive weeks. Ambulatory BP monitoring was then carried out to obtain the averaged mean systolic (SBP) and diastolic BP, and BP variability was defined as the standard deviation of consecutive BP values.
Results:
Diurnal SBP variability was significantly increased in the BD group (p = 0.04). However, with the analysis of covariance for age and baseline office BP, the difference was no longer significant (p = 0.17 and p = 0.09, respectively). We conclude that increased BP variability in BD patients is probably due to older age and increased baseline office BP. Increased BP variability may be a risk factor for small-vessel disease, but not for cognitive impairment.
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