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Visit-to-visit blood pressure variability is a risk factor for all-cause mortality and cardiovascular disease: a
Jianqi Wang1, Xubo Shi, Changsheng Ma
1The Cardiovascular Center of Beijing Tongren Hospital, Capital Medical University, Beijing, PR China.
Insights
Visit-to-visit variability (VVV) in systolic blood pressure (BP) is linked to increased risks of cardiovascular disease (CVD) and mortality. Standardized monitoring of BP VVV is recommended for high-risk patients to improve prognosis.
Area of Science:
- Cardiology
- Public Health
- Epidemiology
Background:
- Clinical studies suggest a link between visit-to-visit variability (VVV) of blood pressure (BP) and adverse cardiovascular outcomes.
- Inconsistencies across studies necessitate a comprehensive analysis to clarify this association.
Purpose of the Study:
- To conduct a systematic review and meta-analysis to determine the association between BP VVV and cardiovascular disease (CVD) and all-cause mortality.
Main Methods:
- Searched PubMed and EMBASE databases up to May 18, 2014, for studies on BP VVV, CVD, and mortality.
- Included 23 publications in the meta-analysis, utilizing a random effects model for data synthesis.
Main Results:
- Elevated systolic BP VVV showed significant associations with increased all-cause mortality (RR 1.14, 95% CI: 1.09-1.18).
- Systolic BP VVV was also linked to higher incidence of CVD (RR 1.12, 95% CI: 1.05-1.09), CVD mortality (RR 1.18, 95% CI: 1.09-1.28), coronary heart disease (CHD) incidence (RR 1.12, 95% CI: 1.06-1.19), and stroke incidence (RR 1.34, 95% CI: 1.11-1.61).
Conclusions:
- Modest associations exist between systolic BP VVV and major adverse cardiovascular outcomes across diverse populations.
- Standardized monitoring of BP VVV is crucial for high-risk individuals (e.g., those with diabetes, CKD, or history of stroke) in future clinical studies to better predict patient prognosis.
Objective:
Clinical cohort studies have reported that visit-to-visit variability (VVV) of blood pressure (BP) is associated with cardiovascular disease (CVD) or mortality. However, the results were not consistent in all studies. The current study is, therefore, aimed to conduct a systematic review and meta-analysis to determine the association between VVV of BP and CVD and all-cause mortality.
Method:
PubMed and EMBASE were searched through 18 May 2014, using the following terms: VVV, BP, CVD, coronary heart disease (CHD), myocardial ischemia, stroke, and mortality. Overall, 84 records were identified, and 23 publications were enrolled into the current study. Data were extracted from selected publications, and meta-analysis was performed using a random effect model.
Result:
VVV of SBP was significantly associated with outcomes of all-cause mortality with the relative risk (RR) and 95% confidence interval (CI) 1.14 (1.09, 1.18), CVD incidence (RR = 1.12, 95% CI: 1.05, 1.09), CVD mortality (RR = 1.18, 95% CI: 1.09, 1.28), CHD incidence (RR = 1.12, 95% CI: 1.06, 1.19), and stroke incidence (RR = 1.34, 95% CI: 1.11, 1.61).
Conclusion:
In summary, among the wide heterogenetic population, modest associations between VVV of SBP and all-cause mortality, CVD incidence, CVD mortality, CHD incidence, and stroke incidence were found. Findings of the current study suggested that standardized approaches of monitoring VVV in the high-risk population, including patients with cardiac infarction, diabetes, stroke, and patients with chronic kidney disease or in dialysis, are necessary in designing a prospective clinical study on the association of VVV and patients' prognosis.
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