Association between within-visit systolic blood pressure variability and development of pre-diabetes and diabetes among overweight/obese individuals
- PMID: 29311705
- PMCID: PMC5763512
- DOI: 10.1038/s41371-017-0009-y
Association between within-visit systolic blood pressure variability and development of pre-diabetes and diabetes among overweight/obese individuals
Abstract
Short-term blood pressure variability is associated with pre-diabetes/diabetes cross-sectionally, but there are no longitudinal studies evaluating this association. The objective of this study is to evaluate the association between within-visit systolic and diastolic blood pressure variability and development of pre-diabetes/diabetes longitudinally. The study was conducted among eligible participants from the San Juan Overweight Adults Longitudinal Study (SOALS), who completed the 3-year follow-up exam. Participants were Hispanics, 40-65 years of age, and free of diabetes at baseline. Within-visit systolic and diastolic blood pressure variability was defined as the maximum difference between three measures, taken a few minutes apart, of systolic and diastolic blood pressure, respectively. Diabetes progression was defined as development of pre-diabetes/diabetes over the follow-up period. We computed multivariate incidence rate ratios adjusting for baseline age, gender, smoking, physical activity, waist circumference, and hypertension status. Participants with systolic blood pressure variability ≥10 mmHg compared to those with <10 mmHg, showed higher progression to pre-diabetes/diabetes (RR = 1.77, 95% CI: 1.30-2.42). The association persisted among never smokers. Diastolic blood pressure variability ≥10 mmHg (compared to <10 mmHg) did not show an association with diabetes status progression (RR = 1.20, 95% CI: 0.71-2.01). Additional adjustment of baseline glycemia, C-reactive protein, and lipids (reported dyslipidemia or baseline HDL or triglycerides) did not change the estimates. Systolic blood pressure variability may be a novel independent risk factor and an early predictor for diabetes, which can be easily incorporated into a single routine outpatient visit at none to minimal additional cost.
Conflict of interest statement
The authors have nothing to disclose.
Figures
References
-
- Conway J, Boon N, Davies C, Jones JV, Sleight P. Neural and humoral mechanisms involved in blood pressure variability. Journal of hypertension. 1984;2(2):203–8. - PubMed
-
- Faramawi MF, Delongchamp R, Said Q, Jadhav S, Abouelenien S. Metabolic syndrome is associated with visit-to-visit systolic blood pressure variability in the US adults. Hypertension research : official journal of the Japanese Society of Hypertension. 2014;37(9):875–9. - PubMed
-
- Mancia G, Grassi G. Mechanisms and clinical implications of blood pressure variability. Journal of cardiovascular pharmacology. 2000;35(7 Suppl 4):S15–9. - PubMed
-
- Mokhtar RH, Ayob A, Mohd Noor N. Blood pressure variability in patients with diabetes mellitus. Asian cardiovascular & thoracic annals. 2010;18(4):344–8. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
