TY - JOUR
T1 - Blood pressure variability and risk of heart failure in accord and the VADT
AU - VADT Investigators
AU - Nuyujukian, Daniel S.
AU - Koska, Juraj
AU - Bahn, Gideon
AU - Reaven, Peter D.
AU - Zhou, Jin J.
N1 - Funding Information:
Acknowledgments. The authors acknowledge the contributions of the Hines Veterans Affairs Cooperative Studies Program Coordinating Center. Funding. This work was supported by the Veterans Affairs Cooperative Studies Program. Additional support was received from the National Institutes of Health (grant R01-067690 to P.D.R.), National Heart, Lung, and Blood Institute (grant R01-HL-94775 to P.D.R.), and the National Institute of Diabetes and Digestive and Kidney Diseases (grant K01-DK-106116 to J.J.Z.). Duality of Interest. No potential conflicts of interest relevant to this article were reported. Author Contributions. D.S.N., J.K., P.D.R., and J.J.Z. contributed to the conception and design of the work and interpreted the data. D.S.N., J.K., and P.D.R. wrote the manuscript. D.S.N., J.K., and J.J.Z. conducted data analysis. G.B. advised on statistical methods and participated in acquisition of the data. P.D.R. was a principal investigator in, and is an executive committee member of, the VADT. All authors provided edits and comments on manuscript drafts. All authors approved the final version of the manuscript. D.S.N. and J.J.Z. are the guarantors of this work and, as such, had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
Publisher Copyright:
© 2020 by the American Diabetes Association.
PY - 2020/7
Y1 - 2020/7
N2 - OBJECTIVE Although blood pressure variability is increasingly appreciated as a risk factor for cardiovascular disease, its relationship with heart failure (HF) is less clear. We examined the relationship between blood pressure variability and risk of HF in two cohorts of type 2 diabetes participating in trials of glucose and/or other risk factor management. RESEARCH DESIGN AND METHODS Data were drawn from the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial and the Veterans Affairs Diabetes Trial (VADT). Coefficient of variation (CV) and average real variability (ARV) were calculated for systolic (SBP) and diastolic blood pressure (DBP) along with maximum and cumulative mean SBP and DBP during both trials. RESULTS In ACCORD, CV and ARV of SBP and DBP were associated with increased risk of HF, even after adjusting for other risk factors and mean blood pressure (e.g., CV-SBP: hazard ratio [HR] 1.15, P = 0.01; CV-DBP: HR 1.18, P = 0.003). In the VADT, DBP variability was associated with increased risk of HF (ARV-DBP: HR 1.16, P = 0.001; CV-DBP: HR 1.09, P = 0.04). Further, in ACCORD, those with progressively lower baseline blood pressure demonstrated a stepwise increase in risk of HF with higher CV-SBP, ARV-SBP, and CV-DBP. Effects of blood pressure variability were related to dips, not elevations, in blood pressure. CONCLUSIONS Blood pressure variability is associated with HF risk in individuals with type 2 diabetes, possibly a consequence of periods of ischemia during diastole. These results may have implications for optimizing blood pressure treatment strategies in those with type 2 diabetes.
AB - OBJECTIVE Although blood pressure variability is increasingly appreciated as a risk factor for cardiovascular disease, its relationship with heart failure (HF) is less clear. We examined the relationship between blood pressure variability and risk of HF in two cohorts of type 2 diabetes participating in trials of glucose and/or other risk factor management. RESEARCH DESIGN AND METHODS Data were drawn from the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial and the Veterans Affairs Diabetes Trial (VADT). Coefficient of variation (CV) and average real variability (ARV) were calculated for systolic (SBP) and diastolic blood pressure (DBP) along with maximum and cumulative mean SBP and DBP during both trials. RESULTS In ACCORD, CV and ARV of SBP and DBP were associated with increased risk of HF, even after adjusting for other risk factors and mean blood pressure (e.g., CV-SBP: hazard ratio [HR] 1.15, P = 0.01; CV-DBP: HR 1.18, P = 0.003). In the VADT, DBP variability was associated with increased risk of HF (ARV-DBP: HR 1.16, P = 0.001; CV-DBP: HR 1.09, P = 0.04). Further, in ACCORD, those with progressively lower baseline blood pressure demonstrated a stepwise increase in risk of HF with higher CV-SBP, ARV-SBP, and CV-DBP. Effects of blood pressure variability were related to dips, not elevations, in blood pressure. CONCLUSIONS Blood pressure variability is associated with HF risk in individuals with type 2 diabetes, possibly a consequence of periods of ischemia during diastole. These results may have implications for optimizing blood pressure treatment strategies in those with type 2 diabetes.
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U2 - 10.2337/dc19-2540
DO - 10.2337/dc19-2540
M3 - Article
C2 - 32327422
AN - SCOPUS:85086792885
SN - 0149-5992
VL - 43
SP - 1471
EP - 1478
JO - Diabetes Care
JF - Diabetes Care
IS - 7
ER -