@article{277fdc32f08f450e8d365afebf512d8e,
title = "Visit-to-visit offce blood pressure variability and cardiovascular outcomes in SPRINT (systolic blood pressure intervention trial)",
abstract = "Studies of visit-to-visit offce blood pressure (BP) variability (OBPV) as a predictor of cardiovascular events and death in high-risk patients treated to lower BP targets are lacking. We conducted a post hoc analysis of SPRINT (Systolic Blood Pressure Intervention Trial), a well-characterized cohort of participants randomized to intensive (<120 mmHg) or standard (<140 mmHg) systolic BP targets. We defned OBPV as the coeffcient of variation of the systolic BP using measurements taken during the 3-,6-, 9-, and 12-month study visits. In our cohort of 7879 participants, older age, female sex, black race, current smoking, chronic kidney disease, and coronary disease were independent determinants of higher OBPV. Use of thiazide-type diuretics or dihydropyridine calcium channel blockers was associated with lower OBPV whereas angiotensin-converting enzyme inhibitors or angiotensin receptor blocker use was associated with higher OBPV. There was no difference in OBPV in participants randomized to standard or intensive treatment groups. We found that OBPV had no signifcant associations with the composite end point of fatal and nonfatal cardiovascular events (n=324 primary end points; adjusted hazard ratio, 1.20; 95% confdence interval, 0.85-1.69, highest versus lowest quintile) nor with heart failure or stroke. The highest quintile of OBPV (versus lowest) was associated with all-cause mortality (adjusted hazard ratio, 1.92; confdence interval, 1.22-3.03) although the association of OBPV overall with all-cause mortality was marginal (P=0.07). Our results suggest that clinicians should continue to focus on offce BP control rather than on OBPV unless defnitive benefts of reducing OBPV are shown in prospective trials.",
keywords = "Angiotensin-converting enzyme inhibitors, Blood pressure, Heart failure, Kidney diseases, Mortality",
author = "Chang, {Tara I.} and Reboussin, {David M.} and Chertow, {Glenn M.} and Cheung, {Alfred K.} and Cushman, {William C.} and Kostis, {William J.} and Gianfranco Parati and Dominic Raj and Erik Riessen and Brian Shapiro and Stergiou, {George S.} and Townsend, {Raymond R.} and Konstantinos Tsioufs and Whelton, {Paul K.} and Jeffrey Whittle and Wright, {Jackson T.} and Vasilios Papademetriou",
note = "Funding Information: T.I. Chang is supported by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), 5K23DK095914. The Systolic Blood Pressure Intervention Trial is funded with Federal funds from the National Institutes of Health (NIH), including the National Heart, Lung, and Blood Institute, the NIDDK, the National Institute on Aging, and the National Institute of Neurological Disorders and Stroke (NINDS), under contract numbers HHSN268200900040C, HHSN268200900046C, HHSN268200900047C, HHSN268200900 048C, HHSN268200900049C, and Inter-Agency Agreement Number A-HL-13-002-001. It was also supported, in part, with resources and use of facilities through the Department of Veterans Affairs. The SPRINT (Systolic Blood Pressure Intervention Trial) investigators acknowledge the contribution of study medications (azilsartan and azil-sartan combined with chlorthalidone) from Takeda Pharmaceuticals International, Inc. All components of the SPRINT study protocol were designed and implemented by the investigators. The investigative team collected, analyzed, and interpreted the data. All aspects of article writing and revision were performed by the coauthors. Funding Information: We also acknowledge the support from the following Clinical and Translational Science Awards funded by the National Center for Advancing Translational Sciences: Case Western Reserve University: UL1TR000439; The Ohio State University: UL1RR025755; University of Pennsylvania: UL1RR024134 and UL1TR000003; Boston: UL1RR025771; Stanford: UL1TR000093; Tufts: UL1RR025752, UL1TR000073, and UL1TR001064; University of Illinois: UL1TR000050; University of Pittsburgh: UL1TR000005; UT Southwestern: 9U54TR000017-06; University of Utah: UL1TR000105-05; Vanderbilt University: UL1 TR000445; George Washington University: UL1TR000075; University of California, Davis: UL1 TR000002; University of Florida: UL1 TR000064; University of Michigan: UL1TR000433; Tulane University: P30GM103337 COBRE Award NIGMS. Funding Information: A.K. Cheung is a consultant for Boehringer Ingelheim and a contributor to Up-to-Date. W.C. Cushman has an institutional grant from Eli Lilly and is an uncompensated consultant for Takeda. V. Papademetriou received grants from Astra-Zeneca, Sanofi, DCRI, VA Co-Op studies, and the National Institutes of Health. G.S. Stergiou received honoraria from Boehringer, Mearini, Novartis, Omron, SanofiAventis, Servier, and has research contracts with Bayer and Boehringer. K. Tsioufis has received research grants or honoraria from Medtronic, St. Jude Medical, Bayer, Novartis, Atra-Zeneca, Boehringer, Pfizer, Sanofi, Vianex, and Servier. The other authors report no conflicts. Publisher Copyright: {\textcopyright} 2017 American Heart Association, Inc.",
year = "2017",
doi = "10.1161/HYPERTENSIONAHA.117.09788",
language = "English (US)",
volume = "70",
pages = "751--758",
journal = "Hypertension",
issn = "0194-911X",
publisher = "Lippincott Williams and Wilkins",
number = "4",
}