Blood Pressure Control and the Association With Diabetes Mellitus Incidence

Author:

Roumie Christianne L.12,Hung Adriana M.12,Russell Gregory B.3,Basile Jan4,Kreider Kathryn Evans5,Nord John6,Ramsey Thomas M.7,Rastogi Anjay8,Sweeney Mary Ellen9,Tamariz Leonardo10,Kostis William J.11,Williams Jonathan S.1213,Zias Athena14,Cushman William C.15,

Affiliation:

1. From the VA Tennessee Valley Healthcare System Geriatric Research and Education Clinical Center, Nashville, TN (C.L.R., A.M.H.)

2. Department of Medicine, Vanderbilt University Medical Center, Nashville, TN (C.L.R., A.M.H.)

3. Department of Biostatistics and Data Science, Wake Forest School of Medicine, NC (G.B.R.)

4. Ralph H Johnson VA Medical Center and Medical University of South Carolina, Charleston (J.B.)

5. Division of Endocrinology, Metabolism and Nutrition, Department of Medicine, Duke University School of Nursing, Duke University Medical Center, NC (K.E.K.)

6. Salt Lake City VA Medical Center, Salt Lake City, UT (J.N.)

7. School of Nursing Office of Research and Scholarship, The University of Alabama at Birmingham (T.M.R.)

8. Division of Nephrology, Department of Medicine David Geffen School of Medicine UCLA, Los Angeles, CA (A.R.)

9. Division of Endocrinology, Diabetes and Lipids, Department of Medicine, Emory University and Atlanta VA Medical Center (M.E.S.)

10. Miami Veterans Healthcare and Division of Population Health and Computational Medicine, University of Miami, FL (L.T.)

11. The Cardiovascular Institute at Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ (W.J.K.)

12. Endocrine Unit, VA Boston Healthcare System, Jamaica Plain, MA (J.S.W.)

13. Division of Endocrinology, Diabetes, and Hypertension Harvard Medical School, Brigham and Women’s Hospital, Boston, MA (J.S.W.)

14. Northport Veterans Affairs Medical Center, Northport, NY Renaissance School of Medicine at Stony Brook University (A.Z.)

15. Memphis Veterans Affairs Medical Center and University of Tennessee Health Science Center, Memphis (W.C.C.).

Abstract

The SPRINT (Systolic Blood Pressure Intervention Trial) demonstrated reduced cardiovascular outcomes. We evaluated diabetes mellitus incidence in this randomized trial that compared intensive blood pressure strategy (systolic blood pressure <120 mm Hg) versus standard strategy (<140 mm Hg). Participants were ≥50 years of age, with systolic 130 to 180 mm Hg and increased cardiovascular risk. Participants were excluded if they had diabetes mellitus, polycystic kidney disease, proteinuria >1 g/d, heart failure, dementia, or stroke. Postrandomization exclusions included participants missing blood glucose or ≥126 mg/dL (6.99 mmol/L) or on hypoglycemics. The outcome was incident diabetes mellitus: fasting blood glucose ≥126 mg/dL (6.99 mmol/L), diabetes mellitus self-report, or new use of hypoglycemics. The secondary outcome was impaired fasting glucose (100–125 mg/dL [5.55–6.94 mmol/L]) among those with normoglycemia (<100 mg/dL [5.55 mmol/L]). There were 9361 participants randomized and 981 excluded, yielding 4187 and 4193 participants assigned to intensive and standard strategies. There were 299 incident diabetes mellitus events (2.3% per year) for intensive and 251 events (1.9% per year) for standard, rates of 22.6 (20.2–25.3) versus 19.0 (16.8–21.5) events per 1000 person-years of treatment, respectively (adjusted hazard ratio, 1.19 [95% CI, 0.95–1.49]). Impaired fasting glucose rates were 26.4 (24.9–28.0) and 22.5 (21.1–24.1) per 100 person-years for intensive and standard strategies (adjusted hazard ratio, 1.17 [1.06–1.30]). Intensive treatment strategy was not associated with increased diabetes mellitus but was associated with more impaired fasting glucose. The risks and benefits of intensive blood pressure targets should be factored into individualized patient treatment goals. Clinical Trial Registration— URL: http://www.clinicaltrials.gov . Unique identifier: NCT01206062.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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