Relationship Between Sarcopenia and Intensive Blood Pressure Control Efficacy and Safety: A Secondary Analysis of SPRINT

Author:

Mirzai Saeid1ORCID,Persits Ian2ORCID,Kazibwe Richard3ORCID,Gabani Mohanad1,Seals Austin1,Singleton Matthew J.4ORCID,Rikhi Rishi1ORCID,Chevli Parag A.3ORCID,Carbone Salvatore56ORCID,Tang W.H. Wilson7ORCID,Yeboah Joseph1ORCID,Williamson Jeff D.8,Kitzman Dalane W.18ORCID,Herrington David M.1ORCID,Shapiro Michael D.1ORCID

Affiliation:

1. Section on Cardiovascular Medicine (S.M., M.G., A.S., R.R., J.Y., D.W.K., D.M.H., M.D.S.), Department of Internal Medicine, Wake Forest University School of Medicine, Winston Salem, NC.

2. Department of Internal Medicine (I.P.), Cleveland Clinic, OH.

3. Section on Hospital Medicine (R.K., P.A.C.), Department of Internal Medicine, Wake Forest University School of Medicine, Winston Salem, NC.

4. Section on Cardiovascular Medicine, Department of Medicine, WellSpan Health, York, PA (M.J.S.).

5. Pauley Heart Center, Division of Cardiology, Department of Internal Medicine (S.C.), Virginia Commonwealth University, Richmond.

6. Department of Kinesiology & Health Sciences, College of Humanities & Sciences (S.C.), Virginia Commonwealth University, Richmond.

7. Kaufman Center for Heart Failure Treatment and Recovery, Heart Vascular and Thoracic Institute (W.H.W.T.), Cleveland Clinic, OH.

8. Section on Gerontology and Geriatric Medicine (J.D.W., D.W.K.), Department of Internal Medicine, Wake Forest University School of Medicine, Winston Salem, NC.

Abstract

BACKGROUND: Sarcopenia and hypertension are independently associated with worse cardiovascular disease (CVD) risk and survival. While individuals with sarcopenia may benefit from intensive blood pressure (BP) control, the increased vulnerability of this population raises concerns for potential harm. This study aimed to evaluate clinical and safety outcomes with intensive (target <120 mm Hg) versus standard (<140 mm Hg) systolic BP targets in older hypertensive adults with sarcopenia compared with nonsarcopenic counterparts in the SPRINT (Systolic Blood Pressure Intervention Trial). METHODS: Sarcopenia was defined using surrogates of the lowest sex-stratified median of the sarcopenia index (serum creatinine/cystatin C×100) for muscle wasting and gait speed ≤0.8 m/s for muscle weakness. Outcomes included CVD events, all-cause mortality, and serious adverse events. RESULTS: Of 2571 SPRINT participants with sarcopenia index and gait speed data available (aged ≥75 years), 502 (19.5%) met the criteria for sarcopenia, which was associated with higher risks of CVD events (adjusted hazard ratio, 1.49 [95% CI, 1.15–1.94]; P =0.003) and all-cause mortality (adjusted hazard ratio, 1.46 [95% CI, 1.09–1.94]; P =0.010). In participants with sarcopenia, intensive (versus standard) BP control nearly halved the risk of CVD events (adjusted hazard ratio, 0.57 [95% CI, 0.36–0.88]; P =0.012) without increasing serious adverse events. Similar risk reduction was seen for all-cause mortality in participants with sarcopenia (adjusted hazard ratio, 0.66 [95% CI, 0.41–1.08]; P =0.102), but the effect was only significant in those without chronic kidney disease. CONCLUSIONS: Older hypertensive adults with sarcopenia randomized to intensive BP control experienced a lower risk of CVD without increased adverse events compared with standard BP control. REGISTRATION: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT01206062.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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