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

cardiovascular diseases cystatin C hypertension sarcopenia walking speed

Journal

Hypertension (Dallas, Tex. : 1979)
ISSN: 1524-4563
Titre abrégé: Hypertension
Pays: United States
ID NLM: 7906255

Informations de publication

Date de publication:
17 Jun 2024
Historique:
medline: 17 6 2024
pubmed: 17 6 2024
entrez: 17 6 2024
Statut: aheadofprint

Résumé

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) BP targets in older hypertensive adults with sarcopenia compared with nonsarcopenic counterparts in the SPRINT (Systolic Blood Pressure Intervention Trial). 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. 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]; 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. URL: https://www.clinicaltrials.gov; Unique identifier: NCT01206062.

Sections du résumé

BACKGROUND UNASSIGNED
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) BP targets in older hypertensive adults with sarcopenia compared with nonsarcopenic counterparts in the SPRINT (Systolic Blood Pressure Intervention Trial).
METHODS UNASSIGNED
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 UNASSIGNED
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];
CONCLUSIONS UNASSIGNED
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 UNASSIGNED
URL: https://www.clinicaltrials.gov; Unique identifier: NCT01206062.

Identifiants

pubmed: 38881460
doi: 10.1161/HYPERTENSIONAHA.124.23011
doi:

Banques de données

ClinicalTrials.gov
['NCT01206062']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Saeid Mirzai (S)

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

Ian Persits (I)

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

Richard Kazibwe (R)

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

Mohanad Gabani (M)

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

Austin Seals (A)

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

Matthew J Singleton (MJ)

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

Rishi Rikhi (R)

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

Parag Chevli (P)

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

Salvatore Carbone (S)

Pauley Heart Center, Division of Cardiology, Department of Internal Medicine, Virginia Commonwealth University, Richmond. (S.C.).
Department of Kinesiology & Health Sciences, College of Humanities & Sciences, Virginia Commonwealth University, Richmond. (S.C.).

W H Wilson Tang (WHW)

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

Joseph Yeboah (J)

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

Jeff D Williamson (JD)

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

Dalane W Kitzman (DW)

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

David Herrington (D)

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

Michael D Shapiro (MD)

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

Classifications MeSH