Associations of Sarcopenia and Body Composition Measures With Mortality After Transcatheter Aortic Valve Replacement.

adiposity frailty mortality sarcopenia utility

Journal

Circulation. Cardiovascular interventions
ISSN: 1941-7632
Titre abrégé: Circ Cardiovasc Interv
Pays: United States
ID NLM: 101499602

Informations de publication

Date de publication:
18 Jan 2024
Historique:
medline: 18 1 2024
pubmed: 18 1 2024
entrez: 18 1 2024
Statut: aheadofprint

Résumé

Frailty associates with worse outcomes after transcatheter aortic valve replacement (TAVR). Sarcopenia underlies frailty, but the association between a comprehensive assessment of sarcopenia-muscle mass, strength, and performance-and outcomes after TAVR has not been examined. From a multicenter prospective registry of patients with symptomatic severe aortic stenosis undergoing TAVR, 445 who had a preprocedure computed tomography and clinical assessment of frailty were included. Cross-sectional muscle (psoas and paraspinal) areas were measured on computed tomography and indexed to height. Gait speed and handgrip strength were obtained, and patients were dichotomized into fast versus slow; strong versus weak; and normal versus low muscle mass. As measures of body composition, cross-sectional fat (subcutaneous and visceral) was measured and indexed to height. The frequency of patients who were slow, weak, and had low muscle mass was 56%, 59%, and 42%, respectively. Among the 3 components of sarcopenia, only slower gait speed (muscle performance) was independently associated with increased post-TAVR mortality (adjusted hazard ratio, 1.12 per 0.1 m/s decrease [95% CI, 1.04-1.21]; Among patients with symptomatic severe aortic stenosis and comprehensive sarcopenia and body composition phenotyping, gait speed was the only sarcopenia measure associated with post-TAVR mortality. Lower visceral fat was also associated with increased risk pointing to an obesity paradox also observed in other patient populations. These findings reinforce the clinical utility of gait speed as a measure of risk and a potential target for adjunctive interventions alongside TAVR to optimize clinical outcomes.

Sections du résumé

BACKGROUND UNASSIGNED
Frailty associates with worse outcomes after transcatheter aortic valve replacement (TAVR). Sarcopenia underlies frailty, but the association between a comprehensive assessment of sarcopenia-muscle mass, strength, and performance-and outcomes after TAVR has not been examined.
METHODS UNASSIGNED
From a multicenter prospective registry of patients with symptomatic severe aortic stenosis undergoing TAVR, 445 who had a preprocedure computed tomography and clinical assessment of frailty were included. Cross-sectional muscle (psoas and paraspinal) areas were measured on computed tomography and indexed to height. Gait speed and handgrip strength were obtained, and patients were dichotomized into fast versus slow; strong versus weak; and normal versus low muscle mass. As measures of body composition, cross-sectional fat (subcutaneous and visceral) was measured and indexed to height.
RESULTS UNASSIGNED
The frequency of patients who were slow, weak, and had low muscle mass was 56%, 59%, and 42%, respectively. Among the 3 components of sarcopenia, only slower gait speed (muscle performance) was independently associated with increased post-TAVR mortality (adjusted hazard ratio, 1.12 per 0.1 m/s decrease [95% CI, 1.04-1.21];
CONCLUSIONS UNASSIGNED
Among patients with symptomatic severe aortic stenosis and comprehensive sarcopenia and body composition phenotyping, gait speed was the only sarcopenia measure associated with post-TAVR mortality. Lower visceral fat was also associated with increased risk pointing to an obesity paradox also observed in other patient populations. These findings reinforce the clinical utility of gait speed as a measure of risk and a potential target for adjunctive interventions alongside TAVR to optimize clinical outcomes.

Identifiants

pubmed: 38235547
doi: 10.1161/CIRCINTERVENTIONS.123.013298
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e013298

Auteurs

Elliot J Stein (EJ)

Department of Medicine, Vanderbilt University Medical Center, Nashville, TN. (E.J.S., C.N.).

Colin Neill (C)

Department of Medicine, Vanderbilt University Medical Center, Nashville, TN. (E.J.S., C.N.).

Sangeeta Nair (S)

Department of Radiology, Vanderbilt University Medical Center, Nashville, TN. (S.N., J.G.T., J.J.C.).

J Greg Terry (JG)

Department of Radiology, Vanderbilt University Medical Center, Nashville, TN. (S.N., J.G.T., J.J.C.).

J Jeffrey Carr (JJ)

Department of Radiology, Vanderbilt University Medical Center, Nashville, TN. (S.N., J.G.T., J.J.C.).

William F Fearon (WF)

Department of Medicine, Division of Cardiology, Stanford Medical Center, Palo Alto, CA (W.F.F., J.B.K.).

Sammy Elmariah (S)

Department of Medicine, Division of Cardiology, University of California San Francisco (S.E.).

Juyong B Kim (JB)

Department of Medicine, Division of Cardiology, Stanford Medical Center, Palo Alto, CA (W.F.F., J.B.K.).

Samir Kapadia (S)

Department of Medicine, Division of Cardiology, Cleveland Clinic Foundation, OH (S.K.).

Dharam J Kumbhani (DJ)

Department of Medicine, Division of Cardiology, University of Texas Southwestern Medical Center, Dallas (D.J.K., A.A.B.).

Linda Gillam (L)

Department of Cardiovascular Medicine, Morristown Medical Center, NJ (L.G.).

Brian Whisenant (B)

Department of Medicine, Division of Cardiology, Intermountain Heart Institute, Murray, UT (B.W.).

Nishath Quader (N)

Department of Medicine, Division of Cardiology, Barnes-Jewish Hospital, St. Louis, MO (N.Q., A.Z., A.V.).

Alan Zajarias (A)

Department of Medicine, Division of Cardiology, Barnes-Jewish Hospital, St. Louis, MO (N.Q., A.Z., A.V.).

Frederick G Welt (FG)

Department of Medicine, Division of Cardiology, University of Utah Hospital, Salt Lake City (F.G.W.).

Anthony A Bavry (AA)

Department of Medicine, Division of Cardiology, University of Texas Southwestern Medical Center, Dallas (D.J.K., A.A.B.).

Megan Coylewright (M)

Department of Cardiovascular Medicine, The Erlanger Heart and Lung Institute, Chattanooga, TN (M.C.).

Robert Piana (R)

Department of Medicine, Division of Cardiology, Vanderbilt University Medical Center, Nashville, TN. (R.P., R.R.M., N.J., B.R.L.).

Ravinder R Mallugari (RR)

Department of Medicine, Division of Cardiology, Vanderbilt University Medical Center, Nashville, TN. (R.P., R.R.M., N.J., B.R.L.).

Anna Vatterott (A)

Department of Medicine, Division of Cardiology, Barnes-Jewish Hospital, St. Louis, MO (N.Q., A.Z., A.V.).

Natalie Jackson (N)

Department of Medicine, Division of Cardiology, Vanderbilt University Medical Center, Nashville, TN. (R.P., R.R.M., N.J., B.R.L.).
Structural Heart and Valve Center, Vanderbilt University Medical Center, Nashville, TN. (N.J., S.H., B.R.L.).

Shi Huang (S)

Structural Heart and Valve Center, Vanderbilt University Medical Center, Nashville, TN. (N.J., S.H., B.R.L.).
Department of Biostatistics, Vanderbilt University School of Medicine, Nashville, TN (S.H.).

Brian R Lindman (BR)

Department of Medicine, Division of Cardiology, Vanderbilt University Medical Center, Nashville, TN. (R.P., R.R.M., N.J., B.R.L.).
Structural Heart and Valve Center, Vanderbilt University Medical Center, Nashville, TN. (N.J., S.H., B.R.L.).

Classifications MeSH