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Quality of Life in Sarcopenia and Frailty

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Abstract

The reduced muscle mass and impaired muscle performance that define sarcopenia in older individuals are associated with increased risk of physical limitation and a variety of chronic diseases. They may also contribute to clinical frailty. A gradual erosion of quality of life (QoL) has been evidenced in these individuals, although much of this research has been done using generic QoL instruments, particularly the SF-36, which may not be ideal in older populations with significant comorbidities. This review and report of an expert meeting presents the current definitions of these geriatric syndromes (sarcopenia and frailty). It then briefly summarizes QoL concepts and specificities in older populations and examines the relevant domains of QoL and what is known concerning QoL decline with these conditions. It calls for a clearer definition of the construct of disability, argues that a disease-specific QoL instrument for sarcopenia/frailty would be an asset for future research, and discusses whether there are available and validated components that could be used to this end and whether the psychometric properties of these instruments are sufficiently tested. It calls also for an approach using utility weighting to provide some cost estimates and suggests that a time trade-off study could be appropriate.

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Emanuele Marzetti, Riccardo Calvani, … on behalf of the SPRINTT Consortium

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Acknowledgement

The authors thank Jeremy Grierson, PhD, for his assistance in preparing the draft of the manuscript from the presentations and discussions of the working group participants.

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Correspondence to René Rizzoli.

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J.-Y. R. has received consulting fees or paid advisory boards for Servier, Novartis, Negma, Lilly, Wyeth, Amgen, Glaxo SmithKline, Roche, Merckle, Nycomed, NPS, Theramex, and UCB; lecture fees from Merck Sharp and Dohme, Lilly, Rottapharm, IBSA, Genevrier, Novartis, Servier, Roche, Glaxo SmithKline, Teijin, Teva, Ebewee Pharma, Zodiac, Analis, Theramex, Nycomed, Novo-Nordisk, and Nolver; Grant support from Bristol Myers Squibb, Merck Sharp and Dohme, Rottapharm, Teva, Lilly, Novartis, Roche, Glaxo SmithKline, Amgen, and Servier. A. C. owns stock in Pfizer. C. C. has a consultant/advisory role to Amgen, Glaxo SmithKline, ABBH, Merck Sharpe and Dohme, Eli Lilly, Pfizer, Novartis, Servier, Medtronic, and Roche. R. F. has had remuneration, has played a consultant/advisory role, and has stock ownership of or funding from Eli Lilly, Dairy Management, Abbott, Pronutrim, Bristol Myers Squibb, Cytokinetics, and Nestec. B. G. has received remuneration from Abbott Nutrition. J. K. has worked with and received funding from many companies and nongovernmental organizations dealing with skeletal metabolism including research funding from the Health Technology Assessment NHS R&D HTA Programme of the UK. B. M. is an employee of and owns stock in Eli Lilly. K. R. has a consultant/advisory role to Eli Lilly. Y. R. has received funding from Eli Lilly, Merck Sharpe and Dohme, Fabre, and Servier. A. S. has received remuneration from Abbott Nutrition, Servier, and Nestle and funding from Glaxo SmithKline. O. B. has received grant support from IBSA, Merck Sharp and Dohme, Nutraveris, Novartis, Pfizer, Rottapharm, Servier, and Theramex; lecture fees from IBSA, Rottapharm, Servier, and SMB; reimbursements for attending meetings from IBSA, Merck Sharp and Dohme, Novartis, Pfizer, Rottapharm, Servier, and Theramex. All other authors have stated that they have no conflict of interest.

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Rizzoli, R., Reginster, JY., Arnal, JF. et al. Quality of Life in Sarcopenia and Frailty. Calcif Tissue Int 93, 101–120 (2013). https://doi.org/10.1007/s00223-013-9758-y

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