Osteoprotegrin (OPG) as a therapeutic target to combat age associated muscle loss.

Lead Research Organisation: Nottingham Trent University
Department Name: School of Science & Technology

Abstract

Background
Osteoprotegerin (OPG) is a circulating factor more commonly associated with the regulation of bone resorption. OPG acts as a decoy receptor to the ligand of the RANK molecule (RANKL). The proportion of RANKL to OPG must remain balanced to maintain bone turnover (Grimaud et al., 2003 Kong et al., 1999; Lacey et al., 1998); OPG is released when RANKL levels are elevated, ensuring bone resorption does not continually occur when RANK/RANKL are bound. OPG is also released from muscle in murine models of degenerative diseases. However, the specific pathway that causes these changes has not been identified (Shen et al., 2017; Dufresne et al., 2016a; Dufresne et al., 2016b; Dufresne et al., 2015).

The Impact of Osteoprotegerin in Ageing
After the age of 50 years old, muscle mass declines by 1-2% per year, with a total decline of ~25% between the ages of 50 and 75 years (Delmonico et al., 2009; Marcell, 2003; LaPier, 1997; Waters et al., 2008). The most recent definition of sarcopenia includes three key parameters; low levels of muscle strength, muscle quality/quantity and physical performance. Muscle quality and quantity are the primary indicators of probable sarcopenia (Cruz-Jentoft et al., 2018). Early diagnosis and treatment of sarcopenia is essential to mitigate the high personal, social and economic burdens that it becomes associated with when left untreated (Cruz-Jentoft et al., 2018).

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Studentship Projects

Project Reference Relationship Related To Start End Student Name
BB/T008369/1 01/10/2020 30/09/2028
2594446 Studentship BB/T008369/1 01/10/2021 30/09/2025