Skeletal Muscle Apoptosis and Physical Performance; Oxidative RNA/DNA Damage and Repair in Aged Human Muscle

Sarcopenia Clinical Trial

Official title: Claude D. Pepper Older Americans Independence Center (OAIC); Skeletal Muscle Apoptosis and Physical Performance; Oxidative RNA/DNA Damage and Repair in Aged Human Muscle

Status Completed

Clinical Trial Summary

The age-related loss of muscle mass and strength, also termed sarcopenia, is a commonly recognized consequence of aging and has been associated with frailty, functional loss, hospitalization, and increased mortality among older people. Sarcopenia and its consequences have a considerable economic impact, since it has been estimated that the healthcare cost attributable to sarcopenia in the US in 2000 was $ 18.5 billions. Preclinical animal models strongly suggest that apoptosis, a programmed cell death, might play a prominent role in the age-related muscle wasting. In specific aim one, the investigators will assess the extent of muscle apoptosis in muscle biopsies obtained from the vastus lateralis muscle of young control subjects (ages 20-35) and high-performance and low-performance older subjects (age range 70-99 years). In specific aim 2, the investigators will investigate the role of Poly (ADP-ribose) polymerase 1 (PARP-1) and apoptosis-inducing factor (AIF) in the induction of skeletal muscle apoptosis. In specific aim 3, the investigators propose to investigate the contribution of the muscle energy deficit, due to the age-related mitochondrial dysfunction, in the development of muscle wasting. Finally, in specific aim 4, the investigators propose to reassess after four years physical performance, muscle mass and the extent of muscle apoptosis, in the high-performing participants, in order to correlate eventual decline in physical function, muscle mass and functional status, with changes in muscle apoptosis and in biochemical parameters in this very old population. Physical performance will be established according to the summary performance score obtained in the Short Form Physical Performance Battery (SPPB). In addition to the SPPB the investigators will also employ hand grip strength and knee extensor strength tests and the investigators will quantify muscle contractile area using 3D magnetic resonance imaging. Disability will be assessed using a self-report questionnaire. These studies will enhance our understanding of the biology and pathophysiology underlying the geriatric syndrome of sarcopenia and provide significant and novel insights that will enable us to identify new potential targets for interventions aimed at preventing and treating sarcopenia and functional impairment in older adults.

Clinical Trial Description

Specific Aims:

Specific Aim 1. To determine the extent of muscle apoptosis during aging in young healthy controls and in high-functioning and low-functioning older subjects. The investigators hypothesize that the observed level of muscle cell apoptosis is associated with physical disability. The investigators will recruit a cohort of ten young control subjects (age 20-35). The investigators will also recruit and stratify a cohort of forty elderly (age 70-99 years) into two distinct categories by set criteria based on their level of physical performance. Subjects with a summary performance score ≥ 11 at the Short Physical Performance Battery (SPPB) (66) will be considered high-functioning. Conversely, subjects with a summary performance score ≤ 7 will be considered low-functioning. In addition to the SPPB, the investigators will also perform the hand grip strength test and the isokinetic knee extensor test, and will implement 3D magnetic resonance imaging (MRI) to precisely quantify the quadriceps contractile area. The investigators will obtain a muscle biopsy for each subject to determine the severity of apoptosis using biochemical and histological analyses (see Methods). Disability will be assessed using a self-report questionnaire. Hence, the investigators will determine the extent muscle apoptosis and the investigators will be able to correlate this to the level of physical disability and muscle mass.

Specific Aim 2. To elucidate the role of Poly(ADP-ribose) polymerase 1 (PARP-1) and apoptosis-inducing factor (AIF) in the induction of apoptosis in human skeletal muscle. The investigators hypothesize that the observed cell loss due to apoptosis is mainly related to a caspase-independent mechanism. The investigators have recently shown that activation of mitochondrial caspase-independent pathway of apoptosis may play a more important role than the caspase-dependent pathway in contributing to nuclear cell death (67). Furthermore, the investigators hypothesize that the PARP-1/AIF pathway of apoptosis might be involved in the age-related muscle wasting process. The investigators will quantitatively assess PARP-1 and AIF and correlate these measures with the extent of muscle apoptosis.

Specific Aim 3. To assess the role of mitochondria dysfunction and energy failure in muscle apoptosis, sarcopenia, and disability. The investigators hypothesize that mitochondrial dysfunction and the resulting reduced production of adenosine triphosphate (ATP) is causally related to sarcopenia, possibly by triggering the apoptosis program. It has been estimated that the mean ATP production in the quadriceps muscle of old human subjects is approximately 50% of that of younger subjects (68), and it has been postulated that energy failure might trigger apoptosis (58). Consistently with these findings, the investigators have recently found that in rats' gastrocnemius muscle, ATP content and the rate of ATP production declined by ~50% with age (59). The investigators will quantitatively assess myocytes' ATP content along with key mitochondrial metabolic enzymes, namely citrate synthase, cytochrome-c-oxidase (COX), ATPase, and aconitase. The investigators will correlate these parameters with the level of apoptosis and with measures of physical performance, disability, and muscle mass.

Specific Aim 4. To correlate changes in physical function and muscle mass with muscle apoptosis and biochemical parameters at follow-up (longitudinal study). After 4 years subjects in the high-performance group will be reevaluated for muscle apoptosis rate, PARP-1 and AIF activity, and energy production. The investigators will correlate these parameters with measures of physical performance and muscle mass assessed by MRI, as well as with self-reported disability. Hence, the investigators will be able to directly correlate an eventual decline in physical performance, muscle mass and functional status at this very old age with changes in muscle apoptosis and in biochemical parameters.

Research Plan:

Using a cross-sectional design (age 20-35 and 70-99 years) the investigators will quantify the level of apoptosis in the vastus lateralis muscle in a healthy (see inclusion/exclusion criteria) population. Apoptosis of irreplaceable post-mitotic cells may be important mechanism in the development of sarcopenia and has not been investigated in healthy humans with age. A variety of chronic diseases have documented cases of apoptosis in human skeletal muscle; i.e., chronic pulmonary diseases (69,70) and patients with heart failure (69,71,72). However, it is essential to establish baseline levels of apoptosis in relatively healthy humans before proceeding to more complex conditions, such as disease conditions and frailty. In addition, the investigators will determine knee extensors strength, the myocyte volume, extra cellular space and the myonuclear domain (cross-sectional muscle area/nucleus) by quantifying the number of nuclei within a cross-sectional area of muscle. This specific aim will establish baseline levels of apoptosis and assess standard measures to assess sarcopenia.

Study design. To accomplish our aims, the investigators propose two separates, yet complementary studies

1. In order to gain insights into changes of the apoptosis potential with age and its contribution to muscle mass and strength loss, the investigators will quantify the level of apoptosis in the vastus lateralis muscle in young (age 20-35 years; N =20), old high-functioning, (age 70-99 years; N = 25), and old low-functioning (age 70-99 years; N = 20) subjects. Muscle biopsy and MRI scan to quantify quadriceps contractile area will be performed in the study participants. Muscle strength will be assessed by hand grip strength test and the isokinetic knee extensor test.

2. Preliminary data on the contribution of skeletal muscle apoptosis to sarcopenia, physical function loss in advanced age will be gathered by quantifying the extent of muscle apoptosis in the vastus lateralis muscle of old (age 70-99 years), high-functioning (N = 25) and low-functioning (N = 20) subjects, along with measures of muscle mass (MRI), muscle strength (hand grip and knee extension test), and overall physical performance (Short Physical Performance Battery, SPPB (67)). In addition, the investigators will collect preliminary data regarding the role mitochondrial-driven apoptosis in muscle wasting and functional loss at old age.

A brief physical exam will be administered to all study participants, and major biological signs (body weight, standing height, body temperature, blood pressure, and pulse) will be recorded. A basic questionnaire regarding participants' health history will also be administered

After four years the old participants will be reevaluated for physical performance, functional status muscle mass (MRI), muscle apoptosis, and biochemical parameters Disability will also be assessed using a self-report disability questionnaire. In order to gain information regarding changes in physical performance and functional status with time and to maximize retention, an annual visit employing SPPB, hand grip and knee extensor testing, will be scheduled for the old participants. ;

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

• Sarcopenia

• NCT number: NCT01644279
• Study type: Observational
• Source: University of Florida
• Status: Completed
• Phase: N/A
• Start date: March 2006
• Completion date: July 2016