Abstract: PO1757
In Vivo Muscle Mitochondrial Function Is Associated with Exercise Capacity and Efficiency in CKD
Session Information
- Health Maintenance, Nutrition, and Metabolism
November 04, 2021 | Location: On-Demand, Virtual Only
Abstract Time: 10:00 AM - 12:00 PM
Category: Health Maintenance, Nutrition, and Metabolism
- 1300 Health Maintenance, Nutrition, and Metabolism
Authors
- Vargas, Chenoa R., University of California Davis Department of Internal Medicine, Sacramento, California, United States
- Begue, Gwenaelle, California State University Sacramento, Sacramento, California, United States
- Rehman, Usman, University of California Davis, Davis, California, United States
- Ahmadi, Armin, University of California Davis, Davis, California, United States
- Kim, Tae Youn, University of California Davis Department of Internal Medicine, Sacramento, California, United States
- Jin, Seung Mi, University of California Davis, Davis, California, United States
- Gamboa, Jorge, Vanderbilt University, Nashville, Tennessee, United States
- Jue, Thomas, University of California Davis, Davis, California, United States
- Roshanravan, Baback, University of California Davis Department of Internal Medicine, Sacramento, California, United States
Background
CKD is associated with skeletal muscle dysfunction increasing risk for frailty. Muscle mitochondrial dysfunction may underly impaired physical performance. The associations of in vivo muscle mitochondrial function with exercise capacity and efficiency in CKD is unknown.
Methods
We recruited 8 diabetic and 6 non-diabetic patients with CKD. Leg muscle mitochondrial oxidative capacity was measured by exercise recovery kinetics of [PCr] using 31Phosphorus Magnetic Resonance Spectroscopy (31P MRS). Cardiorespiratory fitness (CRF, VO2peak), total work, and work efficiency (total work/VO2peak) were assessed by cycle ergometry. We tested associations of 31P MRS measures with endpoints using Pearson correlations.
Results
Participants had a mean age was 61±10yrs, eGFR of 35±12ml/min with 43% females. Faster PCr recovery rate correlated with VO2 peak (r=0.58, p=0.03), total work (r=0.70, p=0.03) and work efficiency (r=0.59, p=0.03) (Figure). Associations of PCr recovery with work and work efficiency were independent of age, sex, and weight (both p=0.03).
Conclusion
Muscle mitochondrial oxidative capacity is a major determinant of exercise efficiency and capacity. Therapeutics targeting muscle mitochondria function in CKD may improve physical performance and CRF.
Funding
- NIDDK Support