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Serum sestrins: potential predictive molecule in human sarcopenia
Sreerag P Rajan1, Masroor Anwar1, Bhrigu Jain1
1Department of Geriatric Medicine, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, 110029, India.
Aging Clinical and Experimental Research
|June 29, 2020
Summary
Sarcopenia, a muscle disease linked to aging, can be diagnosed early. Lower levels of serum sestrin 2 protein indicate sarcopenia in older adults, offering a potential new biomarker for early detection.
Area of Science:
- Gerontology
- Muscle physiology
- Biochemistry
Background:
- Sarcopenia, a decline in skeletal muscle mass and function, is a key factor in aging, frailty, and disability.
- Autophagy, crucial for cellular health, appears impaired in aging skeletal muscle, contributing to sarcopenia.
- Sestrin (Sesn) proteins are vital for inducing autophagy under cellular stress.
Purpose of the Study:
- To identify sarcopenia in older adults using Asian Working Group guidelines (AWGS).
- To establish clinically relevant diagnostic cut-off levels for sarcopenia.
- To investigate the association between sarcopenia and serum levels of antioxidant proteins, Sestrins (Sesns).
Main Methods:
- Recruited 102 older adults from a Geriatric medicine outpatient department.
- Measured serum Sesn levels using Surface Plasmon Resonance (SPR) and validated with immunoblotting.
- Diagnosed 50 participants as sarcopenic based on AWGS criteria.
Main Results:
- Serum Sesn 1 and Sesn 2 levels were significantly lower in sarcopenic individuals compared to non-sarcopenic individuals.
- Receiver Operating Characteristic (ROC) analysis identified Sesn 2 at 10.104 ng/µL as a diagnostic cut-off with 92% sensitivity and 84% specificity.
- Reduced Sesn levels in sarcopenics remained statistically significant even after adjusting for confounding factors.
Conclusions:
- Serum Sesn 2 levels correlate positively with sarcopenia characteristics.
- This study is the first to report serum sestrin concentrations in older adults with sarcopenia.
- Serum sestrin levels may serve as a potential biomarker for early sarcopenia diagnosis.

