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Related Experiment Video

Updated: Nov 4, 2025

The Creation of a Rat Model for Osteosarcopenia via Ovariectomy
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Association Between Interleukin-12 and Sarcopenia.

Yuan-Yuei Chen1,2,3, Tung-Wei Kao3, Yi-Lin Chiu4

  • 1Department of Pathology, Tri-Service General Hospital, School of Medicine, National Defense Medical Center, Taipei, Taiwan, Republic of China.

Journal of Inflammation Research
|May 27, 2021
PubMed
Summary
This summary is machine-generated.

Interleukin-12 (IL-12) may indicate early sarcopenia in older adults. Lower IL-12 levels correlate with muscle weakness and slower gait, suggesting its potential as a diagnostic marker for age-related muscle loss.

Keywords:
IL-12TGF-βgendermacrophagesarcopenia

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Area of Science:

  • Gerontology
  • Immunology
  • Muscle Physiology

Background:

  • Cytokines secreted by macrophages are implicated in skeletal muscle aging.
  • Research is exploring the link between these cytokines and sarcopenia progression in the elderly.

Purpose of the Study:

  • To investigate the impact of specific cytokines on sarcopenia development in an elderly population.
  • To determine if cytokines can serve as early diagnostic indicators for sarcopenia.

Main Methods:

  • Retrospective analysis of 120 elderly adults (≥65 years) from 2015-2019.
  • Sarcopenia assessment based on European Working Group criteria (2019).
  • Utilized Gene Expression Omnibus (GEO) data for macrophages and cytokines, assessing muscle strength, mass, gait speed, TGF-β, and IL-12.

Main Results:

  • Low muscle strength and gait speed were negatively associated with Interleukin-12 (IL-12).
  • Higher sarcopenia severity correlated with lower IL-12 and increased Tumor Growth Factor-beta (TGF-β).
  • Decreased IL-12 and increased TGF-β were linked to diagnosed sarcopenia; higher IL-12 reduced sarcopenia occurrence (OR 0.36).

Conclusions:

  • Interleukin-12 (IL-12) shows potential as an early diagnostic biomarker for sarcopenia in the elderly.
  • Cytokine profiles, particularly IL-12 and TGF-β, are associated with age-related muscle decline.