# Higher Prevalence of Sarcopenia in Knee Osteoarthritis and Its Association with Femoral Intercondylar Cartilage Thickness and Functional Outcomes

## TL;DR

People with knee osteoarthritis are more likely to have sarcopenia, and thicker cartilage in the knee is linked to better muscle function and less pain.

## Contribution

This study identifies a higher prevalence of sarcopenia in knee osteoarthritis and links femoral cartilage thickness to muscle and functional outcomes.

## Key findings

- Sarcopenia prevalence was 41.2% in knee osteoarthritis patients versus 26.3% in controls.
- Thicker femoral intercondylar cartilage correlates with better muscle mass, strength, and mobility in knee osteoarthritis patients.
- Greater cartilage thickness is associated with lower pain and improved functional scores in knee osteoarthritis.

## Abstract

Knee osteoarthritis (KOA) and sarcopenia are prevalent age-related disorders that share common pathophysiological mechanisms such as aging, chronic inflammation, and physical inactivity. Their coexistence may aggravate functional decline and disability. This cross-sectional study aimed to compare the prevalence of sarcopenia between individuals with KOA and matched controls and to explore the relationship between femoral intercondylar cartilage (FIC) thickness and muscle-related parameters. A total of 228 participants (114 KOA, 114 controls) matched by age, sex, and body mass index were enrolled. Assessments included appendicular skeletal muscle mass index (ASMMI), handgrip strength, walking speed, and physical activity. In KOA patients, ultrasound measurements of FIC and quadriceps thickness and the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) were additionally obtained. Sarcopenia prevalence was higher in the KOA group than in controls (41.2% vs. 26.3%, p = 0.017). Greater FIC thickness was associated with higher ASMMI, stronger handgrip strength, faster walking speed, and lower WOMAC pain and total scores. These findings indicate that FIC thickness may serve as a potential structural biomarker linking cartilage integrity with muscle function in KOA.