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MRI-Based Morphometric Comparison of Lower Leg Muscles and Tendons in Individuals With Medial Tibial Stress Syndrome. | LitMetric

MRI-Based Morphometric Comparison of Lower Leg Muscles and Tendons in Individuals With Medial Tibial Stress Syndrome.

Biomed Res Int

Laboratory of Molecular Analysis, Graduate Program in Rehabilitation Science, Faculdade de Ciências da Saúde e Tecnologias, Universidade de Brasília, Brasília, Distrito Federal, Brazil.

Published: December 2024

AI Article Synopsis

Article Abstract

Runners frequently suffer from medial tibial stress syndrome (MTSS), often linked to excessive eccentric muscle contractions causing periosteal traction by the muscles in the deep posterior compartment. However, the effects of MTSS on these muscles and tendons remain underexplored. This study is aimed at investigating changes in muscle and tendon volumes in this compartment, as well as cross-sectional area measurements, using magnetic resonance imaging. Thirty individuals were divided into two groups: MTSS ( = 18; mean age 30.3 ± 12.4) and control ( = 12; age 35.2 ± 9.2). The anterior, deep posterior, superficial posterior, and lateral compartment muscles, along with their respective tendons, were compared between groups, and possible sex differences were also evaluated. The deep posterior compartment showed a significant volume difference of 0.41 cm/kg/ in the MTSS group ( = 0.034), primarily due to the flexor hallucis longus (FHL), which had a 0.55 cm/kg/ greater normalized volume (17.12% greater mean muscle volume) compared to controls ( = 0.023; Cohen = 0.895). No association between sex and MTSS was found ( = 0.752). In conclusion, the FHL muscle exhibited increased normalized volume in the MTSS group compared to controls, with no sex-related differences in MTSS. Clinicians should consider the assessment of FHL muscle volume in routine evaluations of patients presenting with symptoms suggestive of MTSS.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11666316PMC
http://dx.doi.org/10.1155/bmri/8827692DOI Listing

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