Differences in cellular and microstructural properties of the semitendinosus muscle tendon between young and adult patients.

Abstract

BACKGROUND\nPoor outcomes associated with anterior cruciate ligament reconstruction in paediatric patients are a major concern. The tendon structure and its cellular characteristics are key factors that affect the mechanical properties of tendons. This study aimed to evaluate the effects of growth on the cellular and microstructural properties of the tendon of the semitendinosus muscle in humans.\n\n\nMETHODS\nSemitendinosus muscle tendon samples from 76 patients who underwent ligament reconstruction were examined and divided into three groups: immature (10.8\xa0±\xa02.7 years old), young (16.5\xa0±\xa01.8 years old), and adult (35.2\xa0±\xa08.6 years old), based on age and the state of the epiphyseal plate in the distal femur. The number of tendon cells per unit area was assessed, and the major-to-minor-length ratio of the tendon cell nuclei was calculated to evaluate the shape of the nuclei using haematoxylin and eosin staining. The collagen fibril diameter and distribution were determined using electron microscopy.\n\n\nRESULTS\nThe major-to-minor-length ratio of the tendon cell nuclei significantly increased with age (p-value; immature vs. young: 0.018, young vs adult: 0.001, immature vs adult: 0.001). The shape of the tendon cell nuclei was rounder in the immature group and more elongated in the adult group. A significant decrease in the number of tendon cells was observed with age (immature: 565\xa0±\xa0134/mm2, young: 356\xa0±\xa0105/mm2, adult: 272\xa0±\xa081/mm2; p-value: immature vs young: 0.001, young vs adult: 0.012, immature vs adult: 0.001). The mean fibril diameter in the immature group was significantly smaller (p-value: immature vs young: 0.018, young vs adult: 0.001, immature vs adult: 0.001). The distribution of the collagen fibrils changed from right skewed in the immature group to flat in the adult group.\n\n\nCONCLUSIONS\nThe characteristics of the tendon cells and the microstructure of collagen in muscle tendons significantly changed with age.