Abstract

The aim of the present study was to investigate the ultrastructure and content of collagen in uterosacral ligaments and paraurethral tissues in patients with pelvic organ prolapse (POP) and stress urinary incontinence (SUI), analyzing the association between POP and collagen dysfunction. The study comprised three groups: Control, POP and POP with SUI (n=30 per group). Histological characteristics of collagen fiber were observed and the diameters were measured using light and electron microscopy to determine the Type I and Type III collagen content of the main ligament in the urethral specimens. In the POP and POP with SUI groups, observations included diffuse atrophy of smooth muscles, active fibroblast metabolism, swollen mitochondria and visible Golgi apparatus. The collagen fibril diameters in the cardinal ligaments, uterosacral ligaments and paraurethral tissues were significantly greater in the POP and POP with SUI groups compared with those in the control group (P<0.01). In addition, the expression levels of Type I and Type III collagen were significantly lower in the POP and POP with SUI groups when compared with the control group (P<0.01). In the POP with SUI group, pelvic tissues were frail, resulting in smooth muscle bundles comminuting and arranging in a disorganized pattern. Fibroblast and myoblast metabolisms were active and new microvascular cells were weak. However, the collagen fibril diameter increased. Thus, collagen and ultrastructural changes in the pelvic floor may be associated with the development of POP and SUI.

Highlights

  • That the morbidity of POP among females aged >60 years was 25% [3]

  • We hypothesized that changes in the ultrastructure and content of collagen are associated with the angiogenesis of POP

  • Fiber diameter and collagen ultrastructure were investigated in the cardinal ligament, uterosacral ligament and paraurethral tissues of patients with POP

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Summary

Introduction

That the morbidity of POP among females aged >60 years was 25% [3]. Dysfunctions in extracellular matrix (ECM) content form the molecular and biochemical basis for POP. Previous studies have shown that POP and other collagen-associated disorders, including varicose veins and joint hypermobility, may have a common etiology and originate at the molecular level of collagen [4,5,6]. The aim of the present study was to analyze the association between POP and collagen disorders. We hypothesized that changes in the ultrastructure and content of collagen are associated with the angiogenesis of POP. Fiber diameter and collagen ultrastructure were investigated in the cardinal ligament, uterosacral ligament and paraurethral tissues of patients with POP. The results were compared with those of the control group in order to identify the changes in collagen metabolism in POP and to determine the association between POP and collagen changes

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