Title of article :
Role of fascial collagen in stress urinary incontinence, ,
Author/Authors :
Tomasz Rechberger، نويسنده , , Krzysztof Postawski، نويسنده , , Jerzy A. Jakowicki، نويسنده , , Zeenat Gunja-Smith، نويسنده , , J.Frederick Woessner Jr.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 1998
Pages :
4
From page :
1511
To page :
1514
Abstract :
Objectives: Our purpose was to determine whether collagen of the pubocervical fasciae that support the urethrovesical junction undergoes alterations that might contribute to incontinence. Study Design: Pubocervical fascia was collected as a residual tissue in 82 patients, aged 25 to 73 years, during surgical treatment of cystocele (n = 26, no incontinence) or of stress urinary incontinence (n = 56). Measurements were made of collagen content, solubility, and cross-linking and of collagenase activity. Results: Patients treated for incontinence had the same mean age and parity as the control cystocele group. There was a highly significant (20%, P< .0005) decrease in collagen content in fascial tissue from incontinent women. There was no difference in the percentage of acid-soluble (0.7%) and pepsin-soluble (17%) collagen in the 2 groups of patients; this agrees with the lack of significant change in the degree of collagen cross-linking by pyridinoline. Collagenase activity was significant in fascia but did not change in incontinence. Incontinent women had an increased body mass index. Conclusions: The pubocervical fasciae of incontinent women show a diminished content of collagen, but this is not accompanied by changes in collagen solubility or cross-linking or in collagenase activity. This decrease in collagen may contribute to the weakening of support of the bladder neck. (Am J Obstet Gynecol 1998;179:1511-4.)
Keywords :
Stress urinary incontinence , Pyridinoline , collagen , collagenase
Journal title :
American Journal of Obstetrics and Gynecology
Serial Year :
1998
Journal title :
American Journal of Obstetrics and Gynecology
Record number :
643070
Link To Document :
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