C. Falconer et al., PARAURETHRAL CONNECTIVE-TISSUE IN STRESS-INCONTINENT WOMEN AFTER MENOPAUSE, Acta obstetricia et gynecologica Scandinavica, 77(1), 1998, pp. 95-100
Objective. To study whether stress urinary incontinence after menopaus
e is correlated to changes in the paraurethral connective tissue ultra
structure and metabolism. Methods. Transvaginal biopsies were obtained
from the paraurethral connective tissue in stress urinary incontinent
women after menopause with and without estrogen replacement therapy,
and from comparable controls. All the stress-incontinent women underwe
nt urodynamic investigation. In the specimens, collagen concentration,
measured as hydroxyproline, and the degree of extractability by pepsi
n digestion, were quantified. Proteoglycan composition and concentrati
on were analyzed using Alcian Blue precipitation, followed by electrop
horetic separation and quantification. Using Northern blots, mRNA leve
ls for the collagens I and III, the small proteoglycans decorin and bi
glycan, and the large proteoglycan versican, were quantified. Collagen
structure was examined with transmission electron microscopy, and the
diameters of collagen fibrils were analyzed with an interactive image
analysis system (IBAS, Zeiss/Kontron). Results. No significant differ
ence in paraurethral connective tissue biochemistry or ultrastructure
was registered between women with stress incontinence and controls. Es
trogen replacement therapy resulted in a lower collagen concentration
both between the controls (p=0.02) and between the incontinent women (
0.02). In the women with stress incontinence also the extractability b
y pepsin digestion was higher in the group with estrogen treatment (p=
0.004), indicating a decrease in cross-linking. The proteoglycan/colla
gen ratio was higher in the control group with estrogen treatment comp
ared to untreated (p=0.02), but no difference was found between estrog
en treated and untreated incontinent women. The median collagen fibril
diameter was 15% larger in the incontinent group of women without est
rogen therapy compared to the control group and 5% larger when compari
ng the incontinent group on estrogen replacement therapy to the corres
ponding control group. Conclusion. The extracellular matrix of paraure
thral connective tissue in stress urinary incontinent women after meno
pause reacted differently to estrogen replacement therapy compared to
continent controls. In contrast to incontinent women of fertile age no
major changes in collagen metabolism were found in stress urinary inc
ontinent women after menopause.