Abstract
The content and quality of type I collagen in the parametrium of women with and without uterine prolapse was evaluated. Forty-four consecutive patients were selected and divided into two groups: A, 21 women without uterine prolapse, and B, 23 with uterine prolapse. Patients in group A had uterine leiomyoma and were submitted to abdominal hysterectomy; in those from group B, vaginal hysterectomy was performed for correction of the uterine prolapse. During surgery, fragments of the parametrium were removed and processed for immunohistochemical analysis using polyclonal antibodies for type I collagen . A system of computerized digital imaging analysis was used for the quantification of collagen fibers. There was no difference between collagen content in patients either with or without prolapse, nor between pre- and postmenopausal women with prolapse. A modification of the quality of the collagen fiber was observed, it being longer and more compact in the group without uterine prolapse. In contrast, in the group with prolapse, the fibers were shorter and thinner and areas with large spaces between fibers were found at several points of the parametrium. The conclusion was that patients with uterine prolapse have the same type I collagen content as those without, but the quality of the fiber is modified. The hormonal status also did not affect collagen content.
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Carlson KJ, Nichols DH, Schiff I (1993) Indications for hysterectomy. N Engl J Med 328:856–860
Mant J, Painter R, Vessey M (1997) Epidemiology of genital prolapse: observations from the Oxford Family Planning Association Study. Br J Obstet Gynaecol 104:579–585
Bump RC (1992) Racial comparisons and contrasts in urinary incontinence and genital prolapse. Neurourol Urodyn 11:357–358
Norton PA (1993) Pelvic floor disorders: the role of fascia and ligaments. Clin Obstet Gynecol 36:926–938
Handa VL, Harris TA, Ostergard DR (1996) Protecting the pelvic floor: obstetric management to prevent incontinence and pelvic organ prolapse. Obstet Gynecol 88:470–478
DeLancey JO (1993) Anatomy and biomechanics of genital prolapse. Clin Obstet Gynecol 6:897–909
Nimni ME (1983) Collagen: structure, function and metabolism in normal and fibrotic tissues. Semin Arthritis Rheum 13:1–86
Stumpf WE, Sar M, Joshi SG (1974) Estrogen target cells in the skin. Experientia 30:196–199
Schuster S, Black MM, McVitie E (1975) The influence of age and sex on skin thickness, skin collagen and density. Br J Dermatol 93:639–643
Brincat M, Versi E, Moniz CJ, Magos A, DeTreford J, Studd JWW (1987) Skin collagen in postmenopausal women receiving different regimens of estrogen therapy. Obstet Gynecol 70:123–127
Versi E, Cardozo L, Brincat M, Cooper D, Montgomery J, Studd J (1988) Correlation of urethral physiology and skin collagen in postmenopausal women. Br J Obstet Gynaecol 95:147–152
Smith P, Heimer G, Norgen A, Ulmstem U (1990) Steroid hormone receptors in pelvic muscles and ligaments in women. Gynecol Obstet Invest 30:27–30
Phillips JI, Davies J (1980) The comparative morphology of the bladder and urethra in young and old female C57BL/Icffa1 mice. Exp Gerontol 15:551–562
Eika B, Salling LN, Christensen LL, Andersen A, Lauberg S, Danielsen CC (1990) Long-term observation of the detrusor smooth muscle in rats. Its relationship to ovariectomy and estrogen treatment. Urol Res 18:439–442.
Persson K, Svane D, Glavind B, Uvelius B, Forman A, Andesson KE (1996) Effects of ovariectomy on mechanical properties and collagen content in rabbit lower urinary tract smooth muscle. Scand J Urol Nephrol 30:7–14
Sartori MGF, Girão MJBC, Simões MJ, Sartori JP, Baracat EC, Rodrigues de Lima G (2001) Quantitative evaluation of collagen and muscle fibers in the lower urinary tract of castrated and under-hormone replacement female rats. Clin Exp Obstet Gynecol 28:92–96
Falconer C, Ekman-Ordeberg G, Ulmsten U, Westergren-Thorsson G, Barchan K, Masmström A (1996) Changes in paraurethral connective tissue at menopause are counteracted by estrogen. Maturitas 24:197–204
Sayer TR, Dixon JS, Hosker GL, Warrell DW (1990) A study of paraurethral connective tissue in women with stress incontinence of urine. Neurourol Urodyn 9:319–452
Ulmsten U, Ekman G, Giertz G, Malmström A (1987) Different biochemical composition of connective tissue in continent and stress incontinent women. Acta Obstet Gynecol Scand 66:455–457
Bergman A, Elia G, Cheung D, Perelman N, Nimni ME (1994) Biochemical composition of collagen in continent and stress urinary incontinent women. Gynecol Obstet Invest 37:48–51
Takano CC, Girão MJBC, Sartori MGF, Castro RA, Arruda RM, Simões MJ, Baracat EC, Rodrigues de Lima G (2002) Analysis of collagen in parametrium and vaginal apex of women with and without uterine prolapse. Int Urogynecol J Pelvic Floor Dysfunct 13:342–345
Bump RC, Mattiasson A, Bo K et al. (1996) The standardization of terminology of female pelvic organ prolapse and pelvic floor dysfunction. Am J Obstet Gynecol 175:10–17
Mäkinen J, Kähaäri V, Söderströn K, Vuorio E, Hirvönen T (1987) Collagen synthesis in the vaginal connective tissue of patients with and without uterine prolapse. Eur J Obstet Gynecol Reprod Biol 24:319–325
Jackson SR, Avery NC, Tarlton JF, Eckford SD, Abrams P, Bailey AJ (1996) Changes in metabolism of collagen in genitourinary prolapse. Lancet 347:1658–1661
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Editorial Comment: It is widely accepted that the etiology of pelvic organ prolapse is multifactorial, and that multiparity and menopausal status are two of the most important factors that influence the development of pelvic support defects. As the authors note, however, it is currently impossible to accurately predict which patients will ultimately suffer from prolapse. The authors of this paper report on the collagen content and quality of parametrial tissue from women with and without uterine prolapse. Although they found no difference in quantity of collagen between groups (prolapse vs. no prolapse, menopausal vs. premenopausal), they did demonstrate significant changes in the quality of the collagen structure, with shorter and thinner fibers evident in those women with uterine prolapse. Although it would be premature to assume a causal relationship between the collagen changes and the development of prolapse, this finding is intriguing in that analysis of collagen may one day assist physicians in counseling patients regarding such events as delivery mode and prognosis for recurrent prolapse after reconstructive pelvic surgery.
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Barbiero, E.C., Sartori, M.G.F., Girão, M.J.B.C. et al. Analysis of type I collagen in the parametrium of women with and without uterine prolapse, according to hormonal status. Int Urogynecol J 14, 331–334 (2003). https://doi.org/10.1007/s00192-003-1076-x
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DOI: https://doi.org/10.1007/s00192-003-1076-x