Revisão Revisado por pares

Prediction of term and preterm parturition and treatment monitoring by measurement of cervical cross‐linked collagen using light‐induced fluorescence

2005; Informa; Volume: 84; Issue: 6 Linguagem: Inglês

10.1111/j.0001-6349.2005.00806.x

ISSN

1600-0412

Autores

Holger Maul, George R. Saade, Robert E. Garfield,

Tópico(s)

Pelvic floor disorders treatments

Resumo

Acta Obstetricia et Gynecologica ScandinavicaVolume 84, Issue 6 p. 534-536 Free Access Prediction of term and preterm parturition and treatment monitoring by measurement of cervical cross-linked collagen using light-induced fluorescence Holger Maul, Holger Maul From the Division of Reproductive Sciences, The University of Texas Medical Branch Galveston, TX, USA, and Department of Obstetrics and Gynecology, University of Heidelberg, Heidelberg, GermanySearch for more papers by this authorGeorge Saade, George Saade From the Division of Reproductive Sciences, The University of Texas Medical Branch Galveston, TX, USA, andSearch for more papers by this authorRobert E. Garfield, Corresponding Author Robert E. Garfield From the Division of Reproductive Sciences, The University of Texas Medical Branch Galveston, TX, USA, and *Robert E. Garfield Division of Reproductive Sciences Department of Obstetrics and Gynecology The University of Texas Medical Branch Galveston, TX 77555-1062 USA e-mail: rgarfiel@utmb.eduSearch for more papers by this author Holger Maul, Holger Maul From the Division of Reproductive Sciences, The University of Texas Medical Branch Galveston, TX, USA, and Department of Obstetrics and Gynecology, University of Heidelberg, Heidelberg, GermanySearch for more papers by this authorGeorge Saade, George Saade From the Division of Reproductive Sciences, The University of Texas Medical Branch Galveston, TX, USA, andSearch for more papers by this authorRobert E. Garfield, Corresponding Author Robert E. Garfield From the Division of Reproductive Sciences, The University of Texas Medical Branch Galveston, TX, USA, and *Robert E. Garfield Division of Reproductive Sciences Department of Obstetrics and Gynecology The University of Texas Medical Branch Galveston, TX 77555-1062 USA e-mail: rgarfiel@utmb.eduSearch for more papers by this author First published: 18 May 2005 https://doi.org/10.1111/j.0001-6349.2005.00806.xCitations: 15AboutSectionsPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat One of the keys to treating preterm labor is the early detection of changes indicating the onset of parturition. Recently, we have developed a non-invasive method for the objective evaluation of the status of the cervix, where changes in collagen content of the cervix can be detected using an optical system and light-induced autofluorescence (LIF). This system measures the collagen fluorescence in the cervix as an indirect estimate of collagen concentration. Studies of pregnant women during the past few years support the use of this technique. Cervical function and assessment The cervix is composed of smooth muscle (ca. 10%) and a large component of connective tissue (90%) consisting of collagen, elastin, and macromolecular components, which make up the extracellular matrix1-3). Many biochemical and functional changes occur in cervical connective tissue at the end of pregnancy4-7). This process, termed cervical ripening, results in softening, dilatation, and effacement of the cervix. Ripening is required for appropriate progress of labor and delivery of the fetus. Fluorescence spectroscopy of collagen Fluorescence spectroscopy is a widely utilized research tool in the biosciences, primarily because of the amount of information that it can reveal in terms of molecular and physical states8-14). We have used this methodology recently to evaluate the cervix during gestation. The collascope and measurement of cervical ripening Collagen gives characteristic fluorescence whose maximum is around 390 nm. The intrinsic fluorophor is believed to be pyridinoline, which is considered one of the major crosslinks within the primary structure of collagen fibrils (10, 15, 16). In our initial investigations, measurements were obtained from the serosal surface of the medium band of the cervix of rats in vivo. The results showed a decrease in fluorescence intensity decrease in the later gestational days and at parturition corresponding to the decrease in collagen. We also found a drop in collagen fluorescence intensity in rats treated with the anti-progesterone compound RU 38.486 and which delivered prematurely. Further studies of rats With the collascope, we were able to measure the fluorescence signal from the cervix in anaesthetized rats (17). The advantage to this technique is that one can follow cervical changes longitudinally in the same animal under a variety of conditions and treatments (Fig. 1). Figure 1Open in figure viewerPowerPoint Overview of rat cervical collagen fluorescence intensity changes: average values of ratio of collagen peak to reference peak obtained in non-pregnant, various times during pregnancy, during delivery and at various times postpartum in rats. Note the progressive decline in fluorescence with lowest values obtained on day 22 (DL, during labor; NL, non-labor). In the postpartum period, the fluorescence gradually increased from the low value observed during delivery (Fig. 1). These results demonstrate the progressive decline in fluorescence during pregnancy to reach low values during delivery; these findings correlate well with cervical resistance as measured by the slope of stress–strain curves and a decline in cervical collagen content in electron micrographs of ripened versus unripe cervix. In addition, we examined rats at various times prior to and during preterm labor induced with the anti-progesterone onapristone. This study showed that ripening occurred with anti-progesterone treatment and that R5020, a progestin agonist, prevented ripening and preterm birth. We conclude from these studies that the collascope can be used as a non-invasive tool to measure changes in cervical collagen content of the cervix under a variety of conditions. Results of these measurements correspond with known physiological changes in the cervix during pregnancy. Studies of humans We have also initiated human studies with the Collascope (17). Non-pregnant, pregnant, and postpartum human volunteers were recruited for the study. The first step was to establish a longitudinal distribution profile according to the weeks of gestation and postpartum. The cervical external os was gently wiped with rayon-tipped proctoscopic swabs prior to measurements being made. The measuring site was selected at the 12 o'clock position. Fluorescence decreased progressively during the final 15 weeks of pregnancy (Fig. 2). So far, several hundred patients (including nonpregnant patients) have been recruited. Several of the subjects have been measured two or three times during their pregnancy and postpartum. The results show a gradual decrease of the fluorescence as pregnancy approaches term followed by a slow recovery during the postpartum period17-19). Recent studies demonstrated that the collascope could be used for the monitoring of the effect of induction agents on cervical ripening (20). Figure 2Open in figure viewerPowerPoint Cervical fluorescence – pregnant women, during pregnancy, and postpartum: average and single patient data on fluorescent spectra obtained from 40 non-pregnant and pregnant patients at various times of gestation and postpartum. In view of the important role of collagen fibers and their turnover in the process of cervical function during pregnancy, the light-induced autofluorescence of cervical collagen could be a useful tool for evaluating cervical status and monitoring treatment strategies. References 1 Danforth DN. The morphology of the human cervix. Clin Obstet Gynecol 1983; 26: 7– 13.CrossrefCASPubMedGoogle Scholar 2 Woessner JF, Brewer TH. Formation and breakdown of collagen and elastin in the human uterus during pregnancy and postpartum involution. Biochem 1963; J89: 75– 82. CrossrefGoogle Scholar 3 Leppert PC, Keller S, Cerreta J, Mandl I. Conclusive evidence of elastin in the uterine cervix. Am J Obstet Gynecol 1982; 142: 179– 82.CrossrefCASPubMedWeb of Science®Google Scholar 4 Danforth DN, Vies A, Breen M, Weinstein HG, Buckingham JC, Manalo P. The effect of pregnancy and labor on the human cervix. changes in collagen, glycoprotein and glycosaminoglycans. Am J Obstet Gynecol 1986; 120: 641– 51. CrossrefPubMedWeb of Science®Google Scholar 5 Liggins GC. Cervical ripening as an inflammatory reaction. In: DA Ellwood, ABM Anderson, eds. Cervix in Pregnancy and Labour: Clinical and Biochemical Investigation. New York: Churchill Livingstone, 1981: 1– 9. Google Scholar 6 Leppert PC. Anatomy and physiology of cervical ripening. Clin Obstet Gynecol, 1995; 38: 267– 79.CrossrefCASPubMedWeb of Science®Google Scholar 7 Ekman G, Almström H, Granström L, Malmström A, Norman M, Woessner JF Jr. Connective Tissue in Human Cervical Ripening. In: PC Leppert, JF Woessner, eds. The Extracellular Matrix of the Uterus, Cervix and Fetal Membranes: Synthesis Degradation and Hormonal Regulation. New York: Perinatology Press, 1991: 87– 96. Web of Science®Google Scholar 8 Undenfriend S. Fluorescence Assay in Biology and Medicine, Vol. I New York: Academic Press, 1962. Google Scholar 9 Cantor CR, Schimmel PR. Biophysical Chemistry. New York: W.H. Freeman, 1980. Web of Science®Google Scholar 10 Lakowicz JR. Principles of Fluorescence Spectroscopy, 3rd Print. New York: Plenum Press, 1986. Google Scholar 11 Ramanujam N, Mitchell MF, Mahadevan A, Thomsen S, Silva E, Richards-Kortum R. Fluorescence spectroscopy: a diagnostic tool for cervical intrepithelial neoplasia (CIN). Gynecol Oncol 1994; 52: 31– 8.DOI: 10.1006/gyno.1994.1007CrossrefCASPubMedWeb of Science®Google Scholar 12 Lam S, Hung JYC, Kennedy SM, Leriche JC, Vedal S, Nelems B et al. Detection of dysplasia and carcinoma in situ by ratio fluorometry. Am Rev Respir Dis 1992; 146: 1458– 61.CrossrefCASPubMedWeb of Science®Google Scholar 13 Cothren RM, Richards-Kortum RR, Sivak MV, Fitzmaurice M, Rava RP, Boyce GA et al. Gastrointestinal tissue diagnosis by laser induced fluorescence spectroscopy at endoscopy. Gastrontest Endosc 1990; 36: 105– 11. CrossrefPubMedWeb of Science®Google Scholar 14 Schomaker KT, Frisoli JK, Compton CC, Flotte TJ, Richter JM, Nishioka NS et al. Ultraviolet laser-induced fluorescence of colonic tissue: Basic biology and diagnostic potential. Lasers Surg Med 1992; 12: 63– 78.Wiley Online LibraryPubMedWeb of Science®Google Scholar 15 Glassman W, Byam-Smith M, Garfield RE. Changes in rat cervical collagen during gestation and following antiprogesterone treatment as measured in vivo with light induced autofluorescence. Am J Obstet Gynecol 1995; 173: 1550– 6.DOI: 10.1016/0002-9378(95)90648-7CrossrefCASPubMedWeb of Science®Google Scholar 16 Fujimoto D. Isolation and characterization of a fluorescent material in bovine achilles tendon collagen. Biochem Biophysics Res Commun 1977; 76: 1124– 9.DOI: 10.1016/0006-291X(77)90972-XCrossrefCASPubMedWeb of Science®Google Scholar 17 Glassman WS, Liao Q-P, Shi S-Q, Goodrum L, Olson G, Martin E et al. Fluorescence Probe for Cervical Examination during various Reproductive States. Proc SPIE – Adv Fluorescence Sensing Technol III 1997; 2980: 286– 92. CrossrefWeb of Science®Google Scholar 18 Olson G, Goodrum L, Martin E, Saade G, Garfield RE. Noninvasive measurement of cervical collagen content in women approaching delivery. Am J Obstet Gynecol 1998; 178: S91. Google Scholar 19 Maul H, Olson G, Fittkow CT, Saade GR, Garfield RE. Cervical light-induced fluorescence in humans decreases throughout gestation and before delivery: Preliminary observations. Am J Obstet Gynecol 2003; 188: 537– 41.CrossrefPubMedWeb of Science®Google Scholar 20 Fittkow CT, Maul H, Olson G, Martin E, MacKay L, Saade G et al. Light-induced fluorescence of the human cervix decreases after prostaglandin application for induction of labor at term. Eur J Obstet Gynecol Reprod Biol (in press). Google Scholar Citing Literature Volume84, Issue6June 2005Pages 534-536 FiguresReferencesRelatedInformation

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