Abstract

Endometriosis is defined as the presence of endometrial-like tissue outside the uterine cavity and is associated with chronic intra-pelvic inflammation. Its symptoms, which are often severe, have a negative impact on a woman’s quality of life. They include chronic pelvic pain and infertility. It is estimated that about 10% women in their reproductive ages are affected by the disease globally. Currently, diagnostic methods are laparoscopy with histological confirmation and non-invasive such as ultrasound and the quantification of CA-125 biomarker in serum. CA-125 is known to be elevated in endometriosis, however it does not have sufficient diagnostic power as a single biomarker of endometriosis. Due to this, there is a need to determine other antigens that would act as potential biomarkers for endometriosis. It has been observed that Transgelin and T-Plastin are upregulated in endometriosis lesions and in secretory phase of endometrium respectively. There is insufficient data available showing the concentration of T-plastin in serum or plasma in the development of endometriosis. The main objective of this study was to identify whether T-plastin, Transgelin and CA-125 are potential biomarkers in early diagnosis of endometriosis using animal model for endometriosis. The baboon model represents clinically relevant research models for endometriosis. This study compared the levels of T-plastin, Transgelin and CA-125 in the peripheral blood and peritoneal fluid of baboons before and after induction of endometriosis. In this prospective, case-control study, ten female baboons ( Papio anubis , 9-15 kg each) of proven fertility that have had at least one menstruation during captivity, were induced by intra-pelvic injection of menstrual endometrium on day 1 or 2 of menstruation followed by staging laparoscopy. Serum and peritoneal fluid samples were collected prior to induction to serve as controls.T-Plastin, Transgelin and CA-125 were measured using commercially available ELISA Kits. Data was analyzed using non-parametric test and level of significance at p<0.005. T-Plastin and Transgelin had insignificant p values in both peripheral blood and peritoneal fluid while CA-125 showed p=0.0003 in peripheral blood and p=0.0279 in peritoneal fluid. Diagnostic performance of individual biomarkers was determined by Receiver Operating Characteristic (ROC) with the Area under the curve (AUC) equal to 0.5 showing T-Plastin and Transgelin in both serum and peritoneal fluid unreliable for use as biomarkers in endometriosis. CA-125 levels in peritoneal fluid had an AUC of 0.7900 indicating it can be used as potential biomarkers for endometriosis. Key words: Endometriosis, biomarkers, T-Plastin, Transgelin, CA-125, ELISA, Olive Baboons. DOI : 10.7176/ALST/75-06 Publication date :August 31 st 2019

Highlights

  • Endometriosis is a common benign, chronic and multifactorial complex gynecological disease which is estrogen dependent (Sinaii et al, 2008; D'Hooghe, 1997)

  • The study sought to determine the T-plastin, Transgelin and CA125 antigen levels in peripheral blood and peritoneal fluid using ten baboons induced with endometriosis and evaluate their variability as potential biomarkers for the detection of the onset of endometriosis

  • A total of ten baboons induced with endometriosis were evaluated for T plastin, Transgelin and CA-125 concentrations in plasma

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Summary

Introduction

Endometriosis is a common benign, chronic and multifactorial complex gynecological disease which is estrogen dependent (Sinaii et al, 2008; D'Hooghe, 1997). It is characterized by chronic pelvic pain, dysmenorrhea and infertility and defined by presence of endometrial stroma and glands outside the uterine cavity (Nisoile & Donnez, 1997; Farquhar, 2001). A simple, lowcost, non-invasive, fast, accurate and reliable diagnostic test will solve the delay and give light to treatment at early stages of the disease. The study sought to determine the T-plastin, Transgelin and CA125 antigen levels in peripheral blood and peritoneal fluid using ten baboons induced with endometriosis and evaluate their variability as potential biomarkers for the detection of the onset of endometriosis

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