The Role of Galectins in the Non-invasive Diagnosis of Endometriosis

The Role of Galectin-1,3,9 in the the Non-invasive Diagnosis of Endometriosis

Endometriosis is one of the most common infertility-related gynecologic disorder that affect approximately 10-15% of women in reproductive age. The main symptoms are chronic pelvic pain, infertility, dysmenorrhea and dyspareunia. There exists an average diagnostic delay of 7 year but data widely varies between different countries. The current "gold standard" in the diagnosis of endometriosis remains a laparoscopy. Since laparoscopy is an invasive surgical procedure with its potential risk, the development of a non-invasive laboratory test would be of great benefit in the early, clinical management of this diseaseIn the past few years, lectins have become the focus of reproductive immunology, inflammation and autoimmunity. Galectins (Gal) are beta-galactoside binding lectins that play a key role in the regulation of the immune system, cell growth, adhesion, apoptosis, and angiogenesis. Until now 13 different types of galectins have been found in humans, among them Gal-1-4, 7-9 and 12 were detected in the normal endometrium. So far only Gal-1 and Gal-3 have been studied in relation to endometriosis. In a recent pilot study, the investigators have shown that Gal-9 levels are significantly elevated in the serum of endometriosis patients compared to healthy controls. Gal-9 had a high sensitivity (94%) and specificity (93,75%), indicating better diagnostic potential than that of other endometriosis biomarkers and of surgery as the current gold standard.

Study Overview

• Status: Not yet recruiting
• Conditions: Endometriosis; Endometriosis Ovary; Endometriosis Rectovaginal Septum

Detailed Description

Endometriosis is one of the most common infertility-related gynecologic disorder that affect approximately 10-15% of women in reproductive age. The main symptoms are chronic pelvic pain, infertility, dysmenorrhea and dyspareunia. The etiology and pathogenesis of endometriosis has been widely investigated over the past 30 years. Although there are several concepts trying to explain its development, but none of them can be applied for all types of the disease.

The peak incidence of the diagnosis of endometriosis lies between the ages of 25 to 34, although symptoms mostly develop much earlier. There exists an average diagnostic delay of 7 year but data widely varies between different countries: in the is UK 7.9 years, in the US 11.7 years, in Germany and Austria 7 years, in Spain 8 years, in Norway 6.7 years, in Ireland and Belgium 5 years and in Hungary 3.9 years. Such a diagnostic delay is multifactorial, but most importantly due to the lack of non-invasive diagnosis.

The current "gold standard" in the diagnosis of endometriosis remains a laparoscopy with a sensitivity of 79% and a specificity of 94%. Since laparoscopy is an invasive surgical procedure with its potential risk, the development of a non-invasive laboratory test would be of great benefit in the early, clinical management of this disease. Such a biomarker has the enormous potential to improve quality of life, reduce the risks to the patient and the enormous costs to society related to endometriosis.

Until now, several molecules involved in the pathogenesis of endometriosis were investigated as a potential biomarker, however the majority of them have proven inadequate for the diagnosis. In the past few years, lectins have become the focus of reproductive immunology, inflammation and autoimmunity. Galectins (Gal) are beta-galactoside binding lectins that play a key role in the regulation of the immune system, cell growth, adhesion, apoptosis, and angiogenesis. Until now 13 different types of galectins have been found in humans, among them Gal-1-4, 7-9 and 12 were detected in the normal endometrium. So far only Gal-1 and Gal-3 have been studied in relation to endometriosis. It was reported that Gal-1 had a cycle-dependent expression in normal endometrial stromal cells, and its production was significantly elevated in the early pregnancy decidua. In relation to endometriosis, Gal-1 was found to be more abundantly expressed in ectopic endometriotic lesions when compared with the eutopic tissues. Furthermore, the eutopic endometrium of the affected patients showed higher Gal-1 expression than its normal counterparts. In addition to this, similar to Gal-1, Gal-3 was overexpressed in various forms of endometriosis as well as in the eutopic endometrium of diseased women.

The investigators have previously shown that Gal-9 mRNA was markedly overexpressed in the eutopic endometrium of patients with endometriosis in comparison with healthy controls. In addition, the investigators results showed that besides the eutopic endometrium, Gal-9 was also expressed in ectopic implants regardless of the localization of the lesions. The investigators have determined that Gal-9 levels are significantly elevated in the serum of endometriosis patients compared to healthy controls. Gal-9 has a high sensitivity (94%) and specificity (93,75%), indicating better diagnostic potential than that of other endometriosis biomarkers. The optimal cutoff point estimated from the Youden's index was 132 pg/mL, with a sensitivity of 94% and specificity of 93.75%. Using this threshold, the positive predictive value was 97.92% and the negative predictive value was 83.33%, with a prevalence of 75.76%. The diagnostic accuracy of this test was 93.94%, indicating better diagnostic potential than that other already published serum biomarkers.

Based on this previous results, the investigators suggest that Gal-9 is produced by ectopic endometriotic implants, the investigators would like to determine the serum Gal-9 levels one day before and after the surgery and at least 1-6 months later. The investigators aim is to examine the serum Gal-1 and Gal-3 levels in endometriosis patients.

• Study Type: Observational
• Enrollment (Anticipated): 1000

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 20 years to 48 years (Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Female

• Sampling Method: Non-Probability Sample

Study Population

in reproductive age laporoscopically proved endometriosis

Description

Inclusion Criteria:

Histologically proved endometriosis

Exclusion Criteria:

Previous or current hormone therapy

Study Plan

How is the study designed?

Design Details

• Observational Models: Case-Control
• Time Perspectives: Prospective

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort
disease and control

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Development of new non-invasive biomarker for endometriosis	24 months

Collaborators and Investigators

• Sponsor: Semmelweis University
• Collaborators: University of Pecs

Publications and helpful links

General Publications

• Brubel R, Bokor A, Pohl A, Schilli GK, Szereday L, Bacher-Szamuel R, Rigo J Jr, Polgar B. Serum galectin-9 as a noninvasive biomarker for the detection of endometriosis and pelvic pain or infertility-related gynecologic disorders. Fertil Steril. 2017 Dec;108(6):1016-1025.e2. doi: 10.1016/j.fertnstert.2017.09.008.

Study record dates

Study Major Dates

• Study Start (Anticipated): September 1, 2021
• Primary Completion (Anticipated): September 1, 2022
• Study Completion (Anticipated): September 1, 2025

Study Registration Dates

• First Submitted: May 20, 2020
• First Submitted That Met QC Criteria: May 20, 2020
• First Posted (Actual): May 26, 2020

Study Record Updates

• Last Update Posted (Actual): April 15, 2021
• Last Update Submitted That Met QC Criteria: April 12, 2021
• Last Verified: May 1, 2020

More Information

Terms related to this study

• Keywords: Biomarker; Non-invasive diagnosis; Endometriosis; Galectins
• Additional Relevant MeSH Terms: Endometriosis
• Other Study ID Numbers: ENDOGAL

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No