Soluble tumor necrosis factor-alpha receptors in the serum of endometriosis patients
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This study measured serum levels of soluble tumor necrosis factor-alpha receptors in endometriosis patients to assess their potential role in the disease.
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Abstract
INTRODUCTION: We examine serum levels sTNFR-I and sTNFR-II in endometriosis patients, and their role as biomarkers of endometriosis.
MATERIAL AND METHODS: Women were diagnosed with endometriosis during laparoscopy to investigate pelvic pain and/or infertility (N=62). Control group included women with pelvic pain and/or infertility, whose laparoscopy showed no abnormalities (N=55). Serum concentrations of sTNFR-I and sTNFR-II were measured using Bioplex Protein Array system. Non-parametric statistics were used.
RESULTS: Endometriosis patients had significantly higher levels of sTNFR-I than controls (257.46pg/ml, IQR=2.37-1048.92 versus 130.39pg/ml, IQR=0.99-361.1 respectively, P value=0.01). For TNFR-II, difference between women with (232pg/ml, IQR=0.0-624.4), and women without (132.93pg/ml, IQR=0.0-312.81) endometriosis was not significant (P value=0.05). Early stage endometriosis patients had significantly higher level of sTNFR-I (559.13, IQR=1.82-1289.86) and sTNFR-II (248.8, IQR=0-644.65) than control women (P value is 0.01 for TNFR-I and 0.04 for TNFR-II). Levels of sTNFR-I and sTNFR-II were comparable for advanced endometriosis and controls, and between early and advanced endometriosis. As a biomarker for all- stage endometriosis, sTNFR-I produces AUC of 0.62, sensitivity of 61%, and specificity of 47.3%, at a cutoff of 81.87pg/ml. For early stage disease, sTNFR-I yields AUC of 0.68, sensitivity of 60.7%, specificity of 75%, at a cutoff of 351.22pg/ml.
CONCLUSION: sTNFR-I is significantly higher in serum of endometriosis patients than controls. As an endometriosis biomarker, sTNFR-I achieves better performance for early stage disease.
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Cited by (18)
- Molecular Insights Into Endometriosis for Early Detection and Therapeutic Targets 2026
- An overview of endometriosis and molecular target-based therapeutic approach 2025
- Neuroimmunology of Endometriosis-Associated Pain and Its Psychological Aspects 2024
- Immune сheckpoints in the context of external genital endometriosis 2024
- Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family 2023
- The effect of calcineurin signaling inhibition on the treatment of endometriosis in rats 2022
- Accuracy and utility of blood and urine biomarkers for the noninvasive diagnosis of endometriosis: a systematic literature review and meta-analysis 2022
- Novel diagnostic options for endometriosis - Based on the glycome and microbiome 2021
- Role of genes involved in the regulation of apoptosis in the pathogenesis of genital endometriosis. A literature review 2021
- Association between tumor necrosis factor-α gene-1031T/C promoter polymorphism and endometriosis in a European population 2019
- FEATURES OF SYSTEM IMMUNITY IN WOMEN WITH ENDOMETRIOSIS AND GENITAL INFECTION 2019
- Reduced inflammatory state promotes reinnervation of endometriotic-like lesions in TNFRp55 deficient mice 2019
- Noninvasive diagnosis of endometriosis: Review of current peripheral blood and endometrial biomarkers 2018
- Tumor Necrosis Factor and its Soluble Receptors as Potential Diagnostic Markers of Endometriosis 2017
- Stem Cell Markers Describe a Transition From Somatic to Pluripotent Cell States in a Rat Model of Endometriosis 2017
- TNFRp55 deficiency promotes the development of ectopic endometriotic-like lesions in mice 2017
- Decoy receptor 3 promotes cell adhesion and enhances endometriosis development 2017
- Comments on "rhTNFR:Fc Suppresses the Development of Endometriosis in a Mouse Model by Downregulating Cell Proliferation and Invasiveness" 2016
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