Panel of Autoimmune Markers for Noninvasive Diagnosis of Minimal-Mild Endometriosis

Endometriosis, characterized by the presence of endometrial-like tissue at extrauterine sites, is a common, chronic, estrogen-dependent, inflammatory condition associated with pelvic pain, subfertility, dysmenorrhea, and dyspareunia, affecting about 10% of reproductive-age women in any population. T...

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Veröffentlicht in:Reproductive sciences (Thousand Oaks, Calif.) Calif.), 2017-03, Vol.24 (3), p.413-420
Hauptverfasser: Gajbhiye, Rahul, Bendigeri, Trupti, Ghuge, Arun, Bhusane, Kashmira, Begum, Shahina, Warty, Neeta, Sawant, Raj, Padte, Kedar, Humane, Anil, Dasmahapatra, Pramathes, Chauhan, Anahita, Khan, Shagufta
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container_end_page 420
container_issue 3
container_start_page 413
container_title Reproductive sciences (Thousand Oaks, Calif.)
container_volume 24
creator Gajbhiye, Rahul
Bendigeri, Trupti
Ghuge, Arun
Bhusane, Kashmira
Begum, Shahina
Warty, Neeta
Sawant, Raj
Padte, Kedar
Humane, Anil
Dasmahapatra, Pramathes
Chauhan, Anahita
Khan, Shagufta
description Endometriosis, characterized by the presence of endometrial-like tissue at extrauterine sites, is a common, chronic, estrogen-dependent, inflammatory condition associated with pelvic pain, subfertility, dysmenorrhea, and dyspareunia, affecting about 10% of reproductive-age women in any population. The diagnosis of endometriosis is usually delayed on an average by 8 to 11 years leading to significant consequences in terms of disease progression. The current study was aimed to validate enzyme-linked immunosorbent assay based on the epitopes of stomatin-like protein 2, tropomodulin 3 (TMOD3), and tropomyosin 3 (TPM3) for diagnosis of minimal-mild endometriosis (revised American Fertility Society Classification (rAFS) stage I-II) and to compare the performance with the reported markers: cancer antigen (CA) 125, CA19-9, α-enolase, Serine/threonine-protein kinase (PDIK1L), and syntaxin 5. This was a cross-sectional, multicenter study conducted during the year 2012 to 2015. Women with minimal-mild endometriosis (rAFS stage I-II [n = 133]) and healthy controls (n = 104) were screened for 11 novel autoimmune markers and reported markers α-enolase, PDIK1L, syntaxin 5, CA-125, and CA19-9. The sensitivity and diagnostic accuracy of serum antibodies against all the 11 epitopes were higher than that of CA-125, CA19-9, α-enolase, PDIK1L, and syntaxin 5 for diagnosis of rAFS stage I to II endometriosis. The sensitivity of 6 biomarkers (anti-TMOD3b-autoAb, anti-TMOD3c-autoAb, anti-TMOD3d-autoAb, anti-TPM3a-autoAb, anti-TPM3c-autoAb, and anti-TPM3d-autoAb) was higher at the specificity of ≥80% for diagnosis of rAFS stage I to II endometriosis as well as ultrasound-negative endometriosis. Further, logistic regression models of this panel of biomarkers showed increase in sensitivity, specificity, and diagnostic accuracy than individual biomarkers. The panel of 6 autoimmune biomarkers could be useful in setting up of noninvasive diagnostic test for detection of minimal-mild endometriosis.
doi_str_mv 10.1177/1933719116657190
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The diagnosis of endometriosis is usually delayed on an average by 8 to 11 years leading to significant consequences in terms of disease progression. The current study was aimed to validate enzyme-linked immunosorbent assay based on the epitopes of stomatin-like protein 2, tropomodulin 3 (TMOD3), and tropomyosin 3 (TPM3) for diagnosis of minimal-mild endometriosis (revised American Fertility Society Classification (rAFS) stage I-II) and to compare the performance with the reported markers: cancer antigen (CA) 125, CA19-9, α-enolase, Serine/threonine-protein kinase (PDIK1L), and syntaxin 5. This was a cross-sectional, multicenter study conducted during the year 2012 to 2015. Women with minimal-mild endometriosis (rAFS stage I-II [n = 133]) and healthy controls (n = 104) were screened for 11 novel autoimmune markers and reported markers α-enolase, PDIK1L, syntaxin 5, CA-125, and CA19-9. The sensitivity and diagnostic accuracy of serum antibodies against all the 11 epitopes were higher than that of CA-125, CA19-9, α-enolase, PDIK1L, and syntaxin 5 for diagnosis of rAFS stage I to II endometriosis. The sensitivity of 6 biomarkers (anti-TMOD3b-autoAb, anti-TMOD3c-autoAb, anti-TMOD3d-autoAb, anti-TPM3a-autoAb, anti-TPM3c-autoAb, and anti-TPM3d-autoAb) was higher at the specificity of ≥80% for diagnosis of rAFS stage I to II endometriosis as well as ultrasound-negative endometriosis. Further, logistic regression models of this panel of biomarkers showed increase in sensitivity, specificity, and diagnostic accuracy than individual biomarkers. 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subjects Adult
Biomarkers - blood
Blood Proteins
CA-125 Antigen - blood
CA-19-9 Antigen - blood
Cross-Sectional Studies
Endometriosis - blood
Endometriosis - diagnosis
Epitopes
Female
Humans
Membrane Proteins - blood
Phosphopyruvate Hydratase - blood
Protein-Serine-Threonine Kinases - blood
Qa-SNARE Proteins - blood
Sensitivity and Specificity
Tropomodulin - blood
Tropomyosin - blood
title Panel of Autoimmune Markers for Noninvasive Diagnosis of Minimal-Mild Endometriosis
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