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 |
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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. |
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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. The panel of 6 autoimmune biomarkers could be useful in setting up of noninvasive diagnostic test for detection of minimal-mild endometriosis.</description><identifier>EISSN: 1933-7205</identifier><identifier>DOI: 10.1177/1933719116657190</identifier><identifier>PMID: 27485360</identifier><language>eng</language><publisher>United States</publisher><subject>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</subject><ispartof>Reproductive sciences (Thousand Oaks, Calif.), 2017-03, Vol.24 (3), p.413-420</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27485360$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gajbhiye, Rahul</creatorcontrib><creatorcontrib>Bendigeri, Trupti</creatorcontrib><creatorcontrib>Ghuge, Arun</creatorcontrib><creatorcontrib>Bhusane, Kashmira</creatorcontrib><creatorcontrib>Begum, Shahina</creatorcontrib><creatorcontrib>Warty, Neeta</creatorcontrib><creatorcontrib>Sawant, Raj</creatorcontrib><creatorcontrib>Padte, Kedar</creatorcontrib><creatorcontrib>Humane, Anil</creatorcontrib><creatorcontrib>Dasmahapatra, Pramathes</creatorcontrib><creatorcontrib>Chauhan, Anahita</creatorcontrib><creatorcontrib>Khan, Shagufta</creatorcontrib><title>Panel of Autoimmune Markers for Noninvasive Diagnosis of Minimal-Mild Endometriosis</title><title>Reproductive sciences (Thousand Oaks, Calif.)</title><addtitle>Reprod Sci</addtitle><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.</description><subject>Adult</subject><subject>Biomarkers - blood</subject><subject>Blood Proteins</subject><subject>CA-125 Antigen - blood</subject><subject>CA-19-9 Antigen - blood</subject><subject>Cross-Sectional Studies</subject><subject>Endometriosis - blood</subject><subject>Endometriosis - diagnosis</subject><subject>Epitopes</subject><subject>Female</subject><subject>Humans</subject><subject>Membrane Proteins - blood</subject><subject>Phosphopyruvate Hydratase - blood</subject><subject>Protein-Serine-Threonine Kinases - blood</subject><subject>Qa-SNARE Proteins - blood</subject><subject>Sensitivity and Specificity</subject><subject>Tropomodulin - blood</subject><subject>Tropomyosin - blood</subject><issn>1933-7205</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kE1LAzEQhoMgtlbvniRHL6v5zu6x1PoBrQr2viSbiUR3NzXpFvz3brGeHph5eJl5Ebqi5JZSre9oxbmmFaVKyZHkBE0Po0IzIifoPOdPQqSoWHmGJkyLUnJFpuj9zfTQ4ujxfNjF0HVDD3ht0hekjH1M-CX2od-bHPaA74P56GMO-eCvQx860xbr0Dq87F3sYJfCYXuBTr1pM1weOUObh-Vm8VSsXh-fF_NVsZWKFAKgbKQCz5jzXnhlvaWVEZRa73kJ2kJjXak8OOqA-EZ6oQmzjQBOy6biM3TzF7tN8XuAvKu7kBto2_GjOOSalkxpwYRQo3p9VAfbgau3aTw9_dT_PfBfIuVfbg</recordid><startdate>201703</startdate><enddate>201703</enddate><creator>Gajbhiye, Rahul</creator><creator>Bendigeri, Trupti</creator><creator>Ghuge, Arun</creator><creator>Bhusane, Kashmira</creator><creator>Begum, Shahina</creator><creator>Warty, Neeta</creator><creator>Sawant, Raj</creator><creator>Padte, Kedar</creator><creator>Humane, Anil</creator><creator>Dasmahapatra, Pramathes</creator><creator>Chauhan, Anahita</creator><creator>Khan, Shagufta</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201703</creationdate><title>Panel of Autoimmune Markers for Noninvasive Diagnosis of Minimal-Mild Endometriosis</title><author>Gajbhiye, Rahul ; Bendigeri, Trupti ; Ghuge, Arun ; Bhusane, Kashmira ; Begum, Shahina ; Warty, Neeta ; Sawant, Raj ; Padte, Kedar ; Humane, Anil ; Dasmahapatra, Pramathes ; Chauhan, Anahita ; Khan, Shagufta</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p560-4ee8c56ef22dff4f6bfb19a411bff38e7becbd86fed1de0fc5f4702bc4e318c93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Biomarkers - blood</topic><topic>Blood Proteins</topic><topic>CA-125 Antigen - blood</topic><topic>CA-19-9 Antigen - blood</topic><topic>Cross-Sectional Studies</topic><topic>Endometriosis - blood</topic><topic>Endometriosis - diagnosis</topic><topic>Epitopes</topic><topic>Female</topic><topic>Humans</topic><topic>Membrane Proteins - blood</topic><topic>Phosphopyruvate Hydratase - blood</topic><topic>Protein-Serine-Threonine Kinases - blood</topic><topic>Qa-SNARE Proteins - blood</topic><topic>Sensitivity and Specificity</topic><topic>Tropomodulin - blood</topic><topic>Tropomyosin - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gajbhiye, Rahul</creatorcontrib><creatorcontrib>Bendigeri, Trupti</creatorcontrib><creatorcontrib>Ghuge, Arun</creatorcontrib><creatorcontrib>Bhusane, Kashmira</creatorcontrib><creatorcontrib>Begum, Shahina</creatorcontrib><creatorcontrib>Warty, Neeta</creatorcontrib><creatorcontrib>Sawant, Raj</creatorcontrib><creatorcontrib>Padte, Kedar</creatorcontrib><creatorcontrib>Humane, Anil</creatorcontrib><creatorcontrib>Dasmahapatra, Pramathes</creatorcontrib><creatorcontrib>Chauhan, Anahita</creatorcontrib><creatorcontrib>Khan, Shagufta</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Reproductive sciences (Thousand Oaks, Calif.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gajbhiye, Rahul</au><au>Bendigeri, Trupti</au><au>Ghuge, Arun</au><au>Bhusane, Kashmira</au><au>Begum, Shahina</au><au>Warty, Neeta</au><au>Sawant, Raj</au><au>Padte, Kedar</au><au>Humane, Anil</au><au>Dasmahapatra, Pramathes</au><au>Chauhan, Anahita</au><au>Khan, Shagufta</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Panel of Autoimmune Markers for Noninvasive Diagnosis of Minimal-Mild Endometriosis</atitle><jtitle>Reproductive sciences (Thousand Oaks, Calif.)</jtitle><addtitle>Reprod Sci</addtitle><date>2017-03</date><risdate>2017</risdate><volume>24</volume><issue>3</issue><spage>413</spage><epage>420</epage><pages>413-420</pages><eissn>1933-7205</eissn><abstract>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.</abstract><cop>United States</cop><pmid>27485360</pmid><doi>10.1177/1933719116657190</doi><tpages>8</tpages></addata></record> |
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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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