Urinary tissue factor (uTF), tissue factor pathway inhibitor (TFPI) and plasmin as novel biomarkers in early diagnosis of lupus nephritis
Systemic lupus erythematosus (SLE) is an autoimmune inflammatory disease, with multi systematic affection. Lupus nephritis (LN) is the most frequent cause of renal damage in SLE patients with variable presentations that may progress to end stage renal failure. Coagulation disorders are frequently re...
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Veröffentlicht in: | The Egyptian journal of immunology 2024-01, Vol.31 (1), p.143-154 |
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creator | Mustafa, Mohammed H Tony, Effat A E Elgendi, Salwa S Abdelkader, Alaa S Salah, Ayat A Madkour, Rasha A |
description | Systemic lupus erythematosus (SLE) is an autoimmune inflammatory disease, with multi systematic affection. Lupus nephritis (LN) is the most frequent cause of renal damage in SLE patients with variable presentations that may progress to end stage renal failure. Coagulation disorders are frequently reported in SLE and LN with higher mortality rates. Renal biopsy is an invasive process, and the existing indicators for LN diagnosis and activity are unreliable. New urinary biomarkers with significant validity, safety, and accuracy are the current focus of most studies. Our study sought to assess the value of urinary tissue factor (uTF), tissue factor pathway inhibitor (TFPI), and plasmin as biomarkers for the early identification and detection of LN and its activity. This was a cross-sectional study, included 100 subjects (80 SLE patients, and 20 healthy controls), they were recruited from the Internal Medicine department, Rheumatology and Nephrology units and outpatient's clinics at Assiut University hospital between the period of 2020 and 2022. All patients underwent full history taking, clinical evaluation, and activity scoring calculation and laboratory investigations. The results showed that the best diagnostic accuracy of LN was observed with TFPI (90% accuracy, sensitivity 80% and specificity 95% with p 193.2 ng/ml), followed by uTF (75.4% overall accuracy at cut off point of >12.6 ng/ml, sensitivity 90% and specificity 68% with p < 0.001) and plasmin (70.3% accuracy at cut off point of >30.5 ng/ml, sensitivity 55% and specificity 78% with p < 0.001). Urinary TFPI was the best predictor of LN occurrence with odd ratio of 4.34, (p < 0.001). In conclusion urinary TFPI could be used as a diagnostic marker for LN with high accuracy and an early predictor of LN. |
doi_str_mv | 10.55133/eji.310115 |
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Lupus nephritis (LN) is the most frequent cause of renal damage in SLE patients with variable presentations that may progress to end stage renal failure. Coagulation disorders are frequently reported in SLE and LN with higher mortality rates. Renal biopsy is an invasive process, and the existing indicators for LN diagnosis and activity are unreliable. New urinary biomarkers with significant validity, safety, and accuracy are the current focus of most studies. Our study sought to assess the value of urinary tissue factor (uTF), tissue factor pathway inhibitor (TFPI), and plasmin as biomarkers for the early identification and detection of LN and its activity. This was a cross-sectional study, included 100 subjects (80 SLE patients, and 20 healthy controls), they were recruited from the Internal Medicine department, Rheumatology and Nephrology units and outpatient's clinics at Assiut University hospital between the period of 2020 and 2022. All patients underwent full history taking, clinical evaluation, and activity scoring calculation and laboratory investigations. The results showed that the best diagnostic accuracy of LN was observed with TFPI (90% accuracy, sensitivity 80% and specificity 95% with p <0.001 at cutoff point of >193.2 ng/ml), followed by uTF (75.4% overall accuracy at cut off point of >12.6 ng/ml, sensitivity 90% and specificity 68% with p < 0.001) and plasmin (70.3% accuracy at cut off point of >30.5 ng/ml, sensitivity 55% and specificity 78% with p < 0.001). Urinary TFPI was the best predictor of LN occurrence with odd ratio of 4.34, (p < 0.001). In conclusion urinary TFPI could be used as a diagnostic marker for LN with high accuracy and an early predictor of LN.</description><identifier>ISSN: 1110-4902</identifier><identifier>EISSN: 1110-4902</identifier><identifier>DOI: 10.55133/eji.310115</identifier><identifier>PMID: 38224471</identifier><language>eng</language><publisher>Egypt</publisher><subject>Biomarkers ; Cross-Sectional Studies ; Early Diagnosis ; Fibrinolysin ; Humans ; Lipoproteins ; Lupus Erythematosus, Systemic ; Lupus Nephritis - diagnosis ; Thromboplastin</subject><ispartof>The Egyptian journal of immunology, 2024-01, Vol.31 (1), p.143-154</ispartof><rights>Copyright© by the Egyptian Association of Immunologists.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38224471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mustafa, Mohammed H</creatorcontrib><creatorcontrib>Tony, Effat A E</creatorcontrib><creatorcontrib>Elgendi, Salwa S</creatorcontrib><creatorcontrib>Abdelkader, Alaa S</creatorcontrib><creatorcontrib>Salah, Ayat A</creatorcontrib><creatorcontrib>Madkour, Rasha A</creatorcontrib><creatorcontrib>Department of Internal Medicine, Faculty of Medicine, Assiut University, Assiut, Egypt</creatorcontrib><title>Urinary tissue factor (uTF), tissue factor pathway inhibitor (TFPI) and plasmin as novel biomarkers in early diagnosis of lupus nephritis</title><title>The Egyptian journal of immunology</title><addtitle>Egypt J Immunol</addtitle><description>Systemic lupus erythematosus (SLE) is an autoimmune inflammatory disease, with multi systematic affection. Lupus nephritis (LN) is the most frequent cause of renal damage in SLE patients with variable presentations that may progress to end stage renal failure. Coagulation disorders are frequently reported in SLE and LN with higher mortality rates. Renal biopsy is an invasive process, and the existing indicators for LN diagnosis and activity are unreliable. New urinary biomarkers with significant validity, safety, and accuracy are the current focus of most studies. Our study sought to assess the value of urinary tissue factor (uTF), tissue factor pathway inhibitor (TFPI), and plasmin as biomarkers for the early identification and detection of LN and its activity. This was a cross-sectional study, included 100 subjects (80 SLE patients, and 20 healthy controls), they were recruited from the Internal Medicine department, Rheumatology and Nephrology units and outpatient's clinics at Assiut University hospital between the period of 2020 and 2022. All patients underwent full history taking, clinical evaluation, and activity scoring calculation and laboratory investigations. The results showed that the best diagnostic accuracy of LN was observed with TFPI (90% accuracy, sensitivity 80% and specificity 95% with p <0.001 at cutoff point of >193.2 ng/ml), followed by uTF (75.4% overall accuracy at cut off point of >12.6 ng/ml, sensitivity 90% and specificity 68% with p < 0.001) and plasmin (70.3% accuracy at cut off point of >30.5 ng/ml, sensitivity 55% and specificity 78% with p < 0.001). Urinary TFPI was the best predictor of LN occurrence with odd ratio of 4.34, (p < 0.001). In conclusion urinary TFPI could be used as a diagnostic marker for LN with high accuracy and an early predictor of LN.</description><subject>Biomarkers</subject><subject>Cross-Sectional Studies</subject><subject>Early Diagnosis</subject><subject>Fibrinolysin</subject><subject>Humans</subject><subject>Lipoproteins</subject><subject>Lupus Erythematosus, Systemic</subject><subject>Lupus Nephritis - diagnosis</subject><subject>Thromboplastin</subject><issn>1110-4902</issn><issn>1110-4902</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkFFLwzAQx4Mobsw9-S553NDOpMkt7aMMpwNBH7bnkrSpy2ybmrRKP4Lf2rJNEZ_uOH73P-6H0CUlMwDK2K3emRmjhFI4QUNKKQl4TMLTP_0Ajb3fEUJoCGIuxDkasCgMORd0iL42zlTSdbgx3rca5zJtrMOTdr2c3vwb1rLZfsoOm2prlNlj6-XLaoplleG6kL40FZYeV_ZDF1gZW0r3pp3vF7CWruhwZuRrZb3x2Oa4aOu2h3W9daY_dIHOcll4PT7WEdos79eLx-Dp-WG1uHsKUhrHEIi5okAkCM0zUIKDDlPCUxbpKCNSK8gpiXIAEqeRjEEpASSTQjAQKgeesxGaHHJrZ99b7ZukND7VRSErbVufhDHlIRDBeI9eH9DUWe-dzpPamf6pLqEk2etPev3JQX9PXx2DW1Xq7Jf9kc2-AeZSgPI</recordid><startdate>202401</startdate><enddate>202401</enddate><creator>Mustafa, Mohammed H</creator><creator>Tony, Effat A E</creator><creator>Elgendi, Salwa S</creator><creator>Abdelkader, Alaa S</creator><creator>Salah, Ayat A</creator><creator>Madkour, Rasha A</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202401</creationdate><title>Urinary tissue factor (uTF), tissue factor pathway inhibitor (TFPI) and plasmin as novel biomarkers in early diagnosis of lupus nephritis</title><author>Mustafa, Mohammed H ; Tony, Effat A E ; Elgendi, Salwa S ; Abdelkader, Alaa S ; Salah, Ayat A ; Madkour, Rasha A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1995-76b150a57e4d5b745e2c04c38e8d0aeb5f108f5509c8a95bb750da77357bf54f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Biomarkers</topic><topic>Cross-Sectional Studies</topic><topic>Early Diagnosis</topic><topic>Fibrinolysin</topic><topic>Humans</topic><topic>Lipoproteins</topic><topic>Lupus Erythematosus, Systemic</topic><topic>Lupus Nephritis - diagnosis</topic><topic>Thromboplastin</topic><toplevel>online_resources</toplevel><creatorcontrib>Mustafa, Mohammed H</creatorcontrib><creatorcontrib>Tony, Effat A E</creatorcontrib><creatorcontrib>Elgendi, Salwa S</creatorcontrib><creatorcontrib>Abdelkader, Alaa S</creatorcontrib><creatorcontrib>Salah, Ayat A</creatorcontrib><creatorcontrib>Madkour, Rasha A</creatorcontrib><creatorcontrib>Department of Internal Medicine, Faculty of Medicine, Assiut University, Assiut, Egypt</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Egyptian journal of immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mustafa, Mohammed H</au><au>Tony, Effat A E</au><au>Elgendi, Salwa S</au><au>Abdelkader, Alaa S</au><au>Salah, Ayat A</au><au>Madkour, Rasha A</au><aucorp>Department of Internal Medicine, Faculty of Medicine, Assiut University, Assiut, Egypt</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Urinary tissue factor (uTF), tissue factor pathway inhibitor (TFPI) and plasmin as novel biomarkers in early diagnosis of lupus nephritis</atitle><jtitle>The Egyptian journal of immunology</jtitle><addtitle>Egypt J Immunol</addtitle><date>2024-01</date><risdate>2024</risdate><volume>31</volume><issue>1</issue><spage>143</spage><epage>154</epage><pages>143-154</pages><issn>1110-4902</issn><eissn>1110-4902</eissn><abstract>Systemic lupus erythematosus (SLE) is an autoimmune inflammatory disease, with multi systematic affection. Lupus nephritis (LN) is the most frequent cause of renal damage in SLE patients with variable presentations that may progress to end stage renal failure. Coagulation disorders are frequently reported in SLE and LN with higher mortality rates. Renal biopsy is an invasive process, and the existing indicators for LN diagnosis and activity are unreliable. New urinary biomarkers with significant validity, safety, and accuracy are the current focus of most studies. Our study sought to assess the value of urinary tissue factor (uTF), tissue factor pathway inhibitor (TFPI), and plasmin as biomarkers for the early identification and detection of LN and its activity. This was a cross-sectional study, included 100 subjects (80 SLE patients, and 20 healthy controls), they were recruited from the Internal Medicine department, Rheumatology and Nephrology units and outpatient's clinics at Assiut University hospital between the period of 2020 and 2022. All patients underwent full history taking, clinical evaluation, and activity scoring calculation and laboratory investigations. The results showed that the best diagnostic accuracy of LN was observed with TFPI (90% accuracy, sensitivity 80% and specificity 95% with p <0.001 at cutoff point of >193.2 ng/ml), followed by uTF (75.4% overall accuracy at cut off point of >12.6 ng/ml, sensitivity 90% and specificity 68% with p < 0.001) and plasmin (70.3% accuracy at cut off point of >30.5 ng/ml, sensitivity 55% and specificity 78% with p < 0.001). Urinary TFPI was the best predictor of LN occurrence with odd ratio of 4.34, (p < 0.001). In conclusion urinary TFPI could be used as a diagnostic marker for LN with high accuracy and an early predictor of LN.</abstract><cop>Egypt</cop><pmid>38224471</pmid><doi>10.55133/eji.310115</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biomarkers Cross-Sectional Studies Early Diagnosis Fibrinolysin Humans Lipoproteins Lupus Erythematosus, Systemic Lupus Nephritis - diagnosis Thromboplastin |
title | Urinary tissue factor (uTF), tissue factor pathway inhibitor (TFPI) and plasmin as novel biomarkers in early diagnosis of lupus nephritis |
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