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Development of a novel glycated protein‐based fibrosis prediction score for determination of significant liver fibrosis in HCV‐infected patients, a preliminary study
The current study aimed to investigate the diagnostic value of glycated albumin (GA), glycated hemoglobin (HbA1c), and a number of routine biomarkers as noninvasive indicators of liver fibrosis in patients with chronic hepatitis C (CHC). One hundred patients with CHC were subjected to full medical h...
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Published in: | Journal of medical virology 2020-12, Vol.92 (12), p.3525-3533 |
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creator | Abo El‐khair, Salwa M. El‐Alfy, Hatem A. Elsamanoudy, Ayman Z. Elhammady, Dina Abd‐elfattah, Nahed Eldeek, Bassem Farid, Khaled |
description | The current study aimed to investigate the diagnostic value of glycated albumin (GA), glycated hemoglobin (HbA1c), and a number of routine biomarkers as noninvasive indicators of liver fibrosis in patients with chronic hepatitis C (CHC). One hundred patients with CHC were subjected to full medical history and examination, in addition to ultrasound‐guided liver biopsy and histopathological examination for assessment of liver fibrosis stage. GA and HbA1c values, GA/HbA1c ratio, liver function tests, complete blood count, and alpha fetoprotein (AFP) were determined. A novel noninvasive index, dubbed Fibrosis Prediction Score (FPS), was selected for predicting significant liver fibrosis based on total bilirubin, glycated albumin, platelet count, age, and AFP. A validation study for FPS was applied on archival data which include 66 diabetics' patients. The FPS had area under the curve (AUC) of 0.92 for classification of patients with significant fibrosis with 81% sensitivity and 95% specificity. The AUCs of FPS in predicting advanced fibrosis and cirrhosis were 0.86 and 0.82, respectively. Comparison of AST‐to‐platelet ratio index (APRI) and FIB‐4 with FPS indicated increased sensitivity and specificity of FPS over APRI and FIB4 in both significant and advanced fibrosis. FPS has a good sensitivity and specificity for prediction of significant and advanced liver fibrosis in patients with CHC.
Highlights
Progression of hepatitis C virus infection to chronicity is one of the most pressing health problems.
Accurate assessment of liver fibrosis is important to make therapeutic decisions, determine prognosis and to follow‐up disease progression.
Accurate, reproducible and easily applied methods are required for evaluation of hepatic fibrosis.
Fibrosis Prediction Score (FPS), based on five simple variables including AFP, age, glycated albumin, total bilirubin and platelet count, demonstrated better diagnostic power for detection significant and advanced liver fibrosis. |
doi_str_mv | 10.1002/jmv.26204 |
format | article |
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Highlights
Progression of hepatitis C virus infection to chronicity is one of the most pressing health problems.
Accurate assessment of liver fibrosis is important to make therapeutic decisions, determine prognosis and to follow‐up disease progression.
Accurate, reproducible and easily applied methods are required for evaluation of hepatic fibrosis.
Fibrosis Prediction Score (FPS), based on five simple variables including AFP, age, glycated albumin, total bilirubin and platelet count, demonstrated better diagnostic power for detection significant and advanced liver fibrosis.</description><identifier>ISSN: 0146-6615</identifier><identifier>EISSN: 1096-9071</identifier><identifier>DOI: 10.1002/jmv.26204</identifier><identifier>PMID: 32558950</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adult ; Aged ; Albumin ; Albumins ; alpha-Fetoproteins - analysis ; Bile ; Bilirubin ; Biomarkers ; Biomarkers - blood ; Biopsy ; chronic hepatitis C ; Cirrhosis ; Diagnostic systems ; Female ; Fibrosis ; fibrosis prediction score ; glycated albumin ; Glycated Hemoglobin - analysis ; Glycated Serum Albumin ; Glycation End Products, Advanced - blood ; Health problems ; Hemoglobin ; Hepatitis ; Hepatitis C ; Hepatitis C, Chronic - blood ; Hepatitis C, Chronic - complications ; Hepatitis C, Chronic - pathology ; Humans ; Liver ; Liver - pathology ; Liver cirrhosis ; Liver Cirrhosis - blood ; Liver Cirrhosis - diagnosis ; Liver Cirrhosis - pathology ; liver fibrosis ; Liver Function Tests - methods ; Male ; Middle Aged ; Platelet Count ; Platelets ; Predictions ; Sensitivity ; Sensitivity and Specificity ; Serum Albumin - analysis ; Severity of Illness Index ; Ultrasound ; Virology ; Viruses</subject><ispartof>Journal of medical virology, 2020-12, Vol.92 (12), p.3525-3533</ispartof><rights>2020 Wiley Periodicals LLC</rights><rights>2020 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3834-c39b97c5398a24554993b34c2dfafba108a8ce2178c2684829917fd1fb12afa13</cites><orcidid>0000-0001-5449-2723</orcidid></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/32558950$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Abo El‐khair, Salwa M.</creatorcontrib><creatorcontrib>El‐Alfy, Hatem A.</creatorcontrib><creatorcontrib>Elsamanoudy, Ayman Z.</creatorcontrib><creatorcontrib>Elhammady, Dina</creatorcontrib><creatorcontrib>Abd‐elfattah, Nahed</creatorcontrib><creatorcontrib>Eldeek, Bassem</creatorcontrib><creatorcontrib>Farid, Khaled</creatorcontrib><title>Development of a novel glycated protein‐based fibrosis prediction score for determination of significant liver fibrosis in HCV‐infected patients, a preliminary study</title><title>Journal of medical virology</title><addtitle>J Med Virol</addtitle><description>The current study aimed to investigate the diagnostic value of glycated albumin (GA), glycated hemoglobin (HbA1c), and a number of routine biomarkers as noninvasive indicators of liver fibrosis in patients with chronic hepatitis C (CHC). One hundred patients with CHC were subjected to full medical history and examination, in addition to ultrasound‐guided liver biopsy and histopathological examination for assessment of liver fibrosis stage. GA and HbA1c values, GA/HbA1c ratio, liver function tests, complete blood count, and alpha fetoprotein (AFP) were determined. A novel noninvasive index, dubbed Fibrosis Prediction Score (FPS), was selected for predicting significant liver fibrosis based on total bilirubin, glycated albumin, platelet count, age, and AFP. A validation study for FPS was applied on archival data which include 66 diabetics' patients. The FPS had area under the curve (AUC) of 0.92 for classification of patients with significant fibrosis with 81% sensitivity and 95% specificity. The AUCs of FPS in predicting advanced fibrosis and cirrhosis were 0.86 and 0.82, respectively. Comparison of AST‐to‐platelet ratio index (APRI) and FIB‐4 with FPS indicated increased sensitivity and specificity of FPS over APRI and FIB4 in both significant and advanced fibrosis. FPS has a good sensitivity and specificity for prediction of significant and advanced liver fibrosis in patients with CHC.
Highlights
Progression of hepatitis C virus infection to chronicity is one of the most pressing health problems.
Accurate assessment of liver fibrosis is important to make therapeutic decisions, determine prognosis and to follow‐up disease progression.
Accurate, reproducible and easily applied methods are required for evaluation of hepatic fibrosis.
Fibrosis Prediction Score (FPS), based on five simple variables including AFP, age, glycated albumin, total bilirubin and platelet count, demonstrated better diagnostic power for detection significant and advanced liver fibrosis.</description><subject>Adult</subject><subject>Aged</subject><subject>Albumin</subject><subject>Albumins</subject><subject>alpha-Fetoproteins - analysis</subject><subject>Bile</subject><subject>Bilirubin</subject><subject>Biomarkers</subject><subject>Biomarkers - blood</subject><subject>Biopsy</subject><subject>chronic hepatitis C</subject><subject>Cirrhosis</subject><subject>Diagnostic systems</subject><subject>Female</subject><subject>Fibrosis</subject><subject>fibrosis prediction score</subject><subject>glycated albumin</subject><subject>Glycated Hemoglobin - analysis</subject><subject>Glycated Serum Albumin</subject><subject>Glycation End Products, Advanced - blood</subject><subject>Health problems</subject><subject>Hemoglobin</subject><subject>Hepatitis</subject><subject>Hepatitis C</subject><subject>Hepatitis C, Chronic - blood</subject><subject>Hepatitis C, Chronic - complications</subject><subject>Hepatitis C, Chronic - pathology</subject><subject>Humans</subject><subject>Liver</subject><subject>Liver - pathology</subject><subject>Liver cirrhosis</subject><subject>Liver Cirrhosis - blood</subject><subject>Liver Cirrhosis - diagnosis</subject><subject>Liver Cirrhosis - pathology</subject><subject>liver fibrosis</subject><subject>Liver Function Tests - methods</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Platelet Count</subject><subject>Platelets</subject><subject>Predictions</subject><subject>Sensitivity</subject><subject>Sensitivity and Specificity</subject><subject>Serum Albumin - analysis</subject><subject>Severity of Illness Index</subject><subject>Ultrasound</subject><subject>Virology</subject><subject>Viruses</subject><issn>0146-6615</issn><issn>1096-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kcuKFDEUhoMoTju68AUk4EbBnsm1KllKexllxI3OtkilToY0VUmbVLf0zkfwNXwtn8Qz3aOC4CYhJ1--nMNPyGPOzjhj4nw97c5EI5i6Qxac2WZpWcvvkgXjqlk2Ddcn5EGta8aYsULcJydSaG2sZgvy4xXsYMybCdJMc6COpowFej3uvZthoJuSZ4jp57fvvat4DrEvucaKFzBEP8ecaPW5AA250AFmKFNM7lBHX43XKYboHerHuIPyVxATvVhdoTimAP7wFz7DPuoLbAP1Y7wxlT2t83bYPyT3ghsrPLrdT8nnN68_rS6Wlx_fvlu9vFx6aaTC1fa29Vpa44TSWlkre6m8GIILvePMOONB8NZ40RhlhLW8DQMPPRcuOC5PybOjFyf_soU6d1OsHsbRJcjb2gnFtTCKS4no03_Qdd6WhN0hpdtWtVoypJ4fKY9z1wKh25Q44VwdZ91Nfh3m1x3yQ_bJrXHbTzD8IX8HhsD5EfgaR9j_39S9_3B1VP4CDS2pnA</recordid><startdate>202012</startdate><enddate>202012</enddate><creator>Abo El‐khair, Salwa M.</creator><creator>El‐Alfy, Hatem A.</creator><creator>Elsamanoudy, Ayman Z.</creator><creator>Elhammady, Dina</creator><creator>Abd‐elfattah, Nahed</creator><creator>Eldeek, Bassem</creator><creator>Farid, Khaled</creator><general>Wiley Subscription Services, Inc</general><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>7QL</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5449-2723</orcidid></search><sort><creationdate>202012</creationdate><title>Development of a novel glycated protein‐based fibrosis prediction score for determination of significant liver fibrosis in HCV‐infected patients, a preliminary study</title><author>Abo El‐khair, Salwa M. ; 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One hundred patients with CHC were subjected to full medical history and examination, in addition to ultrasound‐guided liver biopsy and histopathological examination for assessment of liver fibrosis stage. GA and HbA1c values, GA/HbA1c ratio, liver function tests, complete blood count, and alpha fetoprotein (AFP) were determined. A novel noninvasive index, dubbed Fibrosis Prediction Score (FPS), was selected for predicting significant liver fibrosis based on total bilirubin, glycated albumin, platelet count, age, and AFP. A validation study for FPS was applied on archival data which include 66 diabetics' patients. The FPS had area under the curve (AUC) of 0.92 for classification of patients with significant fibrosis with 81% sensitivity and 95% specificity. The AUCs of FPS in predicting advanced fibrosis and cirrhosis were 0.86 and 0.82, respectively. Comparison of AST‐to‐platelet ratio index (APRI) and FIB‐4 with FPS indicated increased sensitivity and specificity of FPS over APRI and FIB4 in both significant and advanced fibrosis. FPS has a good sensitivity and specificity for prediction of significant and advanced liver fibrosis in patients with CHC.
Highlights
Progression of hepatitis C virus infection to chronicity is one of the most pressing health problems.
Accurate assessment of liver fibrosis is important to make therapeutic decisions, determine prognosis and to follow‐up disease progression.
Accurate, reproducible and easily applied methods are required for evaluation of hepatic fibrosis.
Fibrosis Prediction Score (FPS), based on five simple variables including AFP, age, glycated albumin, total bilirubin and platelet count, demonstrated better diagnostic power for detection significant and advanced liver fibrosis.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32558950</pmid><doi>10.1002/jmv.26204</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-5449-2723</orcidid></addata></record> |
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subjects | Adult Aged Albumin Albumins alpha-Fetoproteins - analysis Bile Bilirubin Biomarkers Biomarkers - blood Biopsy chronic hepatitis C Cirrhosis Diagnostic systems Female Fibrosis fibrosis prediction score glycated albumin Glycated Hemoglobin - analysis Glycated Serum Albumin Glycation End Products, Advanced - blood Health problems Hemoglobin Hepatitis Hepatitis C Hepatitis C, Chronic - blood Hepatitis C, Chronic - complications Hepatitis C, Chronic - pathology Humans Liver Liver - pathology Liver cirrhosis Liver Cirrhosis - blood Liver Cirrhosis - diagnosis Liver Cirrhosis - pathology liver fibrosis Liver Function Tests - methods Male Middle Aged Platelet Count Platelets Predictions Sensitivity Sensitivity and Specificity Serum Albumin - analysis Severity of Illness Index Ultrasound Virology Viruses |
title | Development of a novel glycated protein‐based fibrosis prediction score for determination of significant liver fibrosis in HCV‐infected patients, a preliminary study |
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