Proposal for a histological scoring and grading system for non-alcoholic fatty liver disease
: Aim/Background: The spectrum of histopathological features in non‐alcoholic fatty liver disease (NAFLD) has been well described. At least two scoring systems have been established. We propose here a system in which numerical scores are obtained using the different features. Methods: Twenty‐five ca...
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Veröffentlicht in: | Liver international 2005-04, Vol.25 (2), p.294-304 |
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description | : Aim/Background: The spectrum of histopathological features in non‐alcoholic fatty liver disease (NAFLD) has been well described. At least two scoring systems have been established. We propose here a system in which numerical scores are obtained using the different features.
Methods: Twenty‐five cases of well‐defined NAFLD were idengified. Two pathologists blinded to idengifiers and clinical data independently scored the liver biopsies twice for portal fibrosis (PF: 0–6), lobular inflammation and necrosis (LIN: 0–3), Mallory bodies (MB: 0–3), hepatocyte ballooning (HB: 0–3), perisinusoidal fibrosis (PSF: 0–3) and fatty change (FC: 1–4). The κ statistic tested observer concordance. Non‐parametric measures of correlation and hierarchical cluster analysis were used to elaborate a grading system.
Results: A broad spectrum of NAFLD was observed. Intra‐ and interobserver concordance was satisfactory. An activity score was created (AS: 0–12) as the sum of LIN, MB, HB and PSF, but not FC. A system for severity of NAFLD was developed: Grade 1 (PF: 0–2 and AS: 0–4), Grade 2 (PF: 3 or AS: 5–7) and Grade 3 (PF: 4–6 or AS: 8–12). Diabetes, elevated alkaline phosphatase and decreased platelets were associated with advanced grade.
Conclusions: This simple, reproducible NAFLD score produces a three‐tier severity grade. This numerical system may prove useful in assessing disease severity and interval changes. |
doi_str_mv | 10.1111/j.1478-3231.2005.01052.x |
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Methods: Twenty‐five cases of well‐defined NAFLD were idengified. Two pathologists blinded to idengifiers and clinical data independently scored the liver biopsies twice for portal fibrosis (PF: 0–6), lobular inflammation and necrosis (LIN: 0–3), Mallory bodies (MB: 0–3), hepatocyte ballooning (HB: 0–3), perisinusoidal fibrosis (PSF: 0–3) and fatty change (FC: 1–4). The κ statistic tested observer concordance. Non‐parametric measures of correlation and hierarchical cluster analysis were used to elaborate a grading system.
Results: A broad spectrum of NAFLD was observed. Intra‐ and interobserver concordance was satisfactory. An activity score was created (AS: 0–12) as the sum of LIN, MB, HB and PSF, but not FC. A system for severity of NAFLD was developed: Grade 1 (PF: 0–2 and AS: 0–4), Grade 2 (PF: 3 or AS: 5–7) and Grade 3 (PF: 4–6 or AS: 8–12). Diabetes, elevated alkaline phosphatase and decreased platelets were associated with advanced grade.
Conclusions: This simple, reproducible NAFLD score produces a three‐tier severity grade. This numerical system may prove useful in assessing disease severity and interval changes.</description><identifier>ISSN: 1478-3223</identifier><identifier>EISSN: 1478-3231</identifier><identifier>DOI: 10.1111/j.1478-3231.2005.01052.x</identifier><identifier>PMID: 15780053</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing</publisher><subject>Adult ; Aged ; Biopsy, Needle ; Cohort Studies ; Disease Progression ; fatty liver ; Fatty Liver - pathology ; Fatty Liver - physiopathology ; Female ; fibrosis ; grade ; Humans ; Immunohistochemistry ; inflammation ; Liver Cirrhosis - pathology ; Liver Cirrhosis - physiopathology ; Liver Function Tests ; Male ; Middle Aged ; non-alcoholic steatohepatitis ; Observer Variation ; Probability ; Retrospective Studies ; score ; Sensitivity and Specificity ; Severity of Illness Index</subject><ispartof>Liver international, 2005-04, Vol.25 (2), p.294-304</ispartof><rights>Copyright Blackwell Munksgaard 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4052-cb1c55dff06f574136880fd4f6b4bf44e254146e58726fcd55d522b223074a6e3</citedby><cites>FETCH-LOGICAL-c4052-cb1c55dff06f574136880fd4f6b4bf44e254146e58726fcd55d522b223074a6e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1478-3231.2005.01052.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1478-3231.2005.01052.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15780053$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mendler, Michel Henry</creatorcontrib><creatorcontrib>Kanel, Gary</creatorcontrib><creatorcontrib>Govindarajan, Sugantha</creatorcontrib><title>Proposal for a histological scoring and grading system for non-alcoholic fatty liver disease</title><title>Liver international</title><addtitle>Liver Int</addtitle><description>: Aim/Background: The spectrum of histopathological features in non‐alcoholic fatty liver disease (NAFLD) has been well described. At least two scoring systems have been established. We propose here a system in which numerical scores are obtained using the different features.
Methods: Twenty‐five cases of well‐defined NAFLD were idengified. Two pathologists blinded to idengifiers and clinical data independently scored the liver biopsies twice for portal fibrosis (PF: 0–6), lobular inflammation and necrosis (LIN: 0–3), Mallory bodies (MB: 0–3), hepatocyte ballooning (HB: 0–3), perisinusoidal fibrosis (PSF: 0–3) and fatty change (FC: 1–4). The κ statistic tested observer concordance. Non‐parametric measures of correlation and hierarchical cluster analysis were used to elaborate a grading system.
Results: A broad spectrum of NAFLD was observed. Intra‐ and interobserver concordance was satisfactory. An activity score was created (AS: 0–12) as the sum of LIN, MB, HB and PSF, but not FC. A system for severity of NAFLD was developed: Grade 1 (PF: 0–2 and AS: 0–4), Grade 2 (PF: 3 or AS: 5–7) and Grade 3 (PF: 4–6 or AS: 8–12). Diabetes, elevated alkaline phosphatase and decreased platelets were associated with advanced grade.
Conclusions: This simple, reproducible NAFLD score produces a three‐tier severity grade. This numerical system may prove useful in assessing disease severity and interval changes.</description><subject>Adult</subject><subject>Aged</subject><subject>Biopsy, Needle</subject><subject>Cohort Studies</subject><subject>Disease Progression</subject><subject>fatty liver</subject><subject>Fatty Liver - pathology</subject><subject>Fatty Liver - physiopathology</subject><subject>Female</subject><subject>fibrosis</subject><subject>grade</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>inflammation</subject><subject>Liver Cirrhosis - pathology</subject><subject>Liver Cirrhosis - physiopathology</subject><subject>Liver Function Tests</subject><subject>Male</subject><subject>Middle Aged</subject><subject>non-alcoholic steatohepatitis</subject><subject>Observer Variation</subject><subject>Probability</subject><subject>Retrospective Studies</subject><subject>score</subject><subject>Sensitivity and Specificity</subject><subject>Severity of Illness Index</subject><issn>1478-3223</issn><issn>1478-3231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtPAyEUhYnRWF9_wbByNyMMMDNduDDGV6yv-OjGhDAMVCodKky1_fcytqlb2XAC57v3cgAAYpTiuI7HKaZFmZCM4DRDiKUII5al8w2ws77YXOuM9MBuCGOEcL_P8DboYVaUESM74O3Bu6kLwkLtPBTw3YTWWTcyMh4F6bxpRlA0NRx5UXc6LEKrJr_uxjWJsNK9O2sk1KJtF9CaL-VhbYISQe2DLS1sUAerfQ-8XJw_n10lg_vL67PTQSJpHDuRFZaM1VqjXLOCYpKXJdI11XlFK02pyhjFNFesLLJcyzp6WZZV8V2ooCJXZA8cLetOvfucqdDyiQlSWSsa5WaB5wUj_aLMo7FcGqV3IXil-dSbifALjhHvkuVj3oXGuwB5lyz_TZbPI3q46jGrJqr-A1dRRsPJ0vBtrFr8uzAfXL92KvLJko8_oOZrXviPOD8pGB_eXXL6SG-G6InwW_IDzCqWhw</recordid><startdate>200504</startdate><enddate>200504</enddate><creator>Mendler, Michel Henry</creator><creator>Kanel, Gary</creator><creator>Govindarajan, Sugantha</creator><general>Blackwell Publishing</general><scope>BSCLL</scope><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>200504</creationdate><title>Proposal for a histological scoring and grading system for non-alcoholic fatty liver disease</title><author>Mendler, Michel Henry ; Kanel, Gary ; Govindarajan, Sugantha</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4052-cb1c55dff06f574136880fd4f6b4bf44e254146e58726fcd55d522b223074a6e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biopsy, Needle</topic><topic>Cohort Studies</topic><topic>Disease Progression</topic><topic>fatty liver</topic><topic>Fatty Liver - pathology</topic><topic>Fatty Liver - physiopathology</topic><topic>Female</topic><topic>fibrosis</topic><topic>grade</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>inflammation</topic><topic>Liver Cirrhosis - pathology</topic><topic>Liver Cirrhosis - physiopathology</topic><topic>Liver Function Tests</topic><topic>Male</topic><topic>Middle Aged</topic><topic>non-alcoholic steatohepatitis</topic><topic>Observer Variation</topic><topic>Probability</topic><topic>Retrospective Studies</topic><topic>score</topic><topic>Sensitivity and Specificity</topic><topic>Severity of Illness Index</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mendler, Michel Henry</creatorcontrib><creatorcontrib>Kanel, Gary</creatorcontrib><creatorcontrib>Govindarajan, Sugantha</creatorcontrib><collection>Istex</collection><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>Liver international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mendler, Michel Henry</au><au>Kanel, Gary</au><au>Govindarajan, Sugantha</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proposal for a histological scoring and grading system for non-alcoholic fatty liver disease</atitle><jtitle>Liver international</jtitle><addtitle>Liver Int</addtitle><date>2005-04</date><risdate>2005</risdate><volume>25</volume><issue>2</issue><spage>294</spage><epage>304</epage><pages>294-304</pages><issn>1478-3223</issn><eissn>1478-3231</eissn><abstract>: Aim/Background: The spectrum of histopathological features in non‐alcoholic fatty liver disease (NAFLD) has been well described. At least two scoring systems have been established. We propose here a system in which numerical scores are obtained using the different features.
Methods: Twenty‐five cases of well‐defined NAFLD were idengified. Two pathologists blinded to idengifiers and clinical data independently scored the liver biopsies twice for portal fibrosis (PF: 0–6), lobular inflammation and necrosis (LIN: 0–3), Mallory bodies (MB: 0–3), hepatocyte ballooning (HB: 0–3), perisinusoidal fibrosis (PSF: 0–3) and fatty change (FC: 1–4). The κ statistic tested observer concordance. Non‐parametric measures of correlation and hierarchical cluster analysis were used to elaborate a grading system.
Results: A broad spectrum of NAFLD was observed. Intra‐ and interobserver concordance was satisfactory. An activity score was created (AS: 0–12) as the sum of LIN, MB, HB and PSF, but not FC. A system for severity of NAFLD was developed: Grade 1 (PF: 0–2 and AS: 0–4), Grade 2 (PF: 3 or AS: 5–7) and Grade 3 (PF: 4–6 or AS: 8–12). Diabetes, elevated alkaline phosphatase and decreased platelets were associated with advanced grade.
Conclusions: This simple, reproducible NAFLD score produces a three‐tier severity grade. This numerical system may prove useful in assessing disease severity and interval changes.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing</pub><pmid>15780053</pmid><doi>10.1111/j.1478-3231.2005.01052.x</doi><tpages>11</tpages></addata></record> |
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subjects | Adult Aged Biopsy, Needle Cohort Studies Disease Progression fatty liver Fatty Liver - pathology Fatty Liver - physiopathology Female fibrosis grade Humans Immunohistochemistry inflammation Liver Cirrhosis - pathology Liver Cirrhosis - physiopathology Liver Function Tests Male Middle Aged non-alcoholic steatohepatitis Observer Variation Probability Retrospective Studies score Sensitivity and Specificity Severity of Illness Index |
title | Proposal for a histological scoring and grading system for non-alcoholic fatty liver disease |
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