{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,2]],"date-time":"2026-03-02T23:09:59Z","timestamp":1772492999380,"version":"3.50.1"},"reference-count":45,"publisher":"Wiley","issue":"11","license":[{"start":{"date-parts":[[2017,10,27]],"date-time":"2017-10-27T00:00:00Z","timestamp":1509062400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["APMIS"],"published-print":{"date-parts":[[2017,11]]},"abstract":"<jats:p>Non\u2010alcoholic fatty liver disease (<jats:styled-content style=\"fixed-case\">NAFLD<\/jats:styled-content>) is an increasingly common cause of chronic liver disease. Till date, liver biopsy remains the gold standard for identification and quantification of the wide histological spectra of<jats:styled-content style=\"fixed-case\">NAFLD<\/jats:styled-content>. Histological scorings are very useful and widely applied for the diagnosis and management in clinical trials and follow\u2010up studies of non\u2010alcoholic steatohepatitis (<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>). However, in view of scarce published literature, there is a need to evaluate them in large cohort of<jats:styled-content style=\"fixed-case\">NAFLD<\/jats:styled-content>. This study was aimed to evaluate the two histological scoring systems (<jats:styled-content style=\"fixed-case\">NAS<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">CRN<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\">SAF<\/jats:styled-content>) in the diagnosis of<jats:styled-content style=\"fixed-case\">NAFLD<\/jats:styled-content>and to assess the role of histological characteristics as injury markers in<jats:styled-content style=\"fixed-case\">NAFLD<\/jats:styled-content>. Retrospective histological study of liver biopsies of 1000 patients diagnosed as<jats:styled-content style=\"fixed-case\">NAFLD<\/jats:styled-content>, between 2010 and 2016, was conducted. Histopathologic evaluation and semiquantiative scoring based on<jats:styled-content style=\"fixed-case\">NAS<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">CRN<\/jats:styled-content>and<jats:styled-content style=\"fixed-case\">SAF<\/jats:styled-content>algorithm and their correlation with serum aminotransferase and fibrosis were performed. Liver biopsies were classified according to the<jats:styled-content style=\"fixed-case\">NAS<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">CRN<\/jats:styled-content>scoring, as<jats:styled-content style=\"fixed-case\">NAS<\/jats:styled-content>&lt;3 (not<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>) in 72 (7.2%),<jats:styled-content style=\"fixed-case\">NAS<\/jats:styled-content>3\u20134 (borderline<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>) in 310 (31%), and<jats:styled-content style=\"fixed-case\">NAS<\/jats:styled-content>\u22655 (definite<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>) in 618 (61.8%), and<jats:styled-content style=\"fixed-case\">SAF<\/jats:styled-content>classified 117 (11.7%) not<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>and 883 (88.3%) definite<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>. There was excellent concordance for definite<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>and not<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>; however, 88.06% of borderline<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>was classified as<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>by<jats:styled-content style=\"fixed-case\">SAF<\/jats:styled-content>. 76.39% by<jats:styled-content style=\"fixed-case\">NAS<\/jats:styled-content>and 78.63% by<jats:styled-content style=\"fixed-case\">SAF<\/jats:styled-content>algorithm who were diagnosed as not<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>showed the presence of fibrosis; however, higher stages of fibrosis were significantly more prevalent in definite<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>, excluding burnt\u2010out cirrhosis. Serum<jats:styled-content style=\"fixed-case\">ALT<\/jats:styled-content>was significantly associated with increasing stages of fibrosis (p\u00a0&lt;\u00a00.001) and the three categories (not<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>, borderline<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>, and definite<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>) when classified as with\/without fibrosis (p\u00a0&lt;\u00a00.001). Steatosis of higher grades, more ballooned cells, and more foci of Lobular Inflammation were found in significantly higher proportion of patients with<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>(p\u00a0&lt;\u00a00.001), with higher fibrosis stages (p\u00a0&lt;\u00a00.001) and higher serum<jats:styled-content style=\"fixed-case\">ALT<\/jats:styled-content>levels (p\u00a0&lt;\u00a00.001).<jats:styled-content style=\"fixed-case\">NAFLD<\/jats:styled-content>classifications based on histological scoring<jats:styled-content style=\"fixed-case\">NAS<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">CRN<\/jats:styled-content>and<jats:styled-content style=\"fixed-case\">SAF<\/jats:styled-content>algorithm are concordant for the category of definite<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>and not<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>, while borderline<jats:styled-content style=\"fixed-case\">NASH<\/jats:styled-content>shows discrepant interpretation. There was highly significant correlation between the<jats:styled-content style=\"fixed-case\">NAS<\/jats:styled-content>and<jats:styled-content style=\"fixed-case\">SAF<\/jats:styled-content>categories with high grades of histological characteristics, with serum<jats:styled-content style=\"fixed-case\">ALT<\/jats:styled-content>and with higher stages of fibrosis. Exclusion of fibrosis is a limitation with both scores.<\/jats:p>","DOI":"10.1111\/apm.12742","type":"journal-article","created":{"date-parts":[[2017,10,27]],"date-time":"2017-10-27T10:48:58Z","timestamp":1509101338000},"page":"962-973","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":49,"title":["Non\u2010alcoholic fatty liver disease \u2013 histological scoring systems: a large cohort single\u2010center, evaluation study"],"prefix":"10.1111","volume":"125","author":[{"given":"Archana","family":"Rastogi","sequence":"first","affiliation":[{"name":"Department of Pathology Institute of Liver &amp; Biliary Sciences Delhi India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Saggere Muralikrishna","family":"Shasthry","sequence":"additional","affiliation":[{"name":"Department of Hepatology Institute of Liver &amp; Biliary Sciences Delhi 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