A quantitative evaluation of liver fibrosis on hepatitis C

To evaluate a degree of liver fibrosis of chronic liver disease quantitatively, we applied the fibrotic ratio (%) that was obtained by calculating fibrotic areas of bioptic liver specimens collected from 102 hepatitis C patients by using computer graphics softwares. The fibrotic ratio increased sign...

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Published inKanzo Vol. 38; no. 6; pp. 349 - 354
Main Authors WAKAHAMA, Osamu, MATSUNAGA, Takashi, NISHIKAWA, Shuji, HIGUCHI, Akifumi, KOIKE, Fumiyuki
Format Journal Article
LanguageJapanese
Published The Japan Society of Hepatology 1997
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ISSN0451-4203
1881-3593
DOI10.2957/kanzo.38.349

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Abstract To evaluate a degree of liver fibrosis of chronic liver disease quantitatively, we applied the fibrotic ratio (%) that was obtained by calculating fibrotic areas of bioptic liver specimens collected from 102 hepatitis C patients by using computer graphics softwares. The fibrotic ratio increased significantly in accordance with the deterioration of chronic liver disease; mean fibrotic ratios of chronic hepatitis (F0, F1, F2, F3: Inuyama 1995), compensate LC, decompensated LC and mortal cases from liver failure were about 0.5%, 3%, 7%, 11%, 17%, 29% and 62% respectively. Mean fibrotic ratios of the patients with splenomegaly, HCC, varices, ascites and hepatic encephalopathy were 24%, 32%, 35%, 38% and 40% respectively. Next we examined the relationships between fibrotic ratio and biochemical liver function tests. The fibrotic ratio correlated not only with fibrotic markers; type 4 collagen 7s and platelet, but also with liver functional markers; prothrombin time, total bilirubin, albumin, ICG R15 and so on. Moreover, the multivariate analysis showed that the fibrotic ratio could be predicted fairly well from the combination of four factors; prothrombin time, total bilirubin, albumin and ICG R15.
AbstractList To evaluate a degree of liver fibrosis of chronic liver disease quantitatively, we applied the fibrotic ratio (%) that was obtained by calculating fibrotic areas of bioptic liver specimens collected from 102 hepatitis C patients by using computer graphics softwares. The fibrotic ratio increased significantly in accordance with the deterioration of chronic liver disease; mean fibrotic ratios of chronic hepatitis (F0, F1, F2, F3: Inuyama 1995), compensate LC, decompensated LC and mortal cases from liver failure were about 0.5%, 3%, 7%, 11%, 17%, 29% and 62% respectively. Mean fibrotic ratios of the patients with splenomegaly, HCC, varices, ascites and hepatic encephalopathy were 24%, 32%, 35%, 38% and 40% respectively. Next we examined the relationships between fibrotic ratio and biochemical liver function tests. The fibrotic ratio correlated not only with fibrotic markers; type 4 collagen 7s and platelet, but also with liver functional markers; prothrombin time, total bilirubin, albumin, ICG R15 and so on. Moreover, the multivariate analysis showed that the fibrotic ratio could be predicted fairly well from the combination of four factors; prothrombin time, total bilirubin, albumin and ICG R15.
Author HIGUCHI, Akifumi
WAKAHAMA, Osamu
MATSUNAGA, Takashi
NISHIKAWA, Shuji
KOIKE, Fumiyuki
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  fullname: KOIKE, Fumiyuki
  organization: Department of Gastroenterology, Sapporo City General Hospital
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References 1) 八橋弘, 矢野右人: 肝細胞癌母地の検討. staging gradingによる予知. 肝臓37: 78, 1996
6) 鈴木宏: 肝硬変の変遷. 肝胆膵26: 173-179, 1993
3) 小俣正男: 新犬山分類によるStaging (Fibrosis) の読み合わせ. 新しい慢性肝炎の分類. 小俣正男編, 南江堂, 東京, 1996, p6-15
7) 渡邊明治: 終末期肝硬変とは?また, その予後の推定は可能か?肝硬変のマネジメント, 水戸廸郎, 谷川久一編, 医学書院, 東京, 1993, p54-64
4) Bianchi L, Gudat F: Chronic hepatitis. In: Pathology of the Liver, Edited by MacSween RNM, Anthony PP, Scheur, PJ, Churchill Livingstone, New York, 1994, p349-395
8) 池田健次, 熊田博光: 肝硬変の経過と予後. 日本臨床52: 63-68, 1993
5) Millward-Sadler GH: Liver cirrhosis. In: Patholgy of the Liver, Edited by MacSween RNM, Anthouy PP, Scheur PJ, Churchill Livingstone, New York, 1994, p397-424
2) 市田文弘, 小俣政男, 辻孝夫, 他: 慢性肝炎の肝組織診断基準一新犬山分類. 第19回犬山シンポジウム, 犬山シンポジウム記録刊行会編, 中外医学社, 東京, 1996, p183-188
References_xml – reference: 2) 市田文弘, 小俣政男, 辻孝夫, 他: 慢性肝炎の肝組織診断基準一新犬山分類. 第19回犬山シンポジウム, 犬山シンポジウム記録刊行会編, 中外医学社, 東京, 1996, p183-188
– reference: 4) Bianchi L, Gudat F: Chronic hepatitis. In: Pathology of the Liver, Edited by MacSween RNM, Anthony PP, Scheur, PJ, Churchill Livingstone, New York, 1994, p349-395
– reference: 1) 八橋弘, 矢野右人: 肝細胞癌母地の検討. staging gradingによる予知. 肝臓37: 78, 1996
– reference: 3) 小俣正男: 新犬山分類によるStaging (Fibrosis) の読み合わせ. 新しい慢性肝炎の分類. 小俣正男編, 南江堂, 東京, 1996, p6-15
– reference: 5) Millward-Sadler GH: Liver cirrhosis. In: Patholgy of the Liver, Edited by MacSween RNM, Anthouy PP, Scheur PJ, Churchill Livingstone, New York, 1994, p397-424
– reference: 7) 渡邊明治: 終末期肝硬変とは?また, その予後の推定は可能か?肝硬変のマネジメント, 水戸廸郎, 谷川久一編, 医学書院, 東京, 1993, p54-64
– reference: 8) 池田健次, 熊田博光: 肝硬変の経過と予後. 日本臨床52: 63-68, 1993
– reference: 6) 鈴木宏: 肝硬変の変遷. 肝胆膵26: 173-179, 1993
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Title A quantitative evaluation of liver fibrosis on hepatitis C
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