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Efficacy of long-term ezetimibe therapy in patients with nonalcoholic fatty liver disease
Background Hyperlipidemia, insulin resistance, and oxidative stress can heavily contribute to the initiation and progression of nonalcoholic fatty liver disease (NAFLD). Currently, there is no established treatment for this disease. Recently, several studies have shown that ezetimibe (EZ), a lipid-l...
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Published in: | Journal of gastroenterology 2011, Vol.46 (1), p.101-107 |
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creator | Park, Hyohun Shima, Toshihide Yamaguchi, Kanji Mitsuyoshi, Hironori Minami, Masahito Yasui, Kohichiroh Itoh, Yoshito Yoshikawa, Toshikazu Fukui, Michiaki Hasegawa, Goji Nakamura, Naoto Ohta, Mitsuhiro Obayashi, Hiroshi Okanoue, Takeshi |
description | Background Hyperlipidemia, insulin resistance, and oxidative stress can heavily contribute to the initiation and progression of nonalcoholic fatty liver disease (NAFLD). Currently, there is no established treatment for this disease. Recently, several studies have shown that ezetimibe (EZ), a lipid-lowering drug, attenuates liver steatosis in an experimental NAFLD model. This study was designed to assess the efficacy of long-term EZ monotherapy in patients with NAFLD. Methods A total of 45 patients with newly diagnosed liver biopsy-proven NAFLD were treated with EZ (10 mg/day) for 24 months. NAFLD-related biochemical parameters, imaging by computerized tomography, and liver biopsy were studied before and after treatment. Results Ezetimibe therapy significantly improved NAFLD-related metabolic parameters including visceral fat area, fasting insulin, homeostasis model assessment of insulin resistance (HOMA-R), triglycerides, total cholesterol, low-density lipoprotein cholesterol (LDL-Ch), oxidative-LDL, the net electronegative charge modified-LDL, profiles of lipoprotein particle size and fatty acids component, and estimated desaturase activity. EZ therapy also significantly lowered serum alanine aminotransferase and high-sensitivity C-reactive protein levels, whereas no significant changes were found in serum type IV collagen 7S, adiponectin, leptin, and resistin levels. Histological features of steatosis grade (P = 0.0003), necroinflammatory grade (P = 0.0456), ballooning score (P = 0.0253), and NAFLD activity score (NAS) (P = 0.0007) were significantly improved from baseline. However, the fibrosis stage was not significantly (P = 0.6547) changed. Conclusion The results in this study suggest that the long-term EZ therapy can lead to improvement in metabolic, biochemical, and histological abnormalities of NAFLD. Therefore, EZ may be a promising agent for treatment of NAFLD. |
doi_str_mv | 10.1007/s00535-010-0291-8 |
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Currently, there is no established treatment for this disease. Recently, several studies have shown that ezetimibe (EZ), a lipid-lowering drug, attenuates liver steatosis in an experimental NAFLD model. This study was designed to assess the efficacy of long-term EZ monotherapy in patients with NAFLD. Methods A total of 45 patients with newly diagnosed liver biopsy-proven NAFLD were treated with EZ (10 mg/day) for 24 months. NAFLD-related biochemical parameters, imaging by computerized tomography, and liver biopsy were studied before and after treatment. Results Ezetimibe therapy significantly improved NAFLD-related metabolic parameters including visceral fat area, fasting insulin, homeostasis model assessment of insulin resistance (HOMA-R), triglycerides, total cholesterol, low-density lipoprotein cholesterol (LDL-Ch), oxidative-LDL, the net electronegative charge modified-LDL, profiles of lipoprotein particle size and fatty acids component, and estimated desaturase activity. EZ therapy also significantly lowered serum alanine aminotransferase and high-sensitivity C-reactive protein levels, whereas no significant changes were found in serum type IV collagen 7S, adiponectin, leptin, and resistin levels. Histological features of steatosis grade (P = 0.0003), necroinflammatory grade (P = 0.0456), ballooning score (P = 0.0253), and NAFLD activity score (NAS) (P = 0.0007) were significantly improved from baseline. However, the fibrosis stage was not significantly (P = 0.6547) changed. Conclusion The results in this study suggest that the long-term EZ therapy can lead to improvement in metabolic, biochemical, and histological abnormalities of NAFLD. Therefore, EZ may be a promising agent for treatment of NAFLD.</description><identifier>ISSN: 0944-1174</identifier><identifier>EISSN: 1435-5922</identifier><identifier>DOI: 10.1007/s00535-010-0291-8</identifier><identifier>PMID: 20658156</identifier><language>eng</language><publisher>Japan: Japan : Springer Japan</publisher><subject>Abdominal Surgery ; Adult ; Anticholesteremic Agents - administration & dosage ; Anticholesteremic Agents - therapeutic use ; Azetidines - administration & dosage ; Azetidines - therapeutic use ; Biliary Tract ; Biomarkers - blood ; Biopsy ; Care and treatment ; Colorectal Surgery ; Development and progression ; Drug Administration Schedule ; Ezetimibe ; Fatty acid metabolism ; Fatty acids ; Fatty liver ; Fatty Liver - blood ; Fatty Liver - drug therapy ; Fatty Liver - pathology ; Female ; Gastroenterology ; Hepatology ; Humans ; Insulin resistance ; Leptin ; lipid metabolism ; Liver - pathology ; Liver Cirrhosis - classification ; Liver Cirrhosis - pathology ; Low density lipoproteins ; Male ; Medical colleges ; Medical research ; Medicine ; Medicine & Public Health ; Medicine, Experimental ; Middle Aged ; NAFLD ; Non-alcoholic Fatty Liver Disease ; Original Article—Liver ; Pancreas ; Surgical Oncology ; Treatment Outcome</subject><ispartof>Journal of gastroenterology, 2011, Vol.46 (1), p.101-107</ispartof><rights>Springer 2010</rights><rights>COPYRIGHT 2011 Springer</rights><rights>Springer 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c514t-b0c8b2d39156e67750afa446bc8362f5835198bbbcb83ee15a80c4391a62d5383</citedby><cites>FETCH-LOGICAL-c514t-b0c8b2d39156e67750afa446bc8362f5835198bbbcb83ee15a80c4391a62d5383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20658156$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Hyohun</creatorcontrib><creatorcontrib>Shima, Toshihide</creatorcontrib><creatorcontrib>Yamaguchi, Kanji</creatorcontrib><creatorcontrib>Mitsuyoshi, Hironori</creatorcontrib><creatorcontrib>Minami, Masahito</creatorcontrib><creatorcontrib>Yasui, Kohichiroh</creatorcontrib><creatorcontrib>Itoh, Yoshito</creatorcontrib><creatorcontrib>Yoshikawa, Toshikazu</creatorcontrib><creatorcontrib>Fukui, Michiaki</creatorcontrib><creatorcontrib>Hasegawa, Goji</creatorcontrib><creatorcontrib>Nakamura, Naoto</creatorcontrib><creatorcontrib>Ohta, Mitsuhiro</creatorcontrib><creatorcontrib>Obayashi, Hiroshi</creatorcontrib><creatorcontrib>Okanoue, Takeshi</creatorcontrib><title>Efficacy of long-term ezetimibe therapy in patients with nonalcoholic fatty liver disease</title><title>Journal of gastroenterology</title><addtitle>J Gastroenterol</addtitle><addtitle>J Gastroenterol</addtitle><description>Background Hyperlipidemia, insulin resistance, and oxidative stress can heavily contribute to the initiation and progression of nonalcoholic fatty liver disease (NAFLD). Currently, there is no established treatment for this disease. Recently, several studies have shown that ezetimibe (EZ), a lipid-lowering drug, attenuates liver steatosis in an experimental NAFLD model. This study was designed to assess the efficacy of long-term EZ monotherapy in patients with NAFLD. Methods A total of 45 patients with newly diagnosed liver biopsy-proven NAFLD were treated with EZ (10 mg/day) for 24 months. NAFLD-related biochemical parameters, imaging by computerized tomography, and liver biopsy were studied before and after treatment. Results Ezetimibe therapy significantly improved NAFLD-related metabolic parameters including visceral fat area, fasting insulin, homeostasis model assessment of insulin resistance (HOMA-R), triglycerides, total cholesterol, low-density lipoprotein cholesterol (LDL-Ch), oxidative-LDL, the net electronegative charge modified-LDL, profiles of lipoprotein particle size and fatty acids component, and estimated desaturase activity. EZ therapy also significantly lowered serum alanine aminotransferase and high-sensitivity C-reactive protein levels, whereas no significant changes were found in serum type IV collagen 7S, adiponectin, leptin, and resistin levels. Histological features of steatosis grade (P = 0.0003), necroinflammatory grade (P = 0.0456), ballooning score (P = 0.0253), and NAFLD activity score (NAS) (P = 0.0007) were significantly improved from baseline. However, the fibrosis stage was not significantly (P = 0.6547) changed. Conclusion The results in this study suggest that the long-term EZ therapy can lead to improvement in metabolic, biochemical, and histological abnormalities of NAFLD. Therefore, EZ may be a promising agent for treatment of NAFLD.</description><subject>Abdominal Surgery</subject><subject>Adult</subject><subject>Anticholesteremic Agents - administration & dosage</subject><subject>Anticholesteremic Agents - therapeutic use</subject><subject>Azetidines - administration & dosage</subject><subject>Azetidines - therapeutic use</subject><subject>Biliary Tract</subject><subject>Biomarkers - blood</subject><subject>Biopsy</subject><subject>Care and treatment</subject><subject>Colorectal Surgery</subject><subject>Development and progression</subject><subject>Drug Administration Schedule</subject><subject>Ezetimibe</subject><subject>Fatty acid metabolism</subject><subject>Fatty acids</subject><subject>Fatty liver</subject><subject>Fatty Liver - blood</subject><subject>Fatty Liver - drug therapy</subject><subject>Fatty Liver - pathology</subject><subject>Female</subject><subject>Gastroenterology</subject><subject>Hepatology</subject><subject>Humans</subject><subject>Insulin resistance</subject><subject>Leptin</subject><subject>lipid metabolism</subject><subject>Liver - pathology</subject><subject>Liver Cirrhosis - classification</subject><subject>Liver Cirrhosis - pathology</subject><subject>Low density lipoproteins</subject><subject>Male</subject><subject>Medical colleges</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Medicine, Experimental</subject><subject>Middle Aged</subject><subject>NAFLD</subject><subject>Non-alcoholic Fatty Liver Disease</subject><subject>Original Article—Liver</subject><subject>Pancreas</subject><subject>Surgical Oncology</subject><subject>Treatment Outcome</subject><issn>0944-1174</issn><issn>1435-5922</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9ks1u1DAUhSMEokPhAdiARResUq7_EmdZVS0gVWIBXbCyHOd6xlUSD7YHNDw9jlJAIIS8sHT9naN7dFxVzymcU4D2TQKQXNZAoQbW0Vo9qDZUlInsGHtYbaAToqa0FSfVk5TuACgHqR5XJwwaqahsNtXnK-e8NfZIgiNjmLd1xjgR_I7ZT75HkncYzf5I_Ez2JnuccyLffN6ROcxmtGEXRm-JMzkfyei_YiSDT2gSPq0eOTMmfHZ_n1a311efLt_VNx_evr-8uKmtpCLXPVjVs4F3ZR1s2laCcUaIpreKN8xJxSXtVN_3tlcckUqjwIqCm4YNkit-Wr1effcxfDlgynryyeI4mhnDIWklgEspQRTy1V_kXTjEkqJAvGulYnSBzlZoa0bUfnYhR2MXS33RUiFV08mFOv8HVc6Ak7dhRufL_A8BXQU2hpQiOr2PfjLxqCnopUy9lqlLmXopUy_JXtzve-gnHH4pfrZXALYCqTzNW4y_A_3P9eUqciZos40-6duPbPkatGMtBc5_ALJOsMQ</recordid><startdate>2011</startdate><enddate>2011</enddate><creator>Park, Hyohun</creator><creator>Shima, Toshihide</creator><creator>Yamaguchi, Kanji</creator><creator>Mitsuyoshi, Hironori</creator><creator>Minami, Masahito</creator><creator>Yasui, Kohichiroh</creator><creator>Itoh, Yoshito</creator><creator>Yoshikawa, Toshikazu</creator><creator>Fukui, Michiaki</creator><creator>Hasegawa, Goji</creator><creator>Nakamura, Naoto</creator><creator>Ohta, Mitsuhiro</creator><creator>Obayashi, Hiroshi</creator><creator>Okanoue, Takeshi</creator><general>Japan : Springer Japan</general><general>Springer Japan</general><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</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>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>2011</creationdate><title>Efficacy of long-term ezetimibe therapy in patients with nonalcoholic fatty liver disease</title><author>Park, Hyohun ; Shima, Toshihide ; Yamaguchi, Kanji ; Mitsuyoshi, Hironori ; Minami, Masahito ; Yasui, Kohichiroh ; Itoh, Yoshito ; Yoshikawa, Toshikazu ; Fukui, Michiaki ; Hasegawa, Goji ; Nakamura, Naoto ; Ohta, Mitsuhiro ; Obayashi, Hiroshi ; Okanoue, Takeshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c514t-b0c8b2d39156e67750afa446bc8362f5835198bbbcb83ee15a80c4391a62d5383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Abdominal Surgery</topic><topic>Adult</topic><topic>Anticholesteremic Agents - administration & dosage</topic><topic>Anticholesteremic Agents - therapeutic use</topic><topic>Azetidines - administration & dosage</topic><topic>Azetidines - therapeutic use</topic><topic>Biliary Tract</topic><topic>Biomarkers - blood</topic><topic>Biopsy</topic><topic>Care and treatment</topic><topic>Colorectal Surgery</topic><topic>Development and progression</topic><topic>Drug Administration Schedule</topic><topic>Ezetimibe</topic><topic>Fatty acid metabolism</topic><topic>Fatty acids</topic><topic>Fatty liver</topic><topic>Fatty Liver - blood</topic><topic>Fatty Liver - drug therapy</topic><topic>Fatty Liver - pathology</topic><topic>Female</topic><topic>Gastroenterology</topic><topic>Hepatology</topic><topic>Humans</topic><topic>Insulin resistance</topic><topic>Leptin</topic><topic>lipid metabolism</topic><topic>Liver - pathology</topic><topic>Liver Cirrhosis - classification</topic><topic>Liver Cirrhosis - pathology</topic><topic>Low density lipoproteins</topic><topic>Male</topic><topic>Medical colleges</topic><topic>Medical research</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Medicine, Experimental</topic><topic>Middle Aged</topic><topic>NAFLD</topic><topic>Non-alcoholic Fatty Liver Disease</topic><topic>Original Article—Liver</topic><topic>Pancreas</topic><topic>Surgical Oncology</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Hyohun</creatorcontrib><creatorcontrib>Shima, Toshihide</creatorcontrib><creatorcontrib>Yamaguchi, Kanji</creatorcontrib><creatorcontrib>Mitsuyoshi, Hironori</creatorcontrib><creatorcontrib>Minami, Masahito</creatorcontrib><creatorcontrib>Yasui, Kohichiroh</creatorcontrib><creatorcontrib>Itoh, Yoshito</creatorcontrib><creatorcontrib>Yoshikawa, Toshikazu</creatorcontrib><creatorcontrib>Fukui, Michiaki</creatorcontrib><creatorcontrib>Hasegawa, Goji</creatorcontrib><creatorcontrib>Nakamura, Naoto</creatorcontrib><creatorcontrib>Ohta, Mitsuhiro</creatorcontrib><creatorcontrib>Obayashi, Hiroshi</creatorcontrib><creatorcontrib>Okanoue, Takeshi</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing & Allied Health Database</collection><collection>Immunology Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Consumer Health Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of gastroenterology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Hyohun</au><au>Shima, Toshihide</au><au>Yamaguchi, Kanji</au><au>Mitsuyoshi, Hironori</au><au>Minami, Masahito</au><au>Yasui, Kohichiroh</au><au>Itoh, Yoshito</au><au>Yoshikawa, Toshikazu</au><au>Fukui, Michiaki</au><au>Hasegawa, Goji</au><au>Nakamura, Naoto</au><au>Ohta, Mitsuhiro</au><au>Obayashi, Hiroshi</au><au>Okanoue, Takeshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy of long-term ezetimibe therapy in patients with nonalcoholic fatty liver disease</atitle><jtitle>Journal of gastroenterology</jtitle><stitle>J Gastroenterol</stitle><addtitle>J Gastroenterol</addtitle><date>2011</date><risdate>2011</risdate><volume>46</volume><issue>1</issue><spage>101</spage><epage>107</epage><pages>101-107</pages><issn>0944-1174</issn><eissn>1435-5922</eissn><abstract>Background Hyperlipidemia, insulin resistance, and oxidative stress can heavily contribute to the initiation and progression of nonalcoholic fatty liver disease (NAFLD). Currently, there is no established treatment for this disease. Recently, several studies have shown that ezetimibe (EZ), a lipid-lowering drug, attenuates liver steatosis in an experimental NAFLD model. This study was designed to assess the efficacy of long-term EZ monotherapy in patients with NAFLD. Methods A total of 45 patients with newly diagnosed liver biopsy-proven NAFLD were treated with EZ (10 mg/day) for 24 months. NAFLD-related biochemical parameters, imaging by computerized tomography, and liver biopsy were studied before and after treatment. Results Ezetimibe therapy significantly improved NAFLD-related metabolic parameters including visceral fat area, fasting insulin, homeostasis model assessment of insulin resistance (HOMA-R), triglycerides, total cholesterol, low-density lipoprotein cholesterol (LDL-Ch), oxidative-LDL, the net electronegative charge modified-LDL, profiles of lipoprotein particle size and fatty acids component, and estimated desaturase activity. EZ therapy also significantly lowered serum alanine aminotransferase and high-sensitivity C-reactive protein levels, whereas no significant changes were found in serum type IV collagen 7S, adiponectin, leptin, and resistin levels. Histological features of steatosis grade (P = 0.0003), necroinflammatory grade (P = 0.0456), ballooning score (P = 0.0253), and NAFLD activity score (NAS) (P = 0.0007) were significantly improved from baseline. However, the fibrosis stage was not significantly (P = 0.6547) changed. Conclusion The results in this study suggest that the long-term EZ therapy can lead to improvement in metabolic, biochemical, and histological abnormalities of NAFLD. Therefore, EZ may be a promising agent for treatment of NAFLD.</abstract><cop>Japan</cop><pub>Japan : Springer Japan</pub><pmid>20658156</pmid><doi>10.1007/s00535-010-0291-8</doi><tpages>7</tpages></addata></record> |
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subjects | Abdominal Surgery Adult Anticholesteremic Agents - administration & dosage Anticholesteremic Agents - therapeutic use Azetidines - administration & dosage Azetidines - therapeutic use Biliary Tract Biomarkers - blood Biopsy Care and treatment Colorectal Surgery Development and progression Drug Administration Schedule Ezetimibe Fatty acid metabolism Fatty acids Fatty liver Fatty Liver - blood Fatty Liver - drug therapy Fatty Liver - pathology Female Gastroenterology Hepatology Humans Insulin resistance Leptin lipid metabolism Liver - pathology Liver Cirrhosis - classification Liver Cirrhosis - pathology Low density lipoproteins Male Medical colleges Medical research Medicine Medicine & Public Health Medicine, Experimental Middle Aged NAFLD Non-alcoholic Fatty Liver Disease Original Article—Liver Pancreas Surgical Oncology Treatment Outcome |
title | Efficacy of long-term ezetimibe therapy in patients with nonalcoholic fatty liver disease |
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