Effect of fructose on markers of non-alcoholic fatty liver disease : a systematic review and meta-analysis of controlled feeding trials
SUBJECTS/METHODS: We searched MEDLINE, EMBASE, CINAHL and the Cochrane Library (through 3 September 2013). We included relevant trials that involved a follow-up of ≥7 days. Two reviewers independently extracted relevant data. Data were pooled by the generic inverse variance method using random effec...
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Veröffentlicht in: | European Journal of Clinical Nutrition 2014, Vol.68 (4), p.416 |
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container_title | European Journal of Clinical Nutrition |
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creator | Chiu, S Sievenpiper, J.L de Souza, R.J Cozma, A.I Mirrahimi, A Carleton, A.J Ha, V Di Buono, M Jenkins, A.L Leiter, L.A Wolever, T.M.S Don-Wauchope, A.C Beyene, J Kendall, C.W.C Jenkins, D.J.A |
description | SUBJECTS/METHODS: We searched MEDLINE, EMBASE, CINAHL and the Cochrane Library (through 3 September 2013). We included relevant trials that involved a follow-up of ≥7 days. Two reviewers independently extracted relevant data. Data were pooled by the generic inverse variance method using random effects models and expressed as standardized mean difference (SMD) for intrahepatocellular lipids (IHCL) and mean difference (MD) for alanine aminotransferase (ALT). Inter-study heterogeneity was assessed (Cochran Q statistic) and quantified ([/.sup.2] statistic). LIMITATIONS: Few trials were available for inclusion, most of which were small, short (≤4 weeks), and of poor quality. Fructose providing excess energy at extreme doses, however, does raise IHCL and ALT, an effect that may be more attributable to excess energy than fructose. Larger, longer and higher-quality trials of the effect of fructose on histopathological NAFLD changes are required. |
doi_str_mv | 10.1038/ejcn.2014.8 |
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We included relevant trials that involved a follow-up of ≥7 days. Two reviewers independently extracted relevant data. Data were pooled by the generic inverse variance method using random effects models and expressed as standardized mean difference (SMD) for intrahepatocellular lipids (IHCL) and mean difference (MD) for alanine aminotransferase (ALT). Inter-study heterogeneity was assessed (Cochran Q statistic) and quantified ([/.sup.2] statistic). LIMITATIONS: Few trials were available for inclusion, most of which were small, short (≤4 weeks), and of poor quality. Fructose providing excess energy at extreme doses, however, does raise IHCL and ALT, an effect that may be more attributable to excess energy than fructose. Larger, longer and higher-quality trials of the effect of fructose on histopathological NAFLD changes are required.</description><identifier>ISSN: 0954-3007</identifier><identifier>DOI: 10.1038/ejcn.2014.8</identifier><language>eng</language><publisher>Nature Publishing Group</publisher><subject>Analysis ; Fatty liver ; Fructose ; Physiological aspects ; Risk factors</subject><ispartof>European Journal of Clinical Nutrition, 2014, Vol.68 (4), p.416</ispartof><rights>COPYRIGHT 2014 Nature Publishing Group</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,780,4476,27902</link.rule.ids></links><search><creatorcontrib>Chiu, S</creatorcontrib><creatorcontrib>Sievenpiper, J.L</creatorcontrib><creatorcontrib>de Souza, R.J</creatorcontrib><creatorcontrib>Cozma, A.I</creatorcontrib><creatorcontrib>Mirrahimi, A</creatorcontrib><creatorcontrib>Carleton, A.J</creatorcontrib><creatorcontrib>Ha, V</creatorcontrib><creatorcontrib>Di Buono, M</creatorcontrib><creatorcontrib>Jenkins, A.L</creatorcontrib><creatorcontrib>Leiter, L.A</creatorcontrib><creatorcontrib>Wolever, T.M.S</creatorcontrib><creatorcontrib>Don-Wauchope, A.C</creatorcontrib><creatorcontrib>Beyene, J</creatorcontrib><creatorcontrib>Kendall, C.W.C</creatorcontrib><creatorcontrib>Jenkins, D.J.A</creatorcontrib><title>Effect of fructose on markers of non-alcoholic fatty liver disease : a systematic review and meta-analysis of controlled feeding trials</title><title>European Journal of Clinical Nutrition</title><description>SUBJECTS/METHODS: We searched MEDLINE, EMBASE, CINAHL and the Cochrane Library (through 3 September 2013). We included relevant trials that involved a follow-up of ≥7 days. Two reviewers independently extracted relevant data. Data were pooled by the generic inverse variance method using random effects models and expressed as standardized mean difference (SMD) for intrahepatocellular lipids (IHCL) and mean difference (MD) for alanine aminotransferase (ALT). Inter-study heterogeneity was assessed (Cochran Q statistic) and quantified ([/.sup.2] statistic). LIMITATIONS: Few trials were available for inclusion, most of which were small, short (≤4 weeks), and of poor quality. Fructose providing excess energy at extreme doses, however, does raise IHCL and ALT, an effect that may be more attributable to excess energy than fructose. 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We included relevant trials that involved a follow-up of ≥7 days. Two reviewers independently extracted relevant data. Data were pooled by the generic inverse variance method using random effects models and expressed as standardized mean difference (SMD) for intrahepatocellular lipids (IHCL) and mean difference (MD) for alanine aminotransferase (ALT). Inter-study heterogeneity was assessed (Cochran Q statistic) and quantified ([/.sup.2] statistic). LIMITATIONS: Few trials were available for inclusion, most of which were small, short (≤4 weeks), and of poor quality. Fructose providing excess energy at extreme doses, however, does raise IHCL and ALT, an effect that may be more attributable to excess energy than fructose. Larger, longer and higher-quality trials of the effect of fructose on histopathological NAFLD changes are required.</abstract><pub>Nature Publishing Group</pub><doi>10.1038/ejcn.2014.8</doi></addata></record> |
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source | Springer Nature - Complete Springer Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Analysis Fatty liver Fructose Physiological aspects Risk factors |
title | Effect of fructose on markers of non-alcoholic fatty liver disease : a systematic review and meta-analysis of controlled feeding trials |
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