The role of hepatokines in NAFLD
Non-alcoholic fatty liver disease (NAFLD) is not only a consequence of insulin resistance, but it is also an important cause of insulin resistance and major non-communicable diseases (NCDs). The close relationship of NAFLD with visceral obesity obscures the role of fatty liver from visceral adiposit...
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Veröffentlicht in: | Cell metabolism 2023-02, Vol.35 (2), p.236-252 |
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creator | Stefan, Norbert Schick, Fritz Birkenfeld, Andreas L. Häring, Hans-Ulrich White, Morris F. |
description | Non-alcoholic fatty liver disease (NAFLD) is not only a consequence of insulin resistance, but it is also an important cause of insulin resistance and major non-communicable diseases (NCDs). The close relationship of NAFLD with visceral obesity obscures the role of fatty liver from visceral adiposity as the main pathomechanism of insulin resistance and NCDs. To overcome this limitation, in analogy to the concept of adipokines, in 2008 we introduced the term hepatokines to describe the role of fetuin-A in metabolism. Since then, several other hepatokines were tested for their effects on metabolism. Here we address the dysregulation of hepatokines in people with NAFLD. Then, we discuss pathophysiological mechanisms of cardiometabolic diseases specifically related to NAFLD by focusing on hepatokine-related organ crosstalk. Finally, we propose how the determination of major hepatokines and adipokines can be used for pathomechanism-based clustering of insulin resistance in NAFLD and visceral obesity to better implement precision medicine in clinical practice.
In this perspective, Stefan et al. address the dysregulation of hepatokines in people with NAFLD. The authors discuss the pathophysiological role of hepatokine-related organ crosstalk in the development of cardiometabolic disorders. Finally, the authors propose how levels of major hepatokines and adipokines may be used for pathomechanism-based clustering of insulin resistance in NAFLD and visceral obesity. |
doi_str_mv | 10.1016/j.cmet.2023.01.006 |
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In this perspective, Stefan et al. address the dysregulation of hepatokines in people with NAFLD. The authors discuss the pathophysiological role of hepatokine-related organ crosstalk in the development of cardiometabolic disorders. Finally, the authors propose how levels of major hepatokines and adipokines may be used for pathomechanism-based clustering of insulin resistance in NAFLD and visceral obesity.</description><identifier>ISSN: 1550-4131</identifier><identifier>EISSN: 1932-7420</identifier><identifier>DOI: 10.1016/j.cmet.2023.01.006</identifier><identifier>PMID: 36754018</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adipokines ; Humans ; Insulin Resistance ; Non-alcoholic Fatty Liver Disease - metabolism ; Obesity, Abdominal</subject><ispartof>Cell metabolism, 2023-02, Vol.35 (2), p.236-252</ispartof><rights>2023 Elsevier Inc.</rights><rights>Copyright © 2023 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-4db86b68bbb827fdddba4fdb8a6fc5a6a4ad69108fc5056a59c10f2090db49543</citedby><cites>FETCH-LOGICAL-c456t-4db86b68bbb827fdddba4fdb8a6fc5a6a4ad69108fc5056a59c10f2090db49543</cites><orcidid>0000-0003-2166-508X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1550413123000062$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36754018$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stefan, Norbert</creatorcontrib><creatorcontrib>Schick, Fritz</creatorcontrib><creatorcontrib>Birkenfeld, Andreas L.</creatorcontrib><creatorcontrib>Häring, Hans-Ulrich</creatorcontrib><creatorcontrib>White, Morris F.</creatorcontrib><title>The role of hepatokines in NAFLD</title><title>Cell metabolism</title><addtitle>Cell Metab</addtitle><description>Non-alcoholic fatty liver disease (NAFLD) is not only a consequence of insulin resistance, but it is also an important cause of insulin resistance and major non-communicable diseases (NCDs). The close relationship of NAFLD with visceral obesity obscures the role of fatty liver from visceral adiposity as the main pathomechanism of insulin resistance and NCDs. To overcome this limitation, in analogy to the concept of adipokines, in 2008 we introduced the term hepatokines to describe the role of fetuin-A in metabolism. Since then, several other hepatokines were tested for their effects on metabolism. Here we address the dysregulation of hepatokines in people with NAFLD. Then, we discuss pathophysiological mechanisms of cardiometabolic diseases specifically related to NAFLD by focusing on hepatokine-related organ crosstalk. Finally, we propose how the determination of major hepatokines and adipokines can be used for pathomechanism-based clustering of insulin resistance in NAFLD and visceral obesity to better implement precision medicine in clinical practice.
In this perspective, Stefan et al. address the dysregulation of hepatokines in people with NAFLD. The authors discuss the pathophysiological role of hepatokine-related organ crosstalk in the development of cardiometabolic disorders. Finally, the authors propose how levels of major hepatokines and adipokines may be used for pathomechanism-based clustering of insulin resistance in NAFLD and visceral obesity.</description><subject>Adipokines</subject><subject>Humans</subject><subject>Insulin Resistance</subject><subject>Non-alcoholic Fatty Liver Disease - metabolism</subject><subject>Obesity, Abdominal</subject><issn>1550-4131</issn><issn>1932-7420</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1PxCAQhonR-P0HPJgevbQOLVCamBjjd7LRi54JhanL2i0rdE3897JZNXrxxMC88wx5CDmiUFCg4nRWmDmORQllVQAtAMQG2aVNVeY1K2Ez1ZxDzmhFd8hejDOASlRNtU12KlFzBlTukuxpilnwPWa-y6a40KN_dQPGzA3Zw8XN5OqAbHW6j3j4de6T55vrp8u7fPJ4e395MckN42LMmW2laIVs21aWdWetbTXr0qMWneFaaKataCjIdAMuNG8Mha6EBmzLGs6qfXK-5i6W7RytwWEMuleL4OY6fCivnfrbGdxUvfh3lVTwWjY8EU6-CMG_LTGOau6iwb7XA_plVGVdM9nUtZQpWq6jJvgYA3Y_eyisgELN1MqtWrlVQFVym4aOf__wZ-RbZgqcrQOYPL07DCoah4NB6wKaUVnv_uN_AlQJihU</recordid><startdate>20230207</startdate><enddate>20230207</enddate><creator>Stefan, Norbert</creator><creator>Schick, Fritz</creator><creator>Birkenfeld, Andreas L.</creator><creator>Häring, Hans-Ulrich</creator><creator>White, Morris F.</creator><general>Elsevier Inc</general><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><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2166-508X</orcidid></search><sort><creationdate>20230207</creationdate><title>The role of hepatokines in NAFLD</title><author>Stefan, Norbert ; Schick, Fritz ; Birkenfeld, Andreas L. ; Häring, Hans-Ulrich ; White, Morris F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-4db86b68bbb827fdddba4fdb8a6fc5a6a4ad69108fc5056a59c10f2090db49543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adipokines</topic><topic>Humans</topic><topic>Insulin Resistance</topic><topic>Non-alcoholic Fatty Liver Disease - metabolism</topic><topic>Obesity, Abdominal</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stefan, Norbert</creatorcontrib><creatorcontrib>Schick, Fritz</creatorcontrib><creatorcontrib>Birkenfeld, Andreas L.</creatorcontrib><creatorcontrib>Häring, Hans-Ulrich</creatorcontrib><creatorcontrib>White, Morris F.</creatorcontrib><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stefan, Norbert</au><au>Schick, Fritz</au><au>Birkenfeld, Andreas L.</au><au>Häring, Hans-Ulrich</au><au>White, Morris F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The role of hepatokines in NAFLD</atitle><jtitle>Cell metabolism</jtitle><addtitle>Cell Metab</addtitle><date>2023-02-07</date><risdate>2023</risdate><volume>35</volume><issue>2</issue><spage>236</spage><epage>252</epage><pages>236-252</pages><issn>1550-4131</issn><eissn>1932-7420</eissn><abstract>Non-alcoholic fatty liver disease (NAFLD) is not only a consequence of insulin resistance, but it is also an important cause of insulin resistance and major non-communicable diseases (NCDs). The close relationship of NAFLD with visceral obesity obscures the role of fatty liver from visceral adiposity as the main pathomechanism of insulin resistance and NCDs. To overcome this limitation, in analogy to the concept of adipokines, in 2008 we introduced the term hepatokines to describe the role of fetuin-A in metabolism. Since then, several other hepatokines were tested for their effects on metabolism. Here we address the dysregulation of hepatokines in people with NAFLD. Then, we discuss pathophysiological mechanisms of cardiometabolic diseases specifically related to NAFLD by focusing on hepatokine-related organ crosstalk. Finally, we propose how the determination of major hepatokines and adipokines can be used for pathomechanism-based clustering of insulin resistance in NAFLD and visceral obesity to better implement precision medicine in clinical practice.
In this perspective, Stefan et al. address the dysregulation of hepatokines in people with NAFLD. The authors discuss the pathophysiological role of hepatokine-related organ crosstalk in the development of cardiometabolic disorders. Finally, the authors propose how levels of major hepatokines and adipokines may be used for pathomechanism-based clustering of insulin resistance in NAFLD and visceral obesity.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>36754018</pmid><doi>10.1016/j.cmet.2023.01.006</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0003-2166-508X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adipokines Humans Insulin Resistance Non-alcoholic Fatty Liver Disease - metabolism Obesity, Abdominal |
title | The role of hepatokines in NAFLD |
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