Pro-Inflammatory Interleukin-18 is Associated with Hepatic Steatosis and Elevated Liver Enzymes in People with HIV Monoinfection
People with HIV (PWH) are at an increased risk of developing nonalcoholic fatty liver disease (NAFLD). Interleukin (IL)-18 is regulated by inflammasomes in response to pathogens and danger signals and has been implicated in both the pathogenesis of NAFLD and HIV disease progression. We hypothesized...
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Veröffentlicht in: | AIDS research and human retroviruses 2021-05, Vol.37 (5), p.385-390 |
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description | People with HIV (PWH) are at an increased risk of developing nonalcoholic fatty liver disease (NAFLD). Interleukin (IL)-18 is regulated by inflammasomes in response to pathogens and danger signals and has been implicated in both the pathogenesis of NAFLD and HIV disease progression. We hypothesized that increased IL-18 may be associated with NAFLD and liver injury in PWH. This was an observational study of 125 PWH and 59 individuals without HIV in the Boston area. Participants with known hepatitis B, hepatitis C, and excessive alcohol use were excluded. IL-18 was measured in serum by enzyme-linked immunosorbent assay. Liver lipid content was assessed by liver-to-spleen computed tomography (CT) attenuation ratio. Aspartate aminotransferase (AST), alanine aminotransferase (ALT), and IL-18 levels were higher in PWH than in controls. In PWH, log(10) IL-18 was associated with log(10)AST (r = 0.34, p = .0001), log(10)ALT (r = 0.33, p = .0002), log(10)HIV RNA (r = 0.29, p = .002), and inversely associated with liver-to-spleen ratio (r = -0.24, p = .02). In addition, log(10) IL-18 was associated with log(10) triglycerides (r = 0.26, p = .003), log(10) MCP-1 (monocyte chemoattractant protein-1; r = 0.33, p = .0004), log(10)caspase-1 (r = 0.35, p < .0001), log(10)LPS (r = 0.28, p = .004), and inversely associated with high-density lipoprotein (r = -0.28, p = .002), and CD4(+)/CD8(+) T cell ratio (r = -0.24, p = .007). In controls without HIV, log(10) IL-18 was also associated with log(10)ALT (r = 0.44, p = .0005). After adjusting for potential confounders, the relationships between IL-18 and AST (p = .004) and ALT (p = .003) remained significant, and the relationship between IL-18 and liver-to-spleen ratio (p = .02). Increased inflammasome activation and subsequent monocyte recruitment in PWH may contribute to the development and progression of NAFLD. Clinical Trials Registration. NCT00455793. |
doi_str_mv | 10.1089/aid.2020.0177 |
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Interleukin (IL)-18 is regulated by inflammasomes in response to pathogens and danger signals and has been implicated in both the pathogenesis of NAFLD and HIV disease progression. We hypothesized that increased IL-18 may be associated with NAFLD and liver injury in PWH. This was an observational study of 125 PWH and 59 individuals without HIV in the Boston area. Participants with known hepatitis B, hepatitis C, and excessive alcohol use were excluded. IL-18 was measured in serum by enzyme-linked immunosorbent assay. Liver lipid content was assessed by liver-to-spleen computed tomography (CT) attenuation ratio. Aspartate aminotransferase (AST), alanine aminotransferase (ALT), and IL-18 levels were higher in PWH than in controls. In PWH, log(10) IL-18 was associated with log(10)AST (r = 0.34, p = .0001), log(10)ALT (r = 0.33, p = .0002), log(10)HIV RNA (r = 0.29, p = .002), and inversely associated with liver-to-spleen ratio (r = -0.24, p = .02). In addition, log(10) IL-18 was associated with log(10) triglycerides (r = 0.26, p = .003), log(10) MCP-1 (monocyte chemoattractant protein-1; r = 0.33, p = .0004), log(10)caspase-1 (r = 0.35, p < .0001), log(10)LPS (r = 0.28, p = .004), and inversely associated with high-density lipoprotein (r = -0.28, p = .002), and CD4(+)/CD8(+) T cell ratio (r = -0.24, p = .007). In controls without HIV, log(10) IL-18 was also associated with log(10)ALT (r = 0.44, p = .0005). After adjusting for potential confounders, the relationships between IL-18 and AST (p = .004) and ALT (p = .003) remained significant, and the relationship between IL-18 and liver-to-spleen ratio (p = .02). Increased inflammasome activation and subsequent monocyte recruitment in PWH may contribute to the development and progression of NAFLD. Clinical Trials Registration. NCT00455793.</description><identifier>ISSN: 0889-2229</identifier><identifier>EISSN: 1931-8405</identifier><identifier>DOI: 10.1089/aid.2020.0177</identifier><identifier>PMID: 33323025</identifier><language>eng</language><publisher>NEW ROCHELLE: Mary Ann Liebert, Inc</publisher><subject>Alanine ; Alanine Transaminase ; Aspartate aminotransferase ; Attenuation ; CD4 antigen ; CD8 antigen ; Cell activation ; Clinical trials ; Computed tomography ; Cytokines ; Enzyme-linked immunosorbent assay ; Fatty liver ; Hepatitis ; Hepatitis B ; Hepatitis C ; HIV ; HIV Infections - complications ; Human immunodeficiency virus ; Humans ; Immunology ; Infectious Diseases ; Inflammasomes ; Inflammation ; Interleukin 18 ; Life Sciences & Biomedicine ; Lipids ; Liver ; Liver - diagnostic imaging ; Liver diseases ; Lymphocytes ; Lymphocytes T ; Monocyte chemoattractant protein ; Monocyte chemoattractant protein 1 ; Monocytes ; Non-alcoholic Fatty Liver Disease ; Pathogenesis ; Science & Technology ; Spleen ; Steatosis ; Triglycerides ; Virology</subject><ispartof>AIDS research and human retroviruses, 2021-05, Vol.37 (5), p.385-390</ispartof><rights>Copyright Mary Ann Liebert, Inc. May 2021</rights><rights>Copyright 2021, Mary Ann Liebert, Inc., publishers 2021 Mary Ann Liebert, Inc., publishers</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>8</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000613494400001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c415t-9039b654b256a12a7107ba28f60e78fd01dd3c1f1f95cd677c643b6c3b78fc93</citedby><cites>FETCH-LOGICAL-c415t-9039b654b256a12a7107ba28f60e78fd01dd3c1f1f95cd677c643b6c3b78fc93</cites><orcidid>0000-0002-2336-2958</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,27928,27929</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33323025$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sim, Jae H.</creatorcontrib><creatorcontrib>Sherman, Julia B.</creatorcontrib><creatorcontrib>Stanley, Takara L.</creatorcontrib><creatorcontrib>Corey, Kathleen E.</creatorcontrib><creatorcontrib>Fitch, Kathleen V.</creatorcontrib><creatorcontrib>Looby, Sara E.</creatorcontrib><creatorcontrib>Robinson, Jake A.</creatorcontrib><creatorcontrib>Lu, Michael T.</creatorcontrib><creatorcontrib>Burdo, Tricia H.</creatorcontrib><creatorcontrib>Lo, Janet</creatorcontrib><title>Pro-Inflammatory Interleukin-18 is Associated with Hepatic Steatosis and Elevated Liver Enzymes in People with HIV Monoinfection</title><title>AIDS research and human retroviruses</title><addtitle>AIDS RES HUM RETROV</addtitle><addtitle>AIDS Res Hum Retroviruses</addtitle><description>People with HIV (PWH) are at an increased risk of developing nonalcoholic fatty liver disease (NAFLD). Interleukin (IL)-18 is regulated by inflammasomes in response to pathogens and danger signals and has been implicated in both the pathogenesis of NAFLD and HIV disease progression. We hypothesized that increased IL-18 may be associated with NAFLD and liver injury in PWH. This was an observational study of 125 PWH and 59 individuals without HIV in the Boston area. Participants with known hepatitis B, hepatitis C, and excessive alcohol use were excluded. IL-18 was measured in serum by enzyme-linked immunosorbent assay. Liver lipid content was assessed by liver-to-spleen computed tomography (CT) attenuation ratio. Aspartate aminotransferase (AST), alanine aminotransferase (ALT), and IL-18 levels were higher in PWH than in controls. In PWH, log(10) IL-18 was associated with log(10)AST (r = 0.34, p = .0001), log(10)ALT (r = 0.33, p = .0002), log(10)HIV RNA (r = 0.29, p = .002), and inversely associated with liver-to-spleen ratio (r = -0.24, p = .02). In addition, log(10) IL-18 was associated with log(10) triglycerides (r = 0.26, p = .003), log(10) MCP-1 (monocyte chemoattractant protein-1; r = 0.33, p = .0004), log(10)caspase-1 (r = 0.35, p < .0001), log(10)LPS (r = 0.28, p = .004), and inversely associated with high-density lipoprotein (r = -0.28, p = .002), and CD4(+)/CD8(+) T cell ratio (r = -0.24, p = .007). In controls without HIV, log(10) IL-18 was also associated with log(10)ALT (r = 0.44, p = .0005). After adjusting for potential confounders, the relationships between IL-18 and AST (p = .004) and ALT (p = .003) remained significant, and the relationship between IL-18 and liver-to-spleen ratio (p = .02). Increased inflammasome activation and subsequent monocyte recruitment in PWH may contribute to the development and progression of NAFLD. Clinical Trials Registration. NCT00455793.</description><subject>Alanine</subject><subject>Alanine Transaminase</subject><subject>Aspartate aminotransferase</subject><subject>Attenuation</subject><subject>CD4 antigen</subject><subject>CD8 antigen</subject><subject>Cell activation</subject><subject>Clinical trials</subject><subject>Computed tomography</subject><subject>Cytokines</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Fatty liver</subject><subject>Hepatitis</subject><subject>Hepatitis B</subject><subject>Hepatitis C</subject><subject>HIV</subject><subject>HIV Infections - complications</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Immunology</subject><subject>Infectious Diseases</subject><subject>Inflammasomes</subject><subject>Inflammation</subject><subject>Interleukin 18</subject><subject>Life Sciences & Biomedicine</subject><subject>Lipids</subject><subject>Liver</subject><subject>Liver - diagnostic imaging</subject><subject>Liver diseases</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Monocyte chemoattractant protein</subject><subject>Monocyte chemoattractant protein 1</subject><subject>Monocytes</subject><subject>Non-alcoholic Fatty Liver Disease</subject><subject>Pathogenesis</subject><subject>Science & Technology</subject><subject>Spleen</subject><subject>Steatosis</subject><subject>Triglycerides</subject><subject>Virology</subject><issn>0889-2229</issn><issn>1931-8405</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>HGBXW</sourceid><sourceid>EIF</sourceid><recordid>eNqNkc-LEzEUxwdR3O7q0asEvAgyNb9mMrkIS6luoeKCi9eQybxxs84kNcl0qaf9001tLerJ0wu8z_u-PD5F8YLgOcGNfKttN6eY4jkmQjwqZkQyUjYcV4-LGW4aWVJK5VlxHuMdxlhSWj0tzhhjlGFazYqH6-DLlesHPY46-bBDK5cgDDB9s64kDbIRXcbojdUJOnRv0y26go1O1qDPCfJIzIR2HVoOsP3FrO0WAlq6H7sRIrIOXYPfDHCcXX1BH73z1vVgkvXuWfGk10OE58d6Udy8X94srsr1pw-rxeW6NJxUqZSYybaueEurWhOqBcGi1bTpawyi6TtMuo4Z0pNeVqarhTA1Z21tWJu7RrKL4t0hdjO1I3QGXAp6UJtgRx12ymur_u44e6u--q1qCKGCNDng9TEg-O8TxKRGGw0Mg3bgp6goF7hmnAmc0Vf_oHd-Ci5fp2hFKcecVSRT5YEywccYoD99hmC1V6uyWrVXq_ZqM__yzwtO9G-XGXhzAO6h9X00FpyBE5bl14RxyXl-4f365v_phU16L2vhJ5fYT0tBwTo</recordid><startdate>20210501</startdate><enddate>20210501</enddate><creator>Sim, Jae H.</creator><creator>Sherman, Julia B.</creator><creator>Stanley, Takara L.</creator><creator>Corey, Kathleen E.</creator><creator>Fitch, Kathleen V.</creator><creator>Looby, Sara E.</creator><creator>Robinson, Jake A.</creator><creator>Lu, Michael T.</creator><creator>Burdo, Tricia H.</creator><creator>Lo, Janet</creator><general>Mary Ann Liebert, Inc</general><general>Mary Ann Liebert, Inc., publishers</general><scope>BLEPL</scope><scope>DTL</scope><scope>HGBXW</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>7QL</scope><scope>7T2</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2336-2958</orcidid></search><sort><creationdate>20210501</creationdate><title>Pro-Inflammatory Interleukin-18 is Associated with Hepatic Steatosis and Elevated Liver Enzymes in People with HIV Monoinfection</title><author>Sim, Jae H. ; Sherman, Julia B. ; Stanley, Takara L. ; Corey, Kathleen E. ; Fitch, Kathleen V. ; Looby, Sara E. ; Robinson, Jake A. ; Lu, Michael T. ; Burdo, Tricia H. ; Lo, Janet</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-9039b654b256a12a7107ba28f60e78fd01dd3c1f1f95cd677c643b6c3b78fc93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alanine</topic><topic>Alanine Transaminase</topic><topic>Aspartate aminotransferase</topic><topic>Attenuation</topic><topic>CD4 antigen</topic><topic>CD8 antigen</topic><topic>Cell activation</topic><topic>Clinical trials</topic><topic>Computed tomography</topic><topic>Cytokines</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Fatty liver</topic><topic>Hepatitis</topic><topic>Hepatitis B</topic><topic>Hepatitis C</topic><topic>HIV</topic><topic>HIV Infections - complications</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Immunology</topic><topic>Infectious Diseases</topic><topic>Inflammasomes</topic><topic>Inflammation</topic><topic>Interleukin 18</topic><topic>Life Sciences & Biomedicine</topic><topic>Lipids</topic><topic>Liver</topic><topic>Liver - diagnostic imaging</topic><topic>Liver diseases</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Monocyte chemoattractant protein</topic><topic>Monocyte chemoattractant protein 1</topic><topic>Monocytes</topic><topic>Non-alcoholic Fatty Liver Disease</topic><topic>Pathogenesis</topic><topic>Science & Technology</topic><topic>Spleen</topic><topic>Steatosis</topic><topic>Triglycerides</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sim, Jae H.</creatorcontrib><creatorcontrib>Sherman, Julia B.</creatorcontrib><creatorcontrib>Stanley, Takara L.</creatorcontrib><creatorcontrib>Corey, Kathleen E.</creatorcontrib><creatorcontrib>Fitch, Kathleen V.</creatorcontrib><creatorcontrib>Looby, Sara E.</creatorcontrib><creatorcontrib>Robinson, Jake A.</creatorcontrib><creatorcontrib>Lu, Michael T.</creatorcontrib><creatorcontrib>Burdo, Tricia H.</creatorcontrib><creatorcontrib>Lo, Janet</creatorcontrib><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Web of Science - Science Citation Index Expanded - 2021</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>AIDS research and human retroviruses</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sim, Jae H.</au><au>Sherman, Julia B.</au><au>Stanley, Takara L.</au><au>Corey, Kathleen E.</au><au>Fitch, Kathleen V.</au><au>Looby, Sara E.</au><au>Robinson, Jake A.</au><au>Lu, Michael T.</au><au>Burdo, Tricia H.</au><au>Lo, Janet</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pro-Inflammatory Interleukin-18 is Associated with Hepatic Steatosis and Elevated Liver Enzymes in People with HIV Monoinfection</atitle><jtitle>AIDS research and human retroviruses</jtitle><stitle>AIDS RES HUM RETROV</stitle><addtitle>AIDS Res Hum Retroviruses</addtitle><date>2021-05-01</date><risdate>2021</risdate><volume>37</volume><issue>5</issue><spage>385</spage><epage>390</epage><pages>385-390</pages><issn>0889-2229</issn><eissn>1931-8405</eissn><abstract>People with HIV (PWH) are at an increased risk of developing nonalcoholic fatty liver disease (NAFLD). Interleukin (IL)-18 is regulated by inflammasomes in response to pathogens and danger signals and has been implicated in both the pathogenesis of NAFLD and HIV disease progression. We hypothesized that increased IL-18 may be associated with NAFLD and liver injury in PWH. This was an observational study of 125 PWH and 59 individuals without HIV in the Boston area. Participants with known hepatitis B, hepatitis C, and excessive alcohol use were excluded. IL-18 was measured in serum by enzyme-linked immunosorbent assay. Liver lipid content was assessed by liver-to-spleen computed tomography (CT) attenuation ratio. Aspartate aminotransferase (AST), alanine aminotransferase (ALT), and IL-18 levels were higher in PWH than in controls. In PWH, log(10) IL-18 was associated with log(10)AST (r = 0.34, p = .0001), log(10)ALT (r = 0.33, p = .0002), log(10)HIV RNA (r = 0.29, p = .002), and inversely associated with liver-to-spleen ratio (r = -0.24, p = .02). In addition, log(10) IL-18 was associated with log(10) triglycerides (r = 0.26, p = .003), log(10) MCP-1 (monocyte chemoattractant protein-1; r = 0.33, p = .0004), log(10)caspase-1 (r = 0.35, p < .0001), log(10)LPS (r = 0.28, p = .004), and inversely associated with high-density lipoprotein (r = -0.28, p = .002), and CD4(+)/CD8(+) T cell ratio (r = -0.24, p = .007). In controls without HIV, log(10) IL-18 was also associated with log(10)ALT (r = 0.44, p = .0005). After adjusting for potential confounders, the relationships between IL-18 and AST (p = .004) and ALT (p = .003) remained significant, and the relationship between IL-18 and liver-to-spleen ratio (p = .02). Increased inflammasome activation and subsequent monocyte recruitment in PWH may contribute to the development and progression of NAFLD. Clinical Trials Registration. NCT00455793.</abstract><cop>NEW ROCHELLE</cop><pub>Mary Ann Liebert, Inc</pub><pmid>33323025</pmid><doi>10.1089/aid.2020.0177</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-2336-2958</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alanine Alanine Transaminase Aspartate aminotransferase Attenuation CD4 antigen CD8 antigen Cell activation Clinical trials Computed tomography Cytokines Enzyme-linked immunosorbent assay Fatty liver Hepatitis Hepatitis B Hepatitis C HIV HIV Infections - complications Human immunodeficiency virus Humans Immunology Infectious Diseases Inflammasomes Inflammation Interleukin 18 Life Sciences & Biomedicine Lipids Liver Liver - diagnostic imaging Liver diseases Lymphocytes Lymphocytes T Monocyte chemoattractant protein Monocyte chemoattractant protein 1 Monocytes Non-alcoholic Fatty Liver Disease Pathogenesis Science & Technology Spleen Steatosis Triglycerides Virology |
title | Pro-Inflammatory Interleukin-18 is Associated with Hepatic Steatosis and Elevated Liver Enzymes in People with HIV Monoinfection |
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