{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,25]],"date-time":"2026-06-25T17:13:22Z","timestamp":1782407602397,"version":"3.54.5"},"reference-count":34,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2018,7,16]],"date-time":"2018-07-16T00:00:00Z","timestamp":1531699200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100007671","name":"Fundaci\u00f3n para la Investigaci\u00f3n y la Prevenci\u00f3n del Sida en Espa\u00f1a","doi-asserted-by":"publisher","award":["FIPSE 24640\/07"],"award-info":[{"award-number":["FIPSE 24640\/07"]}],"id":[{"id":"10.13039\/501100007671","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100004587","name":"Instituto de Salud Carlos III","doi-asserted-by":"publisher","award":["FIS PI070430"],"award-info":[{"award-number":["FIS PI070430"]}],"id":[{"id":"10.13039\/501100004587","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Clinical Endocrinology"],"published-print":{"date-parts":[[2018,10]]},"abstract":"<jats:title>Summary<\/jats:title><jats:sec><jats:title>Objective<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content> infection is associated with an increased risk of cardiovascular disease. Irisin is a miokyne secreted by skeletal muscle, which may influence insulin homeostasis, nonalcoholic fatty liver disease (<jats:styled-content style=\"fixed-case\">NAFLD<\/jats:styled-content>) and atherosclerosis. Our objective was to evaluate the relationships between serum irisin, insulin homeostasis, <jats:styled-content style=\"fixed-case\">NAFLD<\/jats:styled-content> and subclinical atherosclerosis in <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u2010infected males.<\/jats:p><\/jats:sec><jats:sec><jats:title>Design<\/jats:title><jats:p>Cross\u2010sectional study in a cohort of <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u2010infected patients.<\/jats:p><\/jats:sec><jats:sec><jats:title>Patients<\/jats:title><jats:p>Inclusion criteria: men older than 18\u00a0years; antiretroviral therapy (<jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content>) \u2010na\u00efve or on effective <jats:styled-content style=\"fixed-case\">ART<\/jats:styled-content> (&lt;50 <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content>\u20101 <jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\u00a0copies\/<jats:styled-content style=\"fixed-case\">mL<\/jats:styled-content>) without changes in the previous 6\u00a0months; no diabetes or hepatitis C.<\/jats:p><\/jats:sec><jats:sec><jats:title>Measurements<\/jats:title><jats:p>Irisin was measured by enzymatic immunoassay (Phoenix Pharmaceuticals), insulin sensitivity by homeostasis model assessment of insulin resistance (<jats:styled-content style=\"fixed-case\">HOMA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">IR<\/jats:styled-content>), as well as the 2\u2010hour continuous infusion of glucose with model assessment (<jats:styled-content style=\"fixed-case\">CIGMA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">HOMA<\/jats:styled-content>). Hepatic steatosis was measured by 1\u2010H magnetic resonance spectroscopy, subclinical atherosclerosis by evaluation of carotid intima\u2010media thickness (C\u2010<jats:styled-content style=\"fixed-case\">IMT<\/jats:styled-content>), measured by Ultrasonography.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Eight nine men (age 42.0\u00a0\u00b1\u00a08.3\u00a0years, duration of <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content> infection 7.9\u00a0\u00b1\u00a05.6\u00a0years, <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4 count 547\u00a0\u00b1\u00a0279\u00a0cells\/<jats:styled-content style=\"fixed-case\">mL<\/jats:styled-content>) were included. Circulating irisin was positively related to <jats:styled-content style=\"fixed-case\">HOMA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">IR<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">CIGMA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">HOMA<\/jats:styled-content>, hepatic triglyceride content, and to <jats:styled-content style=\"fixed-case\">VAT<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">SAT<\/jats:styled-content> ratio. Higher irisin concentrations were associated with higher C\u2010<jats:styled-content style=\"fixed-case\">IMT<\/jats:styled-content>, although this association did not persist in multivariate analysis. Lipodystrophy and a higher baseline <jats:styled-content style=\"fixed-case\">PAI<\/jats:styled-content>\u20101 concentration were independently associated with C\u2010<jats:styled-content style=\"fixed-case\">IMT<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>In male <jats:styled-content style=\"fixed-case\">HIV<\/jats:styled-content> patients without diabetes, higher irisin concentrations are positively associated with insulin resistance, <jats:styled-content style=\"fixed-case\">NAFLD<\/jats:styled-content> and subclinical atherosclerosis. However, waist\u2010hip\u2010ratio is the main determinant of insulin resistance, and <jats:styled-content style=\"fixed-case\">PAI<\/jats:styled-content>\u20101 and lipodystrophy were the strongest determinants of <jats:styled-content style=\"fixed-case\">IMT<\/jats:styled-content> in this population.<\/jats:p><\/jats:sec>","DOI":"10.1111\/cen.13800","type":"journal-article","created":{"date-parts":[[2018,6,27]],"date-time":"2018-06-27T06:49:32Z","timestamp":1530082172000},"page":"414-423","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":20,"title":["High Irisin levels in nondiabetic <scp>HIV<\/scp>\u2010infected males are associated with insulin resistance, nonalcoholic fatty liver disease, and subclinical atherosclerosis"],"prefix":"10.1111","volume":"89","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-8670-6404","authenticated-orcid":false,"given":"Oscar","family":"Moreno\u2010Perez","sequence":"first","affiliation":[{"name":"Endocrinology and Nutrition Service University General Hospital of Alicante  Alicante Spain"},{"name":"Department of Clinical Medicine University Miguel Hernandez  Alicante Spain"},{"name":"Instituto de Investigaci\u00f3n Sanitaria y Biom\u00e9dica de Alicante (ISABIAL \u2013 FISABIO)  Alicante Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rebeca","family":"Reyes\u2010Garcia","sequence":"additional","affiliation":[{"name":"Bone Metabolism Unit (RETICEF) UGC Endocrinolog\u00eda y Nutrici\u00f3n Complejo Hospitalario Universitario de Granada Instituto de Investigaci\u00f3n Biosanitaria ibs  Granada Spain"},{"name":"Endocrinology Service Complejo Hospitalario Torrecardenas  Almeria 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