{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,14]],"date-time":"2026-08-14T04:12:17Z","timestamp":1786680737738,"version":"build-2736575974"},"reference-count":44,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2015,7,27]],"date-time":"2015-07-27T00:00:00Z","timestamp":1437955200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Oral Pathology Medicine"],"published-print":{"date-parts":[[2016,3]]},"abstract":"<jats:sec><jats:title>Background<\/jats:title><jats:p>Oral lichen planus (<jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>) is a chronic mucocutaneous disease, inflammatory and autoimmune in character, in which the pathogenesis is not fully understood. Psychological stress has also been implicated in triggering or exacerbating the disease.<\/jats:p><\/jats:sec><jats:sec><jats:title>Objective<\/jats:title><jats:p>The aim of this study was to evaluate the psychological profile, sleep, and salivary biological markers\u2014cortisol, immunoglobin<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>(<jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>g<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>), and adiponectin \u2013 in patients with oral lichen planus (<jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>).<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>The sample consisted of 65 patients (33 with<jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>and 32 control patients). Patients completed hospital anxiety and depression scales (<jats:styled-content style=\"fixed-case\">HADD<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\">HADA<\/jats:styled-content>). Questionnaires were used to assess sleepiness: the<jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>ittsburgh sleep quality index (<jats:styled-content style=\"fixed-case\">PSQI<\/jats:styled-content>) and the<jats:styled-content style=\"fixed-case\">E<\/jats:styled-content>pworth sleepiness scale (<jats:styled-content style=\"fixed-case\">ESS<\/jats:styled-content>). A visual analog scale (<jats:styled-content style=\"fixed-case\">VAS<\/jats:styled-content>) was used for rating pain. Unstimulated whole saliva was evaluated, together with total proteins: cortisol,<jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>g<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>, and adiponectin.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Patients with<jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>obtained significantly higher<jats:styled-content style=\"fixed-case\">HADA<\/jats:styled-content>and<jats:styled-content style=\"fixed-case\">PSQI<\/jats:styled-content>scores than control subjects (<jats:italic>P<\/jats:italic>\u00a0=\u00a00.001,<jats:italic>P<\/jats:italic>\u00a0=\u00a00.012, respectively). Total salivary protein (flow at rest) analysis found that total proteins were higher in the<jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>group (<jats:italic>P<\/jats:italic>\u00a0=\u00a00.001). In the<jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>group,<jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>g<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>was 80.3\u00a0\u00b1\u00a051.3 vs. the control group 48.9\u00a0\u00b1\u00a032.8 (<jats:italic>P<\/jats:italic>\u00a0=\u00a00.005). Mean cortisol was 0.5\u00a0\u00b1\u00a00.3\u00a0\u03bcg\/dl in the<jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>group vs. 0.4\u00a0\u00b1\u00a00.2\u00a0\u03bcg\/dl in the control group (<jats:italic>P<\/jats:italic>\u00a0=\u00a00.010). The<jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>group showed a correlation between the<jats:styled-content style=\"fixed-case\">HADA<\/jats:styled-content>variable and pain (<jats:italic>r<\/jats:italic>\u00a0=\u00a00.358;<jats:italic>P<\/jats:italic>\u00a0=\u00a00.041),<jats:styled-content style=\"fixed-case\">HADD<\/jats:styled-content>(<jats:italic>r<\/jats:italic>\u00a0=\u00a00.568;<jats:italic>P<\/jats:italic>\u00a0=\u00a00.001), and<jats:styled-content style=\"fixed-case\">PSQI<\/jats:styled-content>(<jats:italic>r<\/jats:italic>\u00a0=\u00a00.537;<jats:italic>P<\/jats:italic>\u00a0=\u00a00.001).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">OLP<\/jats:styled-content>patients presented worse psychological profiles and sleep disturbances, as well as higher values for<jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>g<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>, cortisol, and total proteins than control subjects.<\/jats:p><\/jats:sec>","DOI":"10.1111\/jop.12345","type":"journal-article","created":{"date-parts":[[2015,7,28]],"date-time":"2015-07-28T05:14:56Z","timestamp":1438060496000},"page":"211-217","source":"Crossref","is-referenced-by-count":52,"title":["Oral lichen planus: salival biomarkers cortisol, immunoglobulin<scp>A<\/scp>, adiponectin"],"prefix":"10.1111","volume":"45","author":[{"given":"Pia","family":"Lopez\u2010Jornet","sequence":"first","affiliation":[{"name":"Oral Medicine University Dental Clinic University of Murcia Murcia Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Cristina Aznar","family":"Cayuela","sequence":"additional","affiliation":[{"name":"Oral Medicine University Dental Clinic University of Murcia Murcia 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