{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,9]],"date-time":"2026-01-09T15:56:19Z","timestamp":1767974179120,"version":"3.49.0"},"reference-count":44,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2016,7,19]],"date-time":"2016-07-19T00:00:00Z","timestamp":1468886400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"AstraZeneca SA"},{"name":"Nycomed Hellas SA"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neurogastroenterology Motil"],"published-print":{"date-parts":[[2017,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Functional dyspepsia (<jats:styled-content style=\"fixed-case\">FD<\/jats:styled-content>) susceptibility might be influenced by polymorphisms of genes related to inflammation (<jats:italic><jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>14<\/jats:italic>,<jats:italic> macrophage migration inhibitory factor<\/jats:italic> [<jats:italic><jats:styled-content style=\"fixed-case\">MIF<\/jats:styled-content><\/jats:italic>]), motor (<jats:italic><jats:styled-content style=\"fixed-case\">GNB<\/jats:styled-content>3<\/jats:italic>), and sensory dysfunction (<jats:italic><jats:styled-content style=\"fixed-case\">GNB<\/jats:styled-content>3, <jats:styled-content style=\"fixed-case\">TRPV<\/jats:styled-content>1<\/jats:italic>). We examined the association between <jats:italic><jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>14<\/jats:italic> rs2569190, <jats:italic><jats:styled-content style=\"fixed-case\">GNB<\/jats:styled-content>3<\/jats:italic> rs5443, <jats:italic><jats:styled-content style=\"fixed-case\">MIF<\/jats:styled-content><\/jats:italic> rs222747, and <jats:italic><jats:styled-content style=\"fixed-case\">TRPV<\/jats:styled-content>1<\/jats:italic> rs755622 gene polymorphisms with <jats:styled-content style=\"fixed-case\">FD<\/jats:styled-content> (Rome III criteria) in the Greek population.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>We genotyped 174 dyspeptics (115 with epigastric pain syndrome; 41% <jats:italic>Helicobacter pylori<\/jats:italic> positive) and 181 controls using polymerase chain reaction\u2010based methods and we measured disease symptoms\u2019 burden with a modified Gastrointestinal Symptoms Related Scale.<\/jats:p><\/jats:sec><jats:sec><jats:title>Key Results<\/jats:title><jats:p>Homozygous for the <jats:styled-content style=\"fixed-case\">TT<\/jats:styled-content> genotype and the T allele of the <jats:italic><jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>14<\/jats:italic> gene were significantly associated (<jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content> [95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>]) with <jats:styled-content style=\"fixed-case\">FD<\/jats:styled-content> (2.65 [1.42\u20134.94] and 1.67 [1.23\u20132.26], respectively). The <jats:styled-content style=\"fixed-case\">CT<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> TT<\/jats:styled-content> genotypes, and T allele frequencies of <jats:italic><jats:styled-content style=\"fixed-case\">GNB<\/jats:styled-content>3<\/jats:italic> showed also significant association with <jats:styled-content style=\"fixed-case\">FD<\/jats:styled-content> (2.18 [1.35\u20133.54], 3.46 [1.30\u20139.23], and 2.18 [1.48\u20133.19]). While heterozygous <jats:styled-content style=\"fixed-case\">GC <\/jats:styled-content><jats:italic><jats:styled-content style=\"fixed-case\">MIF<\/jats:styled-content><\/jats:italic> genotype was more common in dyspeptics (1.67 [1.07\u20132.60]), homozygous <jats:styled-content style=\"fixed-case\">CC<\/jats:styled-content> genotype and the C allele of <jats:italic><jats:styled-content style=\"fixed-case\">TRPV<\/jats:styled-content>1<\/jats:italic> gene were more prevalent in controls (0.47 [0.25\u20130.87] and 0.69 [0.51\u20130.92], respectively). None of the gene polymorphism was related either to dyspepsia clinical syndrome type or to the <jats:italic>H. pylori<\/jats:italic> infection. Among dyspeptics, <jats:italic><jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>14 <\/jats:italic><jats:styled-content style=\"fixed-case\">TT<\/jats:styled-content> genotype was related to lower epigastric pain burden score (<jats:italic>p<\/jats:italic>&lt;.011); <jats:italic><jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>14 <\/jats:italic><jats:styled-content style=\"fixed-case\">CT<\/jats:styled-content> genotype was related to higher epigastric burning and nausea burden scores (<jats:italic>p<\/jats:italic>&lt;.04) while belching score was lower (<jats:italic>p<\/jats:italic>=.027) in <jats:italic><jats:styled-content style=\"fixed-case\">MIF<\/jats:styled-content><\/jats:italic> <jats:styled-content style=\"fixed-case\">CG<\/jats:styled-content> dyspeptics.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion &amp; Inferences<\/jats:title><jats:p>Functional dyspepsia susceptibility is related to <jats:italic><jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>14<\/jats:italic>,<jats:italic> <jats:styled-content style=\"fixed-case\">GNB<\/jats:styled-content>3<\/jats:italic>,<jats:italic> <jats:styled-content style=\"fixed-case\">MIF<\/jats:styled-content><\/jats:italic>, and <jats:italic><jats:styled-content style=\"fixed-case\">TRPV<\/jats:styled-content>1<\/jats:italic> gene polymorphisms, while <jats:italic><jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>14<\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">MIF<\/jats:styled-content><\/jats:italic> gene variants are also associated with dyspepsia symptoms burden.<\/jats:p><\/jats:sec>","DOI":"10.1111\/nmo.12913","type":"journal-article","created":{"date-parts":[[2016,7,19]],"date-time":"2016-07-19T10:58:23Z","timestamp":1468925903000},"source":"Crossref","is-referenced-by-count":20,"title":["Functional dyspepsia susceptibility is related to <i><scp>CD<\/scp>14<\/i>,<i><scp>GNB<\/scp>3<\/i>,<i><scp>MIF<\/scp><\/i>, and <i><scp>TRPV<\/scp>1<\/i> gene polymorphisms in the Greek population"],"prefix":"10.1111","volume":"29","author":[{"given":"K.","family":"Triantafyllou","sequence":"first","affiliation":[{"name":"Hepatogastroenterology Unit Second Department of Internal Medicine Research institute and Diabetes Center Attikon University General Hospital Medical School National and Kapodistrian University  Athens Greece"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Kourikou","sequence":"additional","affiliation":[{"name":"Hepatogastroenterology Unit Second Department of Internal Medicine Research institute and Diabetes Center Attikon University General Hospital Medical School National and Kapodistrian University  Athens Greece"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Gazouli","sequence":"additional","affiliation":[{"name":"Laboratory of Biology Medical School National and Kapodistrian University  Athens Greece"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G. 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