{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T00:44:40Z","timestamp":1787013880822,"version":"build-2736575974"},"reference-count":36,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2017,11,17]],"date-time":"2017-11-17T00:00:00Z","timestamp":1510876800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/100000062","name":"National Institute of Diabetes and Digestive and Kidney Diseases","doi-asserted-by":"publisher","award":["K23DK84413\u20104"],"award-info":[{"award-number":["K23DK84413\u20104"]}],"id":[{"id":"10.13039\/100000062","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000062","name":"National Institute of Diabetes and Digestive and Kidney Diseases","doi-asserted-by":"publisher","award":["T32 DK007130"],"award-info":[{"award-number":["T32 DK007130"]}],"id":[{"id":"10.13039\/100000062","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000062","name":"National Institute of Diabetes and Digestive and Kidney Diseases","doi-asserted-by":"publisher","award":["R01DK097317"],"award-info":[{"award-number":["R01DK097317"]}],"id":[{"id":"10.13039\/100000062","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000062","name":"National Institute of Diabetes and Digestive and Kidney Diseases","doi-asserted-by":"publisher","award":["2P30DK052574"],"award-info":[{"award-number":["2P30DK052574"]}],"id":[{"id":"10.13039\/100000062","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Aliment Pharmacol Ther"],"published-print":{"date-parts":[[2018,1]]},"abstract":"<jats:title>Summary<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      Genetic polymorphisms in G\u2010protein beta\u20103 subunit (\n                      <jats:styled-content style=\"fixed-case\">GN<\/jats:styled-content>\n                      \u03b23) and beta\u20102 adrenergic receptor (\n                      <jats:styled-content style=\"fixed-case\">ADRB<\/jats:styled-content>\n                      2) are associated with pain and gut hypersensitivity, which can overlap with gastroesophageal reflux disease (\n                      <jats:styled-content style=\"fixed-case\">GERD<\/jats:styled-content>\n                      ).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Aim<\/jats:title>\n                    <jats:p>\n                      To evaluate relationships between single nucleotide polymorphisms (\n                      <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>\n                      s) within\n                      <jats:styled-content style=\"fixed-case\">GN<\/jats:styled-content>\n                      \u03b23 and\n                      <jats:styled-content style=\"fixed-case\">ADRB<\/jats:styled-content>\n                      2 systems, and reflux symptom burden,\n                      <jats:styled-content style=\"fixed-case\">GERD<\/jats:styled-content>\n                      phenotypes from ambulatory reflux monitoring, and quality of life.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Symptomatic adults undergoing ambulatory reflux testing were recruited and phenotyped based on acid burden and symptom reflux association; major oesophageal motor disorders and prior foregut surgery were exclusions. A comparison asymptomatic control cohort was also identified. Subjects and controls completed questionnaires assessing symptom burden on visual analog scales, short\u2010form health survey\u201036 (\n                      <jats:styled-content style=\"fixed-case\">SF<\/jats:styled-content>\n                      \u201036), and Beck Anxiety and Depression Inventories (\n                      <jats:styled-content style=\"fixed-case\">BAI<\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">BDI<\/jats:styled-content>\n                      ). Genotyping was performed from saliva samples; 6\n                      <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>\n                      s selected from each of the two genes of interest were compared.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Saliva from 151 study subjects (55.3 \u00b1 1.2 years, 63.6% F) and 60 control subjects (50.9 \u00b1 2.2 years, 66.7%) had sufficient genetic material for genotyping. Study subjects had higher symptom burden, worse total and physical health, and higher anxiety scores compared to controls (\n                      <jats:italic>P<\/jats:italic>\n                      \u2264 .002). Tested\n                      <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>\n                      s within\n                      <jats:styled-content style=\"fixed-case\">ADRB<\/jats:styled-content>\n                      2 were similar between study subjects and controls (\n                      <jats:italic>P<\/jats:italic>\n                      &gt; .09). Study subjects with recessive alleles in 3\n                      <jats:styled-content style=\"fixed-case\">GN<\/jats:styled-content>\n                      \u03b23\n                      <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>\n                      s (Rs2301339, Rs5443, and Rs5446) had worse symptom severity (\n                      <jats:italic>P<\/jats:italic>\n                      = .011), worse mental health (\n                      <jats:italic>P<\/jats:italic>\n                      = .03), and higher depression scores (\n                      <jats:italic>P<\/jats:italic>\n                      = .005) despite no associations with\n                      <jats:styled-content style=\"fixed-case\">GERD<\/jats:styled-content>\n                      phenotypes or reflux metrics.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      Genetic variation within\n                      <jats:styled-content style=\"fixed-case\">GN<\/jats:styled-content>\n                      \u03b23 predicts oesophageal symptom burden and affect, but not oesophageal acid burden or symptom association with reflux episodes.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/apt.14414","type":"journal-article","created":{"date-parts":[[2017,11,17]],"date-time":"2017-11-17T02:16:43Z","timestamp":1510885003000},"page":"289-297","source":"Crossref","is-referenced-by-count":14,"title":["Genetic risk factors for perception of symptoms in\n                    <scp>GERD<\/scp>\n                    : an observational cohort study"],"prefix":"10.1111","volume":"47","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-7214-5901","authenticated-orcid":false,"given":"A.","family":"Patel","sequence":"first","affiliation":[{"name":"Duke University School of Medicine Durham VA Medical Center Durham NC USA"},{"name":"Division of Gastroenterology Washington University School of Medicine St. Louis MO USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S.","family":"Hasak","sequence":"additional","affiliation":[{"name":"Division of Gastroenterology Washington University School of Medicine St. Louis MO USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"B. D.","family":"Nix","sequence":"additional","affiliation":[{"name":"Division of Gastroenterology Washington University School of Medicine St. Louis MO USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1586-199X","authenticated-orcid":false,"given":"G. S.","family":"Sayuk","sequence":"additional","affiliation":[{"name":"Division of Gastroenterology Washington University School of Medicine St. Louis MO USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4152-5191","authenticated-orcid":false,"given":"R. D.","family":"Newberry","sequence":"additional","affiliation":[{"name":"Division of Gastroenterology Washington University School of Medicine St. Louis MO USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3388-0660","authenticated-orcid":false,"given":"C. 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