{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T19:34:01Z","timestamp":1786649641412,"version":"build-2736575974"},"reference-count":31,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","license":[{"start":{"date-parts":[[2025,1,1]],"date-time":"2025-01-01T00:00:00Z","timestamp":1735689600000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2025,1]]},"abstract":"<jats:title>Abstract:<\/jats:title>\n                  <jats:sec>\n                    <jats:title>BACKGROUND:<\/jats:title>\n                    <jats:p>LINC01492 polymorphism has been implicated in the susceptibility of large artery atherosclerotic (LAA) stroke; however, a dearth of systematic research exists regarding this association in the Asian population at present.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>SUBJECTS AND METHODS:<\/jats:title>\n                    <jats:p>This study enrolled Han Chinese patients with LAA stroke (n = 428) and age- and sex-matched controls (n = 434). We employed dominant, recessive, and codominant genetic models to analyze the distribution of alleles and genotypes for 14 tag single nucleotide polymorphisms (SNPs) in LINC01492. Furthermore, we quantified the transcript levels of LINC01492 as well as concentrations of inflammatory factors (interleukin [IL]-1\u03b2, IL-6, IL-8, IL-10, IL-18, tumor necrosis factor alpha, and CCL18). In addition, we explored the association between these SNPs and levels of inflammatory factors.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>RESULTS:<\/jats:title>\n                    <jats:p>\n                      The rs10990654 AA genotype of LINC01492 was markedly associated with a heightened risk of LAA stroke (odds ratio [OR] = 6.403, 95% confidence interval [CI] = 1.180\u201334.734,\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      = 0.031). Conversely, both the GG genotype of rs10990654 (OR = 0.614, 95% CI = 0.384\u20130.980,\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      = 0.041) and the GG genotype of rs16922693 (OR = 0.518, 95% CI = 0.313\u20130.857,\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      = 0.010) were identified as being linked to a reduced risk in this study population. In addition, the transcription level of LINC01492 was markedly reduced in patients compared to controls. Furthermore, significant variations were observed in IL-10 and IL-18 levels across genotypes at LINC01492 polymorphism loci among patients.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>CONCLUSIONS:<\/jats:title>\n                    <jats:p>The genetic polymorphisms and transcript levels of LINC01492 exhibit an association with susceptibility to LAA stroke, and the available evidence suggests that this association may be mediated through IL-10 and IL-18.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>TRIAL REGISTRATION:<\/jats:title>\n                    <jats:p>The trial was registered with the Chinese Clinical Trial Registry (www.chictr.org.cn) under trial registration number ChiCTR2000032684.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.4103\/bc.bc_42_24","type":"journal-article","created":{"date-parts":[[2025,3,22]],"date-time":"2025-03-22T20:32:50Z","timestamp":1742675570000},"page":"48-56","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":3,"title":["LINC01492 is associated with susceptibility to large atherosclerotic stroke and levels of inflammatory factors"],"prefix":"10.4103","volume":"11","author":[{"given":"Jianyu","family":"Liu","sequence":"first","affiliation":[{"name":"Department of Neurology, The Affiliated Hospital of Southwest Jiaotong University, The Third People\u2019s Hospital of Chengdu, Chengdu, China"},{"name":"Medical Research Center, The Affiliated Hospital of Southwest Jiaotong University, The Third People\u2019s Hospital of Chengdu, Chengdu, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Da","family":"Liu","sequence":"additional","affiliation":[{"name":"Department of Clinical Medicine, North Sichuan Medical College, Nanchong, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xing","family":"Guo","sequence":"additional","affiliation":[{"name":"Institute of Biomedical Engineering, College of Medicine, Southwest Jiaotong University, Chengdu, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Li","family":"Zhou","sequence":"additional","affiliation":[{"name":"Department of Neurology, The First People\u2019s Hospital of Neijiang, Neijiang, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zhiyao","family":"Xu","sequence":"additional","affiliation":[{"name":"College of Medicine, Southwest Jiaotong University, Chengdu, Sichuan, China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hua","family":"Liu","sequence":"additional","affiliation":[{"name":"Department of Neurology, The Affiliated Hospital of Southwest Jiaotong University, The Third People\u2019s Hospital of Chengdu, Chengdu, China"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2025,3,21]]},"reference":[{"key":"R1-20250324","doi-asserted-by":"crossref","first-page":"143","DOI":"10.1038\/nrm.2017.104","article-title":"The functions and unique features of long intergenic non-coding RNA","volume":"19","author":"Ransohoff","year":"2018","journal-title":"Nat Rev Mol Cell Biol"},{"key":"R2-20250324","doi-asserted-by":"crossref","first-page":"695","DOI":"10.1016\/S1474-4422(16)00102-2","article-title":"The Stroke Genetics Network (SiGN) and the International Stroke Genetics Consortium (ISGC). 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