Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/17182
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dc.contributor.authorMakruasi N.
dc.contributor.authorE-Kobon T.
dc.contributor.authorWannaiampikul S.
dc.contributor.authorTanunyutthawongse C.
dc.contributor.authorSangsawangchot P.
dc.contributor.authorKhuancharee K.
dc.contributor.authorChansiri K.
dc.date.accessioned2022-03-10T13:16:36Z-
dc.date.available2022-03-10T13:16:36Z-
dc.date.issued2021
dc.identifier.issn1252208
dc.identifier.other2-s2.0-85116001423
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/17182-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85116001423&doi=10.35755%2fjmedassocthai.2021.S03.00020&partnerID=40&md5=e31152e32155f86d6a91c69a8db8329d
dc.description.abstractBackground: Although genome-wide association studies have been conducted to investigate the association between genomic loci associated with urate concentrations and gout in a large population. However, there is a lack of information in the Thai population. Objective: To identify the new genetic predisposition of hyperuricemia (HUA) and gout in non-communicable disease patients (NCDs). Materials and Methods: A whole-genome sequencing (WGS) using the Illumina HiSeq X Ten platform (Macrogen, Korea) was performed on the genomic DNA of 4 adult men (HUA, gout, early-onset gout, and normal subjects) who selected from 250 individuals of Gout among Thai Population Study. Then the candidate gene was identified the association of HUA in Thai NCDs patients (n=550). Results: The data set comprised 118,599 single-nucleotide variants were selected in all 4 participants. The missense Ala17Thr (G>A) GLUT9 mutation was found only in early-onset gout. The synonymous Pro1146Pro, A>G RREB1 mutation was identified in HUA and gout. WGS also identified synonymous Ile223Ile (C>T) ABCC4) and non-synonymous Ala2872Thr (G>A) LRP2 mutation in patients with HUA, early-onset gout, and gout. Because a missense of LRP2 (rs2228171) was found in the HUA subject. Thus the frequencies and association of rs2228171 in patients with HUA, hypertension, diabetes mellitus, heart disease, obesity, dyslipidemia, and stroke by using polymerase chain reaction and DNA sequencing analysis were investigated. Seventy-eight of 550 NCDs patients were selected. As result, an association between LRP2 and HUA was not found. The genotypes GA (adjusted OR 0.11, p=0.040), AA (adjusted OR 0.05, p=0.017) were associated with hypertension. However, the effect of rs2228171 in hypertension was still controversial due to the small population. Conclusion: Our study is the first cross-sectional study of the rs2228171 related HUA in Thai NCDs patients. Furthermore, the study will be done to clarify the effect of rs2228171 and metabolic diseases such as hypertension. © JOURNAL OF THE MEDICAL ASSOCIATION OF THAILAND, 2021.
dc.languageen
dc.subjecturate transporter
dc.subjectAlzheimer disease
dc.subjectArticle
dc.subjectbody mass
dc.subjectbrain ischemia
dc.subjectcardiovascular disease
dc.subjectcardiovascular risk
dc.subjectcerebrovascular accident
dc.subjectclinical article
dc.subjectcommunicable disease
dc.subjectcoronary artery disease
dc.subjectdiabetes mellitus
dc.subjectdisease predisposition
dc.subjectDNA polymorphism
dc.subjectdyslipidemia
dc.subjectgene frequency
dc.subjectgene mutation
dc.subjectgenetic analysis
dc.subjectgenetic polymorphism
dc.subjectgenetic predisposition
dc.subjectgenetic susceptibility
dc.subjectgenetic variation
dc.subjectglucose blood level
dc.subjectheterozygosity
dc.subjecthuman
dc.subjecthyperlipidemia
dc.subjecthypertension
dc.subjecthyperuricemia
dc.subjectkidney function
dc.subjectmetabolic disorder
dc.subjectmissense mutation
dc.subjectnon communicable disease
dc.subjectobesity
dc.subjectpolymerase chain reaction
dc.subjectwhole exome sequencing
dc.titleExome sequencing identifying LRP2 gene (rs2228171) related hyperuricemia in thai patients with non-communicable diseases
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationJournal of the Medical Association of Thailand. Vol 104, No.9 (2021), p.S51-S64
dc.identifier.doi10.35755/jmedassocthai.2021.S03.00020
Appears in Collections:Scopus 1983-2021

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