Publication:
Exome sequencing identifying LRP2 gene (rs2228171) related hyperuricemia in thai patients with non-communicable diseases

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.date.issuedBE2564
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.format.mimetypeapplication/pdf
dc.identifier.citationJournal of the Medical Association of Thailand. Vol 104, No.9 (2021), p.S51-S64
dc.identifier.doi10.35755/jmedassocthai.2021.S03.00020
dc.identifier.issn1252208
dc.identifier.other2-s2.0-85116001423
dc.identifier.urihttps://hdl.handle.net/20.500.14740/3921
dc.language.isoeng
dc.rights.holderScopus
dc.subject.otherUrate transporter
dc.subject.otherAlzheimer disease
dc.subject.otherArticle
dc.subject.otherBody mass
dc.subject.otherBrain ischemia
dc.subject.otherCardiovascular disease
dc.subject.otherCardiovascular risk
dc.subject.otherCerebrovascular accident
dc.subject.otherClinical article
dc.subject.otherCommunicable disease
dc.subject.otherCoronary artery disease
dc.subject.otherDiabetes mellitus
dc.subject.otherDisease predisposition
dc.subject.otherDNA polymorphism
dc.subject.otherDyslipidemia
dc.subject.otherGene frequency
dc.subject.otherGene mutation
dc.subject.otherGenetic analysis
dc.subject.otherGenetic polymorphism
dc.subject.otherGenetic predisposition
dc.subject.otherGenetic susceptibility
dc.subject.otherGenetic variation
dc.subject.otherGlucose blood level
dc.subject.otherHeterozygosity
dc.subject.otherHuman
dc.subject.otherHyperlipidemia
dc.subject.otherHypertension
dc.subject.otherHyperuricemia
dc.subject.otherKidney function
dc.subject.otherMetabolic disorder
dc.subject.otherMissense mutation
dc.subject.otherNon communicable disease
dc.subject.otherObesity
dc.subject.otherPolymerase chain reaction
dc.subject.otherWhole exome sequencing
dc.titleExome sequencing identifying LRP2 gene (rs2228171) related hyperuricemia in thai patients with non-communicable diseases
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85116001423&doi=10.35755%2fjmedassocthai.2021.S03.00020&partnerID=40&md5=e31152e32155f86d6a91c69a8db8329d

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