{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Lv HY"],"funding":["Taizhou Science and Technology Planning Project","Initial Scientific Research Fund for PhD from Taizhou Hospital of Zhejiang Province","Zhejiang Basic Public Welfare Research Project"],"pagination":["7256"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10160091"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["13(1)"],"pubmed_abstract":["In the sulfotransferase (SULT) superfamily, members of the SULT1 family mainly catalyse the sulfonation reaction of phenolic compounds, which is involved in the phase II metabolic detoxification process and plays a key role in endocrine homeostasis. A coding variant rs1059491 in the SULT1A2 gene has been reported to be associated with childhood obesity. This study aimed to investigate the association of rs1059491 with the risk of obesity and cardiometabolic abnormalities in adults. This case‒control study included 226 normal weight, 168 overweight and 72 obese adults who underwent a health examination in Taizhou, China. Genotyping of rs1059491 was performed by Sanger sequencing in exon 7 of the SULT1A2 coding region. Chi-squared tests, one-way ANOVA, and logistic regression models were app"],"journal":["Scientific reports"],"pubmed_title":["Association of SULT1A2 rs1059491 with obesity and dyslipidaemia in southern Chinese adults."],"pmcid":["PMC10160091"],"funding_grant_id":["1802ky01","LGF20H260013","2018BSKYQDJJ15"],"pubmed_authors":["Lv HY","Li C","Ye YF","Chen LH","Tung TH","Shi G","Chen YH","Zhang M"],"additional_accession":[]},"is_claimable":false,"name":"Association of SULT1A2 rs1059491 with obesity and dyslipidaemia in southern Chinese adults.","description":"In the sulfotransferase (SULT) superfamily, members of the SULT1 family mainly catalyse the sulfonation reaction of phenolic compounds, which is involved in the phase II metabolic detoxification process and plays a key role in endocrine homeostasis. A coding variant rs1059491 in the SULT1A2 gene has been reported to be associated with childhood obesity. This study aimed to investigate the association of rs1059491 with the risk of obesity and cardiometabolic abnormalities in adults. This case‒control study included 226 normal weight, 168 overweight and 72 obese adults who underwent a health examination in Taizhou, China. Genotyping of rs1059491 was performed by Sanger sequencing in exon 7 of the SULT1A2 coding region. Chi-squared tests, one-way ANOVA, and logistic regression models were app","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 May","modification":"2026-04-30T12:31:16.311Z","creation":"2024-10-15T05:13:59.801Z"},"accession":"S-EPMC10160091","cross_references":{"pubmed":["37142702"],"doi":["10.1038/s41598-023-34296-4"]}}