Tainá Gomes Diniz, Caroline Severo de Assis, Bruno Rafael Virginio de Sousa, Kamila Sabino Batista, Alexandre Sérgio Silva, Isabella Wanderley de Queiroga Evangelista, Marina Gonçalves Monteiro Viturino, Yuri Mangueira do Nascimento, Evandro Ferreira da Silva, Josean Fechine Tavares, Mussara Gomes Cavalcanti Alves Monteiro, Carla Patricia Novaes Dos Santos Fechine, Anauara Lima E Silva, Darlene Camati Persuhn
{"title":"Analysis of metabolites associated with ADIPOQ genotypes in individuals with type 2 diabetes mellitus.","authors":"Tainá Gomes Diniz, Caroline Severo de Assis, Bruno Rafael Virginio de Sousa, Kamila Sabino Batista, Alexandre Sérgio Silva, Isabella Wanderley de Queiroga Evangelista, Marina Gonçalves Monteiro Viturino, Yuri Mangueira do Nascimento, Evandro Ferreira da Silva, Josean Fechine Tavares, Mussara Gomes Cavalcanti Alves Monteiro, Carla Patricia Novaes Dos Santos Fechine, Anauara Lima E Silva, Darlene Camati Persuhn","doi":"10.1038/s41598-024-79686-4","DOIUrl":null,"url":null,"abstract":"<p><p>Diabetes mellitus (DM) is a significant public health problem and it is known that the identification of molecular markers involved in glycemic control can impact disease control. Although the rs266729 polymorphism located in the promoter of the adiponectin gene (ADP) has been shown to be a candidate for involvement in glycemic control, the genotypic groups have never been characterized in terms of metabolomic aspects. Objective: Analyze the metabolites present in the rs266729 genotype groups. 127 diabetic individuals were compared according to the rs266729 genotype groups CC and GC + GG (RFLP-PCR). Blood plasma metabolites were classified by nuclear magnetic resonance (NMR), and the metabolic pathways of each group using the MetaboAnalyst tool. Insulin therapy (p = 0.049) was more frequent in the GC + GG rs266729 group. Lactate, alanine, glutamine, aspartate, lipid, lysine, isoleucine, citrulline, cholesterol, and fucose impacted the CC group and aspartate, beta-glucose, glutamate, pyruvate, proline, and 2-oxoglutarate impacted the CG + GG group. The glucose-alanine pathway, malate-aspartate transport, and urea cycle impacted the CC group (D-glucose, glutamic acid, L-alanine, oxoglutaric acid, and pyruvic acid). The glutamine/glutamate ratio is likely to be related to the causes of rs266729 influencing the risk of diabetes.</p>","PeriodicalId":21811,"journal":{"name":"Scientific Reports","volume":null,"pages":null},"PeriodicalIF":3.8000,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Scientific Reports","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41598-024-79686-4","RegionNum":2,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Diabetes mellitus (DM) is a significant public health problem and it is known that the identification of molecular markers involved in glycemic control can impact disease control. Although the rs266729 polymorphism located in the promoter of the adiponectin gene (ADP) has been shown to be a candidate for involvement in glycemic control, the genotypic groups have never been characterized in terms of metabolomic aspects. Objective: Analyze the metabolites present in the rs266729 genotype groups. 127 diabetic individuals were compared according to the rs266729 genotype groups CC and GC + GG (RFLP-PCR). Blood plasma metabolites were classified by nuclear magnetic resonance (NMR), and the metabolic pathways of each group using the MetaboAnalyst tool. Insulin therapy (p = 0.049) was more frequent in the GC + GG rs266729 group. Lactate, alanine, glutamine, aspartate, lipid, lysine, isoleucine, citrulline, cholesterol, and fucose impacted the CC group and aspartate, beta-glucose, glutamate, pyruvate, proline, and 2-oxoglutarate impacted the CG + GG group. The glucose-alanine pathway, malate-aspartate transport, and urea cycle impacted the CC group (D-glucose, glutamic acid, L-alanine, oxoglutaric acid, and pyruvic acid). The glutamine/glutamate ratio is likely to be related to the causes of rs266729 influencing the risk of diabetes.
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