Evidence map›Paper›PMID 39543306›Full record

ArticleScientific reports2024

Analysis of metabolites associated with ADIPOQ genotypes in individuals with type 2 diabetes mellitus.

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 and 4 more

Abstract read
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Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Tainá Gomes DinizPost-Graduate Program in Nutrition Science, Federal University of Paraiba, Joao Pessoa, Brazil.
Caroline Severo de AssisPost-Graduate Program in Nutrition Science, Federal University of Paraiba, Joao Pessoa, Brazil.
Bruno Rafael Virginio de SousaPost-Graduate Program in Nutrition Science, Federal University of Paraiba, Joao Pessoa, Brazil.
Kamila Sabino BatistaSemi Arid National Institute - INSA/MCTI, Campina Grande, Paraíba, CEP: 58434-700, Brazil.
Alexandre Sérgio SilvaDepartment of Physical Education, Federal University of Paraiba (UFPB), Joao Pessoa, PB, Brazil.
Isabella Wanderley de Queiroga EvangelistaOphthalmology, Otolaryngology and Oral and Maxillofacial Surgery Unit, Lauro Wanderley University Hospital, Federal University of Paraiba, Joao Pessoa, Brazil.
Marina Gonçalves Monteiro ViturinoOphthalmology, Otolaryngology and Oral and Maxillofacial Surgery Unit, Lauro Wanderley University Hospital, Federal University of Paraiba, Joao Pessoa, Brazil.
Yuri Mangueira do NascimentoPost-Graduate Program in Natural and Synthetic Bioactive Products, Federal University of Paraiba, Joao Pessoa, Brazil.
Evandro Ferreira da SilvaInstitute for Research in Drugs and Medicines - IPeFarM, Federal University of Paraíba, João Pessoa, PB, 58051-900, Brazil.
Josean Fechine TavaresInstitute for Research in Drugs and Medicines - IPeFarM, Federal University of Paraíba, João Pessoa, PB, 58051-900, Brazil.
Mussara Gomes Cavalcanti Alves MonteiroNutritionist and Course Coordinator at Colleges Três Marias and EESAP, João Pessoa, PB, Brazil.
Carla Patricia Novaes Dos Santos FechineThe University Center of João Pessoa, João Pessoa, PB, Brazil.
Anauara Lima E SilvaPost-Graduate Program in Natural and Synthetic Bioactive Products, Federal University of Paraiba, Joao Pessoa, Brazil.
Darlene Camati PersuhnDepartment of Molecular Biology/CCEN, Federal University of Paraiba (UFPB), Joao Pessoa, PB, Brazil. darlenecp@hotmail.com.ORCID 0000-0001-5291-5454

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

AdiponectinDiabetes Mellitus, Type 2GenotypeAdultAgedFemaleHumansMaleMetabolomeMetabolomicsMiddle AgedPolymorphism, Single NucleotideAdiponectinADIPOQ protein, humanAdiponectinMetabolomicsNMRrs266729Type 2 Diabetes Mellitus

Identifiers

PMID39543306
PMCPMC11564893

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.