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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Predictive metabolomic signatures of end-stage renal disease: A multivariate analysis of population-based data

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Autor(es):
Silva, Robson E. [1] ; Baldim, Joao L. [2] ; Chagas-Paula, Daniela A. [3] ; Soares, Marisi G. [3] ; Lago, Joao H. G. [2] ; Goncalves, V, Reggiani ; Novaes, Romulo D. [4]
Número total de Autores: 7
Afiliação do(s) autor(es):
[1] Univ Fed Alfenas, Sch Med, BR-37130001 Alfenas, MG - Brazil
[2] Fed Univ ABC, Ctr Human & Nat Sci, BR-09210580 Santo Andre, SP - Brazil
[3] Univ Fed Alfenas, Inst Chem, BR-37130001 Alfenas, MG - Brazil
[4] Univ Fed Alfenas, Inst Biomed Sci, Dept Struct Biol, Rua Gabriel Monteiro da Silva 700, BR-37130001 Alfenas, MG - Brazil
Número total de Afiliações: 4
Tipo de documento: Artigo Científico
Fonte: Biochimie; v. 152, p. 14-30, SEP 2018.
Citações Web of Science: 1
Resumo

The variability of molecular signatures and predictive low molecular weight markers of chronic kidney disease (CKD) in different populations are poorly understood. Thus, in a large sample with 4763 people we compare the molecular signatures and metabolites with diagnostic relevance in plasma and urine of CKD patients of different geographical origins. From an integrated model based on dynamic networks and multivariate statistics, metabolites with predictive value obtained from targeted and untargeted molecular analysis, interactions between metabolic pathways affected by CKD, and the methodological quality of metabolomic studies were analyzed. The metabolites 3-methylhistidine, citrulline, kynurenine, p-cresol sulfate, urea, and citrate presented consistent expression in all population groups. Only increased kynurenine and p-cresol sulfate in plasma samples obtained acceptable scores as CKD bio-markers, independent of geographic origin. Metabolites such as leucine, alanine, isoleucine, serine, histidine, and citrate were nodal points, indicating that protein metabolism pathways are similarly impaired in Asian, European and North American patients. Based on our integrated model, we show that the metabolome of CKD patients exhibits a strong geographic influence, leading to unique metabolic signatures. Contrary to the likelihood of molecular similarities between geographically distinct populations, metabolic convergences in protein metabolism pathways and the molecules kynurenine and p-cresol sulfate were relevant as general predictors of CKD. In general, the quality assessment indicated that the current evidence is based on research models with variable methodological quality, whose limitations described in this study should be considered in the refinement of molecular approaches. (C) 2018 Elsevier B.V. and Societe Francaise de Biochimie et Biologie Moleculaire (SFBBM). All rights reserved. (AU)

Processo FAPESP: 16/19269-8 - Indução metabólica guiada por análises genômicas em Burkholderia thailandensis para a biossíntese de produtos naturais com atividade antimicrobiana
Beneficiário:Joao Luiz Baldim Zanin
Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado