Interleukin-18 promoter −137 G/C polymorphism (rs187238) is associated with biochemical markers of renal function and cardiovascular disease in type 2 diabetes patients

[Display omitted] •Association between −137G/C IL-18 gene polymorphism and cardiovascular disease in T2DM Brazilian population.•An increased IL-18 production in carriers of CC −137 genotype for the −137G/C polymorphism compared to the GG or GC carriers.•High creatinine and albuminuria levels were as...

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Veröffentlicht in:Clinical biochemistry 2020-06, Vol.80, p.1-7
Hauptverfasser: Cavalcante, Jânio Emanuel Andrade, de Sousa, Ederson Laurindo Holanda, de Oliveira Rodrigues, Raphael, de Almeida Viana, Glautemberg, Duarte Gadelha, Daniel, de Carvalho, Manoela Montenegro Dias, Sousa, Duaran Lopes, Silva, Allysson Jordan Xavier, Filho, Raimundo Rigoberto Barbosa Xavier, Fernandes, Virgínia Oliveira, Montenegro Júnior, Renan Magalhães, de Sousa Alves, Renata, Meneses, Gdayllon Cavalcante, Sampaio, Tiago Lima, Queiroz, Maria Goretti Rodrigues
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Sprache:eng
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Zusammenfassung:[Display omitted] •Association between −137G/C IL-18 gene polymorphism and cardiovascular disease in T2DM Brazilian population.•An increased IL-18 production in carriers of CC −137 genotype for the −137G/C polymorphism compared to the GG or GC carriers.•High creatinine and albuminuria levels were associated with CC −137 genotype. Interleukin-18 (IL-18), a proinflammatory and proatherogenic cytokine, has been associated with type 2 diabetes, metabolic syndrome, stroke and coronary artery disease. Some studies have indicated that the IL-18 promoter −137 G/C polymorphism seems to be associated with changes in the IL-18 expression and may contribute to the development of cardiovascular disease (CVD). The aim of this study was to evaluate the association between −137 G/C polymorphism and the levels of IL-18, biochemical markers for cardiovascular disorders, anthropometric profile and cardiovascular disease in Brazilian patients with type 2 diabetes (T2DM). Design & Methods. Study subjects comprised 125 T2DM patients undergoing follow-up at a reference endocrinology service in northeastern Brazil. The −137G/C polymorphism in the IL-18 gene and serum IL-18 levels were determined by using allele-specific polymerase chain reaction (PCR) and enzyme-linked immune assay (ELISA), respectively. The anthropometric parameters were assessed using a Body Composition Monitor with Scale, and the laboratory data were measured using an automatic analyzer as well as spectrophotometric analysis. Results. The genotype distribution of IL-18 –137 G/C genetic polymorphism was significantly different among T2DM patients with and without CVD. The results show an association between the CC genotype of −137G/C polymorphism and CVD in T2DM patients (p 
ISSN:0009-9120
1873-2933
DOI:10.1016/j.clinbiochem.2020.03.011