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1.
Arch. endocrinol. metab. (Online) ; 62(5): 523-529, Oct. 2018. tab, graf
Artigo em Inglês | LILACS | ID: biblio-983791

RESUMO

ABSTRACT Objective: Recently, a new obesity index (A Body Shape Index, ABSI) based on waist circumference (WC) was developed, and high ABSI corresponds to a more central concentration of body volume. It is well known that central obesity is closely linked with insulin resistance (IR). Therefore, our study aimed to examine the discriminatory power of ABSI for IR in Chinese adults and elderly without diabetes. Subjects and methods: In 2007, a cross-sectional study was made. In this study, 570 individuals without diabetes were available for analysis (male: 56.1%, mean age: 62.3 ± 6.5 years). Insulin resistance was assessed by homeostasis model assessment (HOMA-IR). Areas under the receiver operating characteristic (ROC) curves were determined to identify variables/models that could predict insulin resistance. Results: ABSI was associated with IR, the cut-off points was 0.0785 m11/6kg-2/3 to identifying IR and the area under the ROC (AUC) curve was 0.618 (95%CI: 0.561-0.675), which was not better than body mass index BMI (AUC = 0.753; 95%CI: 0.706-0.801), WC (AUC = 0.749; 95%CI: 0.700-0.797), and fasting plasma glucose (FPG, AUC = 0.752; 95%CI: 0.705-0.799). Furthermore, combination with ABSI could improve the discriminatory power of other variables for IR. The AUC curve increased from 0.753 to 0.771for BMI, 0.749 to 0.754 for WC, 0.752 to 0.769 for FPG, respectively. Conclusions: ABSI is associated with IR in the general Chinese adults and elderly without diabetes, but the discriminatory power for IR is poor. It is recommended that ABSI be used in combination with other variables.


Assuntos
Humanos , Masculino , Feminino , Pessoa de Meia-Idade , Idoso , Resistência à Insulina/fisiologia , Índice de Massa Corporal , Tamanho Corporal/fisiologia , Padrões de Referência , Valores de Referência , Somatotipos , Glicemia/análise , Resistência à Insulina/etnologia , China , Estudos Transversais , Fatores de Risco , Sensibilidade e Especificidade , Estatísticas não Paramétricas , Povo Asiático , Tamanho Corporal/etnologia , Homeostase/fisiologia
2.
Braz. j. med. biol. res ; 45(3): 273-283, Mar. 2012. ilus, tab
Artigo em Inglês | LILACS | ID: lil-618048

RESUMO

Chronic atrophic gastritis (CAG) is a very common gastritis and one of the major precursor lesions of gastric cancer, one of the most common cancers worldwide. The molecular mechanism underlying CAG is unclear, but its elucidation is essential for the prevention and early detection of gastric cancer and appropriate intervention. A combination of two-dimensional gel electrophoresis and mass spectrometry was used in the present study to analyze the differentially expressed proteins. Samples from 21 patients (9 females and 12 males; mean age: 61.8 years) were used. We identified 18 differentially expressed proteins in CAG compared with matched normal mucosa. Eight proteins were up-regulated and 10 down-regulated in CAG when compared with the same amounts of proteins in individually matched normal gastric mucosa. Two novel proteins, proteasome activator subunit 1 (PSME1), which was down-regulated in CAG, and ribosomal protein S12 (RPS12), which was up-regulated in CAG, were further investigated. Their expression was validated by Western blot and RT-PCR in 15 CAG samples matched with normal mucosa. The expression level of RPS12 was significantly higher in CAG than in matched normal gastric mucosa (P < 0.05). In contrast, the expression level of PSME1 in CAG was significantly lower than in matched normal gastric mucosa (P < 0.05). This study clearly demonstrated that there are some changes in protein expression between CAG and normal mucosa. In these changes, down-regulation of PSME1 and up-regulation of RPS12 could be involved in the development of CAG. Thus, the differentially expressed proteins might play important roles in CAG as functional molecules.


Assuntos
Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Mucosa Gástrica/química , Gastrite Atrófica/metabolismo , Proteínas Musculares/genética , Proteômica , Complexo de Endopeptidases do Proteassoma/genética , Proteínas Ribossômicas/metabolismo , Western Blotting , Doença Crônica , Regulação para Baixo , Eletroforese em Gel Bidimensional , Mucosa Gástrica/patologia , Gastrite Atrófica/genética , Helicobacter pylori , Espectrometria de Massas , Proteínas Musculares/metabolismo , Complexo de Endopeptidases do Proteassoma/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Proteínas Ribossômicas/genética , Regulação para Cima
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