ABSTRACT
OBJECTIVE: In order to elucidate the interrelationship of adipokines in glucose hemiostasis, we determined the concentration of visfatin and adipsin in blood samples in patients with type 2 diabetes and age-matched controls after an overnight fast. SUBJECTS AND METHODS: We enrolled 37 patients with known type 2 diabetes -21 males and 16 females, aged 62.95 ± 15.72 years and 43 controls- 28 males and 15 females, aged 60.79 ± 12.67 years. Blood samples were collected after an overnight fast and routine biochemical parameters such as glucose, cholesterol, HDL, LDL, triglycerides along with Hb1Ac, insulin and c-peptide, in addition to circulating visfatin and adipsin were determined in all samples. Data were considered significant at a level of p < 0.05. RESULTS: In patients with type 2 diabetes, circulating adipsin levels were decreased and inversely related with glucose levels while circulating visfatin was increased significantly in the fasting state. CONCLUSION: These results implicate the adipokines adipsin and visfatin as possible participants in the pathogenesis of type 2 diabetes.
Subject(s)
Complement Factor D/metabolism , Diabetes Mellitus, Type 2/blood , Fasting/blood , Nicotinamide Phosphoribosyltransferase/blood , Aged , Aged, 80 and over , Case-Control Studies , Complement Factor D/analysis , Female , Glucose Tolerance Test , Humans , Male , Middle AgedABSTRACT
La evaluación de la actividad de anti-C3d en reactivos de Coombs poliespecíficos, con los procedimientos clásicos presenta, según la experiencia de los autores, dificultades técnicas y falta de reproductibilidad. El objetivo de este trabajo fue describir una técnica para controlar la actividad de los reactivos antiglobulina humana (AGH) poliespecíficos y monoespecíficos anti-C3d, utilizando glóbulos rojos de carnero (GRc) sensibilizados con fragmentos de complemento (C'). La obtención de GRc sensibilizados con C3d, se evaluó con reactivos de calidad certificada por la firma comercial. Se obtuvieron reacciones de aglutinación francamente positivas con reactivos de Coombs poliespecíficos y con reactivos anti-C3d, -C3d monoespecíficos. La sensibilidad, especificidad y sencillez de esta técnica induce a proponerla dentro del protocolo de Control de Calidad de los antisueros AGH poliespecíficos y anti-C3d, -C3d, utilizados de rutina en los Servicios de Medicina Transfusional
Subject(s)
Humans , Complement C3b Inactivator Proteins/analysis , Coombs Test , In Vitro Techniques , Antibodies, Anti-Idiotypic/analysis , Blood Banks/trends , Complement C3d/analysis , Complement Factor D/analysis , Complement System Proteins , Coombs Test , Complement Hemolytic Activity Assay/methods , Quality ControlABSTRACT
La evaluación de la actividad de anti-C3d en reactivos de Coombs poliespecíficos, con los procedimientos clásicos presenta, según la experiencia de los autores, dificultades técnicas y falta de reproductibilidad. El objetivo de este trabajo fue describir una técnica para controlar la actividad de los reactivos antiglobulina humana (AGH) poliespecíficos y monoespecíficos anti-C3d, utilizando glóbulos rojos de carnero (GRc) sensibilizados con fragmentos de complemento (C). La obtención de GRc sensibilizados con C3d, se evaluó con reactivos de calidad certificada por la firma comercial. Se obtuvieron reacciones de aglutinación francamente positivas con reactivos de Coombs poliespecíficos y con reactivos anti-C3d, -C3d monoespecíficos. La sensibilidad, especificidad y sencillez de esta técnica induce a proponerla dentro del protocolo de Control de Calidad de los antisueros AGH poliespecíficos y anti-C3d, -C3d, utilizados de rutina en los Servicios de Medicina Transfusional (AU)
Subject(s)
Humans , In Vitro Techniques , Coombs Test/methods , Complement C3b Inactivator Proteins/analysis , Quality Control , Complement Hemolytic Activity Assay/methods , Complement Factor D/analysis , Complement System Proteins , Complement C3d/analysis , Blood Banks/trends , Coombs Test/methods , Antibodies, Anti-Idiotypic/analysisABSTRACT
Serum hemolytic factor D activity, an important component of the ACP, was measured in patients with SR-INS. The mean serum factor D hemolytic activity of patients with SR-INS in relapse was significantly reduced compared to the mean of the control group. Twenty-one of 27 SR-INS patients in relapse (78%) had reduced serum factor D activity. In contrast, the mean serum factor D hemolytic activity of SR-INS patients in remission was not significantly different from that in the control group. Factor D hemolytic activity was also reduced in other types of renal disease with the nephrotic syndrome. Serum factor D values were highly correlated with the serum albumin concentration. Although hemolytic factor D activity could not be detected in the urine, the low molecular weight and the significant correlation with serum albumin concentration suggest that urinary loss is responsible for the low serum levels of factor D. Deficient serum values of factor D may contribute to the increased susceptibility of SR-INS patients in relapse to bacterial infections with organisms which activate the ACP.