ABSTRACT
Background: Matrix metalloproteinase-10 (MMP-10) levels increase progressively starting from early diabetic kidney disease (DKD) stages. Vitamin D3 (vitD3) deficit is associated with a higher risk of diabetic microangiopathy. Reduced MMP-10 expression has been observed after exposure to vitD3. Aim: to assess how vitD3 status is related to MMP-10 levels in patients with Type 2 diabetes (T2D). Methods: 256 patients with T2D were included in this cross-sectional study. Demographic, clinical and serum MMP-10 and 25-hydroxyvitamin D3 (25(OH)D3) levels were collected from each patient. The association between MMP-10 and (25(OH)D3) levels was assessed using a correlation analysis and fitting a multivariate linear regression model. Results: Serum MMP-10 levels were inversely correlated with circulating 25(OH)D3 (rho = −0.25; p < 0.001). In the subgroup analysis this correlation was significant in patients with DKD (rho = −0.28; p = 0.001) and in subjects with vitD3 deficit (rho = −0.24; p = 0.005). In the regression model adjusted for kidney function, body adiposity, smoking and vitD supplementation MMP-10 levels were 68.7 pg/mL lower in patients with 25(OH)D3 > 20 ng/mL, with respect to ≤20 ng/mL (p = 0.006). Conclusions: vitD3 repletion status is an independent predictor of MMP-10 levels in T2D patients. Perhaps, high 25(OH)D3 values should be targeted in these patients in order to prevent vascular complications.
Subject(s)
Calcifediol , Diabetes Mellitus, Type 2 , Cross-Sectional Studies , Diabetes Mellitus, Type 2/complications , Humans , Matrix Metalloproteinase 10 , Vitamin D/analogs & derivatives , VitaminsABSTRACT
Matrix metalloproteinases have been implicated in diabetic microvascular complications. However, little is known about the pathophysiological links between MMP-10 and the renin-angiotensin system (RAS) in diabetic kidney disease (DKD). We tested the hypothesis that MMP-10 may be up-regulated in early stage DKD, and could be down-regulated by angiotensin II receptor blockade (telmisartan). Serum MMP-10 and TIMP-1 levels were measured in 268 type 2 diabetic subjects and 111 controls. Furthermore, histological and molecular analyses were performed to evaluate the renal expression of Mmp10 and Timp1 in a murine model of early type 2 DKD (db/db) after telmisartan treatment. MMP-10 (473 ± 274 pg/ml vs. 332 ± 151; p = 0.02) and TIMP-1 (573 ± 296 ng/ml vs. 375 ± 317; p < 0.001) levels were significantly increased in diabetic patients as compared to controls. An early increase in MMP-10 and TIMP-1 was observed and a further progressive elevation was found as DKD progressed to end-stage renal disease. Diabetic mice had 4-fold greater glomerular Mmp10 expression and significant albuminuria compared to wild-type, which was prevented by telmisartan. MMP-10 and TIMP-1 are increased from the early stages of type 2 diabetes. Prevention of MMP-10 upregulation observed in diabetic mice could be another protective mechanism of RAS blockade in DKD.
Subject(s)
Angiotensin II Type 1 Receptor Blockers/pharmacology , Diabetes Mellitus, Experimental/complications , Diabetes Mellitus, Type 2/complications , Diabetic Nephropathies/drug therapy , Matrix Metalloproteinase 10/chemistry , Renin-Angiotensin System/drug effects , Telmisartan/pharmacology , Aged , Animals , Case-Control Studies , Cross-Sectional Studies , Diabetic Nephropathies/enzymology , Diabetic Nephropathies/etiology , Female , Humans , Male , Matrix Metalloproteinase 10/metabolism , Mice , Mice, Inbred C57BL , Middle Aged , PrognosisABSTRACT
The flash glucose monitoring (FGM) system FreeStyle Libre® is a device that measures interstitial glucose in a very simple way and indicates direction and speed of glucose change. This allows persons with diabetes to prevent hypoglycemic and hyperglycemic events. Scientific evidence indicates that the system can improve glycemic control and quality of life. To obtain the maximum benefit, it is necessary to properly handle glucose values and trends. Due to the generalization of the system use, the purpose of the document is to provide recommendations for the optimal use of the device, not only in the management of glucose values and trends but also in the prevention of hypoglycemia, actuation in exercise, special situations, and retrospective analysis of the glucose data, among others.
Subject(s)
Blood Glucose Self-Monitoring/instrumentation , Blood Glucose/analysis , Diabetes Mellitus, Type 1/blood , Hypoglycemia/prevention & control , Quality of Life , Diabetes Mellitus, Type 1/drug therapy , Humans , Hypoglycemia/chemically induced , Hypoglycemic Agents/administration & dosage , Hypoglycemic Agents/adverse effects , Insulin/administration & dosage , Insulin/adverse effects , Retrospective StudiesABSTRACT
The hormone glucagon-like peptide-1 (GLP-1) is synthesized and secreted by L cells in the small intestine in response to food ingestion. After reaching the general circulation it has a half-life of 2-3 minutes due to degradation by the enzyme dipeptidyl peptidase-4. Its physiological role is directed to control plasma glucose concentration, though GLP-1 also plays other different metabolic functions following nutrient absorption. Biological activities of GLP-1 include stimulation of insulin biosynthesis and glucose-dependent insulin secretion by pancreatic beta cell, inhibition of glucagon secretion, delay of gastric emptying and inhibition of food intake. GLP-1 is able to reduce plasma glucose levels in patients with type 2 diabetes and also can restore beta cell sensitivity to exogenous secretagogues, suggesting that the increasing GLP-1 concentration may be an useful therapeutic strategy for the treatment of patients with type 2 diabetes.
Subject(s)
Diabetes Mellitus, Type 2/physiopathology , Glucagon-Like Peptide 1/physiology , Glucose/metabolism , Animals , Blood Glucose/analysis , Carbohydrate Metabolism, Inborn Errors/physiopathology , Clinical Trials as Topic , Diabetes Mellitus, Type 2/metabolism , Eating/physiology , Gastric Emptying/physiology , Gastric Inhibitory Polypeptide/physiology , Glucagon/metabolism , Glucagon-Like Peptide 1/agonists , Glucagon-Like Peptide 1/therapeutic use , Glucagon-Like Peptide-1 Receptor , Homeostasis , Humans , Hyperglycemia/physiopathology , Incretins/physiology , Insulin/metabolism , Insulin Secretion , Insulin-Secreting Cells/metabolism , Malabsorption Syndromes/physiopathology , Mice , Mice, Knockout , Models, Biological , Obesity/physiopathology , Receptors, Glucagon/deficiency , Receptors, Glucagon/physiologyABSTRACT
The hormone glucagon-like peptide-1 (GLP-1) is synthesized and secreted by L cells in the small intestine in response to food ingestion. After reaching the general circulation it has a half-life of 2-3 minutes due to degradation by the enzyme dipeptidyl peptidase-4. Its physiological role is directed to control plasma glucose concentration, though GLP-1 also plays other different metabolic functions following nutrient absorption. Biological activities of GLP-1 include stimulation of insulin biosynthesis and glucose-dependent insulin secretion by pancreatic beta cell, inhibition of glucagon secretion, delay of gastric emptying and inhibition of food intake. GLP-1 is able to reduce plasma glucose levels in patients with type 2 diabetes and also can restore beta cell sensitivity to exogenous secretagogues, suggesting that the increasing GLP-1 concentration may be an useful therapeutic strategy for the treatment of patients with type 2 diabetes.
Subject(s)
Diabetes Mellitus, Type 2/physiopathology , Glucagon-Like Peptide 1/metabolism , Biomarkers/metabolism , Blood Glucose/metabolism , Diabetes Mellitus, Type 2/drug therapy , Diabetes Mellitus, Type 2/metabolism , Gastric Inhibitory Polypeptide/metabolism , Glucagon-Like Peptide 1/agonists , Glucagon-Like Peptide 1/therapeutic use , Humans , Hypoglycemic Agents/therapeutic use , Incretins/therapeutic use , Insulin/metabolismABSTRACT
El péptido similar al glucagón-1 (GLP-1) es una hormona intestinal sintetizada en las células L intestinales cuya secreción depende de la presencia de nutrientes en la luz del intestino delgado. Una vez que el GLP-1 alcanza la circulación, tiene una vida media de unos pocos minutos, debido a la rápida degradación por parte de la enzima dipeptidil peptidasa-4 (DPP-4). Su función fisiológica se fundamenta en el control de la concentración sanguínea de glucosa, aunque desempeña múltiples funciones en la homeostasis metabólica después de la absorción de nutrientes. Las actividades biológicas del GLP-1 incluyen la estimulación de la secreción de insulina dependiente de la glucosa y la biosíntesis de insulina, la inhibición de la secreción de glucagón y del vaciado gástrico, y la inhibición de la ingesta de alimentos. El hallazgo de que el GLP-1 reduce los niveles plasmáticos de glucosa en pacientes con diabetes mellitus, junto con otros datos que sugieren que el GLP-1 puede restaurar la sensibilidad de las células beta a secretagogos exógenos, sugiere que aumentar la señalización del GLP-1 es una estrategia útil para el tratamiento de pacientes con diabetes mellitus tipo 2 (AU)
The hormone glucagon-like peptide-1 (GLP-1) is synthesized and secreted by L cells in the small intestine in response to food ingestion. After reaching the general circulation it has a half-life of 2-3 minutes due to degradation by the enzyme dipeptidyl peptidase-4. Its physiological role is directed to control plasma glucose concentration, though GLP-1 also plays other different metabolic functions following nutrient absorption. Biological activities of GLP-1 include stimulation of insulin biosynthesis and glucose-dependent insulin secretion by pancreatic beta cell, inhibition of glucagon secretion, delay of gastric emptying and inhibition of food intake. GLP-1 is able to reduce plasma glucose levels in patients with type 2 diabetes and also can restore beta cell sensitivity to exogenous secretagogues, suggesting that the increasing GLP-1 concentration may be an useful therapeutic strategy for the treatment of patients with type 2 diabetes (AU)
