Controversy about the relative efficacy of dipeptidyl peptidase IV inhibitors.SCHEEN, André ![]() in Diabetologia (2012), 55 Detailed reference viewed: 6 (0 ULg) Decreased baroreflex gain more strongly predicts microalbuminuria and increased pulsatile stress than decreased rr e/i ratio in patients with type 1 diabetesSCHEEN, André ; MARCHAND, Monique ; PHILIPS, Jean-Christophe ![]() in Diabetologia (2011), 54(s1), 104 Detailed reference viewed: 8 (2 ULg) Cardiovascular risk factors and complications associated with impaired renal function and albuminuria in insulin-treated type 2 diabetes; SCHEEN, André ; et alin Diabetologia (2011) Detailed reference viewed: 4 (0 ULg) Hyperglycaemic clamp test for diabetes risk assessment in IA-2-antibody-positive relatives of type 1 diabetic patients; ; et al in Diabetologia (2010), 53 AIMS/HYPOTHESIS: The aim of the study was to investigate the use of hyperglycaemic clamp tests to identify individuals who will develop diabetes among insulinoma-associated protein-2 antibody (IA-2A ... [more ▼] AIMS/HYPOTHESIS: The aim of the study was to investigate the use of hyperglycaemic clamp tests to identify individuals who will develop diabetes among insulinoma-associated protein-2 antibody (IA-2A)-positive first-degree relatives (IA-2A(+) FDRs) of type 1 diabetic patients. METHODS: Hyperglycaemic clamps were performed in 17 non-diabetic IA-2A(+) FDRs aged 14 to 33 years and in 21 matched healthy volunteers (HVs). Insulin and C-peptide responses were measured during the first (5-10 min) and second (120-150 min) release phase, and after glucagon injection (150-160 min). Clamp-induced C-peptide release was compared with C-peptide release during OGTT. RESULTS: Seven (41%) FDRs developed diabetes 3-63 months after their initial clamp test. In all phases they had lower C-peptide responses than non-progressors (p < 0.05) and HVs (p < 0.002). All five FDRs with low first-phase release also had low second-phase release and developed diabetes 3-21 months later. Two of seven FDRs with normal first-phase but low second-phase release developed diabetes after 34 and 63 months, respectively. None of the five FDRs with normal C-peptide responses in all test phases has developed diabetes so far (follow-up 56 to 99 months). OGTT-induced C-peptide release also tended to be lower in progressors than in non-progressors or HVs, but there was less overlap in results between progressors and the other groups using the clamp. CONCLUSIONS/INTERPRETATION: Clamp-derived functional variables stratify risk of diabetes in IA-2A(+) FDRs and may more consistently identify progressors than OGTT-derived variables. A low first-phase C-peptide response specifically predicts impending diabetes while a low second-phase response may reflect an earlier disease stage [less ▲] Detailed reference viewed: 8 (2 ULg) Is the ADA/EASD algorithm for the management of type 2 diabetes (January 2009) based on evidence or opinion? A critical analysis.; ; et al in Diabetologia (2010) The ADA and the EASD recently published a consensus statement for the medical management of hyperglycaemia in patients with type 2 diabetes. The authors advocate initial treatment with metformin ... [more ▼] The ADA and the EASD recently published a consensus statement for the medical management of hyperglycaemia in patients with type 2 diabetes. The authors advocate initial treatment with metformin monotherapy and lifestyle modification, followed by addition of basal insulin or a sulfonylurea if glycaemic goals are not met (tier 1 recommendations). All other glucose-lowering therapies are relegated to a secondary (tier 2) status and only recommended for selected clinical settings. In our view, this algorithm does not offer physicians and patients the appropriate selection of options to individualise and optimise care with a view to sustained control of blood glucose and reduction both of diabetes complications and cardiovascular risk. This paper critically assesses the basis of the ADA/EASD algorithm and the resulting tiers of treatment options. [less ▲] Detailed reference viewed: 36 (1 ULg) Poor glycaemic control in secondary care insulin treated patients correlates with bad process indicators; ; et al in Diabetologia (2010), 53(s407), 1018 Detailed reference viewed: 10 (0 ULg) Patients with type 1 diabetes have similar increased pulsatility stress at comparable age of 50 yearsScheen, André ; Philips, Jean-Christophe ; Marchand, Monique ![]() in Diabetologia (2010), 53 Detailed reference viewed: 9 (0 ULg) Rosiglitazone: to be or not to be?Scheen, André ![]() in Diabetologia (2009), 52(7), 1448-50 Detailed reference viewed: 16 (2 ULg) Induction of nuclear factor-kappaB and its downstream genes by TNF-alpha and IL-1beta has a pro-apoptotic role in pancreatic beta cells; ; et al in Diabetologia (2008), 51 IL-1beta and TNF-alpha contribute to pancreatic beta cell death in type 1 diabetes. Both cytokines activate the transcription factor nuclear factor-kappaB (NF-kappaB), but recent observations suggest that ... [more ▼] IL-1beta and TNF-alpha contribute to pancreatic beta cell death in type 1 diabetes. Both cytokines activate the transcription factor nuclear factor-kappaB (NF-kappaB), but recent observations suggest that NF-kappaB blockade prevents IL-1beta + IFN-gamma- but not TNF-alpha + IFN-gamma-induced beta cell apoptosis. The aim of the present study was to compare the effects of IL-1beta and TNF-alpha on cell death and the pattern of NF-kappaB activation and global gene expression in beta cells. METHODS: Cell viability was measured after exposure to IL-1beta or to TNF-alpha alone or in combination with IFN-gamma, and blockade of NF-kappaB activation or protein synthesis. INS-1E cells exposed to IL-1beta or TNF-alpha in time course experiments were used for IkappaB kinase (IKK) activation assay, detection of p65 NF-kappaB by immunocytochemistry, real-time RT-PCR and microarray analysis. RESULTS: Blocking NF-kappaB activation protected beta cells against IL-1beta + IFNgamma- or TNFalpha + IFNgamma-induced apoptosis. Blocking de novo protein synthesis did not increase TNF-alpha- or IL-1beta-induced beta cell death, in line with the observations that cytokines induced the expression of the anti-apoptotic genes A20, Iap-2 and Xiap to a similar extent. Microarray analysis of INS-1E cells treated with IL-1beta or TNF-alpha showed similar patterns of gene expression. IL-1beta, however, induced a higher rate of expression of NF-kappaB target genes putatively involved in beta cell dysfunction and death and a stronger activation of the IKK complex, leading to an earlier translocation of NF-kappaB to the nucleus. CONCLUSIONS/INTERPRETATION: NF-kappaB activation in beta cells has a pro-apoptotic role following exposure not only to IL-1beta but also to TNF-alpha. The more marked beta cell death induced by IL-1beta is explained at least in part by higher intensity NF-kappaB activation, leading to increased transcription of key target genes. [less ▲] Detailed reference viewed: 81 (17 ULg) Permanent use of a continuous glucose monitor significantly reduces hypoglycemia and HbA1c in type 1 diabetic patients treated by insulin pump with high occurrence of hypoglycemia.RADERMECKER, Régis ; Saint-Remy, Annie ; et alin Diabetologia (2008), 51 Detailed reference viewed: 28 (1 ULg) Glycaemic and blood pressure control seems harder to improve than lipid control in type 2 diabetic patients: comparison of two surveys over 5 years in Belgium.PAQUOT, Nicolas ; ; SCHEEN, André et alin Diabetologia (2008), 51(suppl 1), 71155 Detailed reference viewed: 6 (0 ULg) ACE I/D polymorphism predicts end stage renal disease and or mortality in type I diabetic patients except for those with already advanced nephropathy: the follow up of the Genesis/Genediab Studies; ; et al in Diabetologia (2007, September), 50(Suppl. 1), 157-158 Detailed reference viewed: 12 (0 ULg) Rimonabant improves cardiometabolic risk factors in overweight/obese patients with poorly controlled type 2 diabetes (HbA(1c)>= 8%) on monotherapy with metformin or sulfonylureasScheen, André ; ; et alin Diabetologia (2006, September), 49(Suppl. 1), 483-484 Detailed reference viewed: 13 (0 ULg) Long-term glycaemic effects of pioglitazone in triple oral therapy: Results from PROactive; Scheen, André ![]() in Diabetologia (2006, September), 49(Suppl. 1), 488-489 Detailed reference viewed: 38 (0 ULg) Pioglitazone reduces insulin requirements and improves glycaemic control in insulin-treated patients with type 2 diabetes: results from PROactive; ; Scheen, André ![]() in Diabetologia (2006, September), 49(Suppl. 1), 489 Detailed reference viewed: 10 (0 ULg) Arterial pulse pressure increases according to diabetes duration, independently of age in patients with type 1 diabetesPHILIPS, Jean-Christophe ; MARCHAND, Monique ; WEEKERS, Laurent et alin Diabetologia (2005), 48(suppl 1), 318958 Detailed reference viewed: 7 (2 ULg) Influence of blood glucose control on the progression of cardiac autonomic neuropathy in Type 1 diabetes.PHILIPS, Jean-Christophe ; MARCHAND, Monique ; et alin Diabetologia (2004), 47(suppl 1), 368-3691029 Detailed reference viewed: 5 (2 ULg)![]() Thymic IGF-2 and central self-tolerance of the insulin family: a basis for the development of a negative vaccine against type 1 diabetesGeenen, Vincent ; ; et alin Diabetologia (2003), 46 (Suppl. 2) Detailed reference viewed: 12 (0 ULg) A potent diazoxide analogue activating ATP-sensitive K+ channels and inhibiting insulin release; ; et al in Diabetologia (2000), 43 Detailed reference viewed: 1 (0 ULg)![]() A potent diazoxide analogue activating ATP-sensitive K+ channels and inhibiting insulin release; ; et al in Diabetologia (2000), 43 suppl. 1 Detailed reference viewed: 2 (0 ULg) |
||