Literature DB >> 17883249

beta-cell function and anti-diabetic pharmacotherapy.

Stefano Del Prato1, Cristina Bianchi, Piero Marchetti.   

Abstract

Type 2 diabetes is a chronic disease characterized by progressive worsening of glycaemic control as indicated by the United Kingdom Prospective Diabetes Study (UKPDS). The progressive nature of the disease is mainly due to continuous loss of beta-cell mass and function. Though much of this loss is due to intrinsic defects of the beta-cell several factors may accelerate such process. These include the metabolic environment where hyperglycaemia and increased circulating free-fatty acid exert a toxic effect on the beta-cell. Therefore, tight metabolic control may prevent not only the risk of long-term diabetic complication but also preserve beta-cell function. Several therapeutic agents are currently used for treatment of type 2 diabetic patients. However, their effect on maintenance of beta-cell function has not been yet systematically reviewed. By literature searching we have then analysed in detail the effect of sulfonylureas and non-sulfonylureic secretagogues, incretin-mimetics, insulin sensitizers, alpha-glucosidase inhibitors, and insulin on beta-cell function. Moreover, promising future approaches aiming at preserving beta-cell function and mass are discussed. (c) 2007 John Wiley & Sons, Ltd.

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Year:  2007        PMID: 17883249     DOI: 10.1002/dmrr.770

Source DB:  PubMed          Journal:  Diabetes Metab Res Rev        ISSN: 1520-7552            Impact factor:   4.876


  23 in total

1.  Hydrogen sulphide protects mouse pancreatic β-cells from cell death induced by oxidative stress, but not by endoplasmic reticulum stress.

Authors:  S Taniguchi; L Kang; T Kimura; I Niki
Journal:  Br J Pharmacol       Date:  2011-03       Impact factor: 8.739

Review 2.  The role of incretin therapy at different stages of diabetes.

Authors:  Simona Cernea
Journal:  Rev Diabet Stud       Date:  2011-11-10

3.  Pancreatic β cell dedifferentiation in diabetes and redifferentiation following insulin therapy.

Authors:  Zhiyu Wang; Nathaniel W York; Colin G Nichols; Maria S Remedi
Journal:  Cell Metab       Date:  2014-04-17       Impact factor: 27.287

Review 4.  Emerging treatment options for type 2 diabetes.

Authors:  Milan K Piya; Abd A Tahrani; Anthony H Barnett
Journal:  Br J Clin Pharmacol       Date:  2010-11       Impact factor: 4.335

Review 5.  Hyperinsulinism and diabetes: genetic dissection of beta cell metabolism-excitation coupling in mice.

Authors:  Maria Sara Remedi; Colin G Nichols
Journal:  Cell Metab       Date:  2009-12       Impact factor: 27.287

Review 6.  Beta-cell failure in type 2 diabetes mellitus.

Authors:  Cristina Lencioni; Roberto Lupi; Stefano Del Prato
Journal:  Curr Diab Rep       Date:  2008-06       Impact factor: 4.810

Review 7.  Therapeutic Concentrations of Metformin: A Systematic Review.

Authors:  Farshad Kajbaf; Marc E De Broe; Jean-Daniel Lalau
Journal:  Clin Pharmacokinet       Date:  2016-04       Impact factor: 6.447

Review 8.  Pancreatic β-cell identity in diabetes.

Authors:  M S Remedi; C Emfinger
Journal:  Diabetes Obes Metab       Date:  2016-09       Impact factor: 6.577

Review 9.  Pharmacology and therapeutic implications of current drugs for type 2 diabetes mellitus.

Authors:  Abd A Tahrani; Anthony H Barnett; Clifford J Bailey
Journal:  Nat Rev Endocrinol       Date:  2016-06-24       Impact factor: 43.330

Review 10.  Changing the treatment paradigm for type 2 diabetes.

Authors:  Stefano Del Prato; Giuseppe Penno; Roberto Miccoli
Journal:  Diabetes Care       Date:  2009-11       Impact factor: 19.112

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