Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Beta Cell Centric Approach in the Management of Diabetes


Affiliations
1 President-Medical & Regulatory Affairs, Dept. of Scientific;, India
2 Deputy General Manager-Medical, Dept. of Scientific, India
3 Assistant General Manager-Medical, Dept. of Scientific;, India
4 Senior Executive-Scientific, Dept. of Scientific, Aristo Pharmaceuticals Private Limited,, India
     

   Subscribe/Renew Journal


Type 2 Diabetes (T2DM) is a complex, progressive, chronic metabolic disorder that is mainly characterized by hyperglycemia. The decline in β-cell function and insulin resistance still remains the major pathophysiological mechanisms of disease progression. By the time T2DM is diagnosed, the β-cell function is already lost halfway, which further declines each year thereafter. The majority of the currently present therapy focuses more on achieving glycemic targets without dealing with the deteriorating β-cell function. Various classes of drugs in managing T2DM aids in improving β-cell function and proliferation including newer agents like Glucagon Like Polypeptide-1 Receptor Agonist (GLP-1RA), Sodium-Glucose Co-Transporter-2 inhibitors (SGLT2i) and Dipeptidyl-Peptidase 4 inhibitors (DPP4i). This review highlights the fate of β-cell function during T2DM progression and the therapeutic approach for β-cell preservation with special emphasis on DPP4i.

Keywords

Type 2 Diabetes (T2DM), β-cell preservation, Dipeptidyl-Peptidase 4 inhibitors (DPP4i), Sitagliptin.
Subscription Login to verify subscription
User
Notifications
Font Size


  • Saisho Y. An emerging new concept for the management of type 2 diabetes with a paradigm shift from the glucose-centric to beta cell-centric concept of diabetes - an Asian perspective. Expert Opin Pharmacother. 2020;21(13):1565-78. DOI: 10.1080/14656566.2020.1776262. PMID: 32521177
  • Cerf ME. Beta cell dysfunction and insulin resistance. Front Endocrinol (Lausanne). 2013;27;4:37. DOI: 10.3389/fendo. 2013.00037. PMID: 23542897; PMCID: PMC3608918.
  • Wysham C, Shubrook J. Beta-cell failure in type 2 diabetes: mechanisms, markers, and clinical implications. Postgrad Med. 2020;132(8):676-86. DOI: 10.1080/00325481.2020.1771047. Epub 2020 Jun 16. PMID: 32543261.
  • DeFronzo RA, Abdul-Ghani MA. Preservation of β-cell function: the key to diabetes prevention. J Clin Endocrinol Metab. 2011;96(8):2354-66. DOI: 10.1210/jc.2011-0246. Epub 2011 Jun 22. PMID: 21697254.
  • Talchai C, Xuan S, Lin HV, Sussel L, Accili D. Pancreatic β cell dedifferentiation as a mechanism of diabetic β cell failure. Cell. 2012;150(6):1223-34. DOI: 10.1016/j.cell.2012.07.029. PMID: 22980982; PMCID: PMC3445031.
  • Dhillon S. Sitagliptin: a review of its use in the management of type 2 diabetes mellitus. Drugs. 2010;70(4):489-512. DOI: 10.2165/11203790-000000000-00000. PMID: 20205490.
  • Jung KY, Kim KM, Lim S. Therapeutic Approaches for Preserving or Restoring Pancreatic β-Cell Function and Mass. Diabetes Metab J. 2014;38(6):426-36. DOI: 10.4093/ dmj.2014.38.6.426. PMID: 25541605; PMCID: PMC4273028.
  • Marchetti P, Suleiman M, De Luca C, Baronti W, Bosi E, Tesi M, Marselli L. A direct look at the dysfunction and pathology of the β cells in human type 2 diabetes. Semin Cell Dev Biol. 2020;103:83-93. DOI: 10.1016/j.semcdb.2020.04.005. Epub 2020 May 13. PMID: 32417220.
  • Matveyenko AV, Butler PC. Relationship between beta-cell mass and diabetes onset. Diabetes Obes Metab. 2008;10 Suppl 4(0 4):23-31. DOI: 10.1111/j.1463-1326.2008.00939.x. PMID: 18834430; PMCID: PMC3375862.
  • Wajchenberg BL. Beta-cell failure in diabetes and preservation by clinical treatment. Endocr Rev. 2007;28(2):187- 218. DOI: 10.1210/10.1210/er.2006-0038. Epub 2007 Mar 12. PMID: 17353295.
  • Swisa A, Glaser B, Dor Y. Metabolic Stress and Compromised Identity of Pancreatic Beta Cells. Front Genet. 2017;8:21. DOI: 10.3389/fgene.2017.00021. PMID: 28270834; PMCID: PMC5318414.
  • Lyu X, Zhu X, Zhao B, Du L, Chen D, Wang C, Liu G, Ran X. Effects of dipeptidyl peptidase-4 inhibitors on beta-cell function and insulin resistance in type 2 diabetes: meta-analysis of randomized controlled trials. Sci Rep. 2017;7:44865. DOI: 10.1038/srep44865. PMID: 28322294; PMCID: PMC5359588.
  • Scott LJ. Sitagliptin: A Review in Type 2 Diabetes. Drugs. 2017;77(2):209-24. DOI: 10.1007/s40265-016-0686-9. PMID: 28078647.
  • Mohan V, Yang W, Son HY, Xu L, Noble L, Langdon RB, Amatruda JM, Stein PP, Kaufman KD. Efficacy and safety of sitagliptin in the treatment of patients with type 2 diabetes in China, India, and Korea. Diabetes Res Clin Pract. 2009;83(1):106-16. DOI: 10.1016/j.diabres.2008.10.009. Epub 2008 Dec 20. PMID: 19097665.
  • Aschner P, Kipnes MS, Lunceford JK, Sanchez M, Mickel C, Williams-Herman DE; Sitagliptin Study 021 Group. Effect of the dipeptidyl peptidase-4 inhibitor sitagliptin as monotherapy on glycemic control in patients with type 2 diabetes. Diabetes Care. 2006;29(12):2632-7. DOI: 10.2337/dc06-0703. PMID: 17130196.
  • Le TD, Nguyen NTP, Nguyen ST, Tran HTT, Nguyen LTH, Duong HH, Nguyen HM, Do BN. Sitagliptin Increases Beta- Cell Function and Decreases Insulin Resistance in Newly Diagnosed Vietnamese Patients with Type 2 Diabetes Mellitus. Diabetes Metab Syndr Obes. 2020 Jun;13:2119 127. DOI: 10.2147/DMSO.S255071. PMID: 32606870; PMCID: PMC7310979.
  • Williams-Herman D, Johnson J, Teng R, Golm G, Kaufman KD, Goldstein BJ, Amatruda JM. Efficacy and safety of sitagliptin and metformin as initial combination therapy and as monotherapy over 2 years in patients with type 2 diabetes. Diabetes Obes Metab. 2010;12(5):442-51. DOI: 10.1111/j.1463- 1326.2010.01204.x. PMID: 20415693.
  • Charbonnel B, Karasik A, Liu J, Wu M, Meininger G; Sitagliptin Study 020 Group. Efficacy and safety of the dipeptidyl peptidase-4 inhibitor sitagliptin added to ongoing metformin therapy in patients with type 2 diabetes inadequately controlled with metformin alone. Diabetes Care. 2006;29(12):2638-43. DOI: 10.2337/dc06-0706. PMID: 17130197.
  • Holst JJ, Gromada J. Role of incretin hormones in the regulation of insulin secretion in diabetic and nondiabetic humans. Am J Physiol Endocrinol Metab. 2004;287(2):E199-206. DOI: 10.1152/ajpendo.00545.2003. PMID: 15271645.

Abstract Views: 187

PDF Views: 0




  • Beta Cell Centric Approach in the Management of Diabetes

Abstract Views: 187  |  PDF Views: 0

Authors

Dr. Manish Maladkar
President-Medical & Regulatory Affairs, Dept. of Scientific;, India
Dr. Shrikant Patil
Deputy General Manager-Medical, Dept. of Scientific, India
Dr. Ashok Yadav
Assistant General Manager-Medical, Dept. of Scientific;, India
Charul Lautre
Senior Executive-Scientific, Dept. of Scientific, Aristo Pharmaceuticals Private Limited,, India

Abstract


Type 2 Diabetes (T2DM) is a complex, progressive, chronic metabolic disorder that is mainly characterized by hyperglycemia. The decline in β-cell function and insulin resistance still remains the major pathophysiological mechanisms of disease progression. By the time T2DM is diagnosed, the β-cell function is already lost halfway, which further declines each year thereafter. The majority of the currently present therapy focuses more on achieving glycemic targets without dealing with the deteriorating β-cell function. Various classes of drugs in managing T2DM aids in improving β-cell function and proliferation including newer agents like Glucagon Like Polypeptide-1 Receptor Agonist (GLP-1RA), Sodium-Glucose Co-Transporter-2 inhibitors (SGLT2i) and Dipeptidyl-Peptidase 4 inhibitors (DPP4i). This review highlights the fate of β-cell function during T2DM progression and the therapeutic approach for β-cell preservation with special emphasis on DPP4i.

Keywords


Type 2 Diabetes (T2DM), β-cell preservation, Dipeptidyl-Peptidase 4 inhibitors (DPP4i), Sitagliptin.

References