Literature DB >> 19543848

Is the current therapeutic armamentarium in diabetes enough to control the epidemic and its consequences? What are the current shortcomings?

Dario Giugliano1, Eberhard Standl, Tina Vilsbøll, John Betteridge, Riccardo Bonadonna, Ian W Campbell, Gerit-Holger Schernthaner, Bart Staels, Antonia Trichopoulou, Eduardo Farinaro.   

Abstract

The prevalence of diabetes is expected to rise together with an increase in morbidity and a reduction in life expectancy. A leading cause of death is cardiovascular disease, and hypertension and diabetes are additive risk factors for this complication. Selected treatment options should neither increase cardiovascular risk in patients with diabetes, nor increase risk of hyperglycaemia in patients with hypertension. The efficacy of present antihyperglycaemic agents is limited and new therapies, such as incretin-targeted agents, are under development. Even though most patients do not achieve glycated haemoglobin targets, trial data show that such interventions reduce the incidence of macrovascular events; however, intensive lowering may be detrimental in patients with existing cardiovascular disease. Currently available oral drugs do not address the key driver of type 2 diabetes--loss of functional beta-cell mass. In the future, new oral treatments must improve this, whilst providing durable blood glucose control and long-term tolerability.

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Year:  2009        PMID: 19543848     DOI: 10.1007/s00592-009-0134-3

Source DB:  PubMed          Journal:  Acta Diabetol        ISSN: 0940-5429            Impact factor:   4.280


  7 in total

1.  Designed inhibitors of insulin-degrading enzyme regulate the catabolism and activity of insulin.

Authors:  Malcolm A Leissring; Enrico Malito; Sabrine Hedouin; Lael Reinstatler; Tomoko Sahara; Samer O Abdul-Hay; Shakeel Choudhry; Ghulam M Maharvi; Abdul H Fauq; Malwina Huzarska; Philip S May; Sungwoon Choi; Todd P Logan; Benjamin E Turk; Lewis C Cantley; Marika Manolopoulou; Wei-Jen Tang; Ross L Stein; Gregory D Cuny; Dennis J Selkoe
Journal:  PLoS One       Date:  2010-05-07       Impact factor: 3.240

2.  Deletion of insulin-degrading enzyme elicits antipodal, age-dependent effects on glucose and insulin tolerance.

Authors:  Samer O Abdul-Hay; Dongcheul Kang; Melinda McBride; Lilin Li; Ji Zhao; Malcolm A Leissring
Journal:  PLoS One       Date:  2011-06-09       Impact factor: 3.240

3.  An in silico insight into novel therapeutic interaction of LTNF peptide-LT10 and design of structure based peptidomimetics for putative anti-diabetic activity.

Authors:  Sonali Gopichand Chavan; Deepti Dileep Deobagkar
Journal:  PLoS One       Date:  2015-03-27       Impact factor: 3.240

4.  Synthesis and biological evaluation of glucagon-like peptide-1 receptor agonists.

Authors:  Yu-Juan Zhang; Liu-Lan Shen; Hyae-Gyeong Cheon; Yong-Nan Xu; Jin-Hyun Jeong
Journal:  Arch Pharm Res       Date:  2013-11-01       Impact factor: 4.946

5.  Interaction of herbal compounds with biological targets: a case study with berberine.

Authors:  Xiao-Wu Chen; Yuan Ming Di; Jian Zhang; Zhi-Wei Zhou; Chun Guang Li; Shu-Feng Zhou
Journal:  ScientificWorldJournal       Date:  2012-11-13

6.  First human dose-escalation study with remogliflozin etabonate, a selective inhibitor of the sodium-glucose transporter 2 (SGLT2), in healthy subjects and in subjects with type 2 diabetes mellitus.

Authors:  Anita Kapur; Robin O'Connor-Semmes; Elizabeth K Hussey; Robert L Dobbins; Wenli Tao; Marcus Hompesch; Glenn A Smith; Joseph W Polli; Charles D James; Imao Mikoshiba; Derek J Nunez
Journal:  BMC Pharmacol Toxicol       Date:  2013-05-13       Impact factor: 2.483

7.  Controlled Release of Pyrimidine Compound Using Polymeric Coated ZIF-8 Metal-Organic Framework as Glucagon-Like Peptide-1 Receptor Agonist Carrier.

Authors:  Shaikha S AlNeyadi; Naheed Amir; Mohammad A Ghattas; Noor Atatreh; Shaikha S Alketbi; Ruba Al Ajeil; Abdu Adem
Journal:  Molecules       Date:  2020-09-20       Impact factor: 4.411

  7 in total

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