Effects of vildagliptin, a DPP-4 inhibitor, in elderly diabetic patients with mild cognitive impairment

[Display omitted] •DPP-4i showed beneficial effects on glycaemia and cognitive impairment.•DPP-4i reduce hypoglycemic events and the related damage on cognitive function.•We evaluated the effect of vildagliptin on MMSE in diabetic elderly with MCI.•Our results showed a stable MMSE in patients after...

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Veröffentlicht in:Archives of gerontology and geriatrics 2019-09, Vol.84, p.103896-103896, Article 103896
Hauptverfasser: Borzì, Antonio Maria, Condorelli, Giovanni, Biondi, Antonio, Basile, Francesco, Vicari, Enzo Saretto Dante, Buscemi, Carola, Luca, Salvatore, Vacante, Marco
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Sprache:eng
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Zusammenfassung:[Display omitted] •DPP-4i showed beneficial effects on glycaemia and cognitive impairment.•DPP-4i reduce hypoglycemic events and the related damage on cognitive function.•We evaluated the effect of vildagliptin on MMSE in diabetic elderly with MCI.•Our results showed a stable MMSE in patients after treatment with vildagliptin. There is an unclear association between type 2 diabetes and mild cognitive impairment in the elderly. Both diseases are more prevalent in the older adults compared to the younger counterpart. Some anti-diabetic drugs seem to influence positively the evolution of mild cognitive impairment. This retrospective study investigated the effect of vildagliptin, an inhibitor of the enzyme dipeptidyl peptidase-4 (DPP-4), on the cognitive functioning of elderly diabetic patients with mild cognitive impairment (MCI) documented at mini mental state examination (MMSE). We included 60 diabetic elderly people which were divided in 2 groups: Group A, 30 patients with HbA1c (glycated hemoglobin) ≤7.5% and treated with metformin, and Group B, 30 patients with HbA1c >7.5%, and treated with metformin plus vildagliptin. We collected data on MMSE, fasting plasma glucose (FPG) and HbA1c at baseline and after 180 ± 10 days from the beginning of treatment. The two groups exhibited significantly different values in FPG (P 
ISSN:0167-4943
1872-6976
DOI:10.1016/j.archger.2019.06.001