Clinical audit of patients using DPP4 inhibitors in longstanding type 2 diabetes
Abstract Aims Dipeptidyl peptidase-4 inhibitors (DPP 4i) are oral hypoglycemic agents and are supposed to be beneficial in the early stages of diabetes. In this study, we evaluated the role of DPP4i in long standing type 2 diabetes mellitus (T2DM). Materials and methods This retrospective data analy...
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Published in | Diabetes & metabolic syndrome clinical research & reviews Vol. 9; no. 4; pp. 277 - 279 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier Ltd
01.10.2015
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Subjects | |
Online Access | Get full text |
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Summary: | Abstract Aims Dipeptidyl peptidase-4 inhibitors (DPP 4i) are oral hypoglycemic agents and are supposed to be beneficial in the early stages of diabetes. In this study, we evaluated the role of DPP4i in long standing type 2 diabetes mellitus (T2DM). Materials and methods This retrospective data analysis was conducted from the patient records. All the patients (T2DM > 5 years; Age > 50 years; Gliptin use > 12 months) were divided into 2 groups based on the duration of T2DM: Group A (< 10 years) and Group B (> 10 years). We excluded patients with type 1 diabetes and drug default of more than one month. Our primary objective was to study the change in HbA1c and secondary objectives were change in body weight and insulin requirement. Data are presented as mean ± S.D and comparison between the groups was done using Mann–Whitney and Fisher's exact tests. Results The study participants ( n =501) had a mean age (64.2 ± 8.2 yr), diabetes duration (10.1 ± 4.9 yr), body weight (65.3 ± 9.5 kg), BMI (23.4 ± 3.9 kg/m2 ) and HbA1c of 9.7 ± 1.3%. The use of gliptins resulted in similar HbA1c reduction between the groups ( p = 0.8405) and greater reduction of insulin requirement in group B ( p = 0.0433) at the end of one year. Body weight and hypoglycemia episodes did not differ between the groups. Conclusion DPP4 inhibitors give similar benefit irrespective of the duration of diabetes and our data gives reassurance about their role in long standing diabetes. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1871-4021 1878-0334 |
DOI: | 10.1016/j.dsx.2014.04.031 |