Abstract
Aims
The purpose of this study was to clarify the predictive clinical characteristics of therapy switching from sitagliptin to dulaglutide in patients with type 2 diabetes mellitus.
Methods
This single-center, open-label, investigator-initiated pilot study was conducted in 40 patients with type 2 diabetes mellitus. The patients, who had been treated with 50 mg sitagliptin daily for at least 6 months were switched to 0.75 mg dulaglutide weekly.
Results
A total of 36 patients could be followed for 24 weeks of treatment with dulaglutide. They were assessed for several clinical parameters before the start of and 24 weeks after the study. Multiple linear regression analysis was used to search for independent predictors of reduction of hemoglobin A1c (HbA1c) levels after 24 weeks of treatment switching from sitagliptin to dulaglutide. Dulaglutide administration for 24 weeks resulted in significant reductions in fasting plasma glucose (FPG), HbA1c, and low-density lipoprotein cholesterol (LDL-C) levels. In addition, baseline HbA1c, FPG, body mass index (BMI), and age were significantly correlated with the change in HbA1c levels (ΔHbA1c). Furthermore, multiple linear regression analysis revealed that BMI and age significantly correlated with ΔHbA1c.
Conclusion
In summary, our prospective 24-week study showed that baseline low BMI and old age are significantly useful in predicting the HbA1c-lowering effect of switching from sitagliptin to dulaglutide.
Trial Registration
UMIN Clinical Trials Registry (UMIN000023245).
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TI contributed to the conception and design of the work. TI, TK, and MY contributed to the acquisition, analysis, and interpretation of data for the work. TI drafted the manuscript. TI, TK, and MY critically revised the manuscript for important intellectual content. All gave final approval and agree to be accountable for all aspects of work ensuring integrity and accuracy.
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All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1964 and later revision.
Informed consent
Informed consent or substitute for it was obtained from all patients for being included in the study.
Conflict of interests
The authors declare that they have no competing interests.
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Iwasaki, T., Kessoku, T., Higurashi, T. et al. Low body mass index and old age are useful in predicting the hemoglobin A1c-lowering effect of switching from sitagliptin to dulaglutide in Japanese patients with type 2 diabetes mellitus: a single-center, open-label, single-arm, pilot study. Diabetol Int 9, 189–195 (2018). https://doi.org/10.1007/s13340-018-0348-0
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DOI: https://doi.org/10.1007/s13340-018-0348-0