Cargando…

A Real-World Observational Study Evaluating the Probability of Glycemic Control with Basal Insulin or Glucagon-Like Peptide-1 Receptor Agonist in Japanese Patients with Type 2 Diabetes

INTRODUCTION: The effectiveness of basal insulin (BI) or glucagon-like peptide-1 receptor agonists (GLP-1 RAs) in providing glycemic control in patients with type 2 diabetes (T2D) in Japanese routine practice is not well known. This real-world observational study evaluated the probability of achievi...

Descripción completa

Detalles Bibliográficos
Autores principales: Baxter, Mike, Morimoto, Yukiko, Tamiwa, Masami, Hattori, Masakatsu, Peng, Xuejun Victor, Lubwama, Robert, Maegawa, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7324466/
https://www.ncbi.nlm.nih.gov/pubmed/32445125
http://dx.doi.org/10.1007/s13300-020-00836-8
_version_ 1783551948575735808
author Baxter, Mike
Morimoto, Yukiko
Tamiwa, Masami
Hattori, Masakatsu
Peng, Xuejun Victor
Lubwama, Robert
Maegawa, Hiroshi
author_facet Baxter, Mike
Morimoto, Yukiko
Tamiwa, Masami
Hattori, Masakatsu
Peng, Xuejun Victor
Lubwama, Robert
Maegawa, Hiroshi
author_sort Baxter, Mike
collection PubMed
description INTRODUCTION: The effectiveness of basal insulin (BI) or glucagon-like peptide-1 receptor agonists (GLP-1 RAs) in providing glycemic control in patients with type 2 diabetes (T2D) in Japanese routine practice is not well known. This real-world observational study evaluated the probability of achieving glycemic control in Japanese patients with T2D uncontrolled by oral antidiabetic drugs (OADs) who initiated BI or GLP-1 RA therapy. METHODS: Patients with T2D aged ≥ 18 years initiating BI or GLP-1 RA therapy following treatment with OADs were selected from real-world data (RWD) retrieved from a large electronic medical record database in Japan, using data from 01 January 2010 to 30 June 2019. Patients were required to have glycated hemoglobin (HbA1c) ≥ 7% within 90 days prior to the first prescription of BI or GLP-1 RA. The probability of reaching first HbA1c < 7% was assessed over a 24-month period in cohorts of patients who initiated BI (n = 3477) or GLP-1 RA (n = 780) and in subcohorts by number of OADs at baseline (1, 2, or ≥ 3), HbA1c at baseline (≥ 7 to < 8%, ≥ 8 to < 9%, or ≥ 9%), and age (< 65 or ≥ 65 years). RESULTS: Mean (standard deviation) baseline HbA1c was 9.4% (1.8%) and 8.8% (1.4%) in patients initiating BI or GLP-1 RA therapy, respectively. The cumulative probability of achieving glycemic control was 50.1% with BI and 60.3% with GLP-1 RA therapy, respectively, at 12 months, and 60.8% and 66.6%, respectively, at 24 months. Quarterly (3-month intervals) conditional probabilities of achieving glycemic control decreased over time and were < 10% after 12 months. Patients with more OADs or higher HbA1c at baseline had a lower probability of achieving glycemic control. CONCLUSION: Among Japanese patients with T2D who initiated BI or GLP-1 RA therapy after treatment with OADs, the probability of reaching first glycemic control diminished over time. Further therapy intensification is warranted in patients who do not achieve glycemic control within 6–12 months with BI or GLP-1 RA, particularly those with high HbA1c or taking multiple OADs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13300-020-00836-8) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-7324466
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Springer Healthcare
record_format MEDLINE/PubMed
spelling pubmed-73244662020-07-07 A Real-World Observational Study Evaluating the Probability of Glycemic Control with Basal Insulin or Glucagon-Like Peptide-1 Receptor Agonist in Japanese Patients with Type 2 Diabetes Baxter, Mike Morimoto, Yukiko Tamiwa, Masami Hattori, Masakatsu Peng, Xuejun Victor Lubwama, Robert Maegawa, Hiroshi Diabetes Ther Original Research INTRODUCTION: The effectiveness of basal insulin (BI) or glucagon-like peptide-1 receptor agonists (GLP-1 RAs) in providing glycemic control in patients with type 2 diabetes (T2D) in Japanese routine practice is not well known. This real-world observational study evaluated the probability of achieving glycemic control in Japanese patients with T2D uncontrolled by oral antidiabetic drugs (OADs) who initiated BI or GLP-1 RA therapy. METHODS: Patients with T2D aged ≥ 18 years initiating BI or GLP-1 RA therapy following treatment with OADs were selected from real-world data (RWD) retrieved from a large electronic medical record database in Japan, using data from 01 January 2010 to 30 June 2019. Patients were required to have glycated hemoglobin (HbA1c) ≥ 7% within 90 days prior to the first prescription of BI or GLP-1 RA. The probability of reaching first HbA1c < 7% was assessed over a 24-month period in cohorts of patients who initiated BI (n = 3477) or GLP-1 RA (n = 780) and in subcohorts by number of OADs at baseline (1, 2, or ≥ 3), HbA1c at baseline (≥ 7 to < 8%, ≥ 8 to < 9%, or ≥ 9%), and age (< 65 or ≥ 65 years). RESULTS: Mean (standard deviation) baseline HbA1c was 9.4% (1.8%) and 8.8% (1.4%) in patients initiating BI or GLP-1 RA therapy, respectively. The cumulative probability of achieving glycemic control was 50.1% with BI and 60.3% with GLP-1 RA therapy, respectively, at 12 months, and 60.8% and 66.6%, respectively, at 24 months. Quarterly (3-month intervals) conditional probabilities of achieving glycemic control decreased over time and were < 10% after 12 months. Patients with more OADs or higher HbA1c at baseline had a lower probability of achieving glycemic control. CONCLUSION: Among Japanese patients with T2D who initiated BI or GLP-1 RA therapy after treatment with OADs, the probability of reaching first glycemic control diminished over time. Further therapy intensification is warranted in patients who do not achieve glycemic control within 6–12 months with BI or GLP-1 RA, particularly those with high HbA1c or taking multiple OADs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13300-020-00836-8) contains supplementary material, which is available to authorized users. Springer Healthcare 2020-05-22 2020-07 /pmc/articles/PMC7324466/ /pubmed/32445125 http://dx.doi.org/10.1007/s13300-020-00836-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Original Research
Baxter, Mike
Morimoto, Yukiko
Tamiwa, Masami
Hattori, Masakatsu
Peng, Xuejun Victor
Lubwama, Robert
Maegawa, Hiroshi
A Real-World Observational Study Evaluating the Probability of Glycemic Control with Basal Insulin or Glucagon-Like Peptide-1 Receptor Agonist in Japanese Patients with Type 2 Diabetes
title A Real-World Observational Study Evaluating the Probability of Glycemic Control with Basal Insulin or Glucagon-Like Peptide-1 Receptor Agonist in Japanese Patients with Type 2 Diabetes
title_full A Real-World Observational Study Evaluating the Probability of Glycemic Control with Basal Insulin or Glucagon-Like Peptide-1 Receptor Agonist in Japanese Patients with Type 2 Diabetes
title_fullStr A Real-World Observational Study Evaluating the Probability of Glycemic Control with Basal Insulin or Glucagon-Like Peptide-1 Receptor Agonist in Japanese Patients with Type 2 Diabetes
title_full_unstemmed A Real-World Observational Study Evaluating the Probability of Glycemic Control with Basal Insulin or Glucagon-Like Peptide-1 Receptor Agonist in Japanese Patients with Type 2 Diabetes
title_short A Real-World Observational Study Evaluating the Probability of Glycemic Control with Basal Insulin or Glucagon-Like Peptide-1 Receptor Agonist in Japanese Patients with Type 2 Diabetes
title_sort real-world observational study evaluating the probability of glycemic control with basal insulin or glucagon-like peptide-1 receptor agonist in japanese patients with type 2 diabetes
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7324466/
https://www.ncbi.nlm.nih.gov/pubmed/32445125
http://dx.doi.org/10.1007/s13300-020-00836-8
work_keys_str_mv AT baxtermike arealworldobservationalstudyevaluatingtheprobabilityofglycemiccontrolwithbasalinsulinorglucagonlikepeptide1receptoragonistinjapanesepatientswithtype2diabetes
AT morimotoyukiko arealworldobservationalstudyevaluatingtheprobabilityofglycemiccontrolwithbasalinsulinorglucagonlikepeptide1receptoragonistinjapanesepatientswithtype2diabetes
AT tamiwamasami arealworldobservationalstudyevaluatingtheprobabilityofglycemiccontrolwithbasalinsulinorglucagonlikepeptide1receptoragonistinjapanesepatientswithtype2diabetes
AT hattorimasakatsu arealworldobservationalstudyevaluatingtheprobabilityofglycemiccontrolwithbasalinsulinorglucagonlikepeptide1receptoragonistinjapanesepatientswithtype2diabetes
AT pengxuejunvictor arealworldobservationalstudyevaluatingtheprobabilityofglycemiccontrolwithbasalinsulinorglucagonlikepeptide1receptoragonistinjapanesepatientswithtype2diabetes
AT lubwamarobert arealworldobservationalstudyevaluatingtheprobabilityofglycemiccontrolwithbasalinsulinorglucagonlikepeptide1receptoragonistinjapanesepatientswithtype2diabetes
AT maegawahiroshi arealworldobservationalstudyevaluatingtheprobabilityofglycemiccontrolwithbasalinsulinorglucagonlikepeptide1receptoragonistinjapanesepatientswithtype2diabetes
AT baxtermike realworldobservationalstudyevaluatingtheprobabilityofglycemiccontrolwithbasalinsulinorglucagonlikepeptide1receptoragonistinjapanesepatientswithtype2diabetes
AT morimotoyukiko realworldobservationalstudyevaluatingtheprobabilityofglycemiccontrolwithbasalinsulinorglucagonlikepeptide1receptoragonistinjapanesepatientswithtype2diabetes
AT tamiwamasami realworldobservationalstudyevaluatingtheprobabilityofglycemiccontrolwithbasalinsulinorglucagonlikepeptide1receptoragonistinjapanesepatientswithtype2diabetes
AT hattorimasakatsu realworldobservationalstudyevaluatingtheprobabilityofglycemiccontrolwithbasalinsulinorglucagonlikepeptide1receptoragonistinjapanesepatientswithtype2diabetes
AT pengxuejunvictor realworldobservationalstudyevaluatingtheprobabilityofglycemiccontrolwithbasalinsulinorglucagonlikepeptide1receptoragonistinjapanesepatientswithtype2diabetes
AT lubwamarobert realworldobservationalstudyevaluatingtheprobabilityofglycemiccontrolwithbasalinsulinorglucagonlikepeptide1receptoragonistinjapanesepatientswithtype2diabetes
AT maegawahiroshi realworldobservationalstudyevaluatingtheprobabilityofglycemiccontrolwithbasalinsulinorglucagonlikepeptide1receptoragonistinjapanesepatientswithtype2diabetes