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The effectiveness of insulin glargine 300 U/mL among type 2 diabetes patients: Analysis of a real‐world data in Israel
AIMS: Randomized controlled trials have shown that insulin glargine 300 U/mL (Gla‐300) has a more stable and prolonged glucose lowering effect among patients with type 2 diabetes (T2DM) compared to insulin glargine 100 U/mL (Gla‐100), resulting in a reduced risk of hypoglycaemia while maintaining a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375096/ https://www.ncbi.nlm.nih.gov/pubmed/32704550 http://dx.doi.org/10.1002/edm2.124 |
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author | Melzer Cohen, Cheli Banon, Tamar Shalev, Varda Chodick, Gabriel |
author_facet | Melzer Cohen, Cheli Banon, Tamar Shalev, Varda Chodick, Gabriel |
author_sort | Melzer Cohen, Cheli |
collection | PubMed |
description | AIMS: Randomized controlled trials have shown that insulin glargine 300 U/mL (Gla‐300) has a more stable and prolonged glucose lowering effect among patients with type 2 diabetes (T2DM) compared to insulin glargine 100 U/mL (Gla‐100), resulting in a reduced risk of hypoglycaemia while maintaining a similar efficacy of lowering HbA(1c). We aimed to investigate if the effectiveness of Gla‐300 is reproducible in real‐world settings. MATERIAL AND METHODS: In this retrospective cohort study, data from a large state‐mandated health organization were used to identify adult T2DM patients who were previously on insulin and initiated Gla‐300 therapy between 6/ 2016 and 12/2017. Changes in HbA(1c) levels, body weight and insulin dose were calculated from baseline period and over a follow‐up period of 180 days. Documented hypoglycaemia events were also explored. RESULTS: A total of 1797 patients were included in this study with a mean age of 64.2 (SD = ±11.0y), baseline HbA(1c) was 8.7 ± 1.6% and 42.5% were females. Among all patients with HbA(1c) measurement during follow‐up (n = 1508), HbA(1c) was significantly reduced by −0.6% (95% CI −0.6,−0.5; P < .001) from baseline, with a significant reduction in body weight (−0.4 kg; P = <.001). Additionally, a significant (P = .04) reduction of 40.5% in patients with hypoglycaemia events was recorded during follow‐up period, from 2.1% (n = 37) at the baseline period to 1.2% (n = 22). CONCLUSIONS: This real‐world study supports evidence from RCTs regarding the effectiveness of Gla‐300 among T2DM patients by improving glycaemic control. |
format | Online Article Text |
id | pubmed-7375096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73750962020-07-22 The effectiveness of insulin glargine 300 U/mL among type 2 diabetes patients: Analysis of a real‐world data in Israel Melzer Cohen, Cheli Banon, Tamar Shalev, Varda Chodick, Gabriel Endocrinol Diabetes Metab Original Research Articles AIMS: Randomized controlled trials have shown that insulin glargine 300 U/mL (Gla‐300) has a more stable and prolonged glucose lowering effect among patients with type 2 diabetes (T2DM) compared to insulin glargine 100 U/mL (Gla‐100), resulting in a reduced risk of hypoglycaemia while maintaining a similar efficacy of lowering HbA(1c). We aimed to investigate if the effectiveness of Gla‐300 is reproducible in real‐world settings. MATERIAL AND METHODS: In this retrospective cohort study, data from a large state‐mandated health organization were used to identify adult T2DM patients who were previously on insulin and initiated Gla‐300 therapy between 6/ 2016 and 12/2017. Changes in HbA(1c) levels, body weight and insulin dose were calculated from baseline period and over a follow‐up period of 180 days. Documented hypoglycaemia events were also explored. RESULTS: A total of 1797 patients were included in this study with a mean age of 64.2 (SD = ±11.0y), baseline HbA(1c) was 8.7 ± 1.6% and 42.5% were females. Among all patients with HbA(1c) measurement during follow‐up (n = 1508), HbA(1c) was significantly reduced by −0.6% (95% CI −0.6,−0.5; P < .001) from baseline, with a significant reduction in body weight (−0.4 kg; P = <.001). Additionally, a significant (P = .04) reduction of 40.5% in patients with hypoglycaemia events was recorded during follow‐up period, from 2.1% (n = 37) at the baseline period to 1.2% (n = 22). CONCLUSIONS: This real‐world study supports evidence from RCTs regarding the effectiveness of Gla‐300 among T2DM patients by improving glycaemic control. John Wiley and Sons Inc. 2020-03-24 /pmc/articles/PMC7375096/ /pubmed/32704550 http://dx.doi.org/10.1002/edm2.124 Text en © 2020 The Authors. Endocrinology, Diabetes & Metabolism published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Articles Melzer Cohen, Cheli Banon, Tamar Shalev, Varda Chodick, Gabriel The effectiveness of insulin glargine 300 U/mL among type 2 diabetes patients: Analysis of a real‐world data in Israel |
title | The effectiveness of insulin glargine 300 U/mL among type 2 diabetes patients: Analysis of a real‐world data in Israel |
title_full | The effectiveness of insulin glargine 300 U/mL among type 2 diabetes patients: Analysis of a real‐world data in Israel |
title_fullStr | The effectiveness of insulin glargine 300 U/mL among type 2 diabetes patients: Analysis of a real‐world data in Israel |
title_full_unstemmed | The effectiveness of insulin glargine 300 U/mL among type 2 diabetes patients: Analysis of a real‐world data in Israel |
title_short | The effectiveness of insulin glargine 300 U/mL among type 2 diabetes patients: Analysis of a real‐world data in Israel |
title_sort | effectiveness of insulin glargine 300 u/ml among type 2 diabetes patients: analysis of a real‐world data in israel |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375096/ https://www.ncbi.nlm.nih.gov/pubmed/32704550 http://dx.doi.org/10.1002/edm2.124 |
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