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The Evolution of Insulin Glargine and its Continuing Contribution to Diabetes Care
The epoch-making discovery of insulin heralded a new dawn in the management of diabetes. However, the earliest, unmodified soluble insulin preparations were limited by their short duration of action, necessitating multiple daily injections. Initial attempts to protract the duration of action of insu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4045187/ https://www.ncbi.nlm.nih.gov/pubmed/24866023 http://dx.doi.org/10.1007/s40265-014-0226-4 |
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author | Hilgenfeld, Rolf Seipke, Gerhard Berchtold, Harald Owens, David R. |
author_facet | Hilgenfeld, Rolf Seipke, Gerhard Berchtold, Harald Owens, David R. |
author_sort | Hilgenfeld, Rolf |
collection | PubMed |
description | The epoch-making discovery of insulin heralded a new dawn in the management of diabetes. However, the earliest, unmodified soluble insulin preparations were limited by their short duration of action, necessitating multiple daily injections. Initial attempts to protract the duration of action of insulin involved the use of various additives, including vasoconstrictor substances, which met with limited success. The subsequent elucidation of the chemical and three-dimensional structure of insulin and its chemical synthesis and biosynthesis allowed modification of the insulin molecule itself, resulting in insulin analogs that are designed to mimic normal endogenous insulin secretion during both fasting and prandial conditions. Insulin glargine was the first once-daily, long-acting insulin analog to be introduced into clinical practice more than 10 years ago and is specifically designed to provide basal insulin requirements. It has a prolonged duration of action and no distinct insulin peak, making it suitable for once-daily administration and reducing the risk of nocturnal hypoglycemia that is seen with intermediate-acting insulins. Insulin glargine can be used in combination with prandial insulin preparations and non-insulin anti-diabetic agents according to individual requirements. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s40265-014-0226-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4045187 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-40451872014-06-05 The Evolution of Insulin Glargine and its Continuing Contribution to Diabetes Care Hilgenfeld, Rolf Seipke, Gerhard Berchtold, Harald Owens, David R. Drugs Review Article The epoch-making discovery of insulin heralded a new dawn in the management of diabetes. However, the earliest, unmodified soluble insulin preparations were limited by their short duration of action, necessitating multiple daily injections. Initial attempts to protract the duration of action of insulin involved the use of various additives, including vasoconstrictor substances, which met with limited success. The subsequent elucidation of the chemical and three-dimensional structure of insulin and its chemical synthesis and biosynthesis allowed modification of the insulin molecule itself, resulting in insulin analogs that are designed to mimic normal endogenous insulin secretion during both fasting and prandial conditions. Insulin glargine was the first once-daily, long-acting insulin analog to be introduced into clinical practice more than 10 years ago and is specifically designed to provide basal insulin requirements. It has a prolonged duration of action and no distinct insulin peak, making it suitable for once-daily administration and reducing the risk of nocturnal hypoglycemia that is seen with intermediate-acting insulins. Insulin glargine can be used in combination with prandial insulin preparations and non-insulin anti-diabetic agents according to individual requirements. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s40265-014-0226-4) contains supplementary material, which is available to authorized users. Springer International Publishing 2014-05-28 2014 /pmc/articles/PMC4045187/ /pubmed/24866023 http://dx.doi.org/10.1007/s40265-014-0226-4 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by-nc/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Review Article Hilgenfeld, Rolf Seipke, Gerhard Berchtold, Harald Owens, David R. The Evolution of Insulin Glargine and its Continuing Contribution to Diabetes Care |
title | The Evolution of Insulin Glargine and its Continuing Contribution to Diabetes Care |
title_full | The Evolution of Insulin Glargine and its Continuing Contribution to Diabetes Care |
title_fullStr | The Evolution of Insulin Glargine and its Continuing Contribution to Diabetes Care |
title_full_unstemmed | The Evolution of Insulin Glargine and its Continuing Contribution to Diabetes Care |
title_short | The Evolution of Insulin Glargine and its Continuing Contribution to Diabetes Care |
title_sort | evolution of insulin glargine and its continuing contribution to diabetes care |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4045187/ https://www.ncbi.nlm.nih.gov/pubmed/24866023 http://dx.doi.org/10.1007/s40265-014-0226-4 |
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