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Physiologic Insulin Resensitization as a Treatment Modality for Insulin Resistance Pathophysiology
Prevalence of type 2 diabetes increased from 2.5% of the US population in 1990 to 10.5% in 2018. This creates a major public health problem, due to increases in long-term complications of diabetes, including neuropathy, retinopathy, nephropathy, skin ulcers, amputations, and atherosclerotic cardiova...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836751/ https://www.ncbi.nlm.nih.gov/pubmed/35163806 http://dx.doi.org/10.3390/ijms23031884 |
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author | Greenway, Frank Loveridge, Brian Grimes, Richard M. Tucker, Tori R. Alexander, Michael Hepford, Scott A. Fontenot, Justin Nobles-James, Candi Wilson, Carol Starr, Adam M. Abdelsaid, Mohammed Lewis, Stanley T. Lakey, Jonathan R. T. |
author_facet | Greenway, Frank Loveridge, Brian Grimes, Richard M. Tucker, Tori R. Alexander, Michael Hepford, Scott A. Fontenot, Justin Nobles-James, Candi Wilson, Carol Starr, Adam M. Abdelsaid, Mohammed Lewis, Stanley T. Lakey, Jonathan R. T. |
author_sort | Greenway, Frank |
collection | PubMed |
description | Prevalence of type 2 diabetes increased from 2.5% of the US population in 1990 to 10.5% in 2018. This creates a major public health problem, due to increases in long-term complications of diabetes, including neuropathy, retinopathy, nephropathy, skin ulcers, amputations, and atherosclerotic cardiovascular disease. In this review, we evaluated the scientific basis that supports the use of physiologic insulin resensitization. Insulin resistance is the primary cause of type 2 diabetes. Insulin resistance leads to increasing insulin secretion, leading to beta-cell exhaustion or burnout. This triggers a cascade leading to islet cell destruction and the long-term complications of type 2 diabetes. Concurrent with insulin resistance, the regular bursts of insulin from the pancreas become irregular. This has been treated by the precise administration of insulin more physiologically. There is consistent evidence that this treatment modality can reverse the diabetes-associated complications of neuropathy, diabetic ulcers, nephropathy, and retinopathy, and that it lowers HbA1c. In conclusion, physiologic insulin resensitization has a persuasive scientific basis, significant treatment potential, and likely cost benefits. |
format | Online Article Text |
id | pubmed-8836751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88367512022-02-12 Physiologic Insulin Resensitization as a Treatment Modality for Insulin Resistance Pathophysiology Greenway, Frank Loveridge, Brian Grimes, Richard M. Tucker, Tori R. Alexander, Michael Hepford, Scott A. Fontenot, Justin Nobles-James, Candi Wilson, Carol Starr, Adam M. Abdelsaid, Mohammed Lewis, Stanley T. Lakey, Jonathan R. T. Int J Mol Sci Review Prevalence of type 2 diabetes increased from 2.5% of the US population in 1990 to 10.5% in 2018. This creates a major public health problem, due to increases in long-term complications of diabetes, including neuropathy, retinopathy, nephropathy, skin ulcers, amputations, and atherosclerotic cardiovascular disease. In this review, we evaluated the scientific basis that supports the use of physiologic insulin resensitization. Insulin resistance is the primary cause of type 2 diabetes. Insulin resistance leads to increasing insulin secretion, leading to beta-cell exhaustion or burnout. This triggers a cascade leading to islet cell destruction and the long-term complications of type 2 diabetes. Concurrent with insulin resistance, the regular bursts of insulin from the pancreas become irregular. This has been treated by the precise administration of insulin more physiologically. There is consistent evidence that this treatment modality can reverse the diabetes-associated complications of neuropathy, diabetic ulcers, nephropathy, and retinopathy, and that it lowers HbA1c. In conclusion, physiologic insulin resensitization has a persuasive scientific basis, significant treatment potential, and likely cost benefits. MDPI 2022-02-08 /pmc/articles/PMC8836751/ /pubmed/35163806 http://dx.doi.org/10.3390/ijms23031884 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Greenway, Frank Loveridge, Brian Grimes, Richard M. Tucker, Tori R. Alexander, Michael Hepford, Scott A. Fontenot, Justin Nobles-James, Candi Wilson, Carol Starr, Adam M. Abdelsaid, Mohammed Lewis, Stanley T. Lakey, Jonathan R. T. Physiologic Insulin Resensitization as a Treatment Modality for Insulin Resistance Pathophysiology |
title | Physiologic Insulin Resensitization as a Treatment Modality for Insulin Resistance Pathophysiology |
title_full | Physiologic Insulin Resensitization as a Treatment Modality for Insulin Resistance Pathophysiology |
title_fullStr | Physiologic Insulin Resensitization as a Treatment Modality for Insulin Resistance Pathophysiology |
title_full_unstemmed | Physiologic Insulin Resensitization as a Treatment Modality for Insulin Resistance Pathophysiology |
title_short | Physiologic Insulin Resensitization as a Treatment Modality for Insulin Resistance Pathophysiology |
title_sort | physiologic insulin resensitization as a treatment modality for insulin resistance pathophysiology |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836751/ https://www.ncbi.nlm.nih.gov/pubmed/35163806 http://dx.doi.org/10.3390/ijms23031884 |
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