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Psoriasis Exacerbates the State of Insulin Resistance in Patients with Type 2 Diabetes
PURPOSE: Although psoriasis (PsO) is highly associated with insulin resistance (IR), the role of PsO on activity of insulin secretion or its action in diabetic patients has not been explored. MATERIALS AND METHODS: In-patient data on type 2 diabetes (T2D) with or without PsO from 2016–2019 in our ho...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165100/ https://www.ncbi.nlm.nih.gov/pubmed/34079317 http://dx.doi.org/10.2147/DMSO.S312420 |
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author | Wen, Song Liu, Congying Li, Yanyan Pan, Junhong Nguyen, Thiquynhnga Zhou, Ligang |
author_facet | Wen, Song Liu, Congying Li, Yanyan Pan, Junhong Nguyen, Thiquynhnga Zhou, Ligang |
author_sort | Wen, Song |
collection | PubMed |
description | PURPOSE: Although psoriasis (PsO) is highly associated with insulin resistance (IR), the role of PsO on activity of insulin secretion or its action in diabetic patients has not been explored. MATERIALS AND METHODS: In-patient data on type 2 diabetes (T2D) with or without PsO from 2016–2019 in our hospital were analyzed. Data for 42 diabetic patients with PsO were compared with that of the control group (T2D only). Blood examinations with reference to the levels of fasting blood glucose, C-peptide, insulin, HbA1c, plasma lipids, lipoproteins, and kidney function were explored. HOMA-IR and HOMA-β models were established to explore IR and pancreatic β-cell function. RESULTS: HOMA-IR level was significantly higher (P=0.0003<0.05) in patients with PsO compared with the controls. Although the durations of diabetes in patients with PsO were significantly shorter compared with that of patients with diabetes only (P=0.012<0.05), analysis of mean BMI, eGFR, plasma lipids, and lipoprotein showed no significant differences. Analysis of the level of fasting glucose and HOMA-β showed no statistical differences between the two groups. On the other hand, the levels of C-peptide of PsO group were significantly high in both fasting state (P=0.0182<0.05) and after glucose challenge (P=0.0011<0.01). CONCLUSION: The findings of this study show that under the same fasting conditions, patients with PsO may have relatively preserved pancreatic β-cell function, and PsO significantly increases IR. |
format | Online Article Text |
id | pubmed-8165100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-81651002021-06-01 Psoriasis Exacerbates the State of Insulin Resistance in Patients with Type 2 Diabetes Wen, Song Liu, Congying Li, Yanyan Pan, Junhong Nguyen, Thiquynhnga Zhou, Ligang Diabetes Metab Syndr Obes Original Research PURPOSE: Although psoriasis (PsO) is highly associated with insulin resistance (IR), the role of PsO on activity of insulin secretion or its action in diabetic patients has not been explored. MATERIALS AND METHODS: In-patient data on type 2 diabetes (T2D) with or without PsO from 2016–2019 in our hospital were analyzed. Data for 42 diabetic patients with PsO were compared with that of the control group (T2D only). Blood examinations with reference to the levels of fasting blood glucose, C-peptide, insulin, HbA1c, plasma lipids, lipoproteins, and kidney function were explored. HOMA-IR and HOMA-β models were established to explore IR and pancreatic β-cell function. RESULTS: HOMA-IR level was significantly higher (P=0.0003<0.05) in patients with PsO compared with the controls. Although the durations of diabetes in patients with PsO were significantly shorter compared with that of patients with diabetes only (P=0.012<0.05), analysis of mean BMI, eGFR, plasma lipids, and lipoprotein showed no significant differences. Analysis of the level of fasting glucose and HOMA-β showed no statistical differences between the two groups. On the other hand, the levels of C-peptide of PsO group were significantly high in both fasting state (P=0.0182<0.05) and after glucose challenge (P=0.0011<0.01). CONCLUSION: The findings of this study show that under the same fasting conditions, patients with PsO may have relatively preserved pancreatic β-cell function, and PsO significantly increases IR. Dove 2021-05-26 /pmc/articles/PMC8165100/ /pubmed/34079317 http://dx.doi.org/10.2147/DMSO.S312420 Text en © 2021 Wen et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Wen, Song Liu, Congying Li, Yanyan Pan, Junhong Nguyen, Thiquynhnga Zhou, Ligang Psoriasis Exacerbates the State of Insulin Resistance in Patients with Type 2 Diabetes |
title | Psoriasis Exacerbates the State of Insulin Resistance in Patients with Type 2 Diabetes |
title_full | Psoriasis Exacerbates the State of Insulin Resistance in Patients with Type 2 Diabetes |
title_fullStr | Psoriasis Exacerbates the State of Insulin Resistance in Patients with Type 2 Diabetes |
title_full_unstemmed | Psoriasis Exacerbates the State of Insulin Resistance in Patients with Type 2 Diabetes |
title_short | Psoriasis Exacerbates the State of Insulin Resistance in Patients with Type 2 Diabetes |
title_sort | psoriasis exacerbates the state of insulin resistance in patients with type 2 diabetes |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165100/ https://www.ncbi.nlm.nih.gov/pubmed/34079317 http://dx.doi.org/10.2147/DMSO.S312420 |
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