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Hydroxychloroquine improves insulin sensitivity in obese non-diabetic individuals
INTRODUCTION: Hydroxychloroquine (HCQ) is a common disease modifying therapy for the treatment of rheumatoid arthritis (RA). Prior research suggests that HCQ may reduce the risk of diabetes mellitus in patients with RA. To investigate the mechanism of this effect, we examined the effect of HCQ on in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446518/ https://www.ncbi.nlm.nih.gov/pubmed/22676348 http://dx.doi.org/10.1186/ar3868 |
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author | Mercer, Emileigh Rekedal, Laura Garg, Rajesh Lu, Bing Massarotti, Elena M Solomon, Daniel H |
author_facet | Mercer, Emileigh Rekedal, Laura Garg, Rajesh Lu, Bing Massarotti, Elena M Solomon, Daniel H |
author_sort | Mercer, Emileigh |
collection | PubMed |
description | INTRODUCTION: Hydroxychloroquine (HCQ) is a common disease modifying therapy for the treatment of rheumatoid arthritis (RA). Prior research suggests that HCQ may reduce the risk of diabetes mellitus in patients with RA. To investigate the mechanism of this effect, we examined the effect of HCQ on insulin resistance, insulin sensitivity, and pancreatic β-cell secretion of insulin in non-diabetic, obese subjects. METHODS: We recruited 13 obese, non-diabetic subjects without systemic inflammatory conditions for an open-label longitudinal study of HCQ 6.5 mg per kilogram per day for six weeks. Subjects underwent an oral glucose tolerance test at three time points: 0 weeks (pre-treatment with HCQ), 6 weeks (at the end of the HCQ treatment), and 12 weeks (6 weeks post HCQ-treatment). The Matsuda Insulin Sensitivity Index (ISI), HOMA-IR, and HOMA-B were compared across time-points. RESULTS: The mean age of the cohort was 49 years, 77% females and median body mass index was 36.1 kg/m(2). After 6 weeks of HCQ therapy, ISI increased from a median (interquartile range) of 4.5 (2.3-7.8) to 8.9 (3.7-11.4) with a p-value of 0.040, and HOMA-IR decreased from a median of 2.1 (1.6-5.4) to 1.8 (1.02-2.1) with a p-value of 0.09. All these variables returned toward baseline at week 12. CONCLUSION: HCQ use for 6 weeks in non diabetic obese subjects was associated with a significant increase in ISI and trends toward reduced insulin resistance and insulin secretion. These data suggest that HCQ, a common medication used to treat RA, possesses beneficial effects upon insulin sensitization. Further study of the insulin sensitizing effects of HCQ in patients with RA is warranted. |
format | Online Article Text |
id | pubmed-3446518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34465182012-09-21 Hydroxychloroquine improves insulin sensitivity in obese non-diabetic individuals Mercer, Emileigh Rekedal, Laura Garg, Rajesh Lu, Bing Massarotti, Elena M Solomon, Daniel H Arthritis Res Ther Research Article INTRODUCTION: Hydroxychloroquine (HCQ) is a common disease modifying therapy for the treatment of rheumatoid arthritis (RA). Prior research suggests that HCQ may reduce the risk of diabetes mellitus in patients with RA. To investigate the mechanism of this effect, we examined the effect of HCQ on insulin resistance, insulin sensitivity, and pancreatic β-cell secretion of insulin in non-diabetic, obese subjects. METHODS: We recruited 13 obese, non-diabetic subjects without systemic inflammatory conditions for an open-label longitudinal study of HCQ 6.5 mg per kilogram per day for six weeks. Subjects underwent an oral glucose tolerance test at three time points: 0 weeks (pre-treatment with HCQ), 6 weeks (at the end of the HCQ treatment), and 12 weeks (6 weeks post HCQ-treatment). The Matsuda Insulin Sensitivity Index (ISI), HOMA-IR, and HOMA-B were compared across time-points. RESULTS: The mean age of the cohort was 49 years, 77% females and median body mass index was 36.1 kg/m(2). After 6 weeks of HCQ therapy, ISI increased from a median (interquartile range) of 4.5 (2.3-7.8) to 8.9 (3.7-11.4) with a p-value of 0.040, and HOMA-IR decreased from a median of 2.1 (1.6-5.4) to 1.8 (1.02-2.1) with a p-value of 0.09. All these variables returned toward baseline at week 12. CONCLUSION: HCQ use for 6 weeks in non diabetic obese subjects was associated with a significant increase in ISI and trends toward reduced insulin resistance and insulin secretion. These data suggest that HCQ, a common medication used to treat RA, possesses beneficial effects upon insulin sensitization. Further study of the insulin sensitizing effects of HCQ in patients with RA is warranted. BioMed Central 2012 2012-06-07 /pmc/articles/PMC3446518/ /pubmed/22676348 http://dx.doi.org/10.1186/ar3868 Text en Copyright ©2012 Mercer et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Mercer, Emileigh Rekedal, Laura Garg, Rajesh Lu, Bing Massarotti, Elena M Solomon, Daniel H Hydroxychloroquine improves insulin sensitivity in obese non-diabetic individuals |
title | Hydroxychloroquine improves insulin sensitivity in obese non-diabetic individuals |
title_full | Hydroxychloroquine improves insulin sensitivity in obese non-diabetic individuals |
title_fullStr | Hydroxychloroquine improves insulin sensitivity in obese non-diabetic individuals |
title_full_unstemmed | Hydroxychloroquine improves insulin sensitivity in obese non-diabetic individuals |
title_short | Hydroxychloroquine improves insulin sensitivity in obese non-diabetic individuals |
title_sort | hydroxychloroquine improves insulin sensitivity in obese non-diabetic individuals |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446518/ https://www.ncbi.nlm.nih.gov/pubmed/22676348 http://dx.doi.org/10.1186/ar3868 |
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