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Serum IL-23 significantly decreased in obese patients with psoriatic arthritis six months after a structured weight loss intervention
INTRODUCTION: Patients with psoriatic arthritis (PsA) are frequently obese. We have previously shown decreased disease activity in patients with PsA with a body mass index (BMI) ≥ 33 kg/m(2) following weight loss treatment with Very Low Energy Diet (VLED), resulting in a median weight loss of 18.6%...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373368/ https://www.ncbi.nlm.nih.gov/pubmed/37501212 http://dx.doi.org/10.1186/s13075-023-03105-8 |
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author | Landgren, A. J. Jonsson, C. A. Bilberg, A. Eliasson, B. Torres, L. Dehlin, M. Jacobsson, L. T. H. Gjertsson, I. Larsson, I. Klingberg, E. |
author_facet | Landgren, A. J. Jonsson, C. A. Bilberg, A. Eliasson, B. Torres, L. Dehlin, M. Jacobsson, L. T. H. Gjertsson, I. Larsson, I. Klingberg, E. |
author_sort | Landgren, A. J. |
collection | PubMed |
description | INTRODUCTION: Patients with psoriatic arthritis (PsA) are frequently obese. We have previously shown decreased disease activity in patients with PsA with a body mass index (BMI) ≥ 33 kg/m(2) following weight loss treatment with Very Low Energy Diet (VLED), resulting in a median weight loss of 18.6% at six months (M6) after baseline (BL). In this study we assessed the effects of VLED on cytokines and adipokines at M6 in the same patients with PsA and controls (matched on sex, age and weight). METHODS: VLED (640 kcal/day) during 12 or 16 weeks, depending on BL BMI < 40 or ≥ 40 kg/m(2), was taken and followed by an energy-restricted diet. Cytokines and adipokines were measured with Magnetic Luminex Assays at BL and M6. RESULTS: Serum interleukin (IL)-23, (median (interquartile range) 0.40 (0.17–0.54) ng/mL vs. 0.18 (0.10–0.30) ng/mL, p < 0.001) and leptin (26.28 (14.35–48.73) ng/mL vs. 9.25 (4.40–16.24) ng/mL, p < 0.001) was significantly decreased in patients with PsA. Serum total (tot)-adiponectin and high molecular weight (HMW) adiponectin increased significantly. Similar findings were found in controls. Also, in patients with PsA, ∆BMI was positively correlated with ∆IL-23 (r(S) = 0.671, p < 0.001). In addition, significant positive correlations were found between ΔBMI and ΔDisease Activity Score (DAS28CRP), ΔCRP, Δtumor necrosis factor (TNF)-α, ΔIL-13, ∆IL-17 and Δleptin, and negative correlations between ΔBMI and Δtot-adiponectin. CONCLUSIONS: Weight loss was associated with decreased levels of leptin and cytokines, in particular IL-23. These findings may partly explain the anti-inflammatory effect of weight reduction in PsA. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT02917434, registered on September 21, 2016, retrospectively registered. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-023-03105-8. |
format | Online Article Text |
id | pubmed-10373368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103733682023-07-28 Serum IL-23 significantly decreased in obese patients with psoriatic arthritis six months after a structured weight loss intervention Landgren, A. J. Jonsson, C. A. Bilberg, A. Eliasson, B. Torres, L. Dehlin, M. Jacobsson, L. T. H. Gjertsson, I. Larsson, I. Klingberg, E. Arthritis Res Ther Research INTRODUCTION: Patients with psoriatic arthritis (PsA) are frequently obese. We have previously shown decreased disease activity in patients with PsA with a body mass index (BMI) ≥ 33 kg/m(2) following weight loss treatment with Very Low Energy Diet (VLED), resulting in a median weight loss of 18.6% at six months (M6) after baseline (BL). In this study we assessed the effects of VLED on cytokines and adipokines at M6 in the same patients with PsA and controls (matched on sex, age and weight). METHODS: VLED (640 kcal/day) during 12 or 16 weeks, depending on BL BMI < 40 or ≥ 40 kg/m(2), was taken and followed by an energy-restricted diet. Cytokines and adipokines were measured with Magnetic Luminex Assays at BL and M6. RESULTS: Serum interleukin (IL)-23, (median (interquartile range) 0.40 (0.17–0.54) ng/mL vs. 0.18 (0.10–0.30) ng/mL, p < 0.001) and leptin (26.28 (14.35–48.73) ng/mL vs. 9.25 (4.40–16.24) ng/mL, p < 0.001) was significantly decreased in patients with PsA. Serum total (tot)-adiponectin and high molecular weight (HMW) adiponectin increased significantly. Similar findings were found in controls. Also, in patients with PsA, ∆BMI was positively correlated with ∆IL-23 (r(S) = 0.671, p < 0.001). In addition, significant positive correlations were found between ΔBMI and ΔDisease Activity Score (DAS28CRP), ΔCRP, Δtumor necrosis factor (TNF)-α, ΔIL-13, ∆IL-17 and Δleptin, and negative correlations between ΔBMI and Δtot-adiponectin. CONCLUSIONS: Weight loss was associated with decreased levels of leptin and cytokines, in particular IL-23. These findings may partly explain the anti-inflammatory effect of weight reduction in PsA. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT02917434, registered on September 21, 2016, retrospectively registered. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-023-03105-8. BioMed Central 2023-07-27 2023 /pmc/articles/PMC10373368/ /pubmed/37501212 http://dx.doi.org/10.1186/s13075-023-03105-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Landgren, A. J. Jonsson, C. A. Bilberg, A. Eliasson, B. Torres, L. Dehlin, M. Jacobsson, L. T. H. Gjertsson, I. Larsson, I. Klingberg, E. Serum IL-23 significantly decreased in obese patients with psoriatic arthritis six months after a structured weight loss intervention |
title | Serum IL-23 significantly decreased in obese patients with psoriatic arthritis six months after a structured weight loss intervention |
title_full | Serum IL-23 significantly decreased in obese patients with psoriatic arthritis six months after a structured weight loss intervention |
title_fullStr | Serum IL-23 significantly decreased in obese patients with psoriatic arthritis six months after a structured weight loss intervention |
title_full_unstemmed | Serum IL-23 significantly decreased in obese patients with psoriatic arthritis six months after a structured weight loss intervention |
title_short | Serum IL-23 significantly decreased in obese patients with psoriatic arthritis six months after a structured weight loss intervention |
title_sort | serum il-23 significantly decreased in obese patients with psoriatic arthritis six months after a structured weight loss intervention |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373368/ https://www.ncbi.nlm.nih.gov/pubmed/37501212 http://dx.doi.org/10.1186/s13075-023-03105-8 |
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