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Evaluation of interleukins 37 and 38 and vitamin D status in the serum of women with Graves' disease

BACKGROUND: Graves' disease (GD) is an autoimmune thyroid disorder and recent studies have proposed a role for interleukin (IL)‐37, IL‐38, and vitamin D (VitD) in the pathophysiology of disease. Therefore, this study investigated the expression of IL‐37, IL‐38, and VitD in the serum of GD patie...

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Autores principales: Ibrahim, Hiba Y., Sulaiman, Ghassan M., Al‐shammaa, Mohamed S., Ad'hiah, Ali H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9756989/
https://www.ncbi.nlm.nih.gov/pubmed/36397279
http://dx.doi.org/10.1002/jcla.24776
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author Ibrahim, Hiba Y.
Sulaiman, Ghassan M.
Al‐shammaa, Mohamed S.
Ad'hiah, Ali H.
author_facet Ibrahim, Hiba Y.
Sulaiman, Ghassan M.
Al‐shammaa, Mohamed S.
Ad'hiah, Ali H.
author_sort Ibrahim, Hiba Y.
collection PubMed
description BACKGROUND: Graves' disease (GD) is an autoimmune thyroid disorder and recent studies have proposed a role for interleukin (IL)‐37, IL‐38, and vitamin D (VitD) in the pathophysiology of disease. Therefore, this study investigated the expression of IL‐37, IL‐38, and VitD in the serum of GD patients and correlations of their levels with some demographic and clinical characteristics. METHODS: Serum IL‐37, IL‐38, and VitD levels were evaluated in 90 women with GD and 93 control women using enzyme‐linked immunosorbent assay kits. Depending on therapy, six patients were newly diagnosed (ND; untreated), and 50 patients were receiving only carbimazole (CMZ), while 34 patients were also on CMZ but also received one (31 patients), two (one patient), or three (two patients) doses of radioactive iodine (RAI). RESULTS: IL‐37 levels were significantly higher in GD patients than in controls, while IL‐38 and VitD levels were significantly decreased. As indicated by the area under the curve (AUC), receiver operating characteristic curve analysis demonstrated the potential of IL‐37, IL‐38, and VitD as biomarkers to distinguish GD patients from controls (AUC = 0.953, 0.959, and 0.793, respectively). Multinomial logistic regression analysis showed that altered levels of IL‐37, IL‐38, and VitD were most likely associated with the pathogenesis of GD. IL‐37 was negatively correlated with IL‐38 and VitD, while IL‐38 and VitD were positively correlated. CONCLUSION: Serum Il‐37 levels were upregulated in women with GD, while IL‐38 and VitD levels showed downregulated levels. The latter two were positively correlated while they showed a negative correlation with IL‐37.
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spelling pubmed-97569892022-12-20 Evaluation of interleukins 37 and 38 and vitamin D status in the serum of women with Graves' disease Ibrahim, Hiba Y. Sulaiman, Ghassan M. Al‐shammaa, Mohamed S. Ad'hiah, Ali H. J Clin Lab Anal Research Articles BACKGROUND: Graves' disease (GD) is an autoimmune thyroid disorder and recent studies have proposed a role for interleukin (IL)‐37, IL‐38, and vitamin D (VitD) in the pathophysiology of disease. Therefore, this study investigated the expression of IL‐37, IL‐38, and VitD in the serum of GD patients and correlations of their levels with some demographic and clinical characteristics. METHODS: Serum IL‐37, IL‐38, and VitD levels were evaluated in 90 women with GD and 93 control women using enzyme‐linked immunosorbent assay kits. Depending on therapy, six patients were newly diagnosed (ND; untreated), and 50 patients were receiving only carbimazole (CMZ), while 34 patients were also on CMZ but also received one (31 patients), two (one patient), or three (two patients) doses of radioactive iodine (RAI). RESULTS: IL‐37 levels were significantly higher in GD patients than in controls, while IL‐38 and VitD levels were significantly decreased. As indicated by the area under the curve (AUC), receiver operating characteristic curve analysis demonstrated the potential of IL‐37, IL‐38, and VitD as biomarkers to distinguish GD patients from controls (AUC = 0.953, 0.959, and 0.793, respectively). Multinomial logistic regression analysis showed that altered levels of IL‐37, IL‐38, and VitD were most likely associated with the pathogenesis of GD. IL‐37 was negatively correlated with IL‐38 and VitD, while IL‐38 and VitD were positively correlated. CONCLUSION: Serum Il‐37 levels were upregulated in women with GD, while IL‐38 and VitD levels showed downregulated levels. The latter two were positively correlated while they showed a negative correlation with IL‐37. John Wiley and Sons Inc. 2022-11-17 /pmc/articles/PMC9756989/ /pubmed/36397279 http://dx.doi.org/10.1002/jcla.24776 Text en © 2022 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Ibrahim, Hiba Y.
Sulaiman, Ghassan M.
Al‐shammaa, Mohamed S.
Ad'hiah, Ali H.
Evaluation of interleukins 37 and 38 and vitamin D status in the serum of women with Graves' disease
title Evaluation of interleukins 37 and 38 and vitamin D status in the serum of women with Graves' disease
title_full Evaluation of interleukins 37 and 38 and vitamin D status in the serum of women with Graves' disease
title_fullStr Evaluation of interleukins 37 and 38 and vitamin D status in the serum of women with Graves' disease
title_full_unstemmed Evaluation of interleukins 37 and 38 and vitamin D status in the serum of women with Graves' disease
title_short Evaluation of interleukins 37 and 38 and vitamin D status in the serum of women with Graves' disease
title_sort evaluation of interleukins 37 and 38 and vitamin d status in the serum of women with graves' disease
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9756989/
https://www.ncbi.nlm.nih.gov/pubmed/36397279
http://dx.doi.org/10.1002/jcla.24776
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