Dergiler / Turkish Journal of Medical Sciences / 2022 / Cilt: 52 - Sayı: 3

The relationship between elevated plasma zonulin levels and Hashimoto’s thyroiditis

Sayfa
605–612
Yayın Tarihi
2022-11-05
DOI
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Conclusion: Zonulin is a possible biomarker candidate that may link intestinal permeability with the etiology of autoimmune diseases.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Background/aim: Hashimoto thyroiditis (HT) is one of the most prevalent autoimmune diseases.
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Temel Bulgular & Veri:Materials and methods: We compared 77 HT patients with 66 age-gender and BMI-matched healthy individuals in the case of plasma zonulin levels.
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Sonuç & Katkı:Conclusion: Zonulin is a possible biomarker candidate that may link intestinal permeability with the etiology of autoimmune diseases.
🔬Tür:Modelleme & Sayısal Simülasyon
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Background/aim: Hashimoto thyroiditis (HT) is one of the most prevalent autoimmune diseases. The intestine microbiota is strongly associated with autoimmune diseases. Zonulin, a modulator of tight junctions that controls the selective permeability of the intestine can induce an elevation in gut permeability. We aimed to investigate the association of plasma zonulin levels with HT. Materials and methods: We compared 77 HT patients with 66 age-gender and BMI-matched healthy individuals in the case of plasma zonulin levels. Plasma zonulin levels were measured by ELISA. The statistical analyses were performed using Student’s t-test and chisquare tests. The predictive power was investigated using univariate and multivariate logistic regression analysis. Results: We found that the increase in plasma zonulin levels in the HT group was statistically significant compared to the control group (p < 0.001). The regression analysis showed that urea, anti-thyroid peroxidase, aspartate aminotransferase, thyroid-stimulating hormone, free T3, and serum zonulin levels were found to be associated with HT in both univariate and multivariate models (p < 0.05). Conclusion: Zonulin is a possible biomarker candidate that may link intestinal permeability with the etiology of autoimmune diseases.

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Bu Makaleye Atıf Yap

DEMİR, E., YENMİŞ, G., KUMBASAR, A., DEMİR, B., ŞAHTİYANCI, B., ÖZKAN, H., UTKU, İ. K., ÖNAL, B. (2022). The relationship between elevated plasma zonulin levels and Hashimoto’s thyroiditis. Turkish Journal of Medical Sciences, Cilt: 52 - Sayı: 3, 605–612. https://ajindex.com/articles/609206

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Kaynakça (3)

  1. Shoenfeld Y, Cervera R, Gershwin ME. Diagnostic criteria in autoimmune diseases. Berlin: Springer Science & Business Media; 2010
  2. Fröhlich E, Wahl R. Microbiota and Thyroid Interaction in Health and Disease. Trends Endocrinol Metabolism 2019;30 (8): 479- 490. Epub 2019 Jun 27. doi: 10.1016/j.tem.2019.05.008 3. Nacamulli D, Petricca D, Mian C, C Betterle. Selenium and autoimmune thyroiditis. J Endocrinol Investigation 2013; 36 (10): 8–14
  3. Aghini-Lombardi F, Antonangeli L, Martino E, P Vitti, D Maccherini et al. The spectrum of thyroid disorders in an iodine-defcient community: the Pescopagano survey. The Journal of Clinical Endocrinology and Metabolism 1999; 84 (2): 561–566. doi: 10.1210/jcem.84.2.5508 5. Hollowell JG, Staehling NW, Flanders WD, Hannon WH, Gunter EW et al. Serum TSH, T(4), and thyroid antibodies in the United States population (1988 to 1994): National Health and Nutrition Examination Survey (NHANES III). The Journal of Clinical Endocrinology and Metabolism 2002; 87 (2): 489- 99. doi: 10.1210/jcem.87.2.8182 6. Serena G, Camhi S, Sturgeon C, Yan S, Fasano A. The role of gluten in celiac disease and type 1 diabetes. Nutrients 2015; 7 (9): 7143-7162. doi: 10.3390/nu7095329 7. Fasano A. Physiological, pathological, and therapeutic implications of zonulin-mediated intestinal barrier modulation: living life on the edge of the wall. The American Journal of Pathology 2008; 173 (5): 1243–1252. doi:10.2353/ajpath.2008.080192 8. Lee, V. Membrane transporters. European Journal of Pharmaceutical Sciences 2000; 11 (2): 41–50. doi: 10.1016/ s0928-0987(00)00163-9 9. Young, VB. The intestinal microbiota in health and disease. Current Opinion in Gastroenterology 2012; 28 (1): 63–69. doi: 10.1097/MOG.0b013e32834d61e9 10. Kerakada N, Ganesh M, Meer MC. Prevalence of iodine deficiency among multinodular goiter patients: a South Indian study. International Surgery Journal 2017; 4 (2): 680–684. doi: 10.18203/2349-2902.isj20170213 11. Leung, AM. and Braverman, LE. Consequences of excess iodine. Nature Reviews Endocrinology 2014; 10 (3): 136–142. doi: 10.1038/nrendo.2013.251 12. Kunc M, Gabrych A, Witkowski JM. Microbiome impact on metabolism and function of sex, thyroid, growth and parathyroid hormones. Acta Biochimica Polonica 2016; 63 (2): 189–201. doi: 10.18388/abp.2015_1093 13. Rook GAW, Brunet LR. Microbes, immunoregulation, and the gut. Gut 2005; 54 (3): 317-320. doi: 10.1136/gut.2004.053785 14. Garcia-Castillo V, Enrique Sanhueza, Eileen McNerney,