Thyroid status and TNF-alpha in post-reproductive women with COVID-19 and 12 months after the disease
https://doi.org/10.29413/ABS.2023-8.2.4
Abstract
The aim. To assess the thyroid status and its relationship with tumor necrosis factor alpha (TNF-alpha) in post-reproductive women in the acute phase of the COVID-19 of moderate course and 12 months after the disease.
Materials and methods. 85 women aged 45 to 69 years were divided into groups: women without COVID-19, not vaccinated, with no antibodies to COVID-19 (IgG) – control group (n = 15); women in the acute phase of COVID-19 of a moderate course, accompanied by pneumonia – main group (n = 57); patients from the main group who agreed to be examined 12 months after having COVID-19 (n = 14); women with IgG in blood who deny any symptoms of COVID-19 in the last 12 months – asymptomatic COVID-19 (n = 13). Using hormone replacement therapy and the presence of thyroid disease in history were the exclusion criteria from the study.
Results. 75.4 % of patients with COVID-19 had euthyroidism, 12.3 % had subclinical hyperthyroidism. An increase of free thyroxine (free T4) level in women with COVID-19 as compared to the control group (p = 0.004) and the group with asymptomatic COVID-19 (p = 0.054) was found. There was no statistically significant difference in the level of thyroid stimulating hormone between the groups. The level of C-reactive protein in women with COVID-19 was naturally higher as compared to the control group (p = 0.009) and the group of asymptomatic patients (p = 0.001). A lower TNF-alpha level was found in the group of patients without clinical signs of COVID-19 as compared to the control group (p = 0.007) and the group with COVID-19 (p = 0.00007). The analysis of correlation relationships revealed a positive correlation between of free T4 and TNF-alpha levels in women with COVID-19 (r = 0.38, p = 0.004).
Conclusions. The moderate course of COVID-19 in the post-reproductive women is associated with an increase of free T4 level, which positively correlates with TNF-alpha level. Twelve months after COVID-19, thyroid status in women remains at the level of the acute phase of the disease.
About the Authors
N. V. SemenovaRussian Federation
Natalya V. Semenova – Dr. Sc. (Biol.), Leading Research Officer at the Laboratory of Pathophysiology.
Timiryazeva str. 16, Irkutsk 664003
S. I. Kolesnikov
Russian Federation
Sergey I. Kolesnikov – Dr. Sc. (Med.), Academician of the RAS, Chief Scientific Officer, Scientific Centre for Family Health and Human Reproduction Problems; Professor, Lomonosov Moscow State University.
Timiryazeva str. 16, Irkutsk 664003
E. V. Vyrupaeva
Russian Federation
Ekaterina V. Vyrupaeva – Postgraduate.
Timiryazeva str. 16, Irkutsk 664003
l. F. Sholokhov
Russian Federation
Leonid F. Sholokhov – Dr. Sc. (Med.), Professor, Head of the Laboratory of Physiology and Pathology of the Endocrine System.
Timiryazeva str. 16, Irkutsk 664003
L. V. Rychkova
Russian Federation
Lyubov V. Rychkova – Dr. Sc. (Med.), Corresponding Member of the RAS, Director.
Timiryazeva str. 16, Irkutsk 664003
А. G. Petrova
Russian Federation
Alla G. Petrova – Dr. Sc. (Med.), Professor, Head of the Laboratory of Infectology and Immunoprophylaxis.
Timiryazeva str. 16, Irkutsk 664003
M. R. Akhmedzyanova
Russian Federation
Margarita R. Akhmedzyanova – Junior Research Officer at the Laboratory of Physiology and Pathology of the Endocrine System.
Timiryazeva str. 16, Irkutsk 664003
M. A. Darenskaya
Russian Federation
Marina A. Darenskaya – Dr. Sc. (Biol.), Leading Research Officer at the Laboratory of Pathophysiology.
Timiryazeva str. 16, Irkutsk 664003
L. I. Kolesnikova
Russian Federation
Lyubov I. Kolesnikova – Dr. Sc. (Med.), Professor, Academician of the RAS, Scientific Advisor.
Timiryazeva str. 16, Irkutsk 664003
References
1. Weiss P, Murdoch DR. Clinical course and mortality risk of severe COVID-19. Lancet. 2020; 395(10229): 1014-1015. doi: 10.1016/S0140-6736(20)30633-4
2. Starodubov VI, Beregovykh VV, Akimkin VG, Semenenko TA, Ugleva SV, Avdeev SN, et al. COVID-19 in Russia: Evolution of views on the pandemic. Report I. Annals of the Russian Academy of Medical Sciences. 2022; 77(3): 199-207. (In Russ.). doi: 10.15690/vramn2118
3. Zhang J, Wang X, Jia X, Li J, Hu K, Chen G, et al. Risk factors for disease severity, unimprovement, and mortality in COVID-19 patients in Wuhan, China. Clin Microbiol Infect. 2020; 26(6): 767-772. doi: 10.1016/j.cmi.2020.04.012
4. Nekaeva ES, Bolshakova AE, Malysheva ES, Galova EA, Makarova EV, Nekrasova TA, et al. Gender characteristics of the novel coronavirus infection (COVID-19) in middle-aged adults. Sovremennye tehnologii v medicine. 2021; 13(4): 16-26. doi: 10.17691/stm2021.13.4.02
5. Prinelli F, Trevisan C, Noale M, Franchini M, Giacomelli A, Cori L, et al. EPICOVID19 Working Group. Sex- and gender-related differences linked to SARS-CoV-2 infection among the participants in the web-based EPICOVID19 survey: the hormonal hypothesis. Maturitas. 2022; 158: 61-69. doi: 10.1016/j.maturitas.2021.11.015
6. Li L, Wang Z. Ovarian aging and osteoporosis. Adv Exp Med Biol. 2018; 1086: 199-215. doi: 10.1007/978-981-13-1117-8_13
7. Leeners B, Geary N, Tobler PN, Asarian L. Ovarian hormones and obesity. Hum Reprod Update. 2017; 23(3): 300-321. doi: 10.1093/humupd/dmw045
8. Newson L. Menopause and cardiovascular disease. Post Reprod Health. 2018; 24(1): 44-49. doi: 10.1177/2053369117749675
9. Labandeira-Garcia JL, Rodriguez-Perez AI, Valenzuela R, Costa-Besada MA, Guerra MJ. Menopause and Parkinson’s disease. Interaction between estrogens and brain renin-angiotensin system in dopaminergic degeneration. Front Neuroendocrinol. 2016; 43: 44-59. doi: 10.1016/j.yfrne.2016.09.003
10. Gietka-Czernel M. The thyroid gland in postmenopausal women: physiology and diseases. Prz Menopauzalny. 2017; 16(2): 33-37. doi: 10.5114/pm.2017.68588
11. Naguib R. Potential relationships between COVID-19 and the thyroid gland: An update. J Int Med Res. 2022; 50(2): 3000605221082898. doi: 10.1177/03000605221082898
12. Yazdanpanah N, Rezaei N. Autoimmune complications of COVID-19. J Med Virol. 2022; 94(1): 54-62. doi: 10.1002/jmv.27292
13. Timofeeva LA, Aleksandrov YuK, Aleshina TN, Yusova MA. Subacute thyroiditis associated with COVID-19. REJR. 2021; 11(3): 15-24. (In Russ.). doi: 10.21569/2222-7415-2021-11-3-15-24
14. Urhan E, Karaca Z, Kara CS, Yuce ZT, Unluhizarci K. The potential impact of COVID-19 on thyroid gland volumes among COVID-19 survivors. Endocrine. 2022; 76: 635-641. doi: 10.1007/s12020-022-03019-6
15. Khoo B, Tan T, Clarke SA, Mills EG, Patel B, Modi M, et al. Thyroid function before, during, and after COVID-19. J Clin Endocrinol Metab. 2021; 106(2): e803-e811. doi: 10.1210/clinem/dgaa830
16. National Institute for Health and Care Excellence. Managing the long-term effects of COVID-19. COVID-19 Rapid Guideline. London, UK; 2020; URL: www.nice.org.uk/guidance/ng188 [date of access: 01.03.2023].
17. Raman B, Cassar MP, Tunnicliffe EM, Filippini N, Griffanti L, Alfaro-Almago F, et al. Medium-term effects of SARS-CoV-2 infection on multiple vital organs, exercise capacity, cognition, quality of life and mental health, post-hospital discharge. EClinicalMedicine. 2021; 31: 100683. doi: 10.1016/j.eclinm.2020.100683
18. Karchevskaya NA, Skorobogach IM, Cherniak AV, Migunova EV, Leshchinskaya OV, Kalmanova EN, et al. Long-term followup study of post-COVID-19 patients. Terapevticheskii arkhiv. 2022; 94(3): 378-388. (In Russ.). doi: 10.26442/00403660.2022.03.201399
19. Jasim S, Gharib H. Thyroid and aging. Endocr Pract. 2018; 24(4): 369-374. doi: 10.4158/EP171796.RA
20. Fallahi P, Ferrari SM, Piaggi S, Luconi M, Cantini G, Gelmini S, et al. The paramount role of cytokines and chemokines in papillary thyroid cancer: A review and experimental results. Immunol Res. 2018; 66(6): 710-722. doi: 10.1007/s12026-018-9056-x
21. Jia F, Wang G, Xu J, Long J, Deng F, Jiang W. Role of tumor necrosis factor-α in the mortality of hospitalized patients with severe and critical COVID-19 pneumonia. Aging (Albany NY). 2021; 13(21): 23895-23912. doi: 10.18632/aging.203663
22. Gong J, Wang DK, Dong H, Xia QS, Huang ZY, Zhao Y, et al. Prognostic significance of low TSH concentration in patients with COVID-19 presenting with non-thyroidal illness syndrome. BMC Endocr Disord. 2021; 21(1): 111. doi: 10.1186/s12902-021-00766-x
23. Chen Y, Li X, Dai Y, Zhang J. The association between COVID-19 and thyroxine levels: A meta-analysis. Front Endocrinol (Lausanne). 2022; 12: 779692. doi: 10.3389/fendo.2021.779692
24. Lui DTW, Lee CH, Chow WS, Lee ACH, Tam AR, Fong CHY, et al. Thyroid dysfunction in relation to immune profile, disease status, and outcome in 191 patients with COVID-19. J Clin Endocrinol Metab. 2021; 106(2): e926-e935. doi: 10.1210/clinem/dgaa813
25. Chen M, Zhou W, Xu W. Thyroid function analysis in 50 patients with COVID-19: A retrospective study. Thyroid. 2021; 31(1): 8-11. doi: 10.1089/thy.2020.0363
26. Kolesnikova LI, Darenskaya MA, Grebenkina LA, Sholokhov LF, Rashidova MA, Dolgikh MI, et al. Thyroid status and antioxidant vitamins in girls of various ethnic groups. Russian Journal of Physiology. 2015; 101(2): 214-221. (In Russ.).
27. Gadotti AC, Lipinski AL, Vasconcellos FT, Marqueze LF, Cunha EB, Campos AC, et al. Susceptibility of the patients infected with SARS-CoV2 to oxidative stress and possible interplay with severity of the disease. Free Radic Biol Med. 2021; 165: 184-190. doi: 10.1016/j.freeradbiomed. 2021.01.044
28. Pincemail J, Cavalier E, Charlier C, Cheramy-Bien JP, Brevers E, Courtois A, et al. Oxidative stress status in COVID-19 patients hospitalized in intensive care unit for severe pneumonia. A pilot study. Antioxidants (Basel). 2021; 10(2): ID257. doi: 10.3390/ antiox10020257
29. Martín-Fernández M, Aller R, Heredia-Rodríguez M, Gómez-Sánchez E, Martínez-Paz P, Gonzalo-Benito H, et al. Lipid peroxidation as a hallmark of severity in COVID-19 patients. Redox Biol. 2021; 48: ID102181. doi: 10.1016/j.redox.2021.102181
30. Rychkova LV, Darenskaya MA, Semenova NV, Kolesnikov SI, Petrova AG, Nikitina OA, et al. Oxidative stress intensity in children and adolescents with a new coronavirus infection. Int J Biomed. 2022; 12(2): 242-246.
31. Semenova NV, Rychkova LV, Darenskaya MA, Kolesnikov SI, Nikitina OA, Petrova AG, et al. Supreoxide dismutase activity in male and female patients of different age with moderate COVID-19. Bull Exp Biol Med. 2022; 173(1): 51-53. doi: 10.1007/s10517-022-05491-6
32. Kravets EB, Urazova OI, Nedosekova YuV, Rogaleva AV. On apoptosis of blood lymphocytes in autoimmune thyroid diseases. Problems of Endocrinology. 2010; 56(3): 16-20. (In Russ.).
33. Díez JJ, Hernanz A, Medina S, Bayón C, Iglesias P. Serum concentrations of tumor necrosis factor-alpha (TNF-alpha) and soluble TNF-alpha receptor p55 in patients with hypothyroidism and hyperthyroidism before and after normalization of thyroid function. Clin Endocrinol (Oxf). 2002; 57(4): 515-521. doi: 10.1046/j.1365-2265.2002.01629.x
34. Topolyanskaya SV. Tumor necrosis factor-alpha and agerelated pathologies. The Russian Archives of Internal Medicine. 2020; 10(6): 414-421. (In Russ.). doi: 10.20514/2226-6704-2020-10-6-414-421
35. Vyrupaeva EV, Semenova NV, Rychkova LV, Petrova AG, Darenskaya MA, Kolesnikov SI, et al. Assessment of the general condition and quality of life of women of post-reproductive age after asymptomatic COVID-19 and 12 months after moderate COVID-19. Acta biomedica scientifica. 2022; 7(5-1): 77-85. (In Russ.). doi: 10.29413/ABS.2022-7.5-1.9
36. Milinković N, Ignjatović S, Žarković M, Jovičić S, Radosavljević B, Singh S, et al. Indirect estimation of age-related reference limits of thyroid parameters: A cross-sectional study of outpatients’ results. Scand J Clin Lab Invest. 2014; 74(5): 378-384. doi: 10.3109/00365513.2014.898324
Review
For citations:
Semenova N.V., Kolesnikov S.I., Vyrupaeva E.V., Sholokhov l.F., Rychkova L.V., Petrova А.G., Akhmedzyanova M.R., Darenskaya M.A., Kolesnikova L.I. Thyroid status and TNF-alpha in post-reproductive women with COVID-19 and 12 months after the disease. Acta Biomedica Scientifica. 2023;8(2):33-42. https://doi.org/10.29413/ABS.2023-8.2.4