|
|
|
National Academy of Medical Sciences of Ukraine State Institution "The National Research Center for Radiation Medicine"
|
ISSN 2313-4607 (Online) ISSN 2304-8336 (Print) |
Problems of Radiation Medicine and Radiobiology |
|
|
|
|
|
|
V. G. Bebeshko, K. M. Bruslova, O. Y. Boyarska, L.O. Lyashenko, N. M. Tsvyetkova,
L. O. Gonchar, T. O. Chernysh, I. V. Trychlib, V. D. Pismenniy, Z. S. Yaroshenko, V. V. Vasylenko
State Institution «National Research Center for Radiation Medicine of the National Academy of Medical
Sciences of Ukraine», 53 Yuriia Illienka St., Kyiv, 04050, Ukraine
ENDOCRINE REGULATION OF ERYTHROID LINEAGE OF HEMATOPOIESIS IN CHILDREN LIVING UNDER A LOW-DOSE RADIATION EXPOSURE AFTER THE CHORNOBYL NPP ACCIDENT
Objective. Elucidation of relationship between the levels of thyroid-stimulating hormone (TSH), free serum thyroxine, serum and urine cortisol and parameters of erythroid lineage of hematopoiesis to estimate the thyroid function
in children of prepubertal, pubertal, and postpubertal age permanently residing under a low-dose radiation exposure
to determine the premorbid state of thyroid function.
Materials and methods. Children aged 3 to 18 years old (n = 203) living in the most intensively radionuclide-contaminated regions of Kyiv, Zhytomyr and Chornihiv oblasts of Ukraine after the Chornobyl NPP accident were
enrolled. Complaints of ossalgia, arthralgia, fatigue, bone fractures in the history, bone dysembryogenetic stigmata,
hypermobility syndrome degree, and types of somatic diseases were taken into account. Peripheral blood count
parameters, biochemical indices of blood serum were studied, namely the levels of total protein, cholesterol, creatinine and alkaline phosphatase activity. Levels of the free thyroxine, pituitary TSH, serum and daily urine cortisol, and
doses of radiation exposure were determined.
Results. The radiation dose values in children ranged from (0.35 ± 0.09) mSv to (0.54 ± 0.12) mSv. There was no
difference between the parameters of erythroid lineage of hematopoiesis depending on radiation dose. At the levels of serum TSH up to 1.0 μIU/ml no correlation was found with cortisol levels; at TSH levels of 1.0–3.0 μIU/ml the
correlation coefficient was r = 0.31; at TSH levels higher than 3.0 μIU/ml the correlation coefficient was r = 0.61
probably indicating a compensatory role of adrenal cortex in children at risk of thyroid disease development. In children with joint hypermobility grade II there was a higher incidence of dentofacial anomalies (χ2 = 6.9), deformities
of lower extremities (χ2 = 6.9), and dental caries (χ2 = 4.3) (p < 0.05). There was a direct correlation between the
serum TSH level (over 3 μIU/ml) and micrognathia (brachygnathia) (r = 0.62) indicating the impact of thyroid disease on dentofacial development. The TSH at a level of upper limit of the reference range values may contribute to
a decreased RBC count in peripheral blood, increased average volume and hemoglobin content in erythrocyte being
associated with the initial manifestations of thyroid dysfunction.
Conclusions. Abnormal endocrine regulation of hematopoiesis affects the connective tissue, stromal microenvironment of bone marrow, and accordingly the erythroid branch of hematopoiesis in children, which may be relevant in
the development and course of oncohematological diseases.
Key words: children, ChNPP accident, low-dose radiation exposure, erythroid lineage of hematopoiesis, TSH, cortisol, joint hypermobility.
Problems of Radiation Medicine and Radiobiology. 2020;25:374-389. doi: 10.33145/2304-8336-2020-25-374-389
full text |
1. Choi SA, An JH, Lee SH, Lee GH, Yang HJ, Jeong PS, et al. Comparative evaluation of hormones and hormone-like molecule in lineage specification of human induced pluripotent stem cells. Int J Stem Cells. 2019;12(2):240-250. doi: 10.15283/ijsc18137.
2. Giannakopoulos A, Lazopoulou N, Pervanidou P, Kanaka-Gantenbein C. The Impact of adiposity and puberty on thyroid function in children and adolescents. Child Obes. 2019;15(6):411-415. doi:10.1089/chi.2019.0025.
3. Jung G, Oh SB, Lee WY, Kim HR, Nam HK, Kim JH, et al. Thyroid function in girls with central precocious puberty. Ann Pediatr Endocrinol Metab. 2019 Jun;24(2):124-128. doi: 10.6065/apem.2019.24.2.124.
4. Dudhia SB, Dudhia BB. Undetected hypothyroidism: A rare dental diagnosis. J Oral Maxillofac Pathol. 2014;18(2):315-319. doi:10.4103/0973-029X.140922.
5. Vucic S, Korevaar TIM, Dhamo B, Jaddoe VWV, Peeters RP, Wolvius EB, Ongkosuwito EM. Thyroid function during early life and dental development. J Dent Res. 2017;96(9):1020-1026. doi: 10.1177/0022034517708551.
6. Aldulaijan HA, Cohen RE, Stellrecht EM, Levine MJ, Yerke LM. Relationship between hypothyroidism and periodontitis: A scoping review. Clin Exp Dent Res. 2020;6(1):147-157. doi:10.1002/cre2.247.
7. Wopereis DM, Du Puy RS, van Heemst D, Walsh JP, Bremner A, Bakker SJL, et al. The Relation between thyroid function and anemia: A pooled analysis of individual participant data. J Clin Endocrinol Metab. 2018;103(10):3658-3667. doi: 10.1210/jc.2018-00481.
8. Omar S, Hadj Taeib S, Kanoun F, Hammami MB, Kamoun S, Ben Romdhane N, Feki M, Slimane H, Kaabachi N. Les anomalies ertyrocytaires au cours des dysthyroidies [Erythrocyte abnormalities in thyroid dysfunction]. Tunis Med. 2010;88(11):783-8. French.
9. Thau L, Gandhi J, Sharma S. Physiology, Cortisol. [Updated 2020 May 29]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK538239/.
10. Thiele S, Hannemann A, Winzer M, Baschant U, Weidner H, Nauck M, et al. Regulation of sclerostin in glucocorticoid-induced osteoporosis (GIO) in mice and humans. Endocr Connect. 2019;8(7):923-934. doi: 10.1530/EC-19-0104.
11. Montero D, Lundby C. Regulation of red blood cell volume with exercise training. Compr Physiol. 2018;9(1):149-164. doi: 10.1002/cphy.c180004.
12. Bresnick EH, Hewitt KJ, Mehta C, Keles S, Paulson RF, Johnson KD. Mechanisms of erythrocyte development and regeneration: implications for regenerative medicine and beyond. Development. 2018;145(1):dev151423. doi: 10.1242/dev.151423.
13. Bebeshko VG, Bruslova KM, Pushkareva TI, Tsvietkova NM, Lyashenko LO, Sergeeva AS, et al. Cortisol level as risk factor for malignant hematologic pathology in children exposed to ionizing radiation after Chornobyl accident. Probl Radiac Med Radiobiol. 2017;22:306-315.
14. Xiang B, Tao R, Liu X, Zhu X, He M, Ma Z, et al. A study of thyroid functions in patients with Cushing's syndrome: a single-center experience. Endocr Connect. 2019;8(8):1176-1185. doi: 10.1530/EC-19-0309.
15. Cannarella R, Barbagallo F, Condorelli RA, Aversa A, La Vignera S, Calogero AE. Osteoporosis from an endocrine perspective: the role of hormonal changes in the elderly. J Clin Med. 2019;8(10):1564. doi: 10.3390/jcm8101564.
16. Bebeshko VG, Bruslova KM, Volodina TT, Lyashenko LO, Tsvetkova NM, Trychlib IV, et al. Features of clinical symptoms and signs, hematological and biochemical parameters in children with joint hypermobility in a late period upon the Chornobyl NPP accident. Probl Radiac Med Radiobiol. 2019;24:322-334. doi: 10.33145/2304-8336-2019-24-322-334.
17. Likhtarov IA, editor. [Retrospective-predicted doses of exposure of the population and general dosimetric passportization in 1997 of the settlements of Ukraine contaminated by Chornobyl accident. Summary data for the 1986–1997 years. Collection 7]. Kyiv: Ministry of Health of Ukraine; 1998. 155 p. Ukrainian.
18. Bebeshko VG, Bruslova KM, Stankevych VV, Tsvietkova NM, Lyashenko LO, Galkina SG, et al. Effect of radiation and non-radiation environmental factors on children hematopoietic system. Probl Radiac Med Radiobiol. 2016;21:191-203.
|
|
| |
|
© 2013 Problems of Radiation Medicine |
| | |
|
|