Selenium status, sex hormones, and thyroid function in young women

Journal of Trace Elements in Medicine and Biology

Volumn 22, Issue 4, 2008, Pages 296-304

  Zagrodzki, Paweł ^a,b   Ratajczak, Ryszard ^c  

^a JAGIELLONIAN UNIVERSITY MEDICAL COLLEGE   (Poland)

^b INSTITUTE OF NUCLEAR PHYSICS   (Poland)

^c Outpatient Clinic for Pediatric Endocrinology   (Poland)

Author keywords

Human reproductive system; Partial least squares method; Selenium; Thyroid function

Indexed keywords

ESTRADIOL; FOLLITROPIN; GLUTATHIONE PEROXIDASE; LIOTHYRONINE; LUTEINIZING HORMONE; PROGESTERONE; SELENIUM; SEX HORMONE; THYROID PEROXIDASE ANTIBODY; THYROTROPIN; THYROXINE;

ADULT; ANTIBODY BLOOD LEVEL; ARTICLE; CONCENTRATION RESPONSE; CORRELATION ANALYSIS; ENZYME ACTIVITY; ESTRADIOL BLOOD LEVEL; FEMALE; FREE LIOTHYRONINE INDEX; FREE THYROXINE INDEX; GENITAL SYSTEM; HORMONE RELEASE; HUMAN; HYPOTHESIS; LUTEAL PHASE; MENARCHE; MENSTRUAL CYCLE; PARTIAL LEAST SQUARES REGRESSION; PRIORITY JOURNAL; THYROID FUNCTION; THYROID WEIGHT;

ADULT; FEMALE; GONADAL STEROID HORMONES; HUMANS; SELENIUM; THYROID FUNCTION TESTS;

EID: 55649091401     PISSN: 0946672X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jtemb.2008.07.001     Document Type: Article

References (54)

1. Zagrodzki P., Ratajczak R., and Wietecha-Posłuszny R. The interaction between selenium status, sex hormones, and thyroid metabolism in adolescent girls during the luteal phase of their menstrual cycle. Biol Trace Elem Res 120 (2007) 51-60
2. Beckett G.J., and Arthur J.R. Selenium and endocrine systems. J Endocrinol 184 (2005) 455-465
3. Köhrle J., Jakob F., Contempré B., and Dumont J.E. Selenium, the thyroid, and the endocrine system. Endocr Rev 26 (2005) 944-984
4. Behne D., Kyriakopoulos A., Meinhold H., and Köhrle J. Identification of type I iodothyronine 5′-deiodinase as a selenoenzyme. Biochem Biophys Res Commun 173 (1990) 1143-1149
5. Salvatore D., Low S.C., Berry M., Maia A.L., Harney J.W., Croteau W., et al. Type 3 iodothyronine deiodinase: cloning, in vitro expression and functional analysis of the placental selenoprotein. J Clin Invest 96 (1995) 2431-2437
6. Salvatore D., Bartha T., Harney J.W., and Larsen P.R. Molecular biological and biochemical characterization of the human type 2 selenodeiodinase. Endocrinology 137 (1996) 3308-3315
7. Davey J.C., Becker K.B., Schneider M.J., St Germain D.L., and Galton V.A. Cloning of a cDNA for the type II iodothyronine deiodinase. J Biol Chem 270 (1995) 26786-26789
8. Beech S.G., Walker S.W., Beckett G.J., Arthur J.R., Nicol F., and Lee D. Effect of selenium depletion on thyroidal type-I iodothyronine deiodinase activity in isolated human thyrocytes and rat thyroid and liver. Analyst 120 (1995) 827-831
9. Corvilain B., Contempre B., Longombe A.O., Goyens P., Gerry-Decoster Ch., Lamy F., et al. Selenium and the thyroid: how the relationship was established. Am J Clin Nutr Supl 57 (1993) 244S-248S
10. Ohwada M., Suzuki M., Ato I., Tsukamoto H., and Watanabe K. Glutathione peroxidase activity in endometrium: effects of sex hormones and cancer. Gynecol Oncol 60 (1996) 277-282
11. Smith A.M., Peng-Hsing C.M., and Medeiros L.C. Generational differences in selenium status of women. Biol Trace Elem Res 75 (2000) 157-165
12. Rudolph N., and Wong S.L. Selenium and glutathione peroxidase activity in maternal and cord plasma and red cells. Pediatr Res 12 (1978) 789-792
13. Behne D., and Wolters W. Selenium content and glutathione peroxidase activity in the plasma and erythrocytes of non-pregnant and pregnant women. J Clin Chem Clin Biochem 17 (1979) 133-135
14. Zachara B.A., Wardak C., Didkowski W., Maciag A., and Marchaluk E. Changes in blood selenium and glutathione concentrations and glutathione peroxidase activity in human pregnancy. Gynecol Obstet Invest 35 (1993) 12-17
15. Joshi J.V., Bhandarkar S.D., Chadha M., Balaiah D., and Shah R. Menstrual irregularities and lactation failure may precede thyroid dysfunction or goitre. J Postgrad Med 39 (1993) 137-141
16. Krassas G.E. Thyroid disease and female reproduction. Fertil Steril 74 (2000) 1063-1070
17. Slebodzinski A.B. Ovarian iodide uptake and triiodothyronine generation in follicular fluid. The enigma of the thyroid ovary interaction. Domest Anim Endocrinol 29 (2005) 97-103
18. Duntas L., and Orgiazzi J. Vitamin E and thyroid disease: a potential link that kindles hope. Biofactors 19 (2003) 131-135
19. Zagrodzki P., Nicol F., McCoy M.A., Smyth J.A., Kennedy D.G., Beckett G.J., et al. Iodine deficiency in cattle: compensatory changes in thyroidal selenoenzymes. Res Vet Sci 64 (1998) 209-211
20. Neve J., Chammart S., and Molle L. Optimization of a direct procedure for the determination of selenium in plasma and erythrocytes using Zeeman effect atomic absorption spectroscopy. Trace Elem Anal Chem Med Biol 4 (1987) 349-358
21. Zagrodzki P., Bartoń H., Walas S., Fołta M., Stompór T., Janusz-Grzybowska E., et al. Selenium status indices, laboratory data, and selected biochemical parameters in end stage renal disease patients. Biol Trace Elem Res 116 (2007) 29-42
22. Clementi S., Cruciani G., and Curti G. Some applications of the partial least-squares method. Anal Chim Acta 191 (1986) 149-160
23. Frank I.E., Feikema J., Constantine N., and Kowalski B.R. Prediction of product quality from spectral data using the partial least-squares method. J Chem Inf Comput Sci 24 (1984) 20-24
24. Boulesteix A.L., and Strimmer K. Partial least squares: a versatile tool for the analysis of high-dimensional genomic data. Brief Bioinf 8 (2007) 32-44
25. Furdal S. Statistical modelling in empirical research (1989), The Institute of Sport, Warsaw [in Polish]
26. Gutekunst R., and Martin-Teichert H. Requirements for goiter surveys and the determination of thyroid size. In: Delange F., Dunn J.T., and Glinoer D. (Eds). Iodine deficiency in Europe. A continuing concern (1993), Plenum Press, New York 109-115
27. Wasowicz W. Selenium in eastern European countries. Poland as an example. In: Carapella SC, Oldfield JE, Palmieri Y, editors. Proceedings of the fifth international symposium on uses of selenium and tellurium, Brussels; 1994, p. 163-70.
28. Baj Z., Zeman K., Majewska E., Wa{ogonek}sowicz W., Skłodowska M., Gromadzińska J., et al. Does the selenium (Se) level and Se-dependent enzyme activity in blood plasma correlate with human lymphocyte subpopulations and functions?. Int J Immunopathol Pharmacol 5 (1992) 13-21
29. Pawłowicz Z., Zachara B.A., Trafikowska U., Macia{ogonek}g A., Marchaluk E., and Nowicki A. Blood selenium concentrations and glutathione peroxidase activities in patients with breast cancer and with advanced gastrointestinal cancer. J Trace Elem Electrolytes Health Dis 5 (1991) 275-277
30. McMaster D., Bell N., Anderson P., and Love A.H.G. Automated measurement of two indicators of human selenium status, and applicability to population studies. Clin Chem 36 (1990) 211-216
31. Thomson C.D., McLachlan S.K., Grant A.M., Paterson E., and Lillico A.J. The effect of selenium on thyroid status in a population with marginal selenium and iodine status. Br J Nutr 94 (2005) 962-968
32. Ha E.J., and Smith A.M. Plasma selenium and plasma and erythrocyte glutathione peroxidase activity increase with estrogen during the menstrual cycle. J Am Coll Nutr 22 (2003) 43-51
33. Massafra C., Gioia D., De Felice C., Picciolini E., De Leo V., Bonifazi M., et al. Effects of estrogens and androgens on erythrocyte antioxidant superoxide dismutase, catalase and glutathione peroxidase activities during the menstrual cycle. J Endocrinol 167 (2000) 447-452
34. Bureau I., Anderson R.A., Arnaud J., Raysiguier Y., Favier A.E., and Roussel A.M. Trace mineral status in post menopausal women: impact of hormonal replacement therapy. J Trace Elem Med Biol 16 (2002) 9-13
35. Terwolbeck K., Behne D., Meinhold H., Menzel H., and Lombeck I. Increased plasma T4-levels in children with low selenium state due to reduced type I iodothyronine 5′deiodinase activity?. J Trace Elem Electrolytes Health Dis 7 (1993) 53-55
36. Kvicala J., Zamrazil V., Soutorova M., and Tomiska F. Correlations between parameters of body selenium status and peripheral thyroid parameters in the low selenium region. Analyst 120 (1995) 959-965
37. Duntas L.H., Mantzou E., and Koutras D.A. Effects of a six month treatment with selenomethionine in patients with autoimmune thyroiditis. Eur J Endocrinol 148 (2003) 389-393
38. Gärtner R., Gasnier B.C.H., Dietrich J.W., Krebs B., and Angstwurm M.W.A. Selenium supplementation in patients with autoimmune thyroiditis decreases thyroid peroxidase antibodies concentrations. J Clin Endocrinol Metab 87 (2005) 1687-1691
39. Negro R., Greco G., Mangieri T., Pezzarossa A., Dazzi D., and Hassan H. The influence of selenium supplementation on postpartum thyroid status in pregnant women with thyroid peroxidase autoantibodies. J Clin Endocrinol Metab 92 (2007) 1263-1268
40. Turker O., Kumanlioglu K., Karapolat I., and Dogan I. Selenium treatment in autoimmune thyroiditis: 9-month follow-up with variable doses. J Endocrinol 190 (2006) 151-156
41. Roti E., Minelli R., Gardini E., Bianconi L., Ronchi A., Gatti A., et al. Selenium administration does not cause thyroid insufficiency in subjects with mild iodine deficiency and sufficient selenium intake. J Endocrinol Invest 16 (1993) 481-484
42. Riese C., Michaelis M., Mentrup B., Gotz F., Kohrle J., Schweizer U., et al. Selenium-dependent pre- and posttranscriptional mechanisms are responsible for sexual dimorphic expression of selenoproteins in murine tissues. Endocrinology 147 (2006) 5883-5892
43. Rush J.W., and Sandiford S.D. Plasma glutathione peroxidase in healthy young adults: influence of gender and physical activity. Clin Biochem 36 (2003) 345-351
44. Serviddio G., Loverro G., Vicino M., Prigigallo F., Grattagliano I., Altomare E., et al. Modulation of endometrial redox balance during the menstrual cycle: relation with sex hormones. J Clin Endocrinol Metab 87 (2002) 2843-2848
45. Ba{ogonek}czyk M., Ruchała M., Gembicki M., and Sowiński J. Changes in thyroid pathology in adolescent youths as a result of new iodine prophylaxis in the Poznań region. A preliminary report. Pediatr Współczes 5 (2005) 167-170 [in Polish]
46. Grzesiuk W., Da{ogonek}browska J., Osikowska-Loksztejn M., Kondracka A., Kolasińska K., and Bar-Andziak E. Effectiveness of iodine prophylaxis in hypertensive patients on salt restricted diet. Pol Arch Med Wewn 63 (2005) 147-154 [in Polish]
47. Naskalski J.W., Drozdz R., Solnica B., Rostworowski W., Szybinski Z., Huszno B., et al. Analytical problems of iodine deficiency examination in Polish Nation-wide deficit control program. Przegl Lek 61 (2004) 1325-1329 [in Polish]
48. Lobanov A.V., Hatfield D.L., and Gladyshev V.N. Reduced reliance on the trace element selenium during evolution of mammals. Genome Biol 9 (2008) R62
49. Xia Y., Hill K.E., Byrne D.W., Xu J., and Burk R.F. Effectiveness of selenium supplements in a low-selenium area of China. Am J Clin Nutr 81 (2005) 829-834
50. Méplan C., Crosley L.K., Nicol F., Beckett G.J., Howie A.F., Hill K.E., et al. Genetic polymorphisms in the human selenoprotein P gene determine the response of selenoprotein markers to selenium supplementation in a gender-specific manner (the SELGEN study). FASEB J 21 (2007) 3063-3074
51. Hollenbach B., Morgenthaler N.G., Struck J., Alonso C., Bergmann A., Köhrle J., et al. New assay for the measurement of selenoprotein P as a sepsis biomarker from serum. J Trace Elem Med Biol 22 (2008) 24-32
52. Falnoga I., Kobal A.B., Stibilj V., and Horvat M. Selenoprotein P in subjects exposed to mercury and other stress situations such as physical load or metal chelation treatment. Biol Trace Elem Res 89 (2002) 25-33
53. Burk R.F., Hill K.E., and Motley A.K. Selenoprotein metabolism and function: evidence for more than one function for selenoprotein P. J Nutr 133 (2003) 1517S-1520S
54. Bosschaerts T., Guilliams M., Noel W., Hérin M., Burk R.F., Hill K.E., et al. Alternatively activated myeloid cells limit pathogenicity associated with African trypanosomiasis through the IL-10 inducible gene selenoprotein P. J Immunol 180 (2008) 6168-6175