Læknablaðið

Árgangur

Læknablaðið - 01.03.2022, Síða 17

Læknablaðið - 01.03.2022, Síða 17
L ÆKNABL AÐIÐ 2022/108 129 R A N N S Ó K N Heimildir 1. Léger J, Kaguelidou F, Alberti C, et al. Graves‘ disease in children. Best Pract Res Clin Endocrinol Metab 2014; 28: 233­43. 2. Franklyn JA, Boelaert K. Thyrotoxicosis. Lancet 2012; 379: 1155­66. 3. Rodanaki M, Lodefalk M, Forssell K, et al. The Incidence of Childhood Thyrotoxicosis Is Increasing in Both Girls and Boys in Sweden. Horm Res Paediatr 2019; 91: 195­202. 4. Williamson S, Greene SA. Incidence of thyrotoxicosis in childhood: a national population based study in the UK and Ireland. Clin Endocrinol (Oxf) 2010; 72: 358­63. 5. Havgaard Kjær R, Smedegård Andersen M, Hansen D. Increasing Incidence of Juvenile Thyrotoxicosis in Denmark: A Nationwide Study, 1998­2012. Horm Res Paediatr 2015; 84: 102­7. 6. Wong GW, Cheng PS. Increasing incidence of childhood Graves‘ disease in Hong Kong: a follow­up study. Clin Endocrinol (Oxf) 2001; 54: 547­50. 7. Manji N, Carr­Smith JD, Boelaert K, et al. Influences of age, gender, smoking, and family history on autoimmune thyroid disease phenotype. J Clin Endocrinol Metab 2006; 91: 4873­80. 8. Asvold BO, Bjøro T, Nilsen TI, et al. Tobacco smoking and thyroid function: a population­ based study. Arch Intern Med 2007; 167: 1428­32. 9. Lazar L, Kalter­Leibovici O, Pertzelan A, et al. Thyrotoxicosis in prepubertal children compared with pubertal and postpubertal patients. J Clin Endocrinol Metab 2000; 85: 3678­ 82. 10. Shulman DI, Muhar I, Jorgensen EV, et al. Autoimmune hyperthyroidism in prepubertal children and adolescents: comparison of clinical and biochemical features at diagnosis and responses to medical therapy. Thyroid 1997; 7: 755­60. 11. Ross DS, Burch HB, Cooper DS, et al. 2016 American Thyroid Association Guidelines for Diagnosis and Management of Hyperthyroidism and Other Causes of Thyrotoxicosis. Thyroid 2016; 26: 1343­421. 12. Rivkees SA, Mattison DR. Propylthiouracil (PTU) Hepatoxicity in Children and Recommendations for Discontinuation of Use. Int J Pediatr Endocrinol 2009; 2009: 132041. 13. Kaguelidou F, Alberti C, Castanet M, et al. Predictors of autoimmune hyperthyroidism relapse in children after discontinuation of antithyroid drug treatment. J Clin Endocrinol Metab 2008; 93: 3817­26. 14. Samuelsson U, Westerberg L, Aakesson K, et al. Geographical variation in the incidence of type 1 diabetes in the Nordic countries: A study within NordicDiabKids. Pediatr Diabetes 2020; 21: 259­65. 15. Brix TH, Christensen K, Holm NV, et al. A population­based study of Graves‘ disease in Danish twins. Clin Endocrinol (Oxf) 1998; 48: 397­400. 16. Boelaert K, Newby PR, Simmonds MJ, et al. Prevalence and relative risk of other autoimmune diseases in subjects with autoimmune thyroid disease. Am J Med 2010; 123: 183.e1­9. 17. Burch HB, Burman KD, Cooper DS. A 2011 survey of clinical practice patterns in the management of Graves‘ disease. J Clin Endocrinol Metab 2012; 97: 4549­58. 18. Léger J, Gelwane G, Kaguelidou F, et al. Positive impact of long­term antithyroid drug treatment on the outcome of children with Graves‘ disease: national long­term cohort study. J Clin Endocrinol Metab 2012; 97: 110­9. 19. Glaser NS, Styne DM. Predictors of early remission of hyperthyroidism in children. J Clin Endocrinol Metab 1997; 82: 1719­26. 20. Allahabadia A, Daykin J, Holder RL, et al. Age and gender predict the outcome of treatment for Graves‘ hyperthyroidism. J Clin Endocrinol Metab 2000; 85: 1038­42. 21. Vitti P, Rago T, Chiovato L, et al. Clinical features of patients with Graves‘ disease undergoing remission after antithyroid drug treatment. Thyroid 1997; 7: 369­75. 22. Anagnostis P, Adamidou F, Polyzos SA, et al. Predictors of long­term remission in patients with Graves‘ disease: a single center experience. Endocrine 2013; 44: 448­53. 23. Cappelli C, Gandossi E, Castellano M, et al. Prognostic value of thyrotropin receptor antibodies (TRAb) in Graves‘ disease: a 120 months prospective study. Endocr J 2007; 54: 713­20. 24. Mohlin E, Filipsson Nyström H, Eliasson M. Long­term prognosis after medical treatment of Graves‘ disease in a northern Swedish population 2000­2010. Eur J Endocrinol 2014; 170: 419­27. 25. Daukšienė D, Daukša A, Mickuvienė N. Independent pretreatment predictors of Graves‘ disease outcome. Medicina (Kaunas) 2013; 49: 427­34. 26. Wang PW, Chen IY, Juo SH, et al. Genotype and phenotype predictors of relapse of graves‘ disease after antithyroid drug withdrawal. Eur Thyroid J 2013; 1: 251­8. 27. Solomon B, Glinoer D, Lagasse R, et al. Current trends in the management of Graves‘ disease. J Clin Endocrinol Metab 1990; 70: 1518­24. 28. Bahn Chair RS, Burch HB, Cooper DS, et al. Hyperthyroidism and other causes of thyrotoxicosis: management guidelines of the American Thyroid Association and American Association of Clinical Endocrinologists. Thyroid 2011; 21: 593­646. 29. Hardee JT, Barnett AL, Thannoun A, et al. Propylthiouracil­induced hepatotoxicity. West J Med 1996; 165: 144­7. 30. Rivkees SA. 63 years and 715 days to the „boxed warning“: unmasking of the propylthi­ ouracil problem. Int J Pediatr Endocrinol 2010; 658267. 31. Tagami T, Yambe Y, Tanaka T, et al. Short-term effects of β-adrenergic antagonists and methimazole in new­onset thyrotoxicosis caused by Graves‘ disease. Intern Med 2012; 51: 2285­90. 32. Wartofsky L, Glinoer D, Solomon B, et al. Differences and similarities in the diagnosis and treatment of Graves‘ disease in Europe, Japan, and the United States. Thyroid 1991; 1: 129­ 35. 33. Bartalena L, Burch HB, Burman KD, et al. A 2013 European survey of clinical practice patterns in the management of Graves‘ disease. Clin Endocrinol (Oxf) 2016; 84: 115­20. 34. Miccoli P, Vitti P, Rago T, et al. Surgical treatment of Graves‘ disease: subtotal or total thyroidectomy? Surgery 1996; 120: 1020­4; discussion 4­5. 35. Sung TY, Lee YM, Yoon JH, et al. Long­Term Effect of Surgery in Graves‘ Disease: 20 Years Experience in a Single Institution. Int J Endocrinol 2015; 2015: 542641. E N G L I S H S U M M A R Y Þórbergur Atli Þórsson1 Ragnar Bjarnason1,2 Soffía Guðrún Jónasdóttir3 Berglind Jónsdóttir2 1Faculty of Medicine, Department of Health Sciences, University of Iceland, Reykjavík, 2Childrens Hospital Hringurinn, National University Hospital of Iceland, Reykjavík, 3Domus Medica, Reykjavík. Correspondence: Berglind Jónsdóttir, bergljon@landspitali.is Key words: Graves‘ disease‘, pediatric, treatment, Iceland. Graves‘ disease in children and adolescents in Iceland INTRODUCTION: Graves‘ disease is an autoimmune disease in which autoantibodies cause an increase in the production of thyroid hormones, and is the most common cause of thyrotoxicosis in children. Symptoms in children are often more obscure than in adults. The aim of the study is to assess the incidence of Graves’ disease in children and adolescents in Iceland over the span of two decades (2001-2021), and furthermore to investigate if the incidence rate has increased, as well as to describe treatment options and disease recurrence. MATERIAL/METHODS: This retrospective descriptive study included all children diagnosed with Graves‘ disease in the years 2001-2021 in Iceland. Information was obtained from the Directorate of Health‘s drug database and from ICD-10 diagnoses at Landspítali – The National University Hospital. RESULTS: In total, 57 children and adolescents were diagnosed with Graves’, the overall incidence rate was 3.5/100,000 person-years. Gender ratio was 1:2.7 (male : female) and the mean age at diagnosis was 13.6 for boys and 13.9 years for girls. Of those 12 individuals currently receiving drug therapy (21.8%), four patients have had disease relapse. Thirteen patients reached an euthyroid state with medication (23.7%), 25 received treatment with radioactive iodine (45.5%) and 5 underwent surgery (9.1%). Boys were more likely to relapse. Disease recurrence was 31.8%. CONCLUSION: The incidence of Graves‘ disease did not increase during the study period. The disease was more common in girls, although the gender ratio was lower than expected. Antithyroid drugs were the first choice in treatment and radioactive iodine was the most common permanent treatment option. Disease recurrence was common. A possible relationship between the duration of the original drug therapy and disease recurrence should be investigated. doi 10.17992/lbl.2022.03.680

x

Læknablaðið

Beinleiðis leinki

Hvis du vil linke til denne avis/magasin, skal du bruge disse links:

Link til denne avis/magasin: Læknablaðið
https://timarit.is/publication/986

Link til dette eksemplar:

Link til denne side:

Link til denne artikel:

Venligst ikke link direkte til billeder eller PDfs på Timarit.is, da sådanne webadresser kan ændres uden advarsel. Brug venligst de angivne webadresser for at linke til sitet.