Skip to main content
Erschienen in: Journal of Endocrinological Investigation 12/2019

01.12.2019 | Original Article

Prevalence of endocrine disorders and their associated factors in transfusion-dependent thalassemia patients: a historical cohort study in Southern Iran

verfasst von: M. Bordbar, H. Bozorgi, F. Saki, S. Haghpanah, M. Karimi, A. Bazrafshan, O. R. Zekavat

Erschienen in: Journal of Endocrinological Investigation | Ausgabe 12/2019

Einloggen, um Zugang zu erhalten

Abstract

Purpose

Transfusion-dependent beta-thalassemia (TDT) patients suffer from various endocrinopathies. The main contributing factor associated with these complications is iron overload, secondary to frequent blood transfusions. To improve patients’ quality of life, we evaluated the prevalence of endocrine disorders while considering the associated factors for further assessment.

Methods

Seven hundred thirteen transfusion-dependent thalassemia patients with age range 10–62 years were enrolled in this study. Serum calcium, phosphorous, fast blood sugar, ferritin, 25-OH vitamin D, free thyroxin, thyroid-stimulating hormone and parathyroid hormone were assessed. Bone mineral density was measured by dual-energy X-ray absorptiometry.

Results

In total, 86.8% of the TDT patients suffered from at least one endocrinopathy. The prevalence of endocrinopathies in descending order of frequency was low bone mass (72.6%), hypogonadism (44.5%), diabetes mellitus (15.9%), hypoparathyroidism (13.2%), and hypothyroidism (10.7%). Age, body mass index and splenectomy were significantly associated with most of the endocrine disorders.

Conclusion

Endocrine complications are frequently observed in TDT patients. Splenectomy is a major risk factor and should be generally avoided unless it is highly indicated. Periodic surveillance of endocrine function and proper management of iron overload are advised.
Literatur
1.
Zurück zum Zitat De Sanctis V, Elsedfy H, Soliman AT, Elhakim IZ, Soliman NA, Elalaily R et al (2016) Endocrine profile of β-thalassemia major patients followed from childhood to advanced adulthood in a tertiary care center. Indian J Endocrinol Metab 20(4):451CrossRefPubMedPubMedCentral De Sanctis V, Elsedfy H, Soliman AT, Elhakim IZ, Soliman NA, Elalaily R et al (2016) Endocrine profile of β-thalassemia major patients followed from childhood to advanced adulthood in a tertiary care center. Indian J Endocrinol Metab 20(4):451CrossRefPubMedPubMedCentral
2.
Zurück zum Zitat Dhouib NG, Khaled MB, Ouederni M, Besbes H, Kouki R, Mellouli F et al (2018) Growth and endocrine function in Tunisian thalassemia major patients. Mediterr J Hematol Infect Dis 10(1):e2018031CrossRefPubMedPubMedCentral Dhouib NG, Khaled MB, Ouederni M, Besbes H, Kouki R, Mellouli F et al (2018) Growth and endocrine function in Tunisian thalassemia major patients. Mediterr J Hematol Infect Dis 10(1):e2018031CrossRefPubMedPubMedCentral
3.
Zurück zum Zitat De Sanctis V, Soliman AT, Yassin MA, Di Maio S, Daar S, Elsedfy H et al (2018) Hypogonadism in male thalassemia major patients: pathophysiology, diagnosis and treatment. Acta Bio Medica Atenei Parmensis 89(2-S):6–15PubMedPubMedCentral De Sanctis V, Soliman AT, Yassin MA, Di Maio S, Daar S, Elsedfy H et al (2018) Hypogonadism in male thalassemia major patients: pathophysiology, diagnosis and treatment. Acta Bio Medica Atenei Parmensis 89(2-S):6–15PubMedPubMedCentral
4.
Zurück zum Zitat Farmaki K, Tzoumari I, Pappa C, Chouliaras G, Berdoukas V (2010) Normalisation of total body iron load with very intensive combined chelation reverses cardiac and endocrine complications of thalassaemia major. Br J Haematol 148(3):466–475CrossRefPubMed Farmaki K, Tzoumari I, Pappa C, Chouliaras G, Berdoukas V (2010) Normalisation of total body iron load with very intensive combined chelation reverses cardiac and endocrine complications of thalassaemia major. Br J Haematol 148(3):466–475CrossRefPubMed
5.
Zurück zum Zitat De Sanctis V, Soliman AT, Elsedfy H, Skordis N, Kattamis C, Angastiniotis M et al (2013) Growth and endocrine disorders in thalassemia: the international network on endocrine complications in thalassemia (I-CET) position statement and guidelines. Indian J Endocrinol Metab 17(1):8CrossRefPubMedPubMedCentral De Sanctis V, Soliman AT, Elsedfy H, Skordis N, Kattamis C, Angastiniotis M et al (2013) Growth and endocrine disorders in thalassemia: the international network on endocrine complications in thalassemia (I-CET) position statement and guidelines. Indian J Endocrinol Metab 17(1):8CrossRefPubMedPubMedCentral
6.
Zurück zum Zitat Belhoul KM, Bakir ML, Saned M-S, Kadhim AM, Musallam KM, Taher AT (2012) Serum ferritin levels and endocrinopathy in medically treated patients with β thalassemia major. Ann Hematol 91(7):1107–1114CrossRefPubMed Belhoul KM, Bakir ML, Saned M-S, Kadhim AM, Musallam KM, Taher AT (2012) Serum ferritin levels and endocrinopathy in medically treated patients with β thalassemia major. Ann Hematol 91(7):1107–1114CrossRefPubMed
7.
Zurück zum Zitat Gordon CM, Bachrach LK, Carpenter TO, Crabtree N, Fuleihan GE-H, Kutilek S et al (2008) Dual energy X-ray absorptiometry interpretation and reporting in children and adolescents: the 2007 ISCD Pediatric Official Positions. J Clin Densitom 11(1):43–58CrossRefPubMed Gordon CM, Bachrach LK, Carpenter TO, Crabtree N, Fuleihan GE-H, Kutilek S et al (2008) Dual energy X-ray absorptiometry interpretation and reporting in children and adolescents: the 2007 ISCD Pediatric Official Positions. J Clin Densitom 11(1):43–58CrossRefPubMed
8.
Zurück zum Zitat Lim JU, Lee JH, Kim JS, Hwang YI, Kim T-H, Lim SY et al (2017) Comparison of World Health Organization and Asia-Pacific body mass index classifications in COPD patients. Int J Chronic Obstr Pulm Dis 12:2465CrossRef Lim JU, Lee JH, Kim JS, Hwang YI, Kim T-H, Lim SY et al (2017) Comparison of World Health Organization and Asia-Pacific body mass index classifications in COPD patients. Int J Chronic Obstr Pulm Dis 12:2465CrossRef
9.
Zurück zum Zitat De Sanctis V, Al Jaouni SK, Elsedfy H, Karimi M, Mousa S, Soliman AT et al (2015) Selected highlights of the IX international symposium of clinicians for endocrinopathies in Thalassemia and adolescent medicine (ICET-A) on growth, and endocrine complications in Thalassaemia. Rivista Italiana di Medicina dell’Adolescenza-Volume 13(1):1–13 De Sanctis V, Al Jaouni SK, Elsedfy H, Karimi M, Mousa S, Soliman AT et al (2015) Selected highlights of the IX international symposium of clinicians for endocrinopathies in Thalassemia and adolescent medicine (ICET-A) on growth, and endocrine complications in Thalassaemia. Rivista Italiana di Medicina dell’Adolescenza-Volume 13(1):1–13
10.
Zurück zum Zitat Haghpanah S, Jelodari S, Karamifar H, Saki F, Rahimi R, De VS et al (2018) The frequency of hypothyroidism and its relationship with HCV positivity in patients with thalassemia major in southern Iran. Acta Bio Medica Atenei Parmensis 89(1):55–60PubMedPubMedCentral Haghpanah S, Jelodari S, Karamifar H, Saki F, Rahimi R, De VS et al (2018) The frequency of hypothyroidism and its relationship with HCV positivity in patients with thalassemia major in southern Iran. Acta Bio Medica Atenei Parmensis 89(1):55–60PubMedPubMedCentral
11.
Zurück zum Zitat Introduction: Standards of Medical Care in Diabetes-2018 (2018) Diabetes Care 41(Suppl 1):S1–S2 Introduction: Standards of Medical Care in Diabetes-2018 (2018) Diabetes Care 41(Suppl 1):S1–S2
12.
Zurück zum Zitat Laird E, O’halloran AM, Carey D, Healy M, O’connor D, Moore P et al (2017) The prevalence of vitamin D deficiency and the determinants of 25 (OH) D concentration in older Irish adults: data from The Irish Longitudinal Study on Ageing (TILDA). J Gerontol Ser A 73(4):519–525CrossRef Laird E, O’halloran AM, Carey D, Healy M, O’connor D, Moore P et al (2017) The prevalence of vitamin D deficiency and the determinants of 25 (OH) D concentration in older Irish adults: data from The Irish Longitudinal Study on Ageing (TILDA). J Gerontol Ser A 73(4):519–525CrossRef
13.
Zurück zum Zitat Adil A, Sobani ZA, Jabbar A, Adil SN, Awan S (2012) Endocrine complications in patients of beta thalassemia major in a tertiary care hospital in Pakistan. J Pak Med Assoc 62(3):307PubMed Adil A, Sobani ZA, Jabbar A, Adil SN, Awan S (2012) Endocrine complications in patients of beta thalassemia major in a tertiary care hospital in Pakistan. J Pak Med Assoc 62(3):307PubMed
14.
Zurück zum Zitat Gulati R, Bhatia V, Agarwal S (2000) Early onset of endocrine abnormalities in ß-thalassemia major in a developing country. J Pediatr Endocrinol Metab 13(6):651–656CrossRefPubMed Gulati R, Bhatia V, Agarwal S (2000) Early onset of endocrine abnormalities in ß-thalassemia major in a developing country. J Pediatr Endocrinol Metab 13(6):651–656CrossRefPubMed
15.
Zurück zum Zitat De Sanctis V, Soliman AT, Elsefdy H, Soliman N, Bedair E, Fiscina B et al (2018) Bone disease in β thalassemia patients: past, present and future perspectives. Metabolism 80:66–79CrossRefPubMed De Sanctis V, Soliman AT, Elsefdy H, Soliman N, Bedair E, Fiscina B et al (2018) Bone disease in β thalassemia patients: past, present and future perspectives. Metabolism 80:66–79CrossRefPubMed
16.
Zurück zum Zitat Mirhosseini NZ, Shahar S, Ghayour-Mobarhan M, Banihashem A, Kamaruddin NA, Hatef MR et al (2013) Bone-related complications of transfusion-dependent beta thalassemia among children and adolescents. J Bone Miner Metab 31(4):468–476CrossRefPubMed Mirhosseini NZ, Shahar S, Ghayour-Mobarhan M, Banihashem A, Kamaruddin NA, Hatef MR et al (2013) Bone-related complications of transfusion-dependent beta thalassemia among children and adolescents. J Bone Miner Metab 31(4):468–476CrossRefPubMed
17.
Zurück zum Zitat Vogiatzi MG, Autio KA, Mait JE, Schneider R, Lesser M, Giardina PJ (2005) Low bone mineral density in adolescents with β-thalassemia. Ann N Y Acad Sci 1054(1):462–466CrossRefPubMed Vogiatzi MG, Autio KA, Mait JE, Schneider R, Lesser M, Giardina PJ (2005) Low bone mineral density in adolescents with β-thalassemia. Ann N Y Acad Sci 1054(1):462–466CrossRefPubMed
18.
Zurück zum Zitat Pollak RD, Rachmilewitz E, Blumenfeld A, Idelson M, Goldfarb AW (2000) Bone mineral metabolism in adults with β-thalassaemia major and intermedia. Br J Haematol 111(3):902–907 Pollak RD, Rachmilewitz E, Blumenfeld A, Idelson M, Goldfarb AW (2000) Bone mineral metabolism in adults with β-thalassaemia major and intermedia. Br J Haematol 111(3):902–907
19.
Zurück zum Zitat Vogiatzi MG, Macklin EA, Fung EB, Cheung AM, Vichinsky E, Olivieri N et al (2009) Bone disease in thalassemia: a frequent and still unresolved problem. J Bone Miner Res 24(3):543–557CrossRefPubMed Vogiatzi MG, Macklin EA, Fung EB, Cheung AM, Vichinsky E, Olivieri N et al (2009) Bone disease in thalassemia: a frequent and still unresolved problem. J Bone Miner Res 24(3):543–557CrossRefPubMed
20.
Zurück zum Zitat Shamshirsaz A, Bekheirnia M, Kamgar M, Pakbaz Z, Tabatabaie S, Bouzari N et al (2007) Bone mineral density in Iranian adolescents and young adults with β-thalassemia major. Pediatr Hematol Oncol 24(7):469–479CrossRefPubMed Shamshirsaz A, Bekheirnia M, Kamgar M, Pakbaz Z, Tabatabaie S, Bouzari N et al (2007) Bone mineral density in Iranian adolescents and young adults with β-thalassemia major. Pediatr Hematol Oncol 24(7):469–479CrossRefPubMed
21.
Zurück zum Zitat Jensen C, Tuck S, Agnew J, Koneru S, Morris R, Yardumian A et al (1998) High prevalence of low bone mass in thalassaemia major. Br J Haematol 103(4):911–915CrossRefPubMed Jensen C, Tuck S, Agnew J, Koneru S, Morris R, Yardumian A et al (1998) High prevalence of low bone mass in thalassaemia major. Br J Haematol 103(4):911–915CrossRefPubMed
22.
Zurück zum Zitat Poggi M, Sorrentino F, Pugliese P, Smacchia MP, Daniele C, Equitani F et al (2016) Longitudinal changes of endocrine and bone disease in adults with beta-thalassemia major receiving different iron chelators over 5 years. Ann Hematol 95(5):757–763CrossRefPubMed Poggi M, Sorrentino F, Pugliese P, Smacchia MP, Daniele C, Equitani F et al (2016) Longitudinal changes of endocrine and bone disease in adults with beta-thalassemia major receiving different iron chelators over 5 years. Ann Hematol 95(5):757–763CrossRefPubMed
24.
Zurück zum Zitat Di Stefano M, Chiabotto P, Roggia C, Garofalo F, Lala R, Piga A et al (2004) Bone mass and metabolism in thalassemic children and adolescents treated with different iron-chelating drugs. J Bone Miner Metab 22(1):53–57CrossRefPubMed Di Stefano M, Chiabotto P, Roggia C, Garofalo F, Lala R, Piga A et al (2004) Bone mass and metabolism in thalassemic children and adolescents treated with different iron-chelating drugs. J Bone Miner Metab 22(1):53–57CrossRefPubMed
25.
Zurück zum Zitat Olivieri NF, Koren G, Harris J, Khattak S, Freedman MH, Templeton DM et al (1992) Growth failure and bony changes induced by deferoxamine. Am J Pediatr Hematol Oncol 14(1):48–56CrossRefPubMed Olivieri NF, Koren G, Harris J, Khattak S, Freedman MH, Templeton DM et al (1992) Growth failure and bony changes induced by deferoxamine. Am J Pediatr Hematol Oncol 14(1):48–56CrossRefPubMed
26.
Zurück zum Zitat De Sanctis V, Soliman AT, Elsedfy H, Di Maio S, Canatan D, Soliman N et al (2017) Gonadal dysfunction in adult male patients with thalassemia major: an update for clinicians caring for thalassemia. Expert Rev Hematol 10(12):1095–1106CrossRefPubMed De Sanctis V, Soliman AT, Elsedfy H, Di Maio S, Canatan D, Soliman N et al (2017) Gonadal dysfunction in adult male patients with thalassemia major: an update for clinicians caring for thalassemia. Expert Rev Hematol 10(12):1095–1106CrossRefPubMed
27.
Zurück zum Zitat Wu HP, Lin CL, Chang YC, Wu KH, Lei RL, Peng CT et al (2017) Survival and complication rates in patients with thalassemia major in Taiwan. Pediatr Blood Cancer 64(1):135–138CrossRefPubMed Wu HP, Lin CL, Chang YC, Wu KH, Lei RL, Peng CT et al (2017) Survival and complication rates in patients with thalassemia major in Taiwan. Pediatr Blood Cancer 64(1):135–138CrossRefPubMed
28.
Zurück zum Zitat Habeb AM, Al-Hawsawi ZM, Morsy MM, Al-Harbi AM, Osilan AS, Al-Magamsi MS et al (2013) Endocrinopathies in beta-thalassemia major. Prevalence, risk factors, and age at diagnosis in Northwest Saudi Arabia. Saudi Med J 34(1):67–73PubMed Habeb AM, Al-Hawsawi ZM, Morsy MM, Al-Harbi AM, Osilan AS, Al-Magamsi MS et al (2013) Endocrinopathies in beta-thalassemia major. Prevalence, risk factors, and age at diagnosis in Northwest Saudi Arabia. Saudi Med J 34(1):67–73PubMed
29.
Zurück zum Zitat Yaghobi M, Miri-Moghaddam E, Majid N, Bazi A, Navidian A, Kalkali A (2017) Complications of transfusion-dependent beta-thalassemia patients in Sistan and Baluchistan, South-East of Iran. Int J Hematol Oncol Stem Cell Res 11(4):268–272PubMedPubMedCentral Yaghobi M, Miri-Moghaddam E, Majid N, Bazi A, Navidian A, Kalkali A (2017) Complications of transfusion-dependent beta-thalassemia patients in Sistan and Baluchistan, South-East of Iran. Int J Hematol Oncol Stem Cell Res 11(4):268–272PubMedPubMedCentral
30.
Zurück zum Zitat De Sanctis V, Elsedfy H, Soliman AT, Elhakim IZ, Kattamis C, Soliman NA et al (2016) Clinical and biochemical data of adult thalassemia major patients (TM) with multiple endocrine complications (MEC) versus TM patients with normal endocrine functions: a long-term retrospective study (40 years) in a tertiary care center in Italy. Mediterr J Hematol Infect Dis 8(1):e2016022CrossRefPubMedPubMedCentral De Sanctis V, Elsedfy H, Soliman AT, Elhakim IZ, Kattamis C, Soliman NA et al (2016) Clinical and biochemical data of adult thalassemia major patients (TM) with multiple endocrine complications (MEC) versus TM patients with normal endocrine functions: a long-term retrospective study (40 years) in a tertiary care center in Italy. Mediterr J Hematol Infect Dis 8(1):e2016022CrossRefPubMedPubMedCentral
31.
Zurück zum Zitat Bazi A, Harati H, Khosravi-Bonjar A, Rakhshani E, Delaramnasab M (2018) Hypothyroidism and hypoparathyroidism in thalassemia major patients: a study in Sistan and Baluchestan Province, Iran. Int J Endocrinol Metab 16(2):e13228CrossRefPubMedPubMedCentral Bazi A, Harati H, Khosravi-Bonjar A, Rakhshani E, Delaramnasab M (2018) Hypothyroidism and hypoparathyroidism in thalassemia major patients: a study in Sistan and Baluchestan Province, Iran. Int J Endocrinol Metab 16(2):e13228CrossRefPubMedPubMedCentral
32.
Zurück zum Zitat Teawtrakul N, Jetsrisuparb A, Pongudom S, Sirijerachai C, Chansung K, Wanitpongpun C et al (2018) Epidemiologic study of major complications in adolescent and adult patients with thalassemia in Northeastern Thailand: the E-SAAN study phase I. Hematology 23(1):55–60CrossRefPubMed Teawtrakul N, Jetsrisuparb A, Pongudom S, Sirijerachai C, Chansung K, Wanitpongpun C et al (2018) Epidemiologic study of major complications in adolescent and adult patients with thalassemia in Northeastern Thailand: the E-SAAN study phase I. Hematology 23(1):55–60CrossRefPubMed
33.
Zurück zum Zitat Chuncharunee S, Teawtrakul N, Siritanaratkul N, Chueamuangphan N (2019) Review of disease-related complications and management in adult patients with thalassemia: a multi-center study in Thailand. PLoS One 14(3):e0214148CrossRefPubMedPubMedCentral Chuncharunee S, Teawtrakul N, Siritanaratkul N, Chueamuangphan N (2019) Review of disease-related complications and management in adult patients with thalassemia: a multi-center study in Thailand. PLoS One 14(3):e0214148CrossRefPubMedPubMedCentral
34.
Zurück zum Zitat Kolnagou A, Michaelides Y, Kontoghiorghe CN, Kontoghiorghes GJ (2013) The importance of spleen, spleen iron, and splenectomy for determining total body iron load, ferrikinetics, and iron toxicity in thalassemia major patients. Toxicol Mech Methods 23(1):34–41CrossRefPubMed Kolnagou A, Michaelides Y, Kontoghiorghe CN, Kontoghiorghes GJ (2013) The importance of spleen, spleen iron, and splenectomy for determining total body iron load, ferrikinetics, and iron toxicity in thalassemia major patients. Toxicol Mech Methods 23(1):34–41CrossRefPubMed
35.
Zurück zum Zitat Cappellini M-D, Cohen A, Porter J, Taher A, Viprakasit V (2014) Guidelines for the management of transfusion dependent thalassaemia (TDT): thalassaemia. International Federation Nicosia, Cyprus, pp 174–175 Cappellini M-D, Cohen A, Porter J, Taher A, Viprakasit V (2014) Guidelines for the management of transfusion dependent thalassaemia (TDT): thalassaemia. International Federation Nicosia, Cyprus, pp 174–175
36.
Zurück zum Zitat Isik P, Yarali N, Tavil B, Demirel F, Karacam GB, Sac RU et al (2014) Endocrinopathies in Turkish children with Beta thalassemia major: results from a single center study. Pediatr Hematol Oncol 31(7):607–615CrossRefPubMed Isik P, Yarali N, Tavil B, Demirel F, Karacam GB, Sac RU et al (2014) Endocrinopathies in Turkish children with Beta thalassemia major: results from a single center study. Pediatr Hematol Oncol 31(7):607–615CrossRefPubMed
37.
Zurück zum Zitat Altincik A, Akin M (2016) Prevalence of endocrinopathies in Turkish children with beta-thalassemia major: a single-center study. J Pediatr Hematol Oncol 38(5):389–393CrossRefPubMed Altincik A, Akin M (2016) Prevalence of endocrinopathies in Turkish children with beta-thalassemia major: a single-center study. J Pediatr Hematol Oncol 38(5):389–393CrossRefPubMed
38.
Zurück zum Zitat Chern JP, Lin KH, Lu MY, Lin DT, Lin KS, Chen JD et al (2001) Abnormal glucose tolerance in transfusion-dependent beta-thalassemic patients. Diabetes Care 24(5):850–854CrossRefPubMed Chern JP, Lin KH, Lu MY, Lin DT, Lin KS, Chen JD et al (2001) Abnormal glucose tolerance in transfusion-dependent beta-thalassemic patients. Diabetes Care 24(5):850–854CrossRefPubMed
39.
Zurück zum Zitat Najafipour F, Aliasgarzadeh A, Aghamohamadzadeh N, Bahrami A, Mobasri M, Niafar M et al (2008) A cross-sectional study of metabolic and endocrine complications in beta-thalassemia major. Ann Saudi Med 28(5):361–366CrossRefPubMedPubMedCentral Najafipour F, Aliasgarzadeh A, Aghamohamadzadeh N, Bahrami A, Mobasri M, Niafar M et al (2008) A cross-sectional study of metabolic and endocrine complications in beta-thalassemia major. Ann Saudi Med 28(5):361–366CrossRefPubMedPubMedCentral
40.
Zurück zum Zitat Sharma S, Dutt N, Sidhu M, Digra S, Meenia R (2017) Prevalence of hypothyroidism, diabetes mellitus and delayed puberty in patients of thalassemia major in a tertiary care center of Jammu province, Jammu Kashmir, India. Int J Adv Med 4(3):673–677CrossRef Sharma S, Dutt N, Sidhu M, Digra S, Meenia R (2017) Prevalence of hypothyroidism, diabetes mellitus and delayed puberty in patients of thalassemia major in a tertiary care center of Jammu province, Jammu Kashmir, India. Int J Adv Med 4(3):673–677CrossRef
41.
Zurück zum Zitat Pirinççioğlu AG, Gökalp D, Söker M (2017) Parathyroid functions in thalassemia major patients. Ann Clin Endocrinol Metab 1:015–019CrossRef Pirinççioğlu AG, Gökalp D, Söker M (2017) Parathyroid functions in thalassemia major patients. Ann Clin Endocrinol Metab 1:015–019CrossRef
42.
Zurück zum Zitat Tangngam H, Mahachoklertwattana P, Poomthavorn P, Chuansumrit A, Sirachainan N, Chailurkit L et al (2018) Under-recognized hypoparathyroidism in thalassemia. J Clin Res Pediatr Endocrinol 10(4):324–330PubMedPubMedCentral Tangngam H, Mahachoklertwattana P, Poomthavorn P, Chuansumrit A, Sirachainan N, Chailurkit L et al (2018) Under-recognized hypoparathyroidism in thalassemia. J Clin Res Pediatr Endocrinol 10(4):324–330PubMedPubMedCentral
43.
Zurück zum Zitat De Sanctis V, Soliman AT, Canatan D, Elsedfy H, Karimi M, Daar S et al (2018) An ICET—a survey on hypoparathyroidism in patients with thalassaemia major and intermedia: a preliminary report. Acta Biomed 88(4):435–444PubMed De Sanctis V, Soliman AT, Canatan D, Elsedfy H, Karimi M, Daar S et al (2018) An ICET—a survey on hypoparathyroidism in patients with thalassaemia major and intermedia: a preliminary report. Acta Biomed 88(4):435–444PubMed
44.
Zurück zum Zitat El-Din LB, Ebeid FS, Toaima NN, Ibrahim WW (2018) Hypoparathyroidism in children with β-thalassemia major and its relation to iron chelation therapy. Egypt J Haematol 43(2):63CrossRef El-Din LB, Ebeid FS, Toaima NN, Ibrahim WW (2018) Hypoparathyroidism in children with β-thalassemia major and its relation to iron chelation therapy. Egypt J Haematol 43(2):63CrossRef
45.
Zurück zum Zitat Rehim MH, Mustafa S, Rizvi SKA (2017) Correlation between serum TSH and serum ferritin in patients of beta thalassemia major. Pak J Med Health Sci 11(1):266–269 Rehim MH, Mustafa S, Rizvi SKA (2017) Correlation between serum TSH and serum ferritin in patients of beta thalassemia major. Pak J Med Health Sci 11(1):266–269
46.
Zurück zum Zitat Soliman AT, Al Yafei F, Al-Naimi L, Almarri N, Sabt A, Yassin M et al (2013) Longitudinal study on thyroid function in patients with thalassemia major: high incidence of central hypothyroidism by 18 years. Indian J Endocrinol Metab 17(6):1090–1095CrossRefPubMedPubMedCentral Soliman AT, Al Yafei F, Al-Naimi L, Almarri N, Sabt A, Yassin M et al (2013) Longitudinal study on thyroid function in patients with thalassemia major: high incidence of central hypothyroidism by 18 years. Indian J Endocrinol Metab 17(6):1090–1095CrossRefPubMedPubMedCentral
47.
Zurück zum Zitat Jaruratanasirikul S, Wongcharnchailert M, Laosombat V, Sangsupavanich P, Leetanaporn K (2007) Thyroid function in β-thalassemic children receiving hypertransfusions with suboptimal iron-chelating therapy. J Med Assoc Thail 90:1798–1802 Jaruratanasirikul S, Wongcharnchailert M, Laosombat V, Sangsupavanich P, Leetanaporn K (2007) Thyroid function in β-thalassemic children receiving hypertransfusions with suboptimal iron-chelating therapy. J Med Assoc Thail 90:1798–1802
48.
Zurück zum Zitat Abdel-Razek AR, Abdel-Salam A, El-Sonbaty MM, Youness ER (2013) Study of thyroid function in Egyptian children with beta-thalassemia major and beta-thalassemia intermedia. J Egypt Public Health Assoc 88(3):148–152CrossRefPubMed Abdel-Razek AR, Abdel-Salam A, El-Sonbaty MM, Youness ER (2013) Study of thyroid function in Egyptian children with beta-thalassemia major and beta-thalassemia intermedia. J Egypt Public Health Assoc 88(3):148–152CrossRefPubMed
49.
Zurück zum Zitat Azami M, Parizad N, Sayehmiri K (2016) Prevalence of hypothyroidism, hypoparathyroidism and the frequency of regular chelation therapy in patients with thalassemia major in Iran: a systematic review and meta-analysis study. Iran J Pediatr Hematol Oncol 6(4):261–276 Azami M, Parizad N, Sayehmiri K (2016) Prevalence of hypothyroidism, hypoparathyroidism and the frequency of regular chelation therapy in patients with thalassemia major in Iran: a systematic review and meta-analysis study. Iran J Pediatr Hematol Oncol 6(4):261–276
50.
Zurück zum Zitat Malik SA, Syed S, Ahmed N (2010) Frequency of hypothyroidism in patients of b-thalassemia. J Pak Med Assoc 60:17–21PubMed Malik SA, Syed S, Ahmed N (2010) Frequency of hypothyroidism in patients of b-thalassemia. J Pak Med Assoc 60:17–21PubMed
Metadaten
Titel
Prevalence of endocrine disorders and their associated factors in transfusion-dependent thalassemia patients: a historical cohort study in Southern Iran
verfasst von
M. Bordbar
H. Bozorgi
F. Saki
S. Haghpanah
M. Karimi
A. Bazrafshan
O. R. Zekavat
Publikationsdatum
01.12.2019
Verlag
Springer International Publishing
Erschienen in
Journal of Endocrinological Investigation / Ausgabe 12/2019
Elektronische ISSN: 1720-8386
DOI
https://doi.org/10.1007/s40618-019-01072-z

Weitere Artikel der Ausgabe 12/2019

Journal of Endocrinological Investigation 12/2019 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Erhebliches Risiko für Kehlkopfkrebs bei mäßiger Dysplasie

29.05.2024 Larynxkarzinom Nachrichten

Fast ein Viertel der Personen mit mäßig dysplastischen Stimmlippenläsionen entwickelt einen Kehlkopftumor. Solche Personen benötigen daher eine besonders enge ärztliche Überwachung.

Nach Herzinfarkt mit Typ-1-Diabetes schlechtere Karten als mit Typ 2?

29.05.2024 Herzinfarkt Nachrichten

Bei Menschen mit Typ-2-Diabetes sind die Chancen, einen Myokardinfarkt zu überleben, in den letzten 15 Jahren deutlich gestiegen – nicht jedoch bei Betroffenen mit Typ 1.

15% bedauern gewählte Blasenkrebs-Therapie

29.05.2024 Urothelkarzinom Nachrichten

Ob Patienten und Patientinnen mit neu diagnostiziertem Blasenkrebs ein Jahr später Bedauern über die Therapieentscheidung empfinden, wird einer Studie aus England zufolge von der Radikalität und dem Erfolg des Eingriffs beeinflusst.

Costims – das nächste heiße Ding in der Krebstherapie?

28.05.2024 Onkologische Immuntherapie Nachrichten

„Kalte“ Tumoren werden heiß – CD28-kostimulatorische Antikörper sollen dies ermöglichen. Am besten könnten diese in Kombination mit BiTEs und Checkpointhemmern wirken. Erste klinische Studien laufen bereits.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.