Page last updated: 2024-10-25

deferoxamine and Hypothyroidism

deferoxamine has been researched along with Hypothyroidism in 13 studies

Deferoxamine: Natural product isolated from Streptomyces pilosus. It forms iron complexes and is used as a chelating agent, particularly in the mesylate form.
desferrioxamine B : An acyclic desferrioxamine that is butanedioic acid in which one of the carboxy groups undergoes formal condensation with the primary amino group of N-(5-aminopentyl)-N-hydroxyacetamide and the second carboxy group undergoes formal condensation with the hydroxyamino group of N(1)-(5-aminopentyl)-N(1)-hydroxy-N(4)-[5-(hydroxyamino)pentyl]butanediamide. It is a siderophore native to Streptomyces pilosus biosynthesised by the DesABCD enzyme cluster as a high affinity Fe(III) chelator.

Hypothyroidism: A syndrome that results from abnormally low secretion of THYROID HORMONES from the THYROID GLAND, leading to a decrease in BASAL METABOLIC RATE. In its most severe form, there is accumulation of MUCOPOLYSACCHARIDES in the SKIN and EDEMA, known as MYXEDEMA. It may be primary or secondary due to other pituitary disease, or hypothalamic dysfunction.

Research Excerpts

ExcerptRelevanceReference
" In 18 requiring thyroxine supplementation for hypothyroidism, 10 were able to discontinue, and four reduced their thyroxine dose."5.14Normalisation of total body iron load with very intensive combined chelation reverses cardiac and endocrine complications of thalassaemia major. ( Berdoukas, V; Chouliaras, G; Farmaki, K; Pappa, C; Tzoumari, I, 2010)
"In this study, we compared the long-term effects of different iron chelation regimens (deferoxamine, deferiprone, deferoxamine + deferiprone, and deferasirox) in preventing or reversing endocrinopathy (diabetes mellitus, hypothyroidism, or hypogonadism) and bone disease (measured through DEXA) in 165 adults with β-thalassemia major (TM) (mean age 39."3.83Longitudinal changes of endocrine and bone disease in adults with β-thalassemia major receiving different iron chelators over 5 years. ( Daniele, C; Equitani, F; Guitarrini, MR; Losardo, A; Maffei, L; Monti, S; Pasin, M; Poggi, M; Pugliese, P; Smacchia, MP; Sorrentino, F; Terlizzi, F; Toscano, V, 2016)
"Delayed puberty was present in 18."2.72Impact of long-term iron chelation therapy on growth and endocrine functions in thalassaemia. ( De Sanctis, V; Fortini, M; Galati, MC; Gasser, T; Raiola, G; Roos, M, 2006)
"Hypothyroidism is one of the common endocrine complications described in patients with β-thalassemia major (β-TM)."1.51Compliance with Deferoxamine Therapy and Thyroid Dysfunction of Patients with β-Thalassemia Major in Syria. ( Alquobaili, F; Kabalan, Y; Mukhalalaty, Y; Yassouf, MY, 2019)
"We report a case of thalassemia major with biopsy-proven pulmonary iron overload, in which thoracic high-resolution computed tomography revealed a morphological-functional correlation consistent with small airway disease."1.31Pulmonary iron overload in thalassemia major presenting as small airway disease. ( Khong, PL; Lam, WK; Ooi, GC; Trendell-Smith, NJ; Tsang, KW, 2002)
"Three patients had evidence of primary hypothyroidism."1.29Multiple hormone deficiencies in children with hemochromatosis. ( Cassorla, FG; Kamp, GA; Manasco, PK; Munson, PJ; Nienhuis, AW; Oerter, KE, 1993)

Research

Studies (13)

TimeframeStudies, this research(%)All Research%
pre-19903 (23.08)18.7374
1990's2 (15.38)18.2507
2000's4 (30.77)29.6817
2010's4 (30.77)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Yassouf, MY1
Alquobaili, F1
Kabalan, Y1
Mukhalalaty, Y1
Poggi, M1
Sorrentino, F1
Pugliese, P1
Smacchia, MP1
Daniele, C1
Equitani, F1
Terlizzi, F1
Guitarrini, MR1
Monti, S1
Maffei, L1
Losardo, A1
Pasin, M1
Toscano, V1
Farmaki, K1
Tzoumari, I1
Pappa, C1
Chouliaras, G1
Berdoukas, V1
Belhoul, KM1
Bakir, ML1
Saned, MS1
Kadhim, AM1
Musallam, KM1
Taher, AT1
Ooi, GC1
Khong, PL1
Lam, WK1
Trendell-Smith, NJ1
Tsang, KW1
Borgna-Pignatti, C1
Rugolotto, S1
De Stefano, P1
Zhao, H1
Cappellini, MD1
Del Vecchio, GC1
Romeo, MA1
Forni, GL1
Gamberini, MR1
Ghilardi, R1
Piga, A2
Cnaan, A1
De Sanctis, V2
Roos, M1
Gasser, T1
Fortini, M1
Raiola, G1
Galati, MC1
Kidson-Gerber, GL1
Francis, S1
Lindeman, R1
Tuschy, U1
Schmidt, U1
Meinhold, J1
Wutke, K1
Oerter, KE1
Kamp, GA1
Munson, PJ1
Nienhuis, AW1
Cassorla, FG1
Manasco, PK1
Calleja, EM1
Shen, JY1
Lesser, M1
Grady, RW1
New, MI1
Giardina, PJ1
Gabutti, V1
Sacchetti, L1
Sandri, A1
Biginelli, M1
Saracco, P1
Ferri, M1
Vullo, C1
Katz, M1
Wonke, B1
Hoffbrand, VA1
Di Palma, A1
Bagni, B1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Iron-mediated Vascular Disease in Sickle Cell Disease.[NCT01239901]150 participants (Actual)Observational2009-12-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trials

2 trials available for deferoxamine and Hypothyroidism

ArticleYear
Normalisation of total body iron load with very intensive combined chelation reverses cardiac and endocrine complications of thalassaemia major.
    British journal of haematology, 2010, Volume: 148, Issue:3

    Topics: Adolescent; Adult; beta-Thalassemia; Blood Glucose; Cardiomyopathies; Child; Deferiprone; Deferoxami

2010
Impact of long-term iron chelation therapy on growth and endocrine functions in thalassaemia.
    Journal of pediatric endocrinology & metabolism : JPEM, 2006, Volume: 19, Issue:4

    Topics: Adolescent; Adult; beta-Thalassemia; Body Height; Child; Child, Preschool; Deferoxamine; Female; Glu

2006

Other Studies

11 other studies available for deferoxamine and Hypothyroidism

ArticleYear
Compliance with Deferoxamine Therapy and Thyroid Dysfunction of Patients with β-Thalassemia Major in Syria.
    Hemoglobin, 2019, Volume: 43, Issue:3

    Topics: Adolescent; Adult; beta-Thalassemia; Biomarkers; Case-Control Studies; Child; Cross-Sectional Studie

2019
Longitudinal changes of endocrine and bone disease in adults with β-thalassemia major receiving different iron chelators over 5 years.
    Annals of hematology, 2016, Volume: 95, Issue:5

    Topics: Adult; Benzoates; beta-Thalassemia; Chelation Therapy; Deferasirox; Deferiprone; Deferoxamine; Diabe

2016
Serum ferritin levels and endocrinopathy in medically treated patients with β thalassemia major.
    Annals of hematology, 2012, Volume: 91, Issue:7

    Topics: Adolescent; Adult; beta-Thalassemia; Blood Transfusion; Child; Cross-Sectional Studies; Deferoxamine

2012
Pulmonary iron overload in thalassemia major presenting as small airway disease.
    Acta haematologica, 2002, Volume: 108, Issue:1

    Topics: Adult; Airway Obstruction; beta-Thalassemia; Biopsy; Chelation Therapy; Combined Modality Therapy; D

2002
Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine.
    Haematologica, 2004, Volume: 89, Issue:10

    Topics: Adult; Age Factors; Arrhythmias, Cardiac; Blood Transfusion; Chelation Therapy; Cohort Studies; Defe

2004
Management and clinical outcomes of transfusion-dependent thalassaemia major in an Australian tertiary referral clinic.
    The Medical journal of Australia, 2008, Jan-21, Volume: 188, Issue:2

    Topics: Adult; Age Factors; Australia; Cardiomyopathies; Deferiprone; Deferoxamine; Diabetes Mellitus; Drug

2008
[Long-term study in congenital refractory anemia and secondary siderosis].
    Zeitschrift fur die gesamte innere Medizin und ihre Grenzgebiete, 1982, Apr-01, Volume: 37, Issue:7

    Topics: Adolescent; Anemia, Aplastic; Deferoxamine; Dwarfism; Female; Hemosiderosis; Humans; Hypogonadism; H

1982
Multiple hormone deficiencies in children with hemochromatosis.
    The Journal of clinical endocrinology and metabolism, 1993, Volume: 76, Issue:2

    Topics: Adolescent; Child; Deferoxamine; Endocrine System Diseases; Female; Follicle Stimulating Hormone; Go

1993
Survival and morbidity in transfusion-dependent thalassemic patients on subcutaneous desferrioxamine chelation. Nearly two decades of experience.
    Annals of the New York Academy of Sciences, 1998, Jun-30, Volume: 850

    Topics: Adolescent; Adult; Age Factors; beta-Thalassemia; Blood Transfusion; Child; Child, Preschool; Defero

1998
Quality of life and life expectancy in thalassemic patients with complications.
    Progress in clinical and biological research, 1989, Volume: 309

    Topics: Adolescent; Adult; Blood Transfusion; Child; Deferoxamine; Diabetes Mellitus, Type 1; Heart Diseases

1989
Endocrine complications in thalassaemia major.
    Progress in clinical and biological research, 1989, Volume: 309

    Topics: Adolescent; Adult; Blood Transfusion; Deferoxamine; Diabetes Mellitus, Type 1; Female; Humans; Hypog

1989