Page last updated: 2024-10-25

deferoxamine and Hypogonadism

deferoxamine has been researched along with Hypogonadism in 18 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.

Hypogonadism: Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism).

Research Excerpts

ExcerptRelevanceReference
"Deferiprone (L1) was found to have greater efficacy at depleting myocardial iron than desferrioxamine (DFX)."5.32Combined therapy with deferiprone and desferrioxamine successfully regresses severe heart failure in patients with beta-thalassemia major. ( Chang, JS; Peng, CT; Tsai, CH; Wu, KH, 2004)
" We compared the efficacy of oral deferiprone (L1) to subcutaneous desferrioxamine (DFO) chelation therapy for the prevention of major endocrinopathies (growth hormone insufficiency, diabetes mellitus and gonadal dysfunction) among patients with beta-thal major to see if we could offer these patients an easier and more painless way to reduce their body iron load and related endocrine complications."5.12Comparison of oral and subcutaneous iron chelation therapies in the prevention of major endocrinopathies in beta-thalassemia major patients. ( Peng, CT; Tsai, CH; Tsai, FJ; Wang, CH; Wu, KH, 2006)
"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)
"Hypogonadism was noted in 59% of the patients who reached pubertal age, and short stature was found in 36% of patients who reached final height."1.33Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients. ( Carmi, D; Kornreich, L; Miskin, H; Phillip, M; Shalitin, S; Tamary, H; Weintrob, N; Yaniv, I; Zilber, R, 2005)
"Deferiprone (L1) was found to have greater efficacy at depleting myocardial iron than desferrioxamine (DFX)."1.32Combined therapy with deferiprone and desferrioxamine successfully regresses severe heart failure in patients with beta-thalassemia major. ( Chang, JS; Peng, CT; Tsai, CH; Wu, KH, 2004)
"Juvenile hemochromatosis is a rare genetic disorder that causes iron overload."1.31Juvenile hemochromatosis associated with B-thalassemia treated by phlebotomy and recombinant human erythropoietin. ( Brunello, F; Camaschella, C; De Gobbi, M; Mazza, U; Paccotti, P; Pasquero, P, 2000)

Research

Studies (18)

TimeframeStudies, this research(%)All Research%
pre-19905 (27.78)18.7374
1990's2 (11.11)18.2507
2000's9 (50.00)29.6817
2010's2 (11.11)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Picardo, E1
Mitidieri, M1
Minniti, E1
Ambroggio, S1
D'Addato, F1
Benedetto, C1
Gregori, G1
Baù, MG1
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
De Sanctis, V4
PESTEL, M1
Wu, KH2
Chang, JS1
Tsai, CH2
Peng, CT2
Borgna-Pignatti, C1
Rugolotto, S1
De Stefano, P1
Zhao, H1
Cappellini, MD1
Del Vecchio, GC1
Romeo, MA1
Forni, GL1
Gamberini, MR1
Ghilardi, R1
Piga, A1
Cnaan, A1
Shalitin, S1
Carmi, D1
Weintrob, N1
Phillip, M1
Miskin, H1
Kornreich, L1
Zilber, R1
Yaniv, I1
Tamary, H1
Vogiatzi, MG1
Autio, KA1
Mait, JE1
Schneider, R1
Lesser, M1
Giardina, PJ1
Roos, M1
Gasser, T1
Fortini, M1
Raiola, G1
Galati, MC1
Wang, CH1
Tsai, FJ1
Kidson-Gerber, GL1
Francis, S1
Lindeman, R1
Economidou, J1
Tuschy, U1
Schmidt, U1
Meinhold, J1
Wutke, K1
Jensen, CE1
Tuck, SM1
Old, J1
Morris, RW1
Yardumian, A1
Hoffbrand, AV1
Wonke, B2
De Gobbi, M1
Pasquero, P1
Brunello, F1
Paccotti, P1
Mazza, U1
Camaschella, C1
Simon, M1
Bourel, M1
Allegra, A1
Capra, M1
Cuccia, L1
Pulejo, ML1
Raineri, L1
Corselli, F1
Traina, MC1
Giannola, C1
La Grutta, A1
Vullo, C1
Katz, M1
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]

Reviews

4 reviews available for deferoxamine and Hypogonadism

ArticleYear
The first case of breast cancer in thalassemic patient: case report and review of literature.
    Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology, 2015, Volume: 31, Issue:5

    Topics: Adult; beta-Thalassemia; Blood Transfusion; Breast Neoplasms; Carcinoma, Intraductal, Noninfiltratin

2015
Growth and puberty and its management in thalassaemia.
    Hormone research, 2002, Volume: 58 Suppl 1

    Topics: Adolescent; Adult; Amenorrhea; beta-Thalassemia; Body Height; Calcification, Physiologic; Child; Def

2002
Problems related to treatment of beta-thalassaemia major.
    Paediatrician, 1982, Volume: 11, Issue:3-4

    Topics: Adolescent; Adult; Bone Diseases; Child; Child, Preschool; Deferoxamine; Encephalitis; Female; Hormo

1982
[Idiopathic haemochromatosis. I. Clinical, biological and therapeutic aspects (author's transl)].
    La Nouvelle presse medicale, 1979, Mar-10, Volume: 8, Issue:11

    Topics: Bloodletting; Bone Diseases; Cardiomyopathies; Deferoxamine; Diabetes Mellitus; Female; Ferritins; H

1979

Trials

2 trials available for deferoxamine and Hypogonadism

ArticleYear
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
Comparison of oral and subcutaneous iron chelation therapies in the prevention of major endocrinopathies in beta-thalassemia major patients.
    Hemoglobin, 2006, Volume: 30, Issue:2

    Topics: Administration, Oral; Adolescent; Adult; beta-Thalassemia; Chelation Therapy; Child; Combined Modali

2006

Other Studies

12 other studies available for deferoxamine and Hypogonadism

ArticleYear
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
[HEMOCHROMATOSIS].
    La Presse medicale, 1964, Apr-18, Volume: 72

    Topics: Alcoholism; Biopsy; Blood Chemical Analysis; Bloodletting; Chelating Agents; Deferoxamine; Diabetes

1964
Combined therapy with deferiprone and desferrioxamine successfully regresses severe heart failure in patients with beta-thalassemia major.
    Annals of hematology, 2004, Volume: 83, Issue:7

    Topics: Adult; beta-Thalassemia; Cardiovascular Agents; Deferiprone; Deferoxamine; Diabetes Complications; D

2004
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
Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients.
    European journal of haematology, 2005, Volume: 74, Issue:2

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

2005
Low bone mineral density in adolescents with beta-thalassemia.
    Annals of the New York Academy of Sciences, 2005, Volume: 1054

    Topics: Adolescent; Adult; Anthropometry; beta-Thalassemia; Blood Transfusion; Bone Density; Bone Diseases,

2005
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
Incidence of endocrine complications and clinical disease severity related to genotype analysis and iron overload in patients with beta-thalassaemia.
    European journal of haematology, 1997, Volume: 59, Issue:2

    Topics: Adolescent; Adult; beta-Thalassemia; Child; Deferoxamine; Endocrine System Diseases; Female; Genotyp

1997
Juvenile hemochromatosis associated with B-thalassemia treated by phlebotomy and recombinant human erythropoietin.
    Haematologica, 2000, Volume: 85, Issue:8

    Topics: Adrenal Cortex Hormones; Adrenal Insufficiency; Adult; Arrhythmias, Cardiac; beta-Thalassemia; Chela

2000
Hypogonadism in beta-thalassemic adolescents: a characteristic pituitary-gonadal impairment. The ineffectiveness of long-term iron chelation therapy.
    Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology, 1990, Volume: 4, Issue:3

    Topics: Adolescent; Chelation Therapy; Child; Deferoxamine; Dose-Response Relationship, Drug; Estradiol; Fem

1990
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