Literature DB >> 17316339

Effect of hydroxyurea on sperm count, motility and morphology in adult men with sickle cell or myeloproliferative disease.

A Grigg1.   

Abstract

Hydroxyurea (HU) is not infrequently used in patients with sickle cell disease and myeloproliferative disorders. Despite murine data showing adverse effects on sperm counts, motility and morphology, there is little information on the effect of HU on human spermatogenesis. A retrospective review of four adult men who had semen analysis during HU therapy and in three cases after its cessation suggests that HU generally reduces sperm counts and motility and results in abnormal morphology. Cessation of HU in one case with azoospermia resulted in recovery of spermatogenesis; in two of the three cases, however, sperm morphology and mobility remained impaired. Recommendations for fertility management in adult men receiving long-term HU therapy are proposed.

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Year:  2007        PMID: 17316339     DOI: 10.1111/j.1445-5994.2006.01290.x

Source DB:  PubMed          Journal:  Intern Med J        ISSN: 1444-0903            Impact factor:   2.048


  13 in total

Review 1.  Hydroxyurea for children with sickle cell disease.

Authors:  Matthew M Heeney; Russell E Ware
Journal:  Hematol Oncol Clin North Am       Date:  2010-02       Impact factor: 3.722

2.  Pharmacological Induction of Human Fetal Globin Gene in Hydroxyurea-Resistant Primary Adult Erythroid Cells.

Authors:  Yu-Chi Chou; Ruei-Lin Chen; Zheng-Sheng Lai; Jen-Shin Song; Yu-Sheng Chao; Che-Kun James Shen
Journal:  Mol Cell Biol       Date:  2015-05-18       Impact factor: 4.272

Review 3.  Systematic review: Hydroxyurea for the treatment of adults with sickle cell disease.

Authors:  Sophie Lanzkron; John J Strouse; Renee Wilson; Mary Catherine Beach; Carlton Haywood; HaeSong Park; Catherine Witkop; Eric B Bass; Jodi B Segal
Journal:  Ann Intern Med       Date:  2008-05-05       Impact factor: 25.391

Review 4.  Iron and copper in male reproduction: a double-edged sword.

Authors:  Eva Tvrda; Rohan Peer; Suresh C Sikka; Ashok Agarwal
Journal:  J Assist Reprod Genet       Date:  2014-09-23       Impact factor: 3.412

Review 5.  A systematic review of known mechanisms of hydroxyurea-induced fetal hemoglobin for treatment of sickle cell disease.

Authors:  Gift D Pule; Shaheen Mowla; Nicolas Novitzky; Charles S Wiysonge; Ambroise Wonkam
Journal:  Expert Rev Hematol       Date:  2015-09-01       Impact factor: 2.819

6.  Effect of N(Epsilon)-(carboxymethyl)lysine on Laboratory Parameters and Its Association with β S Haplotype in Children with Sickle Cell Anemia.

Authors:  Uche Samuel Ndidi; Corynne Stephanie Ahouefa Adanho; Rayra Pereira Santiago; Sètondji Cocou Modeste Alexandre Yahouédéhou; Sânzio Silva Santana; Vitor Valério Mafili; Thassila Nogueira Pitanga; Cleverson Alves Fonseca; Junia Raquel Dutra Ferreira; Elisângela Vitoria Adorno; Isa Menezes Lyra; Adekunle D Adekile; Cynara Gomes Barbosa; Marilda Souza Goncalves
Journal:  Dis Markers       Date:  2019-09-15       Impact factor: 3.434

7.  Adverse effects of a clinically relevant dose of hydroxyurea used for the treatment of sickle cell disease on male fertility endpoints.

Authors:  Kea M Jones; Mohammad S Niaz; Cynthia M Brooks; Shannon I Roberson; Maria P Aguinaga; Edward R Hills; Valerie Montgomery Rice; Phillip Bourne; Donald Bruce; Anthony E Archibong
Journal:  Int J Environ Res Public Health       Date:  2009-03-16       Impact factor: 3.390

8.  Role of hydroxycarbamide in prevention of complications in patients with sickle cell disease.

Authors:  Nm Wiles; J Howard
Journal:  Ther Clin Risk Manag       Date:  2009-09-24       Impact factor: 2.423

Review 9.  [From Hemoglobin SS to SF: interest of hydroxyurea in the management of sickle cell disease in two Congolese children and review of the literature].

Authors:  Gayllord Mutoke Nkashama; Gray Kanteng A Wakamb; Augustin Mutombo Mulangu; Georges Mutoke Nkashama; Boniface Kabeya Kupa; Oscar Luboya Numbi
Journal:  Pan Afr Med J       Date:  2015-06-15

10.  Hydroxyurea down-regulates BCL11A, KLF-1 and MYB through miRNA-mediated actions to induce γ-globin expression: implications for new therapeutic approaches of sickle cell disease.

Authors:  Gift Dineo Pule; Shaheen Mowla; Nicolas Novitzky; Ambroise Wonkam
Journal:  Clin Transl Med       Date:  2016-04-07
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