Literature DB >> 18255340

Hemophilia, low bone mass, and osteopenia/osteoporosis.

Christopher S Kovacs1.   

Abstract

A recent case series from Australia suggested that children with hemophilia may be more likely to have low bone density or osteopenia than healthy controls. This finding has led to uncertainty among patients and their physicians as to whether treatment with bisphosphonates is indicated to treat osteopenia and prevent osteoporosis in children or young adults with hemophilia. In fact, several studies confirmed that selected patients with hemophilia were shorter, weighed less, had reduced physical activity, and had other factors (hepatitis C and HIV seropositivity) which predict lower peak bone mass. Some of these factors may accelerate loss of bone mass between ages 20 and 50 when bone mass should otherwise be stable, but no study has yet confirmed if this is the case for patients with hemophilia. Treatment with weight-bearing physical activity, physiotherapy and surgery to remobilize diseased joints, and calcium and vitamin D supplementation, can be recommended for anyone at any age. Treatment with an antiresorptive medication (usually a bisphosphonate) is not indicated for low peak bone mass that will otherwise be maintained by the patient between ages 20 and 50. On the other hand, on an individualized basis, treatment with an antiresorptive may be indicated for patients in whom rapid loss of bone mass has been confirmed by sequential BMD measurements, or who have already suffered fragility fractures, or who have reached an age and BMD value that places them into a high-risk category for estimated 10-year fracture risk.

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Year:  2008        PMID: 18255340     DOI: 10.1016/j.transci.2007.12.003

Source DB:  PubMed          Journal:  Transfus Apher Sci        ISSN: 1473-0502            Impact factor:   1.764


  14 in total

Review 1.  Bleeding disorders and reduced bone density.

Authors:  Hassan Mansouritorghabeh; Zahra Rezaieyazdi
Journal:  Rheumatol Int       Date:  2010-05-27       Impact factor: 2.631

2.  Impact of mild versus moderate intensity aerobic walking exercise training on markers of bone metabolism and hand grip strength in moderate hemophilic A patients.

Authors:  Fadwa Al-Ghalib Al-Sharif; Osama Hussien Al-Jiffri; Shehab Mahmoud Abd El-Kader; Eman Mohamed Ashmawy
Journal:  Afr Health Sci       Date:  2014-03       Impact factor: 0.927

Review 3.  Pathological mechanism of joint destruction in haemophilic arthropathy.

Authors:  Haijia Zhu; Yilin Meng; Peijian Tong; Shanxing Zhang
Journal:  Mol Biol Rep       Date:  2020-12-08       Impact factor: 2.316

4.  Evaluation of bone mineral density (BMD) and indicators of bone turnover in patients with hemophilia.

Authors:  Mehmet Dagli; Ali Kutlucan; Sedat Abusoglu; Abdulkadir Basturk; Mehmet Sozen; Leyla Kutlucan; Ali Unlu; Farise Yilmaz
Journal:  Bosn J Basic Med Sci       Date:  2018-05-20       Impact factor: 3.363

5.  Bone mineral density in hemophilia patients.

Authors:  Nader Roushan; Alipasha Meysamie; Mohammadreza Managhchi; Javad Esmaili; Tarane Dormohammadi
Journal:  Indian J Hematol Blood Transfus       Date:  2014-01-22       Impact factor: 0.900

6.  Factor VIII-von Willebrand factor complex inhibits osteoclastogenesis and controls cell survival.

Authors:  Marc Baud'huin; Laurence Duplomb; Stéphane Téletchéa; Céline Charrier; Mike Maillasson; Marc Fouassier; Dominique Heymann
Journal:  J Biol Chem       Date:  2009-09-16       Impact factor: 5.157

7.  Blood-induced bone loss in murine hemophilic arthropathy is prevented by blocking the iRhom2/ADAM17/TNF-α pathway.

Authors:  Coline Haxaire; Narine Hakobyan; Tania Pannellini; Camila Carballo; David McIlwain; Tak W Mak; Scott Rodeo; Suchitra Acharya; Daniel Li; Jackie Szymonifka; Xiangqian Song; Sébastien Monette; Alok Srivastava; Jane E Salmon; Carl P Blobel
Journal:  Blood       Date:  2018-05-18       Impact factor: 22.113

8.  Osteoporosis in haemophilic patient, rehabilitative aspects.

Authors:  Patrizia Franco
Journal:  Clin Cases Miner Bone Metab       Date:  2012-09-30

9.  Hemophilia A and B mice, but not VWF-/-mice, display bone defects in congenital development and remodeling after injury.

Authors:  Sarah Taves; Junjiang Sun; Eric W Livingston; Xin Chen; Jerome Amiaud; Regis Brion; William B Hannah; Ted A Bateman; Dominique Heymann; Paul E Monahan
Journal:  Sci Rep       Date:  2019-10-08       Impact factor: 4.379

10.  Clinical Care of Bone Health in Patients on the Immune Tolerance Induction's Protocols With an Immunosuppressive Agent for Inhibitor Eradication in Hemophilia.

Authors:  Zahra Rezaieyazdi; Hassan Mansouritorghabeh
Journal:  Clin Appl Thromb Hemost       Date:  2020 Jan-Dec       Impact factor: 2.389

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