Literature DB >> 16199706

Bone area and bone mineral content deficits in children with sickle cell disease.

Anne M Buison1, Deborah A Kawchak, Joan I Schall, Kwaku Ohene-Frempong, Virginia A Stallings, Mary B Leonard, Babette S Zemel.   

Abstract

OBJECTIVE: Children with sickle cell disease (SCD) experience poor growth, altered body composition, and delayed maturation. Deficits in bone mineral content (BMC) and bone area (BA) have not been well characterized. The objectives of this study were to assess whole-body BMC (WBBMC) and WBBA in children with SCD, type SS (SCD-SS), compared with healthy control subjects, adjusted for growth and body composition, and to determine the relationships of WBBMC and WBBA to bone age and hematologic parameters in children with SCD-SS.
METHODS: WBBMC, WBBA, and lean mass were measured by dual-energy x-ray absorptiometry in children who were aged 4 to 19 years. Growth, sexual development, and bone age were assessed. Gender-specific z scores for WBBMC relative to age and height were generated from control data.
RESULTS: Ninety children with SCD-SS and 198 healthy control subjects were evaluated. SCD-SS was associated with poor growth. WBBMC was significantly decreased in SCD-SS compared with control subjects, adjusted for age, height, pubertal status, and lean mass. WBBMC relative to age and WBBMC relative to height z scores were -0.95 +/- 0.99 and -0.54 +/- 0.97, respectively, and were associated with hemoglobin and hematocrit levels and history of delayed bone age.
CONCLUSIONS: Children with SCD-SS have significant deficits in WBBMC that persist despite adjustment for poor growth and decreased lean mass. These children may be at increased risk for fragility fractures and suboptimal peak bone mass.

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Year:  2005        PMID: 16199706     DOI: 10.1542/peds.2004-2582

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  17 in total

1.  Markers of bone turnover are associated with growth and development in young subjects with sickle cell anemia.

Authors:  Ellen B Fung; Deborah A Kawchak; Babette S Zemel; Alisha J Rovner; Kwaku Ohene-Frempong; Virginia A Stallings
Journal:  Pediatr Blood Cancer       Date:  2008-03       Impact factor: 3.167

2.  Malnutrition in Sickle Cell Anemia: Implications for Infection, Growth, and Maturation.

Authors:  Hyacinth I Hyacinth; Oluwatoyosi A Adekeye; Christopher S Yilgwan
Journal:  J Soc Behav Health Sci       Date:  2013-01-01

3.  Height-corrected low bone density associates with severe outcomes in sickle cell disease: SCCRIP cohort study results.

Authors:  Oyebimpe O Adesina; James G Gurney; Guolian Kang; Martha Villavicencio; Jason R Hodges; Wassim Chemaitilly; Sue C Kaste; Babette S Zemel; Jane S Hankins
Journal:  Blood Adv       Date:  2019-05-14

4.  Safety and Efficacy of High-dose Daily Vitamin D3 Supplementation in Children and Young Adults With Sickle Cell Disease.

Authors:  Kelly A Dougherty; Chiara Bertolaso; Joan I Schall; Kim Smith-Whitley; Virginia A Stallings
Journal:  J Pediatr Hematol Oncol       Date:  2015-07       Impact factor: 1.289

5.  Microarchitectural and mechanical characterization of the sickle bone.

Authors:  Mykel Green; Idowu Akinsami; Angela Lin; Shereka Banton; Samit Ghosh; Binbin Chen; Manu Platt; Ifeyinwa Osunkwo; Solomon Ofori-Acquah; Robert Guldberg; Gilda Barabino
Journal:  J Mech Behav Biomed Mater       Date:  2015-04-24

Review 6.  Beyond the definitions of the phenotypic complications of sickle cell disease: an update on management.

Authors:  Samir K Ballas; Muge R Kesen; Morton F Goldberg; Gerard A Lutty; Carlton Dampier; Ifeyinwa Osunkwo; Winfred C Wang; Carolyn Hoppe; Ward Hagar; Deepika S Darbari; Punam Malik
Journal:  ScientificWorldJournal       Date:  2012-08-01

7.  Fracture prevalence and relationship to endocrinopathy in iron overloaded patients with sickle cell disease and thalassemia.

Authors:  Ellen B Fung; Paul R Harmatz; Meredith Milet; Thomas D Coates; Alexis A Thompson; Mark Ranalli; Robert Mignaca; Charles Scher; Patricia Giardina; Shanda Robertson; Lynne Neumayr; Elliott P Vichinsky
Journal:  Bone       Date:  2008-03-15       Impact factor: 4.398

8.  Status of vitamin D in children with sickle cell disease living in Madrid, Spain.

Authors:  Carmen Garrido; Elena Cela; Cristina Beléndez; Cristina Mata; Jorge Huerta
Journal:  Eur J Pediatr       Date:  2012-09-05       Impact factor: 3.183

9.  Growth patterns in children with sickle cell anemia during puberty.

Authors:  Melissa Rhodes; Sylvie A Akohoue; Sadhna M Shankar; Irma Fleming; Angel Qi An; Chung Yu; Sari Acra; Maciej S Buchowski
Journal:  Pediatr Blood Cancer       Date:  2009-10       Impact factor: 3.167

10.  Normal muscle oxygen consumption and fatigability in sickle cell patients despite reduced microvascular oxygenation and hemorheological abnormalities.

Authors:  Xavier Waltz; Aurélien Pichon; Nathalie Lemonne; Danièle Mougenel; Marie-Laure Lalanne-Mistrih; Yann Lamarre; Vanessa Tarer; Benoit Tressières; Maryse Etienne-Julan; Marie-Dominique Hardy-Dessources; Olivier Hue; Philippe Connes
Journal:  PLoS One       Date:  2012-12-20       Impact factor: 3.240

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