Literature DB >> 17243130

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

Ellen B Fung1, Deborah A Kawchak, Babette S Zemel, Alisha J Rovner, Kwaku Ohene-Frempong, Virginia A Stallings.   

Abstract

Children with sickle cell anemia (SCA) have low bone mass though bone turnover has not been well described. In this study, growth and pubertal development were assessed twice, 1 year apart, in 80 young subjects with type-SS SCA, while whole body bone mineral content (BMC) and density where measured in a subset (n = 46). Markers of bone turnover were measured at the second visit. Bone formation (alkaline phosphatase) was elevated, whereas bone resorption (deoxypyridinoline) was decreased compared to published data in healthy children. Markers of bone turnover correlated with growth velocity and pubertal development but not with changes in bone mass. (c) 2007 Wiley-Liss, Inc.

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Year:  2008        PMID： 17243130      PMCID： PMC2561913          DOI： 10.1002/pbc.21147

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN： 1545-5009            Impact factor:   3.167


  18 in total

1.  Total and resting energy expenditure in children with sickle cell disease.

Authors:  E M Barden; B S Zemel; D A Kawchak; M I Goran; K Ohene-Frempong; V A Stallings
Journal:  J Pediatr       Date:  2000-01       Impact factor: 4.406

2.  Biochemical markers of bone formation in Thai children and adolescents.

Authors:  La-or Chailurkit; Umaporn Suthutvoravut; Pat Mahachoklertwattana; Somsri Charoenkiatkul; Rajata Rajatanavin
Journal:  Endocr Res       Date:  2005       Impact factor: 1.720

3.  Collagen markers deoxypyridinoline and hydroxylysine glycosides: pediatric reference data and use for growth prediction in growth hormone-deficient children.

Authors:  Frank Rauch; Mareile Georg; Angelika Stabrey; Christina Neu; Werner F Blum; Thomas Remer; Friedrich Manz; Eckhard Schoenau
Journal:  Clin Chem       Date:  2002-02       Impact factor: 8.327

4.  Biochemical markers of bone turnover and the volume and the density of bone in children at different stages of sexual development.

Authors:  S Mora; P Pitukcheewanont; F R Kaufman; J C Nelson; V Gilsanz
Journal:  J Bone Miner Res       Date:  1999-10       Impact factor: 6.741

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

Authors:  Anne M Buison; Deborah A Kawchak; Joan I Schall; Kwaku Ohene-Frempong; Virginia A Stallings; Mary B Leonard; Babette S Zemel
Journal:  Pediatrics       Date:  2005-10       Impact factor: 7.124

6.  Bone mineral density of the lumbar spine and proximal femur is decreased in children with sickle cell anemia.

Authors:  M R Brinker; K A Thomas; S J Meyers; T Texada; J R Humbert; S D Cook; R Gitter
Journal:  Am J Orthop (Belle Mead NJ)       Date:  1998-01

7.  Bone-specific alkaline phosphatase protein, total alkaline phosphatase activity and lactate dehydrogenase in sera of patients with sickle cell disease.

Authors:  D M Bolarin
Journal:  Haematologia (Budap)       Date:  2001

8.  Increased bone turnover is associated with protein and energy metabolism in adolescents with sickle cell anemia.

Authors:  M S Buchowski; F A de la Fuente; P J Flakoll; K Y Chen; E A Turner
Journal:  Am J Physiol Endocrinol Metab       Date:  2001-03       Impact factor: 4.310

9.  Assessment of the bone status of Nigerian children and adolescents with sickle cell disease using calcaneal ultrasound and serum markers of bone metabolism.

Authors:  D J VanderJagt; C Bonnett; S N Okolo; R H Glew
Journal:  Calcif Tissue Int       Date:  2002-07-24       Impact factor: 4.333

10.  Bone disorders in sickle-cell disease.

Authors:  O Onuba
Journal:  Int Orthop       Date:  1993-12       Impact factor: 3.075
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  9 in total

1.  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

2.  Predictors of osteoclast activity in patients with sickle cell disease.

Authors:  Mehdi Nouraie; Kevin Cheng; Xiaomei Niu; Evadne Moore-King; Margaret F Fadojutimi-Akinsi; Caterina P Minniti; Craig Sable; Sohail Rana; Niti Dham; Andrew Campbell; Gregory Ensing; Gregory J Kato; Mark T Gladwin; Oswaldo L Castro; Victor R Gordeuk
Journal:  Haematologica       Date:  2011-05-05       Impact factor: 9.941

3.  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 4.  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

5.  Zinc supplementation improves bone density in patients with thalassemia: a double-blind, randomized, placebo-controlled trial.

Authors:  Ellen B Fung; Janet L Kwiatkowski; James N Huang; Ginny Gildengorin; Janet C King; Elliott P Vichinsky
Journal:  Am J Clin Nutr       Date:  2013-08-14       Impact factor: 7.045

6.  The association of bone mineral density and parathyroid hormone with serum magnesium in adult patients with sickle-cell anaemia.

Authors:  Mohamed F Elshal; Amna E Bernawi; Maryam A Al-Ghamdy; Jalaluddin A Jalal
Journal:  Arch Med Sci       Date:  2012-05-09       Impact factor: 3.318

7.  Frequency and risk factors of endocrine complications in Turkish children and adolescents with sickle cell anemia.

Authors:  Samim Ozen; Selma Unal; Neslihan Erçetin; Bahar Taşdelen
Journal:  Turk J Haematol       Date:  2013-03-05       Impact factor: 1.831

8.  SOCIOECONOMIC AND NUTRITIONAL CHARACTERISTICS OF CHILDREN AND ADOLESCENTS WITH SICKLE CELL ANEMIA: A SYSTEMATIC REVIEW.

Authors:  Amanda Cristina da Silva de Jesus; Tulio Konstantyner; Ianna Karolina Véras Lôbo; Josefina Aparecida Pellegrini Braga
Journal:  Rev Paul Pediatr       Date:  2018 Oct-Dec

Review 9.  Mechanisms of Bone Impairment in Sickle Bone Disease.

Authors:  Paola Giordano; Flavia Urbano; Giuseppe Lassandro; Maria Felicia Faienza
Journal:  Int J Environ Res Public Health       Date:  2021-02-13       Impact factor: 3.390
  9 in total

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