Literature DB >> 18555484

Interpretation of biomarkers of bone metabolism in children: impact of growth velocity and body size in healthy children and chronic disease.

Shamir Tuchman1, Meena Thayu, Justine Shults, Babette S Zemel, Jon M Burnham, Mary B Leonard.   

Abstract

OBJECTIVES: To determine the effects of growth, maturation, and whole body bone mineral content (WB-BMC) accrual on biomarkers of bone formation (bone-specific alkaline phosphatase [BSAP]) and resorption (urine deoxypyridinoline/creatinine [DPD]) in healthy children and children with Crohn's disease. STUDY
DESIGN: BSAP and DPD were measured at baseline, with growth and dual energy x-ray absorptiometry (DXA) WB-BMC measured at baseline and 6 months in 202 control subjects and 110 subjects with Crohn's disease, ages 5 to 21 years. Multivariable linear regression identified determinants of biomarkers in control subjects and subjects with Crohn's disease.
RESULTS: In control subjects, BSAP and DPD were significantly and independently associated with sex, Tanner stage, WB-BMC, height velocity, and WB-BMC accrual rates; these covariates explained 77% to 80% of the variability in the bone biomarkers, respectively. Subjects with Crohn's disease had lower height-for-age (P < .001) and WB-BMC-for-height (P <.05) than control subjects. Crohn's disease was associated with lower BSAP (P < .001) and greater DPD (P < .001), independent of growth, maturation, baseline WB-BMC, and WB-BMC accrual, compared with control subjects.
CONCLUSIONS: These data illustrate the potential confounding effects of growth and WB-BMC on bone metabolism biomarkers in children. After adjustment for these effects, Crohn's disease was associated with lower biomarkers of bone formation and greater bone resorption.

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Year:  2008        PMID: 18555484      PMCID: PMC2683408          DOI: 10.1016/j.jpeds.2008.04.028

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  34 in total

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2.  Serum bone alkaline phosphatase isoenzyme levels in normal children and children with growth hormone (GH) deficiency: a potential marker for bone formation and response to GH therapy.

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3.  Growth and clinical course of children with Crohn's disease.

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Review 5.  Osteoporosis in Children with Chronic Illnesses: Diagnosis, Monitoring, and Treatment.

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8.  Improvements in Bone Density and Structure during Anti-TNF-α Therapy in Pediatric Crohn's Disease.

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9.  Effect of exclusive enteral nutrition on bone turnover in children with Crohn's disease.

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10.  Glucocorticoid effects on changes in bone mineral density and cortical structure in childhood nephrotic syndrome.

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Journal:  J Bone Miner Res       Date:  2013-03       Impact factor: 6.741

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