Literature DB >> 26856247

A genetic factor associated with low final bone mineral density in children after a long-term glucocorticoids treatment.

H-W Park1,2, S Tse1,3, W Yang4, H W Kelly5, S C Kaste6, C-H Pui7, M V Relling4, K G Tantisira1,8.   

Abstract

Treatment with glucocorticoids is associated with lower bone mineral density (BMD). We performed a genome-wide association study to analyze interactive effects between genotypes and cumulative dose of prednisone (PD) over 4.3 years of follow-up period on the final BMD Z-scores in 461 white children from the Childhood Asthma Management Program. No variants met the conventional criteria for genome-wide significance, and thus we looked for evidence of replication. The top 100-ranked single-nucleotide polymorphisms (SNPs) were then carried forward replication in 59 children with acute lymphoblastic leukemia (ALL) exposed to large fixed doses of PD as part of their chemotherapeutic regimen. Among them, rs6461639 (interaction P=1.88 × 10-5 in the CAMP population) showed a significant association with the final BMD Z-scores in the ALL population (P=0.016). The association of the ALL population was only present after correction for the anti-metabolite treatment arm (high vs low dose). We have identified a novel SNP, rs6461639, showing a significant effect on the final BMD Z-scores in two independent pediatric populations after long-term high-dose PD treatment.

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Year:  2016        PMID: 26856247      PMCID: PMC4980282          DOI: 10.1038/tpj.2015.92

Source DB:  PubMed          Journal:  Pharmacogenomics J        ISSN: 1470-269X            Impact factor:   3.550


  32 in total

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2.  Evaluation of Glucocorticoid Therapy in Asthma Children with Small Airway Obstruction Based on CT Features of Deep Learning.

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3.  Identification of a key gene module associated with glucocorticoid- induced derangement in bone mineral density in patients with asthma.

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