Bone metabolism in oxalosis: a single-center study using new imaging techniques and biomarkers

被引:25
作者
Bacchetta, Justine [1 ,2 ,3 ,4 ]
Fargue, Sonia [1 ,3 ,4 ]
Boutroy, Stephanie [2 ,3 ]
Basmaison, Odile [1 ,4 ]
Vilayphiou, Nicolas [2 ,3 ]
Plotton, Ingrid [3 ,4 ,5 ]
Guebre-Egziabher, Fitsum [3 ,4 ,6 ]
Dohin, Bruno [7 ,8 ]
Kohler, Remi [3 ,4 ,7 ]
Cochat, Pierre [1 ,3 ,4 ]
机构
[1] Hop Femme Mere Enfant, Ctr Reference Malad Renales Rares, Serv Nephrol & Rhumatol Pediat, F-69677 Bron, France
[2] INSERM, U831, F-69008 Lyon, France
[3] Univ Lyon, F-69008 Lyon, France
[4] Hosp Civils Lyon, Ctr Hosp Univ CHU Lyon, Lyon, France
[5] Hosp Civils Lyon, Ctr Biol Est, Serv Endocrinol Mol & Malad Rares, Lyon, France
[6] Hop Edouard Herriot, Dept Nephrol, Lyon, France
[7] Hop Femme Mere Enfant, Serv Chirurg Orthoped Pediat, Lyon, France
[8] Univ St Etienne, St Etienne, France
关键词
Bone imaging; Children; FGF23; Primary hyperoxaluria; Skeletal age; PREEMPTIVE LIVER-TRANSPLANTATION; PRIMARY HYPEROXALURIA TYPE-1; OXALATE; DISEASE; CHILDREN;
D O I
10.1007/s00467-010-1453-x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The deposition of calcium oxalate crystals in the kidney and bone is a hallmark of primary hyperoxaluria type 1 (PH1). We report here an evaluation of the bone status of 12 PH1 children based on bone biomarkers [parathyroid hormone, vitamin D, fibroblast growth factor 23 (FGF23)] and radiological assessments (skeletal age, three-dimensional high-resolution peripheral quantitative computed tomography, HR-pQCT) carried out within the framework of a cross-sectional single-center study. The controls consisted of healthy and children with chronic kidney disease already enrolled in local bone and mineral metabolism studies. The mean age (+/- standard deviation) age of the patients was 99 (+/- 63) months. Six children suffered from fracture. Bone maturation was accelerated in five patients, four of whom were < 5 years. The combination of new imaging techniques and biomarkers highlighted new and unexplained features of PH1: advanced skeletal age in young PH1 patients, increased FGF23 levels and decreased total volumetric bone mineral density with bone microarchitecture alteration.
引用
收藏
页码:1081 / 1089
页数:9
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