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Bone Abstracts (2019) 7 P63 | DOI: 10.1530/boneabs.7.P63

ICCBH2019 Poster Presentations (1) (226 abstracts)

Bone geometry and microarchitecture deficits in children with Alagille syndrome

Joseph Kindler 1 , Ellen Mitchell 2 , David Piccoli 1 , Adda Grimberg 1 , Mary Leonard 3 , Kathleen Loomes 1 & Babette Zemel 1

1The Children’s Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA; 2St Christopher’s Hospital for Children and Department of Pediatrics at Drexel University School of Medicine, Philadelphia, PA, USA; 3Stanford School of Medicine, Palo Alto, CA, USA.

Objectives: Alagille syndrome (ALGS) is an autosomal dominant disorder attributed to mutations in the Notch signaling pathway. Children with ALGS are at increased risk for fragility fracture, but the etiology of this disposition is unknown. Our objective was to characterize bone mass, geometry, and microarchitecture in children with ALGS.

Methods: This was a cross-sectional study of 10 children (9 females) ages 8-18 years, with a clinical diagnosis of ALGS. Bone density was assessed via DXA. Tibia trabecular and cortical bone was assessed via pQCT (Stratec XCT 2000) at the distal 3% and 38% sites, respectively. Ultradistal tibia bone microarchitecture was assessed via HR-pQCT (Scanco XtremeCT II). Z-scores were calculated for DXA and pQCT measures. Reference data for the Xtreme CT II HR-pQCT scanner are not yet available, so these measures were descriptively compared to a sample of healthy children ages 5–20 years (n=247). Anthropometrics and labs were also collected.

Results: Based on one-sample t-tests, mean Z-scores for height and weight (both P<0.05), but not DXA bone measures, were negative and significantly different from zero. For pQCT bone measures, Z-scores for total bone mineral content (BMC) at the distal 3% site and cortical BMC, cortical area, and cortical thickness at the distal 38% site were negative and different from zero (all P<0.05). Compared to healthy children, those with ALGS generally had lower trabecular number, greater trabecular separation, and lower bone volume to total volume fraction despite having greater trabecular thickness (measured via HR-pQCT). Overall, bilirubin and bile acids, which are markers of hepatic cholestasis, were associated with poorer bone health. For example, bilirubin was associated with lower trabecular number (Spearman’s rho=−0.86, P=0.014), greater trabecular separation (Spearman’s rho=0.82, P=0.023), and greater cortical pore diameter (Spearman’s rho=0.99, P<0.001) measured via HR-pQCT, and bile acids were associated with lower cortical area measured via pQCT (Spearman’s rho=−0.78, P=0.041) and lower serum insulin-like growth factor 1 (Spearman’s rho=−0.86, P=0.002).

Conclusions: Further investigation is needed to understand the factors contributing to ALGS-related cortical and trabecular bone inadequacies, and the manner in which these deficits contribute to increased fracture risk.

Disclosure: The authors declared no competing interests.

Volume 7

9th International Conference on Children's Bone Health


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