Indexed on: 01 Aug '18Published on: 01 Aug '18Published in: Hepatology
Osteopenia and bone fractures (fx) are significant causes of morbidity in children with cholestatic liver disease. Dual-energy X-ray absorptiometry (DXA) analysis was performed in children with intrahepatic cholestatic diseases who were enrolled in the Longitudinal Study of Genetic Causes of Intrahepatic Cholestasis (LOGIC) in the Childhood Liver Disease Research Network (ChiLDReN). DXA was performed on participants age > 5 years (with native liver) diagnosed with bile acid synthetic disorder (BASD), alpha-1 antitrypsin deficiency (A1AT), chronic intrahepatic cholestasis (CIC), and Alagille syndrome (ALGS). Weight, height, and body mass index Z-scores were lowest in CIC and ALGS. Total bilirubin (TB) and serum bile acids (SBA) were highest in ALGS. Bone mineral density (BMD) and bone mineral content (BMC) Z-scores were significantly lower in CIC and ALGS than in BASD and A1AT (p<0.001). After anthropometric adjustment, bone deficits persisted in CIC but were no longer noted in ALGS. In ALGS, height- and weight-adjusted subtotal BMD and BMC Z-scores were negatively correlated with TB (p<0.001) and SBA (p=0.02). Mean height- and weight-adjusted subtotal BMC Z-scores were lower in ALGS participants with a history of fx. DXA measures did not correlate significantly with biliary diversion status. CIC patients had significant bone deficits that persisted after adjustment for height and weight and generally did not correlate with degree of cholestasis. In ALGS, low BMD and BMC reference Z-scores were explained by poor growth. Anthropometrically-adjusted DXA measures in ALGS correlate with markers of cholestasis and fx history. Reduced bone density in this population is multifactorial and related to growth, degree of cholestasis, fracture vulnerability, and contribution of underlying genetic etiology. This article is protected by copyright. All rights reserved. This article is protected by copyright. All rights reserved.