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. 2019 Jan;69(1):245-257.
doi: 10.1002/hep.30196. Epub 2018 Dec 27.

Bone Density in Children With Chronic Liver Disease Correlates With Growth and Cholestasis

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Bone Density in Children With Chronic Liver Disease Correlates With Growth and Cholestasis

Kathleen M Loomes et al. Hepatology. 2019 Jan.

Abstract

Osteopenia and bone fractures 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 in the Childhood Liver Disease Research Network. DXA was performed on participants aged >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-adjusted and weight-adjusted subtotal BMD and BMC Z scores were negatively correlated with TB (P < 0.001) and SBA (P = 0.02). Mean height-adjusted and weight-adjusted subtotal BMC Z scores were lower in ALGS participants with a history of bone fractures. DXA measures did not correlate significantly with biliary diversion status. Conclusion: 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 bone fracture history. Reduced bone density in this population is multifactorial and related to growth, degree of cholestasis, fracture vulnerability, and contribution of underlying genetic etiology.

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Figures

Figure 1:
Figure 1:. Comparison between DXA Reference and Height- and Weight-Adjusted Z-scores for Total Body minus Head Measurements (Figure 1.1 BMD; Figure 1.2 BMC) for ALGS and CIC disease groups.
The reference line indicates equality between the reference and adjusted Z-scores. Points above the line indicate observations where the Z-score adjusted for height and weight is higher than the reference Z-score. Points below the line indicate observations where the adjusted Z-score is lower than the reference Z-score. [Footnote] *Non-Winsorized BMD values presented Abbreviations: BMC, bone mineral content; BMD, bone mineral density; DXA, dual-energy X-ray absorptiometry.
Figure 1:
Figure 1:. Comparison between DXA Reference and Height- and Weight-Adjusted Z-scores for Total Body minus Head Measurements (Figure 1.1 BMD; Figure 1.2 BMC) for ALGS and CIC disease groups.
The reference line indicates equality between the reference and adjusted Z-scores. Points above the line indicate observations where the Z-score adjusted for height and weight is higher than the reference Z-score. Points below the line indicate observations where the adjusted Z-score is lower than the reference Z-score. [Footnote] *Non-Winsorized BMD values presented Abbreviations: BMC, bone mineral content; BMD, bone mineral density; DXA, dual-energy X-ray absorptiometry.

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