Division of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, University of California San Diego School of Medicine, La Jolla, CA.
Division of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, University of California San Diego School of Medicine, La Jolla, CA; Department of Gastroenterology, Rady Children's Hospital, San Diego, CA.
J Pediatr. 2021 Jun;233:105-111.e3. doi: 10.1016/j.jpeds.2021.01.064. Epub 2021 Feb 3.
To evaluate the relationship between hepatic steatosis and bone mineral density (BMD) in children. In addition, to assess 25-hydroxyvitamin D levels in the relationship between hepatic steatosis and BMD.
A community-based sample of 235 children was assessed for hepatic steatosis, BMD, and serum 25-hydroxyvitamin D. Hepatic steatosis was measured by liver magnetic resonance imaging proton density fat fraction (MRI-PDFF). BMD was measured by whole-body dual-energy x-ray absorptiometry.
The mean age of the study population was 12.5 years (SD 2.5 years). Liver MRI-PDFF ranged from 1.1% to 40.1% with a mean of 9.3% (SD 8.5%). Across this broad spectrum of hepatic fat content, there was a significant negative relationship between liver MRI-PDFF and BMD z score (R = -0.421, P < .001). Across the states of sufficiency, insufficiency, and deficiency, there was a significant negative association between 25-hydroxyvitamin D and liver MRI-PDFF (P < .05); however, there was no significant association between vitamin D status and BMD z score (P = .94). Finally, children with clinically low BMD z scores were found to have higher alanine aminotransferase (P < .05) and gamma-glutamyl transferase (P < .05) levels compared with children with normal BMD z scores.
Across the full range of liver MRI-PDFF, there was a strong negative relationship between hepatic steatosis and BMD z score. Given the prevalence of nonalcoholic fatty liver disease and the critical importance of childhood bone mineralization in protecting against osteoporosis, clinicians should prioritize supporting bone development in children with nonalcoholic fatty liver disease.
评估儿童肝脂肪变性与骨密度(BMD)之间的关系。此外,评估 25-羟维生素 D 水平在肝脂肪变性与 BMD 之间的关系。
对 235 名儿童进行了基于社区的样本评估,评估内容包括肝脂肪变性、BMD 和血清 25-羟维生素 D。肝脂肪变性通过肝脏磁共振成像质子密度脂肪分数(MRI-PDFF)测量。BMD 通过全身双能 X 射线吸收法测量。
研究人群的平均年龄为 12.5 岁(SD 2.5 岁)。肝脏 MRI-PDFF 范围为 1.1%至 40.1%,平均值为 9.3%(SD 8.5%)。在这个广泛的肝脂肪含量范围内,肝脏 MRI-PDFF 与 BMD z 评分之间存在显著的负相关关系(R=-0.421,P<0.001)。在充足、不足和缺乏的状态下,25-羟维生素 D 与肝脏 MRI-PDFF 之间存在显著的负相关关系(P<0.05);然而,维生素 D 状态与 BMD z 评分之间没有显著的关联(P=0.94)。最后,与 BMD z 评分正常的儿童相比,临床 BMD z 评分较低的儿童丙氨酸氨基转移酶(P<0.05)和γ-谷氨酰转移酶(P<0.05)水平较高。
在整个肝脏 MRI-PDFF 范围内,肝脂肪变性与 BMD z 评分之间存在强烈的负相关关系。鉴于非酒精性脂肪性肝病的流行和儿童骨矿物质化对预防骨质疏松症的至关重要性,临床医生应优先支持非酒精性脂肪性肝病儿童的骨骼发育。