Bone microarchitecture evaluated by HR-pQCT in Chinese adolescent and pediatric patients with X-linked hypophosphatemia.

IF 5 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Clinical Endocrinology & Metabolism Pub Date : 2024-11-14 DOI:10.1210/clinem/dgae782
Yushuo Wu, Yisen Yang, Xiaosen Ma, Qianqian Pang, Yue Chi, Ruizhi Jiajue, Wei Liu, Yan Jiang, Ou Wang, Mei Li, Xiaoping Xing, Lijia Cui, Weibo Xia
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Abstract

Context: X-linked hypophosphatemia (XLH) is the most common form of heritable hypophosphatemic rickets. Previous studies have found deteriorated bone microarchitecture in the XLH adults. Detailed studies on the skeletal microarchitecture of XLH adolescent and pediatric patients are still lacking.

Objective: This study aimed to evaluate bone geometry, density, microarchitecture, stiffness in XLH adolescent and pediatric patients by using high-resolution peripheral quantitative computed tomography (HR-pQCT).Method: This study utilized HR-pQCT to assess bone geometry, density, microarchitecture, and stiffness in 106 Chinese adolescent and pediatric patients with XLH.

Result: Compared with the sex- and age-matched controls, XLH patients had significantly higher trabecular area (Tb.Ar), lower total volumetric bone mineral density (Tot.vBMD), lower cortical volumetric BMD (Ct.vBMD), and lower stiffness at both the distal radius and the tibia after adjusting for height and weight. Alkaline phosphatase Z score (ALP-Z), a marker to reflect the disease activity of rickets, was negatively correlated with Ct.vBMD and cortical thickness (Ct.Th) at the distal radius, and Ct.vBMD at the distal tibia, and positively correlated with cortical porosity (Ct.Po) at the distal tibia. We developed an online calculator to estimate Tb.Ar, Ct.vBMD, and stiffness of the distal tibia of XLH adolescent and pediatric patients based on clinical general characteristic and biochemical indicators.

Conclusion: The bone microarchitecture of XLH adolescent and pediatric patients was deteriorated, and ALP-Z was negatively correlated with the skeletal quality of XLH adolescent and pediatric patients, especially in the cortical bone. HR-pQCT parameters can be estimated using clinical characteristics and biochemical indicators, which may assist physicians to monitor the disease progression in areas without HR-pQCT access.

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用 HR-pQCT 评估中国 X 连锁低磷血症青少年和儿童患者的骨微结构。
背景:X 连锁低磷血症(XLH)是遗传性低磷血症佝偻病中最常见的一种。以往的研究发现,XLH 成年人的骨骼微结构恶化。目前仍缺乏对XLH青少年和儿童患者骨骼微结构的详细研究:本研究旨在利用高分辨率外周定量计算机断层扫描(HR-pQCT)评估 XLH 青少年和儿童患者的骨骼几何形状、密度、微结构和硬度:该研究利用高分辨率外周定量计算机断层扫描(HR-pQCT)评估了106名中国XLH青少年和儿童患者的骨几何形状、密度、微结构和硬度:结果:与性别和年龄匹配的对照组相比,XLH患者的骨小梁面积(Tb.Ar)明显增大,总体积骨矿物质密度(Tot.vBMD)降低,皮质体积骨矿物质密度(Ct.vBMD)降低,调整身高和体重后,桡骨远端和胫骨的硬度降低。碱性磷酸酶 Z 评分(ALP-Z)是反映佝偻病疾病活动性的指标,它与桡骨远端皮质容积 BMD 和皮质厚度(Ct.Th)以及胫骨远端皮质容积 BMD 呈负相关,而与胫骨远端皮质孔隙率(Ct.Po)呈正相关。我们开发了一种在线计算器,可根据临床一般特征和生化指标估算XLH青少年和儿童患者的Tb.Ar、Ct.vBMD和胫骨远端硬度:XLH青少年和儿童患者的骨微结构恶化,ALP-Z与XLH青少年和儿童患者的骨骼质量呈负相关,尤其是皮质骨。HR-pQCT参数可通过临床特征和生化指标进行估算,这可能有助于医生在无法获得HR-pQCT的地区监测疾病进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical Endocrinology & Metabolism
Journal of Clinical Endocrinology & Metabolism 医学-内分泌学与代谢
CiteScore
11.40
自引率
5.20%
发文量
673
审稿时长
1 months
期刊介绍: The Journal of Clinical Endocrinology & Metabolism is the world"s leading peer-reviewed journal for endocrine clinical research and cutting edge clinical practice reviews. Each issue provides the latest in-depth coverage of new developments enhancing our understanding, diagnosis and treatment of endocrine and metabolic disorders. Regular features of special interest to endocrine consultants include clinical trials, clinical reviews, clinical practice guidelines, case seminars, and controversies in clinical endocrinology, as well as original reports of the most important advances in patient-oriented endocrine and metabolic research. According to the latest Thomson Reuters Journal Citation Report, JCE&M articles were cited 64,185 times in 2008.
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