Changes in bone density and microarchitecture in adolescents undergoing a first kidney transplantation: a prospective study.

IF 3 3区 医学 Q1 PEDIATRICS
European Journal of Pediatrics Pub Date : 2024-12-01 Epub Date: 2024-10-09 DOI:10.1007/s00431-024-05777-z
Aurélie De Mul, Anne-Laure Sellier Leclerc, Tiphanie Ginhoux, Charlène Levi, Cyrille Confavreux, Manon Aurelle, Aurélie Portefaix, Justine Bacchetta
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引用次数: 0

Abstract

Purpose: Mineral bone disorder associated with chronic kidney disease (CKD-MBD) frequently persists after kidney transplantation (KTx), being due to pre-existing CKD-MBD, immunosuppressive therapies, and post-KTx hypophosphatemia. This study aimed to evaluate bone biomarkers and microarchitecture using high resolution peripheral quantitative computed tomography (HR-pQCT) at the time of KTx and 6 months thereafter and to compare these results with those of matched healthy controls (HC).

Methods: This study presented the single-center subgroup of patients aged between 10 and 18 years included in the prospective "Bone Microarchitecture in the Transplant Patient" study (TRANSOS-NCT02729142). Patients undergoing a first KTx were matched (1:2) with HC from the "Vitamin D, Bones, Nutritional and Cardiovascular Status" cohort (VITADOS) on sex, pubertal stage, and age.

Results: At a median (interquartile range, IQR) age of 15 [13; 16] years, 19 patients (6 girls, 7 pre-emptive KTx, 7 steroid-sparing immunosuppressive strategies) underwent a first KTx, with a median [IQR] parathyroid hormone level of 1.9 [1.4; 2.9] the upper limit of normal (ULN). Higher total and trabecular bone densities, along with superior trabecular microarchitecture, were observed at KTx compared to HC. Six months post-KTx, patients had significantly impaired trabecular parameters at the radius, while results were not significantly different at the weight-bearing tibia, neither cortical parameters at both sites. Six months post-KTx, 6 (32%) patients still present with metabolic acidosis, 10 (53%) persistent hyperparathyroidism (always < 2 ULN), and 5 (26%) elevated FGF23 levels; 11 (58%) received phosphate supplementation.

Conclusions: Bone density and microarchitecture at the time of KTx were superior compared to HC, but radial trabecular bone microarchitecture impairment observed 6 months post-KTx may reflect subtle albeit present post-KTx CKD-MBD. What is Known? • Mineral bone disorder associated with chronic kidney disease (CKD-MBD) frequently persists after kidney transplantation (KTx) and is associated with morbidity. However, biochemical parameters and dual X-ray absorptiometry (DXA) are poor predictors of the underlying bone disease. What is new? • The present study on 19 adolescent KTx recipients with adequate CKD-MBD control at the time of KTx reveals no significant bone disease compared to matched healthy controls. Microarchitecture impairment observes 6 months post-KTx may reflect subtle, albeit present, post-KTx CKD-MBD.

首次接受肾移植的青少年骨密度和微结构的变化:一项前瞻性研究。
目的:与慢性肾脏病(CKD-MBD)相关的矿物质骨紊乱经常在肾移植(KTx)后持续存在,其原因包括肾移植前已存在的CKD-MBD、免疫抑制疗法和肾移植后低磷血症。本研究旨在使用高分辨率外周定量计算机断层扫描(HR-pQCT)评估 KTx 时及其后 6 个月的骨生物标志物和微结构,并将这些结果与匹配的健康对照组(HC)的结果进行比较:本研究介绍了前瞻性 "移植患者骨微结构 "研究(TRANSOS-NCT02729142)中的单中心亚组 10 至 18 岁患者的情况。首次接受 KTx 的患者与 "维生素 D、骨骼、营养和心血管状况 "队列(VITADOS)中的 HC 在性别、青春期阶段和年龄上进行了配对(1:2):中位数(四分位数间距,IQR)年龄为15 [13; 16]岁的19名患者(6名女孩,7名接受了先期KTx,7名采取了类固醇保护免疫抑制策略)接受了首次KTx,甲状旁腺激素水平的中位数[IQR]为正常值上限(ULN)的1.9 [1.4; 2.9]。与 HC 相比,KTx 可观察到更高的总骨密度和骨小梁密度,以及更优越的骨小梁微结构。KTx 术后 6 个月,患者桡骨的骨小梁参数明显受损,而负重胫骨的骨小梁参数和两个部位的皮质参数没有明显差异。KTx 术后 6 个月,仍有 6 名(32%)患者出现代谢性酸中毒,10 名(53%)患者出现持续性甲状旁腺功能亢进(总结论):KTx 时的骨密度和微结构优于 HC,但 KTx 术后 6 个月观察到的桡骨小梁骨微结构损伤可能反映了 KTx 术后 CKD-MBD 虽然存在,但却很微妙。已知信息- 与慢性肾脏病相关的矿物质骨骼紊乱(CKD-MBD)经常在肾移植(KTx)后持续存在,并与发病率相关。然而,生化指标和双 X 射线吸收测定法(DXA)对潜在骨病的预测效果不佳。有什么新发现?- 本研究对 19 名青少年 KTx 受者进行了研究,与匹配的健康对照组相比,他们在接受 KTx 时已充分控制了慢性肾功能衰竭和骨髓增生性疾病,没有发现明显的骨病。KTx 术后 6 个月观察到的微结构损伤可能反映了 KTx 术后 CKD-MBD 的微妙变化,尽管这种变化是存在的。
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来源期刊
CiteScore
5.90
自引率
2.80%
发文量
367
审稿时长
3-6 weeks
期刊介绍: The European Journal of Pediatrics (EJPE) is a leading peer-reviewed medical journal which covers the entire field of pediatrics. The editors encourage authors to submit original articles, reviews, short communications, and correspondence on all relevant themes and topics. EJPE is particularly committed to the publication of articles on important new clinical research that will have an immediate impact on clinical pediatric practice. The editorial office very much welcomes ideas for publications, whether individual articles or article series, that fit this goal and is always willing to address inquiries from authors regarding potential submissions. Invited review articles on clinical pediatrics that provide comprehensive coverage of a subject of importance are also regularly commissioned. The short publication time reflects both the commitment of the editors and publishers and their passion for new developments in the field of pediatrics. EJPE is active on social media (@EurJPediatrics) and we invite you to participate. EJPE is the official journal of the European Academy of Paediatrics (EAP) and publishes guidelines and statements in cooperation with the EAP.
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