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氟[18F]去铁胺 PET/CT 作为成骨不全性骨纤维发育异常的标志物:从分子机制到骨骼疾病的临床应用。

[F]NaF PET/CT as a Marker for Fibrodysplasia Ossificans Progressiva: From Molecular Mechanisms to Clinical Applications in Bone Disorders.

机构信息

Amsterdam UMC location Vrije Universiteit Amsterdam, Department of Endocrinology and Metabolism, De Boelelaan 1117, Amsterdam, The Netherlands.

Amsterdam Movement Sciences, Tissue Function and Regeneration, Amsterdam, The Netherlands.

出版信息

Biomolecules. 2024 Oct 10;14(10):1276. doi: 10.3390/biom14101276.

DOI:10.3390/biom14101276
PMID:39456213
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11505869/
Abstract

Fibrodysplasia ossificans progressiva (FOP) is a rare genetic bone disorder characterized by episodic flare-ups in connective tissue, which are frequently followed by the formation of heterotopic ossification. The absence of available plasma-soluble biomarkers for flare-ups or heterotopic bone formation poses severe challenges to the monitoring of disease activity to measure or predict disease progression. Recently, 18-fluor-sodium fluoride positron emission tomography/computed tomography ([F]NaF PET/CT) was introduced as a potential marker for ossifying FOP activity. This review discusses the pharmacokinetics of [F]NaF in relation to the pathophysiology of FOP, and its use as a marker of local bone metabolism in a variety of bone-related disorders. In addition, the review specifically addresses the applicability of [F]NaF PET/CT imaging in FOP as a monitoring modality.

摘要

进行性骨化性纤维发育不良(FOP)是一种罕见的遗传性骨疾病,其特征是结缔组织间歇性发作,随后常伴有异位骨形成。由于缺乏用于发作或异位骨形成的可用血浆可溶性生物标志物,因此对疾病活动的监测存在严重挑战,无法测量或预测疾病进展。最近,18-氟-氟化钠正电子发射断层扫描/计算机断层扫描([F]NaF PET/CT) 被引入作为骨化性 FOP 活性的潜在标志物。本文综述了[F]NaF 的药代动力学与 FOP 的病理生理学之间的关系,及其在各种与骨骼相关的疾病中作为局部骨骼代谢标志物的用途。此外,该综述特别讨论了[F]NaF PET/CT 成像在 FOP 中的监测作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21c2/11505869/fef92ac1f57d/biomolecules-14-01276-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21c2/11505869/ba4a4d83488f/biomolecules-14-01276-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21c2/11505869/fef92ac1f57d/biomolecules-14-01276-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21c2/11505869/ba4a4d83488f/biomolecules-14-01276-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21c2/11505869/fef92ac1f57d/biomolecules-14-01276-g002.jpg

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本文引用的文献

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Performance of simplified methods for quantification of [F]NaF uptake in fibrodysplasia ossificans progressiva.进行性骨化性纤维发育不良中[F]氟化钠摄取定量简化方法的性能
Front Nucl Med. 2024 Jul 22;4:1406947. doi: 10.3389/fnume.2024.1406947. eCollection 2024.
2
Garetosmab in fibrodysplasia ossificans progressiva: a randomized, double-blind, placebo-controlled phase 2 trial.加雷托单抗治疗进行性骨化性纤维发育不良:一项随机、双盲、安慰剂对照的 2 期临床试验。
Nat Med. 2023 Oct;29(10):2615-2624. doi: 10.1038/s41591-023-02561-8. Epub 2023 Sep 28.
3
The Fibrodysplasia Ossificans Progressiva Physical Function Questionnaire (FOP-PFQ): A patient-reported, disease-specific measure.
纤维发育不良性骨化性肌炎生理功能问卷(FOP-PFQ):一种患者报告的、针对特定疾病的测量方法。
Bone. 2023 Mar;168:116642. doi: 10.1016/j.bone.2022.116642. Epub 2022 Dec 13.
4
Shortened duration whole body F-FDG PET Patlak imaging on the Biograph Vision Quadra PET/CT using a population-averaged input function.在Biograph Vision Quadra PET/CT上使用群体平均输入函数进行缩短时长的全身F-FDG PET Patlak成像。
EJNMMI Phys. 2022 Oct 29;9(1):74. doi: 10.1186/s40658-022-00504-9.
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Protocol paper: a multi-center, double-blinded, randomized, 6-month, placebo-controlled study followed by 12-month open label extension to evaluate the safety and efficacy of Saracatinib in Fibrodysplasia Ossificans Progressiva (STOPFOP).方案论文:一项多中心、双盲、随机、6 个月、安慰剂对照研究,随后进行 12 个月的开放标签扩展,以评估 Saracatinib 在纤维发育不良性骨化进展症(STOPFOP)中的安全性和疗效。
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