Jimenez Macarena, Sheppard Aaron J, Jaimovich Rodrigo, Covarrubias Natalia, Jordan Diego, Quintana Juan Carlos, Contreras Oscar, Zuvic Danisa Ivanovic, Madison Anette, Saboury Babak, Collins Michael T, Florenzano Pablo
Endocrinology Department, School of Medicine, Pontificia Universidad Católica de Chile, Av. Diagonal Paraguay 262, Cuarto Piso, Santiago, Chile.
Center for Translational Research in Endocrinology, School of Medicine, CETREN-UC, Pontificia Universidad Católica de Chile, Santiago, Chile.
Calcif Tissue Int. 2025 Jan 26;116(1):34. doi: 10.1007/s00223-025-01343-3.
X-linked hypophosphatemia (XLH) is a rare metabolic disorder characterized by elevated FGF23 and chronic hypophosphatemia, leading to impaired skeletal mineralization and enthesopathies that are associated with pain, stiffness, and diminished quality of life. The natural history of enthesopathies in XLH remains poorly defined, partly due to absence of a sensitive quantitative tool for assessment and monitoring. This study investigates the utility of 18F-NaF PET/CT scans in characterizing enthesopathies in XLH subjects. In 19 adult XLH subjects, enthesopathy burden was assessed by quantifying calcified sites on CT and 18F-NaF PET uptake at 16 common tendon/ligament insertion locations. Parameters obtained were (1) number of enthesopathy sites, (2) characterization of each site as CT-positive (CT +) and/or PET-positive (PET +), (3) a semiquantitative score based on severity of affected enthesopathies (CT-score and PET-score). Biochemical and self-reported questionnaires results were correlated with 18F-NaF PET/CT parameters. 18F-NaF PET/CT detected at least one enthesopathy in all subjects, with 18F-NaF PET positivity often detected before CT (19.4% of all enthesopathies). Age negatively correlated with the number of PET + /CT- enthesopathies and positively with PET-/CT + enthesopathies. PET-score was positively associated with ALP. While PET-score showed no correlation with any applied survey, CT-score was associated with worse functionality and pain. These associations suggest a progression from an actively mineralizing lesion to a more established, inactive lesion. Overall, although 18F-NaF PET/CT is not yet indicated for routine clinical use, it is a promising research tool for evaluating enthesopathy burden in XLH, offering valuable insights into the disease's progression and potentially enabling early therapeutic assessment.
X连锁低磷血症(XLH)是一种罕见的代谢紊乱疾病,其特征为成纤维细胞生长因子23(FGF23)升高和慢性低磷血症,导致骨骼矿化受损和附着点病,这些疾病与疼痛、僵硬及生活质量下降相关。XLH中附着点病的自然病程仍不清楚,部分原因是缺乏用于评估和监测的敏感定量工具。本研究调查了18F-氟化钠正电子发射断层扫描/计算机断层扫描(18F-NaF PET/CT)在表征XLH患者附着点病方面的效用。在19名成年XLH患者中,通过量化CT上的钙化部位以及16个常见肌腱/韧带附着部位的18F-NaF PET摄取来评估附着点病负担。获得的参数包括:(1)附着点病部位数量;(2)将每个部位表征为CT阳性(CT+)和/或PET阳性(PET+);(3)基于受影响附着点病严重程度的半定量评分(CT评分和PET评分)。生化指标和自我报告问卷结果与18F-NaF PET/CT参数相关。18F-NaF PET/CT在所有受试者中均检测到至少一处附着点病,18F-NaF PET阳性往往比CT更早被检测到(在所有附着点病中占19.4%)。年龄与PET+/CT-附着点病数量呈负相关,与PET-/CT+附着点病数量呈正相关。PET评分与碱性磷酸酶(ALP)呈正相关。虽然PET评分与任何应用的调查均无相关性,但CT评分与功能较差和疼痛相关。这些关联表明从活跃矿化病变向更成熟的非活跃病变进展。总体而言,尽管18F-NaF PET/CT尚未被用于常规临床应用,但它是评估XLH附着点病负担的一种有前景的研究工具,可为疾病进展提供有价值的见解,并可能实现早期治疗评估。