High prevalence of vertebral deformity in tumor-induced osteomalacia associated with impaired bone microstructure

医学 畸形 定量计算机断层扫描 骨矿物 椎骨 骨软化症 骨质疏松症 骨密度 外科 射线照相术 内科学
作者
Xiaolin Ni,Wenmin Guan,Yuanyuan Jiang,X Li,Yue Chi,Qi Pang,W Liu,Ruizhi Jiajue,O Wang,M Li,Xiaoping Xing,Huanwen Wu,Li Huo,Y Liu,Jie Jin,Xi Zhou,Wei Lv,Lian Zhou,Xia Yu,Yiyi Gong,Wei Yu,Weibo Xia
出处
期刊:Journal of Endocrinological Investigation [Springer Nature]
卷期号:46 (3): 487-500 被引量:1
标识
DOI:10.1007/s40618-022-01918-z
摘要

Patients with tumor-induced osteomalacia (TIO) often suffer from irreversible height loss due to vertebral deformity. However, the prevalence of vertebral deformity in TIO patients varies among limited studies. In addition, the distribution and type of vertebral deformity, as well as its risk factors, remain unknown. This study aimed to identify the prevalence, distribution, type and risk factors for vertebral deformity in a large cohort of TIO patients.A total of 164 TIO patients were enrolled in this retrospective study. Deformity in vertebrae T4-L4 by lateral thoracolumbar spine radiographs was evaluated according to the semiquantitative method of Genant. Bone microstructure was evaluated by trabecular bone score (TBS) and high-resolution peripheral QCT (HR-pQCT).Ninety-nine (99/164, 60.4%) patients had 517 deformed vertebrae with a bimodal pattern of distribution (T7-9 and T11-L1), and biconcave deformity was the most common type (267/517, 51.6%). Compared with patients without vertebral deformity, those with vertebral deformity had a higher male/female ratio, longer disease duration, more height loss, lower serum phosphate, higher bone turnover markers, lower TBS, lower areal bone mineral density (aBMD), lower peripheral volumetric BMD (vBMD) and worse microstructure. Lower trabecular vBMD and worse trabecular microstructure in the peripheral bone and lower spine TBS were associated with an increased risk of vertebral deformity independently of aBMD. After adjusting for the number of deformed vertebrae, we found little difference in clinical indexes among the patients with different types of vertebral deformity. However, we found significant correlations of clinical indexes with the number of deformed vertebrae and the spinal deformity index.We reported a high prevalence of vertebral deformity in the largest cohort of TIO patients and described the vertebral deformity in detail for the first time. Risk factors for vertebral deformity included male sex, long disease duration, height loss, abnormal biochemical indexes and bone impairment. Clinical manifestation, biochemical indexes and bone impairment were correlated with the number of deformed vertebrae and degree of deformity, but not the type of deformity.
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