Adipokine dysregulation as an underlying pathology for diffuse ectopic ossification of spinal posterior longitudinal ligament in patients with obesity.

IF 4.9 1区 医学 Q1 CLINICAL NEUROLOGY Spine Journal Pub Date : 2024-09-26 DOI:10.1016/j.spinee.2024.09.023
Masahiko Takahata, Yoshinao Koike, Tsutomu Endo, Shiro Ikegawa, Shiro Imagama, Satoshi Kato, Masahiro Kanayama, Kazuyoshi Kobayashi, Takashi Kaito, Hiroaki Sakai, Yoshiharu Kawaguchi, Itaru Oda, Chikashi Terao, Tomoya Kanto, Hiroshi Taneichi, Norimasa Iwasaki
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Abstract

Background context: Growing evidence suggests that obesity is implicated in the progression of heterotopic ossification of the posterior longitudinal ligament of the spine (OPLL), a major cause of myelopathy in Asians. However, it remains unclear whether dysregulation of adipokine production due to fat accumulation contributes to OPLL progression.

Purpose: To determine whether adipose-derived biochemical signals are associated with OPLL development or severity.

Study design/setting: A nationwide, multicenter, case-control study.

Patient sample: Patients with symptomatic thoracic OPLL (T-OPLL) who received treatment between June 2017 and March 2021 and 111 controls without OPLL.

Outcome measures: OPLL severity index based on whole-spine computed tomography.

Methods: Serum concentrations of adipokines, including leptin (Lep), tumor necrosis factor α (TNFα), and adiponectin (Adpn), as well as the Adpn/Lep ratio-an indicator of adipokine production dysregulation-were compared between the multiple-region OPLL and the single-region OPLL groups. Regression analysis was performed to examine the correlation between adipokine concentrations and OPLL severity index, which was calculated using whole-spine computed tomography images of 77 patients with T-OPLL within 3 years of onset. Using propensity score matching, the adipokine profiles of 59 patients with T-OPLL were compared with those of 59 non-OPLL controls.

Results: Patients with multiple-region OPLL exhibited a higher body mass index (BMI), lower serum Adpn/Lep ratio, and higher serum concentration of osteocalcin (OCN) than those with single-region OPLL. The OPLL severity index exhibited a weak positive correlation with BMI and serum Lep levels and a weak negative correlation with the Adpn/Lep ratio. Serum TNFα and OCN concentrations were significantly higher in patients with T-OPLL than in controls with similar age, sex, and BMI.

Conclusions: Patients with diffuse OPLL over the entire spine are often metabolically obese with low Adpn/Lep ratios. In patients with OPLL, TNFα and OCN serum concentrations were essentially elevated regardless of obesity, suggesting a potential association with OPLL development. Considering the absence of therapeutic drugs for OPLL, the findings presented herein offer valuable insights that can aid in identifying therapeutic targets and formulating strategies to impede its progression.

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肥胖症患者脊柱后纵韧带弥漫性异位骨化的潜在病理机制是脂肪因子失调。
背景情况:越来越多的证据表明,肥胖与脊柱后纵韧带异位骨化(OPLL)的进展有关,OPLL是亚洲人脊髓病的一个主要原因。目的:确定脂肪衍生的生化信号是否与 OPLL 的发展或严重程度有关:患者样本:2017年6月至2021年3月期间接受治疗的有症状胸部OPLL(T-OPLL)患者和111名无OPLL的对照组:基于全脊柱计算机断层扫描的OPLL严重程度指数:比较多区域OPLL组和单区域OPLL组血清中脂肪因子的浓度,包括瘦素(Lep)、肿瘤坏死因子α(TNFα)和脂肪连蛋白(Adpn),以及Adpn/Lep比值(脂肪因子分泌失调的指标)。对 77 名发病 3 年内的 T-OPLL 患者的全脊柱计算机断层扫描图像计算出的 OPLL 严重程度指数进行了回归分析,以检验脂肪因子浓度与 OPLL 严重程度指数之间的相关性。采用倾向得分匹配法,将 59 名 T-OPLL 患者的脂肪因子谱与 59 名非 OPLL 对照组的脂肪因子谱进行了比较:结果:与单区域 OPLL 患者相比,多区域 OPLL 患者的体重指数(BMI)较高,血清 Adpn/Lep 比率较低,血清骨钙素(OCN)浓度较高。OPLL 严重程度指数与 BMI 和血清 Lep 水平呈弱正相关,与 Adpn/Lep 比率呈弱负相关。T-OPLL患者的血清TNFα和OCN浓度明显高于年龄、性别和体重指数相似的对照组:结论:整个脊柱弥漫性OPLL患者通常代谢肥胖,Adpn/Lep比率较低。在 OPLL 患者中,无论肥胖与否,TNFα 和 OCN 的血清浓度基本上都会升高,这表明它们与 OPLL 的发展可能有关。考虑到目前还没有治疗 OPLL 的药物,本文的研究结果提供了有价值的见解,有助于确定治疗目标和制定策略以阻止其发展。
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
Spine Journal
Spine Journal 医学-临床神经学
CiteScore
8.20
自引率
6.70%
发文量
680
审稿时长
13.1 weeks
期刊介绍: The Spine Journal, the official journal of the North American Spine Society, is an international and multidisciplinary journal that publishes original, peer-reviewed articles on research and treatment related to the spine and spine care, including basic science and clinical investigations. It is a condition of publication that manuscripts submitted to The Spine Journal have not been published, and will not be simultaneously submitted or published elsewhere. The Spine Journal also publishes major reviews of specific topics by acknowledged authorities, technical notes, teaching editorials, and other special features, Letters to the Editor-in-Chief are encouraged.
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