早期复杂性区域疼痛综合征的骨转换标志物和 Wnt 信号调节剂。一项预先指定的观察性研究。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-09-01 Epub Date: 2024-07-01 DOI:10.1007/s00223-024-01251-y
Massimo Varenna, Francesco Orsini, Raffaele Di Taranto, Francesca Zucchi, Giovanni Adami, Davide Gatti, Chiara Crotti
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引用次数: 0

摘要

探讨血清中某些骨转换标志物的水平以及Wnt信号转导在CRPS-1中的参与。Query ID="Q1" Text="请检查并确认对文章标题的编辑是否正确"。我们对治疗前招募的早期CRPS-1患者进行了一项观察性研究。在评估临床指标的同时还进行了生化评估。硬骨蛋白、DKK1、CTX-I 和 P1NP 的值与性别年龄匹配的健康对照组(HCs)进行了比较。我们共招募了 34 名确诊为 CRPS-1 的患者(平均年龄为 59.3 ± 10.6 岁,男性/女性各 10/24),中位病程 = 2 周(IQR 1-5);中位 VAS 评分 = 76(IQR 68-80)。足部定位的频率略高于手部定位(18/16)。CTX-I(0.3 ± 0.1 ng/ml vs 0.3 ± 0.1,P = 0.140)在CRPS-1患者和HC之间无统计学差异,而P1NP的平均血清值在CRPS-1患者中明显高于HC(70.0 ± 38.8 ng/ml vs 50.1 ± 13.6,P = 0.005)。CRPS-1 患者的硬骨蛋白和 DKK1 平均水平低于 HCs(硬骨蛋白 28.4 ± 10.8 pmol/l vs 34.1 ± 11.6,p = 0.004;DKK1 12.9 ± 10.8 pmol/l vs 24.1 ± 11.9,p = 0.001)。在骨折诱发的 CRPS-1 亚组中,所有生化评估结果均无明显统计学差异。在疾病定位、病程长短、是否存在痛觉减退、异动症、渗出运动改变以及轻度或中度/重度肿胀方面,均未发现有统计学意义的差异。硬骨素、DKK1水平、基线VAS评分或麦吉尔疼痛问卷评分之间无明显相关性。早期 CRPS-1 的骨骼受累似乎并不依赖于破骨细胞活性的增加。相反,骨形成的血清标志物却增加了。Sclerostin和DKK1的数值均有所下降,这可能表明骨细胞功能普遍丧失:论文编号:2014-001156-28。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bone Turnover Markers and Wnt Signaling Modulators in Early Complex Regional Pain Syndrome. A Pre-specified Observational Study.

Bone Turnover Markers and Wnt Signaling Modulators in Early Complex Regional Pain Syndrome. A Pre-specified Observational Study.

To explore serum levels of some bone turnover markers and the involvement of the Wnt signaling in CRPS-1. Query ID="Q1" Text="Please check and confirm whether the edit made to the article title is in order." We conducted an observational study on patients with early CRPS-1 recruited before any treatment. Clinical measures were assessed together with biochemical evaluation. Values of sclerostin, DKK1, CTX-I, and P1NP were compared with sex-age-matched healthy controls (HCs). We enrolled 34 patients diagnosed with CRPS-1 (mean age 59.3 ± 10.6 years, Male/Female 10/24), median disease duration = 2 weeks (IQR 1-5); median VAS score = 76 (IQR 68-80). Foot localization was slightly more frequent than hand localization (18/16). No statistically significant difference was found between CRPS-1 patients and HCs for CTX-I (0.3 ± 0.1 ng/ml vs 0.3 ± 0.1, p = 0.140), while mean serum values of P1NP were significantly higher in CRPS-1 patients compared to HCs (70.0 ± 38.8 ng/ml vs 50.1 ± 13.6, p = 0.005). Mean levels of sclerostin and DKK1 were lower in CRPS-1 patients vs HCs (sclerostin 28.4 ± 10.8 pmol/l vs 34.1 ± 11.6, p = 0.004; DKK1 12.9 ± 10.8 pmol/l vs 24.1 ± 11.9, p = 0.001). No statistically significant difference was found for all biochemical assessments in a subgroup of fracture-induced CRPS-1. No statistically significant differences were observed according to disease localization, disease duration, presence of hyperalgesia, allodynia, sudomotor alterations, and mild or moderate/severe swelling. No significant correlation emerged between sclerostin, DKK1 levels, baseline VAS score, or McGill Pain Questionnaire score. Bone involvement in early CRPS-1 does not seem to rely on increased osteoclast activity. Conversely, a serum marker of bone formation resulted increased. Both Sclerostin and DKK1 showed decreased values, probably suggesting a widespread osteocyte loss of function.Trial registration number: Eudract Number: 2014-001156-28.

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