Correlation Analysis of Serum G-Protein-Coupled Receptor 4 and Biglycan Levels with the Severity of Intervertebral Disc Degeneration.

IF 1.7 Q2 ORTHOPEDICS
Orthopedic Research and Reviews Pub Date : 2025-07-08 eCollection Date: 2025-01-01 DOI:10.2147/ORR.S525337
Bingjie Gao, Yizhi Cui, Yexiao Qin, Chuncheng Qu, Jiaqi Zhao, Xiaoning Li
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引用次数: 0

Abstract

Objective: To investigate the correlation between serum levels of G protein-coupled receptor 4 (GPR4) and Biglycan (BGN) with the severity of Intervertebral Disc Degeneration (IVDD).

Methods: A total of 162 patients with IVDD treated at our hospital from August 2023 to August 2024 were included. The general information of patients was retrospectively collected. MRI was used to assess IVDD severity using the Pfirrmann grading system. Serum GPR4 and BGN levels were measured by enzyme-linked immunosorbent assay (ELISA). Multiple linear regression analysis was performed to identify risk factors for IVDD severity. Spearman's and Pearson's correlation analyses were used to evaluate the relationships between serum GPR4, BGN, and IVDD severity. Receiver operating characteristic (ROC) curve analysis was used to evaluate the diagnostic value of serum GPR4 and BGN in IVDD.

Results: Significant differences in age and the proportion of diabetic patients as well as serum GPR4 and BGN were found among different Pfirrmann grades (P<0.05). Serum GPR4 levels increased but BGN levels decreased with higher Pfirrmann grades (P<0.05). Multiple linear regression analysis showed that age and serum GPR4 and BGN levels were risk factors for IVDD severity (P<0.05). The results of the correlation analysis showed that serum GPR4 and age were positively correlated with the severity of IVDD (r=0.651, r=0.488, P<0.001), while BGN was negatively correlated with the severity of IVDD (r=-0.591, P<0.001). The results of Spearman correlation analysis showed a negative correlation between serum GPR4 and BGN (P<0.05). ROC curve analysis revealed that the AUC values for the diagnosis of IVDD using serum GPR4 alone, BGN alone, and the combination of GPR4 and BGN were 0.918, 0.811, and 0.919, respectively (P<0.05). Moreover, the combination of GPR4 and BGN demonstrated higher sensitivity and specificity compared to either marker alone.

Conclusions: Serum GPR4 and BGN levels are identified as effective diagnostic indicators for IVDD, with serum GPR4 positively correlated but BGN negatively correlated with the severity of IVDD.

血清g蛋白偶联受体4和Biglycan水平与椎间盘退变严重程度的相关性分析。
目的:探讨血清G蛋白偶联受体4 (GPR4)和Biglycan (BGN)水平与椎间盘退变(IVDD)严重程度的相关性。方法:选取2023年8月至2024年8月在我院治疗的IVDD患者162例。回顾性收集患者的一般资料。MRI采用Pfirrmann分级系统评估IVDD严重程度。采用酶联免疫吸附试验(ELISA)检测血清GPR4和BGN水平。采用多元线性回归分析确定IVDD严重程度的危险因素。采用Spearman和Pearson相关分析评估血清GPR4、BGN和IVDD严重程度之间的关系。采用受试者工作特征(ROC)曲线分析评价血清GPR4、BGN对IVDD的诊断价值。结果:不同Pfirrmann分级患者的年龄、糖尿病患者比例及血清GPR4、BGN差异均有统计学意义(PPPr=0.651, r=0.488, Pr=-0.591), PSpearman相关分析显示血清GPR4、BGN水平与IVDD呈负相关(ppp)。结论:血清GPR4、BGN水平与IVDD的严重程度呈正相关,血清GPR4与IVDD的严重程度呈负相关。
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
Orthopedic Research and Reviews
Orthopedic Research and Reviews Medicine-Orthopedics and Sports Medicine
CiteScore
2.80
自引率
0.00%
发文量
51
审稿时长
16 weeks
期刊介绍: Orthopedic Research and Reviews is an international, peer-reviewed, open-access journal focusing on the patho-physiology of the musculoskeletal system, trauma, surgery and other corrective interventions to restore mobility and function. Advances in new technologies, materials, techniques and pharmacological agents will be particularly welcome. Specific topics covered in the journal include: Patho-physiology and bioengineering, Technologies and materials science, Surgical techniques, including robotics, Trauma management and care, Treatment including pharmacological and non-pharmacological, Rehabilitation and Multidisciplinarian care approaches, Patient quality of life, satisfaction and preference, Health economic evaluations. The journal welcomes submitted papers covering original research, basic science and technology, clinical studies, reviews and evaluations, guidelines, expert opinion and commentary, case reports and extended reports.
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