血清25-羟基维生素D3浓度与腰椎间盘突出症患者情绪障碍的神经机制研究
Study on the Neural Mechanism of Serum 25-Hydroxyvitamin D3 Concentration and Emotional Disorders in Patients with Lumbar Disc Herniation
摘要: 目的:探究血清25-羟基维生素D3[25(OH)D3)]浓度与腰椎间盘突出症(LDH)患者情绪障碍的关联神经机制,为临床干预LDH患者情绪问题提供理论依据。方法:选取2023年8月~2025年8月安徽医科大学第一附属医院收治的64例LDH患者设为LDH组,同期选取64例年龄、性别匹配的健康志愿者设为健康对照(HC)组。收集两组受试者临床资料,采用汉密尔顿抑郁、焦虑量表(HAMD、HAMA)评估情绪状态,视觉模拟评分法(VAS)评估疼痛程度,Oswestry功能障碍指数(ODI)、日本骨科协会腰椎功能评分(JOA)评估腰椎功能;采集空腹静脉血,通过化学发光免疫分析法检测血清25(OH)D3浓度,行高分辨率3D-T1结构磁共振扫描获取全脑灰质体积(GMV)。运用独立样本t检验对比两组各项指标差异,通过Pearson相关、多元线性回归分析,校正混杂因素后探究血清25(OH)D3浓度、差异脑区GMV与情绪评分的相关性。结果:1) 两组年龄、性别、BMI基线资料无统计学差异(P > 0.05);相较于HC组,LDH组血清25(OH)D3浓度、JOA评分显著降低,HAMD、HAMA、VAS、ODI评分均显著升高,差异均有统计学意义(P < 0.001)。2) LDH患者血清25(OH)D3浓度与HAMD、HAMA、VAS、ODI评分呈显著负相关,与JOA评分呈显著正相关(均P < 0.001);校正年龄、性别、BMI后,该独立负相关关系依然成立(均P < 0.001)。3) 相较于HC组,LDH患者左侧颞极部颞上回、左侧颞中回、右侧颞中回等情绪调节相关脑区GMV显著减小(P < 0.05)。4) LDH患者HAMD评分与左侧颞极部颞上回GMV呈负相关,且血清25(OH)D3浓度与该脑区GMV呈显著正相关(均P < 0.05)。结论:LDH患者普遍存在维生素D缺乏(VDD),且伴随明显焦虑、抑郁情绪,此类情绪障碍或与血清25(OH)D3浓度降低、颞叶皮层等情绪调节关键脑区体积减小相关。维生素D (VD)可通过调控特定脑区结构可塑性,对LDH患者情绪障碍起到保护作用,本研究为阐释LDH合并情绪障碍的神经机制提供了影像学依据,也为临床VD筛查、心理评估及补充VD辅助治疗提供了科学支撑。
Abstract: Objective: To explore the neural mechanism underlying the correlation between serum 25-hydroxyvitamin D3 [25(OH)D3] concentration and emotional disorders in patients with lumbar disc herniation (LDH), so as to provide a theoretical basis for the clinical intervention of emotional problems in LDH patients. Methods: Sixty-four LDH patients admitted to the First Affiliated Hospital of Anhui Medical University from August 2023 to August 2025 were selected as the LDH group, and 64 healthy volunteers matched for age and gender were enrolled as the healthy control (HC) group in the same period. Clinical data of all subjects were collected. Emotional status was assessed using the Hamilton Depression Scale (HAMD) and Hamilton Anxiety Scale (HAMA), pain severity was evaluated via the Visual Analogue Scale (VAS), and lumbar function was rated with the Oswestry Disability Index (ODI) and Japanese Orthopaedic Association (JOA) Lumbar Function Score. Fasting venous blood samples were collected, and serum 25(OH)D3 concentration was detected by chemiluminescent immunoassay. High-resolution 3D-T1 structural magnetic resonance imaging was performed to obtain the whole-brain gray matter volume (GMV). The independent-sample t-test was used to compare differences in various indicators between the two groups. Pearson correlation analysis and multiple linear regression analysis were applied to explore the correlations among serum 25(OH)D3 concentration, GMV of differential brain regions and emotional scores after adjusting for confounding factors. Results: 1) There were no statistically significant differences in baseline data including age, gender and BMI between the two groups (P > 0.05). Compared with the HC group, the LDH group presented significantly lower serum 25(OH)D3 concentration and JOA score, and remarkably higher HAMD, HAMA, VAS and ODI scores, with extremely significant differences (P < 0.001). 2) Serum 25(OH)D3 concentration in LDH patients was significantly negatively correlated with HAMD, HAMA, VAS and ODI scores, and positively correlated with JOA score (all P < 0.001). After adjusting for age, gender and BMI, this independent negative correlation still remained (all P < 0.001). 3) Compared with the HC group, LDH patients showed significantly decreased GMV in multiple emotion regulation-related brain regions, such as the left temporal pole superior temporal gyrus, left middle temporal gyrus and right middle temporal gyrus (P < 0.05). 4) In the LDH group, HAMD score was negatively correlated with GMV of the left temporal pole superior temporal gyrus, and serum 25(OH)D3 concentration was significantly positively correlated with GMV of this brain region (both P < 0.05). Conclusions: Vitamin D deficiency (VDD) is prevalent in LDH patients, accompanied by obvious anxiety and depression. Such emotional disorders may be related to decreased serum 25(OH)D3 concentration and reduced volume of key emotion regulation brain regions such as the temporal cortex. Vitamin D (VD) can exert a protective effect on emotional disorders in LDH patients by regulating the structural plasticity of specific brain regions. This study provides imaging evidence for clarifying the neural mechanism of LDH complicated with emotional disorders, and also offers scientific support for clinical VD screening, psychological evaluation and adjuvant therapy with VD supplementation.
文章引用:陈南希, 霍晓征, 房翠瑶, 陈和木. 血清25-羟基维生素D3浓度与腰椎间盘突出症患者情绪障碍的神经机制研究[J]. 临床医学进展, 2026, 16(4): 2209-2218. https://doi.org/10.12677/acm.2026.1641468

参考文献

[1] Vos, T., Allen, C., Arora, M., Barber, R.M., Bhutta, Z.A., Brown, A., et al. (2016) Global, Regional, and National Incidence, Prevalence, and Years Lived with Disability for 310 Diseases and Injuries, 1990-2015: A Systematic Analysis for the Global Burden of Disease Study 2015. The Lancet, 388, 1545-1602. [Google Scholar] [CrossRef] [PubMed]
[2] Stafford, M.A., Peng, P. and Hill, D.A. (2007) Sciatica: A Review of History, Epidemiology, Pathogenesis, and the Role of Epidural Steroid Injection in Management. British Journal of Anaesthesia, 99, 461-473. [Google Scholar] [CrossRef] [PubMed]
[3] Hoy, D., March, L., Brooks, P., Blyth, F., Woolf, A., Bain, C., et al. (2014) The Global Burden of Low Back Pain: Estimates from the Global Burden of Disease 2010 Study. Annals of the Rheumatic Diseases, 73, 968-974. [Google Scholar] [CrossRef] [PubMed]
[4] Pinheiro, M.B., Ferreira, M.L., Refshauge, K., Ordoñana, J.R., Machado, G.C., Prado, L.R., et al. (2015) Symptoms of Depression and Risk of New Episodes of Low Back Pain: A Systematic Review and Meta‐Analysis. Arthritis Care & Research, 67, 1591-1603. [Google Scholar] [CrossRef] [PubMed]
[5] Gatchel, R.J., Polatin, P.B. and Mayer, T.G. (1995) The Dominant Role of Psychosocial Risk Factors in the Development of Chronic Low Back Pain Disability. Spine, 20, 2702-2709. [Google Scholar] [CrossRef] [PubMed]
[6] Matsudaira, K., Takahashi, M., Kawaguchi, M., Hamaguchi, A., Haga, Y. and Koga, T. (2019) Assessment of Risk Factors for Non-Specific Chronic Disabling Low Back Pain in Japanese Workers—Findings from the CUPID (Cultural and Psychosocial Influences on Disability) Study. Industrial Health, 57, 503-510. [Google Scholar] [CrossRef] [PubMed]
[7] Withanage, N.D., Perera, S., Peiris, H. and Athiththan, L.V. (2018) Serum 25-Hydroxyvitamin D, Serum Calcium and Vitamin D Receptor (VDR) Polymorphisms in a Selected Population with Lumbar Disc Herniation—A Case Control Study. PLOS ONE, 13, e0205841. [Google Scholar] [CrossRef] [PubMed]
[8] Eyles, D.W., Smith, S., Kinobe, R., Hewison, M. and McGrath, J.J. (2005) Distribution of the Vitamin D Receptor and 1α-Hydroxylase in Human Brain. Journal of Chemical Neuroanatomy, 29, 21-30. [Google Scholar] [CrossRef] [PubMed]
[9] Kesby, J.P., Cui, X., O’Loan, J., McGrath, J.J., Burne, T.H.J. and Eyles, D.W. (2010) Developmental Vitamin D Deficiency Alters Dopamine-Mediated Behaviors and Dopamine Transporter Function in Adult Female Rats. Psychopharmacology, 208, 159-168. [Google Scholar] [CrossRef] [PubMed]
[10] Holick, M.F., Binkley, N.C., Bischoff-Ferrari, H.A., Gordon, C.M., Hanley, D.A., Heaney, R.P., et al. (2011) Evaluation, Treatment, and Prevention of Vitamin D Deficiency: An Endocrine Society Clinical Practice Guideline. The Journal of Clinical Endocrinology & Metabolism, 96, 1911-1930. [Google Scholar] [CrossRef] [PubMed]
[11] Yan, C., Wang, X., Zuo, X. and Zang, Y. (2016) DPABI: Data Processing & Analysis for (Resting-State) Brain Imaging. Neuroinformatics, 14, 339-351. [Google Scholar] [CrossRef] [PubMed]
[12] Zadro, J., Shirley, D., Ferreira, M., et al. (2017) Mapping the Association between Vitamin D and Low Back Pain: A Systematic Review and Meta-Analysis of Observational Studies. Pain Physician, 7, 611-640. [Google Scholar] [CrossRef
[13] Zolfaghari, F., Faridmoayer, A., Soleymani, B., Taji, M. and Mahabadi, M. (2016) A Survey of Vitamin D Status in Patients with Degenerative Diseases of the Spine. Asian Spine Journal, 10, 834-842. [Google Scholar] [CrossRef] [PubMed]
[14] Dechsupa, S., Yingsakmongkol, W., Limthongkul, W., Singhatanadgige, W., Jitjumnong, M. and Honsawek, S. (2023) Vitamin D Inadequacy Affects Skeletal Muscle Index and Physical Performance in Lumbar Disc Degeneration. International Journal of Molecular Sciences, 24, Article 3152. [Google Scholar] [CrossRef] [PubMed]
[15] 张天龙, 赵继荣, 陈祁青, 等. 腰椎间盘突出症慢性疼痛的脑机制研究进展[J]. 世界科学技术-中医药现代化, 2022, 24(1): 277-282.
[16] 谢权, 肖欢, 孙雯. 血清25-羟基维生素D3浓度与腰痛患者疼痛和功能障碍的相关性[J]. 颈腰痛杂志, 2022, 43(4): 570-572.
[17] He, Y., Wu, Z., Lan, T., Wang, Y., Tian, Y., Chen, X., et al. (2020) The 25(OH)D/VDR Signaling May Play a Role in Major Depression. Biochemical and Biophysical Research Communications, 523, 405-410. [Google Scholar] [CrossRef] [PubMed]
[18] 赵文明. 维生素D、炎症与抑郁症关联的神经机制——基于多模态MRI技术的研究[D]: [博士学位论文]. 合肥: 安徽医科大学, 2024.
[19] 张石盼, 金曼, 倪爱华, 等. 维生素D与抑郁症的相关研究进展[J]. 现代医药卫生, 2023, 39(13): 2267-2271, 2277.
[20] Patrick, R.P. and Ames, B.N. (2014) Vitamin D Hormone Regulates Serotonin Synthesis. Part 1: Relevance for Autism. The FASEB Journal, 28, 2398-2413. [Google Scholar] [CrossRef] [PubMed]
[21] Sabir, M.S., Haussler, M.R., Mallick, S., Kaneko, I., Lucas, D.A., Haussler, C.A., et al. (2018) Optimal Vitamin D Spurs Serotonin: 1,25-Dihydroxyvitamin D Represses Serotonin Reuptake Transport (SERT) and Degradation (MAO-A) Gene Expression in Cultured Rat Serotonergic Neuronal Cell Lines. Genes & Nutrition, 13, Article No. 19. [Google Scholar] [CrossRef] [PubMed]
[22] Croll, P.H., Boelens, M., Vernooij, M.W., van de Rest, O., Zillikens, M.C., Ikram, M.A., et al. (2021) Associations of Vitamin D Deficiency with MRI Markers of Brain Health in a Community Sample. Clinical Nutrition, 40, 72-78. [Google Scholar] [CrossRef] [PubMed]
[23] Navale, S.S., Mulugeta, A., Zhou, A., Llewellyn, D.J. and Hyppönen, E. (2022) Vitamin D and Brain Health: An Observational and Mendelian Randomization Study. The American Journal of Clinical Nutrition, 116, 531-540. [Google Scholar] [CrossRef] [PubMed]
[24] Takamiya, A., Radwan, A., Christiaens, D., Van Cauwenberge, M., Vande Casteele, T., Laroy, M., et al. (2025) Gray and White Matter Differences in the Medial Temporal Lobe in Late-Life Depression: A Multimodal PET-MRI Investigation. Psychological Medicine, 55, e10. [Google Scholar] [CrossRef] [PubMed]
[25] Espinoza Oyarce, D.A., Shaw, M.E., Alateeq, K. and Cherbuin, N. (2020) Volumetric Brain Differences in Clinical Depression in Association with Anxiety: A Systematic Review with Meta-Analysis. Journal of Psychiatry and Neuroscience, 45, 406-429. [Google Scholar] [CrossRef] [PubMed]
[26] Sturm, V.E., Yokoyama, J.S., Seeley, W.W., Kramer, J.H., Miller, B.L. and Rankin, K.P. (2013) Heightened Emotional Contagion in Mild Cognitive Impairment and Alzheimer’s Disease Is Associated with Temporal Lobe Degeneration. Proceedings of the National Academy of Sciences of the United States of America, 110, 9944-9949. [Google Scholar] [CrossRef] [PubMed]