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血清胆红素水平与帕金森病临床症状的相关性研究

王恒杰 朱啸巍 季杜欣 陈岩 张超 刘时华 钟平 曹立

王恒杰, 朱啸巍, 季杜欣, 陈岩, 张超, 刘时华, 钟平, 曹立. 血清胆红素水平与帕金森病临床症状的相关性研究[J]. 中华全科医学, 2025, 23(7): 1123-1126. doi: 10.16766/j.cnki.issn.1674-4152.004079
引用本文: 王恒杰, 朱啸巍, 季杜欣, 陈岩, 张超, 刘时华, 钟平, 曹立. 血清胆红素水平与帕金森病临床症状的相关性研究[J]. 中华全科医学, 2025, 23(7): 1123-1126. doi: 10.16766/j.cnki.issn.1674-4152.004079
WANG Hengjie, ZHU Xiaowei, JI Duxin, CHEN Yan, ZHANG Chao, LIU Shihua, ZHONG Ping, CAO Li. Correlation between serum bilirubin levels and motor symptoms in Parkinson' s disease[J]. Chinese Journal of General Practice, 2025, 23(7): 1123-1126. doi: 10.16766/j.cnki.issn.1674-4152.004079
Citation: WANG Hengjie, ZHU Xiaowei, JI Duxin, CHEN Yan, ZHANG Chao, LIU Shihua, ZHONG Ping, CAO Li. Correlation between serum bilirubin levels and motor symptoms in Parkinson' s disease[J]. Chinese Journal of General Practice, 2025, 23(7): 1123-1126. doi: 10.16766/j.cnki.issn.1674-4152.004079

血清胆红素水平与帕金森病临床症状的相关性研究

doi: 10.16766/j.cnki.issn.1674-4152.004079
基金项目: 

安徽省临床医学研究转化专项项目 202204295107020063

安徽省卫生健康科研项目 AHWJ2022b106

详细信息
    通讯作者:

    曹立,E-mail:caoli2000@yeah.net

  • 中图分类号: R742.5

Correlation between serum bilirubin levels and motor symptoms in Parkinson' s disease

  • 摘要:   目的   探究血清胆红素(BI)水平与帕金森病(PD)临床症状(运动症状、非运动症状)的关系,为揭示PD发病机制及寻找潜在的生物学标志物提供理论依据。   方法   回顾性分析2021年7月—2024年7月于安徽医科大学附属宿州医院就诊的102例PD患者和102例健康体检者(HC)的临床资料。PD患者根据Hoehn-Yahr分期分为早期组(65例)和中晚期组(37例)。比较PD组和HC组、早期组和中晚期组组间总胆红素(TBIL)、直接胆红素(DBIL)、间接胆红素(IBIL)水平,分析血清BI水平与PD患者年龄、运动症状[帕金森病统一评分量表(UPDRS)-Ⅲ评分、Berg平衡量表]和非运动症状(蒙特利尔认知评估量表、汉密尔顿抑郁量表)的相关性。   结果   102例PD组患者中,男性50例,女性52例,年龄为71(64,76)岁。PD组TBIL、DBIL均高于HC组(P < 0.05)。中晚期组TBIL[(16.04±6.73)μmol/L vs. (13.41±4.07)μmol/L, P=0.035]、IBIL[(11.01±5.05)μmol/L vs. (9.16±2.73)μmol/L, P=0.045]水平均高于早期组。Spearman相关分析显示,PD患者的运动症状严重程度(UPDRS-Ⅲ评分)与DBIL(rs=0.325,P < 0.001)水平呈正相关关系。   结论   与健康体检者比较,PD患者的血清DBIL水平明显升高,且与PD运动症状呈正相关关系,通过检测和降低血清DBIL水平等可能对延缓PD运动症状进展有一定的作用。

     

  • 表  1  PD组与HC组研究对象一般资料及血清BI水平比较

    Table  1.   Comparison of general data and serum BI levels between PD group and HC group

    组别 例数 性别[例(%)] 年龄
    [M(P25, P75), 岁]
    有吸烟史
    [例(%)]
    有饮酒史
    [例(%)]
    有糖尿病史
    [例(%)]
    有高血压病史
    [例(%)]
    TBIL
    [M(P25, P75), μmol/L]
    DBIL
    [M(P25, P75), μmol/L]
    IBIL
    [M(P25, P75), μmol/L]
    男性 女性
    PD组 102 50(49.02) 52(50.98) 71(64, 76) 9(8.82) 3(2.94) 22(21.57) 50(49.02) 13.65(10.80, 16.90) 4.20(2.90, 5.40) 9.35(7.20, 11.90)
    HC组 102 44(43.14) 58(56.86) 69(65, 73) 7(6.86) 8(7.84) 28(27.45) 44(43.14) 12.05(9.90, 14.90) 3.30(2.70, 4.00) 8.80(7.10, 11.10)
    统计量 0.710a -1.651b 0.271a 2.402a 0.954a 0.710a -2.498b -4.484b -1.083b
    P 0.399 0.099 0.602 0.121 0.329 0.399 0.012 < 0.001 0.279
    注:a为χ2值,bZ值。
    下载: 导出CSV

    表  2  早期组与中晚期组PD患者血清BI水平比较(μmol/L)

    Table  2.   Comparison of serum BI levels (μmol/L) between early PD and moderate-to-late PD groups (μmol/L)

    组别 例数 TBIL(x±s) DBIL[M(P25, P75)] IBIL(x±s)
    早期组 65 13.41±4.07 4.10(2.80, 4.90) 9.16±2.73
    中晚期组 37 16.04±6.73 4.50(3.30, 6.20) 11.01±5.05
    统计量 2.166a -1.856b 2.062a
    P 0.035 0.063 0.045
    注:at值,bZ值。
    下载: 导出CSV

    表  3  血清BI水平与年龄及各量表评分的相关性分析

    Table  3.   Correlation analysis of serum BI levels with age and various scale scores

    项目 TBIL DBIL IBIL
    统计量 P 统计量 P 统计量 P
    年龄 0.139a 0.162 0.181a 0.068 0.135a 0.175
    UPDRS-Ⅲ评分 0.280a 0.004 0.325a < 0.001 0.248b 0.012
    MoCA评分 -0.066a 0.513 -0.003a 0.973 -0.167b 0.094
    HAMD评分 -0.061a 0.539 -0.082a 0.412 -0.044a 0.660
    BBS评分 -0.225a 0.023 -0.263a 0.008 -0.201a 0.042
    注:ars值,br值。
    下载: 导出CSV
  • [1] ZHU J Q, CUI Y S, ZHANG J J, et al. Temporal trends in the prevalence of Parkinson' s disease from 1980 to 2023: a systematic review and meta-analysis[J]. Lancet Healthy Longev, 2024, 5(7): e464-e479. doi: 10.1016/S2666-7568(24)00094-1
    [2] 刘浩宇, 朋文佳, 芈静, 等. 1990—2019年全球帕金森病疾病负担的APC分析[J]. 中华全科医学, 2024, 22(1): 154-157. doi: 10.16766/j.cnki.issn.1674-4152.003353

    LIU H Y, PENG W J, MI J, et al. APC analysis of the global disease burden of Parkinson' s disease from 1990 to 2019[J]. Chinese Journal of General Practice, 2024, 22(1): 154-157. doi: 10.16766/j.cnki.issn.1674-4152.003353
    [3] CHAKRABARTI S, BISAGLIA M. Oxidative stress and neuroinflammation in Parkinson' s disease: the role of dopamine oxidation products[J]. Antioxidants(Basel), 2023, 12(4): 955. DOI: 10.3390/antiox12040955.
    [4] DIONÍSIO P A, AMARAL J D, RODRIGUES C M P. Oxidative stress and regulated cell death in Parkinson' s disease[J]. Ageing Res Rev, 2021, 67: 101263. DOI: 10.1016/j.arr.2021.101263.
    [5] SADIQ I Z. Free radicals and oxidative stress: signaling mechanisms, redox basis for human diseases, and cell cycle regulation[J]. Curr Mol Med, 2023, 23(1): 13-35. doi: 10.2174/1566524022666211222161637
    [6] LIM D W, LEE J E, LEE C, et al. Natural products and their neuroprotective effects in degenerative brain diseases: a comprehensive review[J]. Int J Mol Sci, 2024, 25(20): 11223. DOI: 10.3390/ijms252011223.
    [7] 焦倩, 姜宏. 帕金森病病因与发病机制研究现状及其诊治意义[J]. 青岛大学学报(医学版), 2021, 57(2): 159-162.

    JIAO Q, JIANG H. Current research on etiology and pathogenesis of Parkinson's disease and significance of its diagnosis and treatment[J]. Journal of Qingdao University(Medical Sciences), 2021, 57(2): 159-162.
    [8] TAHAVVORI A, GARGARI M K, YAZDANI Y, et al. Involvement of antioxidant enzymes in Parkinson' s disease[J]. Pathol Res Pract, 2023, 249: 154757. DOI: 10.1016/j.prp.2023.154757.
    [9] MA L L, SUN L, WANG Y X, et al. Association between HO-1 gene promoter polymorphisms and diseases (review)[J]. Mol Med Rep, 2022, 25(1): 29. DOI: 10.3892/mmr.2021.12545.
    [10] PRZYBYLSKI P, ŻEBROWSKI M, WITKOWSKI W, et al. Antioxidant activity of bilirubin in micellar and liposomal systems is pH-dependent[J]. Antioxidants(Basel), 2024, 13(4): 426. DOI: 10.3390/antiox13040426.
    [11] BIANCO A, DVOŘÁK A, CAPKOVÁ N, et al. The extent of intracellular accumulation of bilirubin determines its anti-or pro-oxidant effect[J]. Int J Mol Sci, 2020, 21(21): 8101. DOI: 10.3390/ijms21218101.
    [12] VITEK L, HINDS T D J R, STEC D E, et al. The physiology of bilirubin: health and disease equilibrium[J]. Trends Mol Med, 2023, 29(4): 315-328. doi: 10.1016/j.molmed.2023.01.007
    [13] MARTÍNEZ A, LÓPEZ-RULL I, FARGALLO J A. To prevent oxidative stress, what about protoporphyrin Ⅸ, biliverdin, and bilirubin?[J]. Antioxidants(Basel), 2023, 12(9): 1662. DOI: 10.3390/antiox12091662.
    [14] HIRVONEN O P, LEHTI M, KYRÖLǍINEN H, et al. Heme oxygenase-1 and blood bilirubin are gradually activated by oral D-glyceric acid[J]. Antioxidants(Basel), 2022, 11(12): 2319. DOI: 10.3390/antiox11122319.
    [15] JAYANTI S, MORETTI R, TIRIBELLI C, et al. Bilirubin: a promising therapy for Parkinson' s disease[J]. Int J Mol Sci, 2021, 22(12): 6223. DOI: 10.3390/ijms22126223.
    [16] 中华医学会神经病学分会帕金森病及运动障碍学组, 中国医师协会神经内科医师分会帕金森病及运动障碍专业. 中国帕金森病的诊断标准(2016版)[J]. 中华神经科杂志, 2016, 49(4): 268-271.

    Chinese society of Parkinson' s disease and movement disorders, Parkinson' s disease and movement disorder section of neurologist branch of Chinese medical doctor association. Diagnostic criteria Parkinson' s disease in China (2016 edition)[J]. Chinese Journal of Neurology, 2016, 49(4): 268-271.
    [17] 赵媛, 刘向, 杨国锋. 血清CD73和帕金森病患者运动障碍相关性研究[J]. 医学研究杂志, 2024, 53(1): 75-79.

    ZHAO Y, LIU X, YANG G F. Correlation between serum CD73 and motor dysfunction in patients with Parkinson's Disease[J]. Journal of Medical Research, 2024, 53(1): 75-79.
    [18] JAYANTI S, VÍTEK L, TIRIBELLI C, et al. The role of bilirubin and the other "yellow players" in neurodegenerative diseases[J]. Antioxidants(Basel), 2020, 9(9): 900. DOI: 10.3390/antiox9090900.
    [19] ZHANG F H, CHEN L H, JIANG K W. Neuroinflammation in bilirubin neurotoxicity[J]. J Integr Neurosci, 2023, 22(1): 9. DOI: 10.31083/j.jin2201009.
    [20] SUN W H, ZHENG J H, MA J J, et al. Increased plasma heme oxygenase-1 levels in patients with early-stage Parkinson' s disease[J]. Front Aging Neurosci, 2021, 13: 621508. DOI: 10.3389/fnagi.2021.621508.
    [21] LIU H W, GONG L N, LAI K, et al. Bilirubin gates the TRPM2 channel as a direct agonist to exacerbate ischemic brain damage[J]. Neuron, 2023, 111(10): 1609-1625. e6 doi: 10.1016/j.neuron.2023.02.022
    [22] ALAHMAD M, ISBEA H, SHITAW E, et al. Nox2-trpm2 coupling promotes Zn2+ inhibition of complex Ⅲ to exacerbate ros production in a cellular model of Parkinson' s disease[J]. Sci Rep, 2024, 14(1): 18431. DOI: 10.1038/s41598-024-66630-9.
    [23] FEI L, LIANG Y T, KINTSCHER U, et al. Coupling of mitochondrial state with active zone plasticity in early brain aging[J]. Redox Biol, 2024, 79: 103454. DOI: 10.1016/j.redox.2024.103454.
    [24] KAZEMI D, HAJISHAH H, CHADEGANIPOUR A S. Association of total bilirubin with motor signs in early Parkinson' s disease in LRRK2 variant carriers[J]. J Mol Neurosci, 2022, 72(11): 2338-2344. doi: 10.1007/s12031-022-02067-x
    [25] GROFIK M, CIBULKA M, OLEKSAKOVA J, et al. Oxidative stress parameters and their relation to motor subtype of Parkinson' s disease and levodopa treatment status[J]. Gen Physiol Biophys, 2023, 42(1): 77-85. doi: 10.4149/gpb_2022051
    [26] JIN J N, LIU X, LI M J, et al. Association between serum bilirubin concentration and Parkinson' s disease: a meta-analysis[J]. Chin Med J(Engl), 2020, 134(6): 655-661.
    [27] QIN X L, ZHANG Q S, SUN L, et al. Lower serum bilirubin and uric acid concentrations in patients with Parkinson' s disease in China[J]. Cell Biochem Biophys, 2015, 72(1): 49-56. doi: 10.1007/s12013-014-0402-x
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  • 收稿日期:  2024-09-19
  • 网络出版日期:  2025-10-25

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