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肌萎缩侧索硬化患者认知功能损害与代谢水平的相关性

豆瑞霞 谷成 张璐璐 梁韫华 张毅

豆瑞霞, 谷成, 张璐璐, 梁韫华, 张毅. 肌萎缩侧索硬化患者认知功能损害与代谢水平的相关性[J]. 中华全科医学, 2025, 23(7): 1119-1122. doi: 10.16766/j.cnki.issn.1674-4152.004078
引用本文: 豆瑞霞, 谷成, 张璐璐, 梁韫华, 张毅. 肌萎缩侧索硬化患者认知功能损害与代谢水平的相关性[J]. 中华全科医学, 2025, 23(7): 1119-1122. doi: 10.16766/j.cnki.issn.1674-4152.004078
DOU Ruixia, GU Cheng, ZHANG Lulu, LIANG Yunhua, ZHANG Yi. Correlation between cognitive impairment and metabolic level in patients with amyotrophic lateral sclerosis[J]. Chinese Journal of General Practice, 2025, 23(7): 1119-1122. doi: 10.16766/j.cnki.issn.1674-4152.004078
Citation: DOU Ruixia, GU Cheng, ZHANG Lulu, LIANG Yunhua, ZHANG Yi. Correlation between cognitive impairment and metabolic level in patients with amyotrophic lateral sclerosis[J]. Chinese Journal of General Practice, 2025, 23(7): 1119-1122. doi: 10.16766/j.cnki.issn.1674-4152.004078

肌萎缩侧索硬化患者认知功能损害与代谢水平的相关性

doi: 10.16766/j.cnki.issn.1674-4152.004078
基金项目: 

科技部科技创新2030-“脑科学与类脑研究”重大项目 2021ZD0201801

甘肃省科技计划项目 23JRRA1290

详细信息
    通讯作者:

    张毅,E-mail:zhangyi9310@21cn.com

  • 中图分类号: R744.8

Correlation between cognitive impairment and metabolic level in patients with amyotrophic lateral sclerosis

  • 摘要:   目的   探索肌萎缩侧索硬化(ALS)患者认知损害与代谢指标的关系,以期提高ALS患者认知损害的早期干预率。   方法   回顾性分析2022年7月—2024年3月在甘肃省人民医院门诊及住院部就诊的36例ALS患者的基本临床资料,收集血肌酐(Cr)、尿酸(UA)、肌酸激酶(CK)、总胆固醇(TC)、甘油三酯(TG)、高/低密度脂蛋白胆固醇(H/LDL-C)等代谢指标,采用Spearman、logistic回归对代谢指标与认知损伤的相关性进行分析。   结果   对36例ALS患者使用简易精神状态检查表(MMSE)评估显示,20例伴发认知功能障碍,认知功能障碍的发生率为55.56%。与非认知障碍组比较,认知障碍组女性占比、ALS患者功能评分量表(ALSFRSr)评分、CK和LDL-C等指标均较高, 教育程度及UA均较低, 差异有统计学意义(P<0.05)。蒙特利尔认知评估量表(MoCA)评估显示,19例伴发认知功能障碍,认知功能障碍的发生率为52.78%。与非认知障碍组比较,认知障碍组女性占比、ALSFRSr评分、CK和LDL-C等指标均较高, 教育程度及UA均较低,差异有统计学意义(P<0.05)。Logistic回归分析显示,女性、高ALSFRSr评分及低UA均为患者认知损害的主要危险因素(P<0.05)。   结论   女性、ALSFRSr评分、血脂、延髓起病、教育水平及UA与ALS患者认知损害相关,对ALS患者应加强以上因素的关注并及时干预。

     

  • 表  1  不同MMSE评分分组ALS患者各项代谢指标比较

    Table  1.   Comparison of metabolic parameters in ALS patients with different MMSE scores

    组别 例数 性别
    (男性/女性,例)
    年龄
    (x±s, 岁)
    延髓起病
    [例(%)]
    起病年龄
    (x±s, 岁)
    教育程度
    [M(P25, P75), 年]
    病程
    (x±s, 年)
    BMI
    (x±s)
    ALSFRSr评分
    [M(P25, P75), 分]
    认知障碍组 20 9/11 59.40±12.12 11(55.00) 56.85±11.90 7.00(5.75, 9.00) 10.42±4.98 22.15±3.46 39.00(35.75, 41.00)
    非认知障碍组 16 14/2 53.75±12.99 9(56.25) 52.12±12.47 10.00(9.00, 12.50) 11.65±5.45 22.48±4.93 22.00(21.75, 25.50)
    统计量 1.350b 1.161b 2.624c 0.766b 0.233b -4.613c
    P 0.014a 0.187 0.999a 0.254 0.008 0.444 0.816 < 0.001
    组别 例数 TC
    (x±s, mmol/L)
    TG[M(P25, P75), mmol/L] CK
    (x±s, mmol/L)
    Cr
    [M(P25, P75), mmol/L]
    UA
    [M(P25, P75), μmol/L]
    LDL-C[M(P25, P75), mmol/L] HDL-C
    (x±s, mmol/L)
    认知障碍组 20 4.26±0.96 1.04(0.77, 1.62) 236.22±136.37 55.05(46.50, 60.20) 275.50(194.25, 298.75) 2.48(1.99, 2.89) 1.15±0.30
    非认知障碍组 16 4.37±0.95 1.30(1.01, 2.01) 116.88±39.11 61.79(50.33, 69.78) 436.79(432.75, 461.25) 1.77(1.22, 1.89) 1.10±0.32
    统计量 0.358b -1.545c 3.734b -0.462c -4.551c -3.004c 0.322b
    P 0.721 0.124 0.001 0.648 < 0.001 0.002 0.750
    注:a为采用Fisher精确检验,bt值,cZ值。
    下载: 导出CSV

    表  2  不同MoCA评分分组ALS患者各项代谢指标比较

    Table  2.   Comparison of metabolic parameters in ALS patients with different MoCA scores

    组别 例数 性别
    (男性/女性,例)
    年龄
    (x±s, 岁)
    延髓起病
    [例(%)]
    起病年龄
    (x±s, 岁)
    教育程度
    [M(P25, P75), 年]
    病程
    (x±s, 年)
    BMI
    (x±s)
    ALSFRSr评分
    [M(P25, P75), 分]
    认知障碍组 19 8/11 58.89±12.23 10(52.63) 56.37±12.02 7.00(5.50, 9.00) 10.42±4.98 21.97±3.45 39.00(36.00, 41.00)
    非认知障碍组 17 15/2 54.65±13.11 10(58.82) 52.94±12.53 10.00(9.00, 12.00) 11.65±5.45 22.67±4.84 22.00(22.00, 25.00)
    统计量 1.013b 0.836b -2.933c 0.689b 0.501b -4.837c
    P 0.006a 0.322 0.749a 0.408 0.003 0.488 0.618 < 0.001
    组别 例数 TC
    (x±s, mmol/L)
    TG[M(P25, P75), mmol/L] CK
    (x±s, mmol/L)
    Cr
    [M(P25, P75), mmol/L]
    UA
    [M(P25, P75), μmol/L]
    LDL-C[M(P25, P75), mmol/L] HDL-C
    (x±s,mmol/L)
    认知障碍组 19 4.30±0.97 1.06(0.77, 1.66) 246.13±132.50 54.40(46.50, 58.25) 275.00(192.50, 288.50) 2.48(2.01, 2.90) 1.15±0.30
    非认知障碍组 17 4.32±0.95 1.29(1.01, 2.01) 112.83±41.39 69.18(51.00, 70.60) 436.59(432.00, 458.00) 1.77(1.23, 1.89) 1.10±0.32
    统计量 0.057b -1.248c 4.163b -0.939c -4.578c -3.392c 0.534b
    P 0.953 0.208 < 0.001 0.346 < 0.001 < 0.001 0.597
    注:a为采用Fisher精确检验,bt值,cZ值。
    下载: 导出CSV

    表  3  MMSE评分评估认知障碍与各代谢指标的Spearman相关分析

    Table  3.   Spearman correlation analysis between cognitive impairment assessed by MMSE score and various metabolic indicators

    项目 r P
    教育程度 -0.446 0.006
    病程 -0.111 0.521
    BMI -0.016 0.925
    Cr -0.081 0.640
    TC -0.046 0.791
    TG -0.264 0.119
    UA -0.772 < 0.001
    LDL-C 0.509 0.002
    CK 0.429 0.009
    下载: 导出CSV

    表  4  MoCA评分评估认知障碍与各代谢指标的Spearman相关分析

    Table  4.   Spearman correlation analysis between cognitive impairment assessed by MoCA score and various metabolic indicators

    因素 r P
    教育程度 -0.498 0.002
    病程 -0.105 0.543
    BMI -0.070 0.686
    Cr -0.161 0.349
    TC 0.019 0.913
    TG -0.215 0.209
    UA -0.777 < 0.001
    LDL-C 0.577 < 0.001
    CK 0.512 0.001
    下载: 导出CSV

    表  5  MMSE评分评估认知障碍相关因素的logistic回归分析

    Table  5.   Logistic regression analysis of factors linked to cognitive impairment based on MMSE scores

    自变量 B SE Waldχ2 P OR 95% CI
    模型1
      女性 2.330 0.880 2.640 0.008 10.310 1.820~58.390
      ALSFRSr评分 0.461 0.154 2.981 0.003 1.590 1.172~2.153
      UA -0.033 0.010 -3.360 < 0.001 0.972 0.953~0.990
    模型2
      高ALSFRSr评分 3.411 1.380 2.470 0.013 30.252 2.024~452.420
      低UA水平 3.313 1.410 2.336 0.019 27.391 1.710~438.172
    注:男性=0,女性=1;连续性变量,以实际值赋值;ALSFRSr评分,低评分=0,高评分=1;UA水平,正常/高UA=0,低UA=1。
    下载: 导出CSV

    表  6  MoCA评分评估认知障碍相关因素的logistic回归分析

    Table  6.   Logistic regression analysis of factors linked to cognitive impairment based on MoCA scores

    变量 B SE Waldχ2 P OR 95% CI
    模型1
      女性 2.149 0.881 2.444 0.015 8.562 1.527~47.963
      ALSFRSr评分 0.367 0.109 3.211 0.001 1.444 1.151~1.814
      UA -0.033 0.010 -3.302 < 0.001 0.970 0.950~0.990
    模型2
      高ALSFRSr评分 4.001 1.366 2.923 0.004 54.873 3.720~808.708
      低UA水平 3.518 1.675 2.091 0.036 33.718 1.259~907.153
    注:男性=0,女性=1;连续性变量,以实际值赋值;ALSFRSr评分,低评分=0,高评分=1;UA水平,正常/高UA=0,低UA=1。
    下载: 导出CSV
  • [1] 李瑞, 王国平. 运动神经元病的诊断与治疗[J]. 中华全科医学, 2019, 17(7): 1073-1074. http://zhqkyx.net/article/id/2df5e613-96c8-4c61-b366-03ed9ccf8ea2

    LI R, WANG G P. Diagnosis and treatment of motor neuronal disease[J]. Chinese Journal of General Practice, 2019, 17(7): 1073-1074. http://zhqkyx.net/article/id/2df5e613-96c8-4c61-b366-03ed9ccf8ea2
    [2] FELDMAN E L, GOUTMAN S A, PETRI S, et al. Amyotrophic lateral sclerosis[J]. The Lancet, 2022, 400(10360): 1363-1380. doi: 10.1016/S0140-6736(22)01272-7
    [3] GOUTMAN S A, HARDIMAN O, AL-CHALABI A, et al. Recent advances in the diagnosis and prognosis of amyotrophic lateral sclerosis[J]. The Lancet, 2022, 21(5): 480-493.
    [4] MEAD R J, SHAN N, REISER H J, et al. Amyotrophic lateral sclerosis: a neurodegenerative disorder poised for successful therapeutic translation[J]. Natrev Drug Discov, 2023, 22(3): 185-212. doi: 10.1038/s41573-022-00612-2
    [5] 张秋丽, 张明. 肌萎缩侧索硬化症患者神经影像学研究进展[J]. 西安交通大学学报(医学版), 2023, 44(5): 668-673.

    ZHANG Q L, ZHANG M. Neuroimaging advances in patients with amyotrophic lateral sclerosis[J]. Journal of Xi'an Jiaotong University(Medical Sciences), 2023, 44(5): 668-673.
    [6] 赵小泉, 卢祖能. 肌萎缩侧索硬化临床特征及预后因素研究进展[J]. 天津医药, 2023, 51(7): 694-697.

    ZHAO X Q, LU Z N. Advances in clinical characteristics and prognostic factors of amyotrophic lateral sclerosis[J]. Tianjin Medical Journal, 2023, 51(7): 694-697.
    [7] 朱思佳, 俞立强, 方琪. 肌萎缩侧索硬化症患者认知损害和行为障碍的影像学研究进展[J]. 中国临床神经科学, 2024, 32(2): 220-227.

    ZHU S J, YU L Q, FANG Q. Multi-dimensional neuroimagings in amyotrophic lateral sclerosis with cognitive and behavioral disorders[J]. Chinese Journal of Clinical Neurosciences, 2024, 32(2): 220-227.
    [8] XIA K L, WITZEL S, WITZEL C, et al. Mutation-specific metabolic profiles in presymptomatic amyotrophic lateral sclerosis[J]. Eur J Neurol, 2023, 30(1): 87-95. doi: 10.1111/ene.15584
    [9] 张一方, 张海鑫, 张纹菱, 等. 基于Meta分析的中国老年人轻度认知障碍风险评估模型的构建与验证[J]. 中华疾病控制杂志, 2023, 27(6): 705-710.

    ZHANG Y F, ZHANG H X, ZHANG W L, et al. Construction and validation of a risk assessment model for mild cognitive impairment in Chinese elderly based on Meta-analysis[J]. Chinese Journal of Disease Control & Prevention, 2023, 27(6): 705-710.
    [10] LEE Y G, PARK M, JEONG S H, et al. Alzheimer' s disease neuroimaging initiative. Effects of baseline serum uric acid and apolipoprotein E4 on longitudinal cognition and cerebral metabolism[J]. Neurobiol Aging, 2021, 106: 223-231. doi: 10.1016/j.neurobiolaging.2021.05.003
    [11] 刘潇, 秦星, 靳娇婷, 等. 肌萎缩侧索硬化症患者抑郁与代谢水平的相关性[J]. 西安交通大学学报(医学版), 2020, 41(6): 816-820.

    LIU X, QIN X, JIN J T, et al. Association between depression and metabolomic biomarkers of patients with amyotrophic lateral sclerosis[J]. Journal of Xi'an Jiaotong University(Medical Sciences), 2020, 41(6): 816-820.
    [12] VAN DAMME P, AL-CHALABI A, ANDERSEN P M, et al. European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERN EURO-NMD)[J]. Eur J Neurol, 2024, 31(6): e16264. DOI: 10.1111/ene.16264.
    [13] 郭晓敏, 魏爱芹, 刘宗伟, 等. 脑小血管病认知障碍患者脑电功率谱变化与中性粒细胞/淋巴细胞比值相关性及临床价值研究[J]. 陕西医学杂志, 2024, 53(3): 361-367.

    GUO X M, WEI A Q, LIU Z W, et al. Relationship between electroencephalographic power spectrum changes and NLR in CSVCI patients and its clinical value[J]. Shaanxi Medical Journal, 2024, 53(3): 361-367.
    [14] 黄晓东, 罗伟良, 梁素琴, 等. 无症状性中重度颈内动脉狭窄患者认知功能障碍的临床研究[J]. 中国处方药, 2022, 20(4): 184-186.

    HUANG X D, LUO W L, LIANG S Q, et al. Correlation between asymptomatic moderate and severe carotid stenosis and cognitive impairment[J]. Journal of China Prescription Drug, 2022, 20(4): 184-186.
    [15] 段倩倩, 张秋丽, 李海宁, 等. 肌萎缩侧索硬化患者丘脑局灶性损伤与认知功能障碍的相关性[J]. 西安交通大学学报(医学版), 2023, 44(5): 688-693.

    DUAN Q Q, ZHANG Q L, LI H N, et al. Focal thalamus alterations and their associations with cognitive impairment in patients with amyotrophic lateral sclerosis[J]. Journal of Xi'an Jiaotong University(Medical Sciences), 2023, 44(5): 688-693.
    [16] BENATAR M, WUU J, MCHUTCHISON C, et al. First International Pre-Symptomatic ALS Workshop. Preventing amyotrophic lateral sclerosis: insights from pre-symptomatic neurodegenerative diseases[J]. Brain, 2022, 145(1): 27-44. doi: 10.1093/brain/awab404
    [17] KACEM I, ABIDA Y, FERCHICHI W, et al. Arabic adaptation of the Edinburgh Cognitive and behavioural Amyotrophic lateral Sclerosis screen(ECAS-AR)[J]. Rev Neurol(Paris), 2022, 178(8): 817-825. doi: 10.1016/j.neurol.2021.12.015
    [18] MOGLIA C, CALVO A, CANOSA A, et al. Cognitive and behavioral features of patients with amyotrophic lateral sclerosis who are carriers of the TARDBP pathogenic variant[J]. Neurology, 2024, 102(4): e208082. DOI: 10.1212/WNL.0000000000208082.
    [19] TELEANU D M, NICULESCU A G, LUNGU I I, et al. An overview of oxidative stress, neuroinflammation, and neurodegenerative diseases[J] Int J Mol Sci, 2022, 23(11): 5938. DOI: 10.3390/ijms23115938.
    [20] KUNITSKAYA N A, ARIEV A L. The role of hyperuricemia in the development of cognitive changes in the elderly[J]. Adv Gerontol, 2022, 35(5): 775-782.
    [21] KORCZOWSKA-ŁACKA I, SŁOWIKOWSKI B, PIEKUT T, et al. Disorders of endogenous and exogenous antioxidants in neurological diseases[J]. Antioxidants(Basel), 2023, 29, 12(10): 1811. DOI: 10.3390/antiox12101811.
    [22] AERQIN Q, JIA S S, SHEN X N, et al. Serum uric acid levels in neurodegenerative disorders: a cross-sectional study[J]. Alzheimers Dis, 2022, 90(2): 761-773. doi: 10.3233/JAD-220432
    [23] NISSEN S E, MENON V, NICHOLLS S J, et al. Bempedoic acid for primary prevention of cardiovascular events in statin-intolerant patients[J]. JAMA, 2023, 330(2): 131-140. doi: 10.1001/jama.2023.9696
    [24] AMES B N, CATHCART R, SCHWIERS E, et al. Uric acid provides an antioxidant defense in humans against oxidant and radical-caused aging and cancer: a hypothesis[J]. Proc Natl Acad Sci U S A, 1981, 78(11): 6858-6862. doi: 10.1073/pnas.78.11.6858
    [25] WALK D, NICHOLSON K, LOCATELLI E, et al. Randomized trial of inosine for urate elevation in amyotrophic lateral sclerosis[J]. Muscle Nerve, 2023, 67(5): 378-386. doi: 10.1002/mus.27807
    [26] 李丽娜, 魏洪娟, 杨雪雯, 等. 中国老年人群阿尔茨海默病疾病负担的年龄-时期-队列分析[J]. 现代预防医学, 2024, 51(10): 1754-1759.

    LI L N, WEI H J, YANG X W, et al. Age period cohort analysis of Alzheimer' s disease burden in the elderly population in China[J]. Modern Preventive Medicine, 2024, 51(10): 1754-1759.
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  • 收稿日期:  2025-01-25
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