留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

血清超敏C反应蛋白与老年人非酒精性脂肪肝的相关性

陈长喜 杜娟 宋健 张丞 李梦婷 李红亮

陈长喜, 杜娟, 宋健, 张丞, 李梦婷, 李红亮. 血清超敏C反应蛋白与老年人非酒精性脂肪肝的相关性[J]. 中华全科医学, 2023, 21(9): 1491-1494. doi: 10.16766/j.cnki.issn.1674-4152.003153
引用本文: 陈长喜, 杜娟, 宋健, 张丞, 李梦婷, 李红亮. 血清超敏C反应蛋白与老年人非酒精性脂肪肝的相关性[J]. 中华全科医学, 2023, 21(9): 1491-1494. doi: 10.16766/j.cnki.issn.1674-4152.003153
CHEN Changxi, DU Juan, SONG Jian, ZHANG Cheng, LI Mengting, LI Hongliang. Study on correlation between serum hypersensitive C-reactive protein and nonalcoholic fatty liver disease in the elderly[J]. Chinese Journal of General Practice, 2023, 21(9): 1491-1494. doi: 10.16766/j.cnki.issn.1674-4152.003153
Citation: CHEN Changxi, DU Juan, SONG Jian, ZHANG Cheng, LI Mengting, LI Hongliang. Study on correlation between serum hypersensitive C-reactive protein and nonalcoholic fatty liver disease in the elderly[J]. Chinese Journal of General Practice, 2023, 21(9): 1491-1494. doi: 10.16766/j.cnki.issn.1674-4152.003153

血清超敏C反应蛋白与老年人非酒精性脂肪肝的相关性

doi: 10.16766/j.cnki.issn.1674-4152.003153
基金项目: 

浙江省医药卫生科技计划项目 2022KY1182

宁波市自然基金项目 2017A610276

宁波市鄞州区农社科类科技项目 2021AS0053

详细信息
    通讯作者:

    李红亮,E-mail:rmlihongliang@nbu.edu.cn

  • 中图分类号: R575.5

Study on correlation between serum hypersensitive C-reactive protein and nonalcoholic fatty liver disease in the elderly

  • 摘要:   目的  探讨血清超敏C反应蛋白(hs-CRP)与老年人非酒精性脂肪肝(NAFLD)间的关系,为防治NAFLD提供依据。  方法  调查2013年3—11月符合研究条件的2 124名年龄60岁及以上宁波市镇海区某石化企业退休员工,测量腰围、血压、体重指数、空腹血糖、尿酸、血脂谱、肝功能、hs-CRP和腹部B超结果。按hs-CRP水平的四分位数分为Q1组为≤0.4 mg/L(n=667),Q2组为>0.4 mg/L~≤0.7 mg/L(n=437),Q3组为>0.7 mg/L~≤1.4 mg/L(n=515),Q4组为>1.4 mg/L(n=505),NAFLD患病危险因素采用logistic回归分析。  结果  老年人NAFLD的患病率为25.8%(548/2 124);随着年龄的增长,患病率逐渐降低差异有统计学意义(P<0.05),Q1、Q2、Q3、Q4组的NAFLD患病率为13.2%(88/667)、24.5%(107/437)、32.6%(168/515)、36.6%(185/505),患病率逐渐增高,差异有统计学意义(χ2=99.246,P<0.001);多因素logistic回归分析显示升高的血清hs-CRP是老年人患NAFLD的危险因素,未校正相关因素前Q2、Q3、Q4分组的NAFLD患病风险分别是Q1的2.133、3.185、3.804倍,校正相关因素后分别是Q1组的1.554、1.828、1.895倍。  结论  升高的血清hs-CRP是老年人NAFLD患病的独立危险因素。

     

  • 表  1  对照组和NAFLD组临床、实验室检查指标比较

    Table  1.   Comparison of clinical and laboratory examination indexes between control group and NAFLD group

    组别 例数 年龄
    (x±s,岁)
    腰围
    (x±s,cm)
    BMI
    (x±s)
    收缩压
    (x±s,mmHg)
    舒张压
    (x±s,mmHg)
    TC
    [M(P25, P75),mmol/L]
    TG
    [M(P25, P75),mmol/L]
    HDL-C
    (x±s,mmol/L)
    对照组 1 576 69.2±7.2 82.9±8.1 23.1±2.7 131.1±16.9 77.7±10.4 4.9(4.3, 5.6) 1.2(0.7, 1.6) 1.6±0.4
    NAFLD组 548 68.3±6.5 90.3±7.8 26.0±2.6 135.9±16.6 80.8±9.9 4.9(4.3, 5.7) 1.6(1.2, 2.2) 1.4±0.3
    t 2.698a 18.533a 20.608a 5.734a 6.144a 0.252b 13.381b 10.727a
    P 0.007 < 0.001 < 0.001 < 0.001 < 0.001 0.801 < 0.001 < 0.001
    组别 例数 LDL-C
    (x±s,mmol/L)
    ALT
    [M(P25, P75),U/L]
    AST
    [M(P25, P75),U/L]
    GGT
    [M(P25, P75),U/L]
    空腹血糖
    (x±s,mmol/L)
    尿酸
    (x±s,μmol/L)
    HbA1c
    [M(P25, P75),%]
    hs-CRP
    [M(P25, P75),mg/L]
    对照组 1 576 2.7±0.8 16(13, 21) 23(19, 26) 20(16, 29) 5.4±0.6 318.8±77.9 5.1(4.8, 5.4) 0.6(0.3, 1.2)
    NAFLD组 548 2.7±0.8 21(16, 29) 24(20, 28) 27(19, 39) 5.5±0.7 360.2±78.2 5.3(4.9, 5.6) 1.0(0.6, 1.9)
    t 0.681a 12.660b 4.222b 10.470b 4.140a 10.712a 5.021b 10.149b
    P 0.496 < 0.001 < 0.001 < 0.001 < 0.001 < 0.001 < 0.001 < 0.001
    注:1 mmHg=0.133 kPa;at值,bZ值。
    下载: 导出CSV

    表  2  不同性别不同hs-CRP浓度组NAFLD患病情况[例(%)]

    Table  2.   Prevalence of NAFLD in different sex groups with different hs-CRP concentrations[cases (%)]

    性别 Q1(n=667) Q2(n=437) Q3(n=515) Q4(n=505) χ2 P
    男性 66(18.8) 77(21.9) 107(30.5) 101(28.8) 52.159 < 0.001
    女性 22(11.2) 30(15.2) 61(31.0) 84(42.6) 60.509 < 0.001
    合计 88(13.2) 107(24.5) 168(32.6) 185(36.6) 99.246 < 0.001
    下载: 导出CSV

    表  3  hs-CRP分层后老年人的临床特征

    Table  3.   Clinical characteristics of the elderly after hs-CRP stratification

    项目 Q1(n=667) Q2(n=437) Q3(n=515) Q4(n=505) 统计量 P
    年龄(x±s,岁) 67.9±6.6 68.5±7.1 69.5±7.0 70.2±7.3 12.196a < 0.001
    腰围(x±s,cm) 82.0±8.3 84.7±8.0 86.5±8.5 86.9±8.8 41.502a < 0.001
    BMI(x±s) 22.8±2.9 23.9±2.6 24.4±2.9 24.7±3.0 48.356a < 0.001
    收缩压(x±s,mmHg) 129.9±16.2 132.3±17.6 133.6±16.7 134.3±16.9 7.974a < 0.001
    舒张压(x±s,mmHg) 77.3±9.8 78.3±9.8 79.2±10.3 79.4±10.6 5.086a 0.002
    TC[M(P25, P75),mmol/L] 4.8(4.2, 5.5) 5.0(4.3, 5.6) 5.0(4.4, 5.7) 5.0(4.4, 5.7) 17.099b 0.001
    TG[M(P25, P75),mmol/L] 1.1(0.8, 1.4) 1.2(0.9, 1.8) 1.4(1.0, 1.9) 1.4(1.0, 1.9) 104.223b < 0.001
    HDL-C(x±s,mmol/L) 1.6±0.4 1.6±0.4 1.5±0.3 1.4±0.3 -19.633a < 0.001
    LDL-C(x±s,mmol/L) 2.6±0.8 2.7±0.7 2.7±0.7 2.8±0.8 10.832a 0.001
    ALT[M(P25, P75),U/L] 17(13, 22) 18(13, 24) 18(14, 24) 17(13, 24) 13.339b 0.004
    AST[M(P25, P75),U/L] 22(19, 27) 23(19, 27) 23(20, 28) 23(19, 27) 9.447b 0.024
    GGT[M(P25, P75),U/L] 19(15, 26) 22(16, 33) 24(18, 34) 25(18, 38) 11.248b < 0.001
    空腹血糖(x±s,mmol/L) 5.4±0.6 5.4±0.6 5.4±0.6 5.5±0.6 1.614a 0.184
    尿酸(x±s,μmol/L) 313.0±70.4 324.7±79.6 339.9±78.8 344.7±88.9 19.453a < 0.001
    HbA1c[M(P25, P75),%] 5.1(4.8, 5.4) 5.2(4.9, 5.5) 5.2(4.8, 5.5) 5.2(4.9, 5.6) 21.524b < 0.001
    注:aF值,bH值。
    下载: 导出CSV

    表  4  老年人NAFLD的患病危险因素的logistic回归分析

    Table  4.   Logistic regression analysis of risk factors for NAFLD in the elderly

    项目 B SE Wald χ2 P OR(95% CI)
    年龄 -0.040 0.009 21.516 <0.001 0.961(0.944~0.977)
    腰围 0.809 0.131 38.104 <0.001 2.245(1.737~2.902)
    体重指数 0.133 1.045 61.524 <0.001 2.842(2.189~3.690)
    收缩压 0.189 0.136 1.950 0.163 1.209(0.926~1.577)
    舒张压 0.072 0.182 0.157 0.692 1.075(0.752~1.536)
    三酰甘油 0.121 0.838 47.677 <0.001 2.312(1.822~2.932)
    高密度脂蛋白 0.215 0.211 1.032 0.310 1.240(0.819~1.876)
    谷丙转氨酶 0.382 0.474 0.651 0.420 1.466(0.579~3.710)
    谷草转氨酶 0.701 0.350 4.004 0.045 2.015(1.014~4.002)
    谷氨酰转肽酶 0.219 0.227 0.924 0.336 1.244(0.797~1.942)
    空腹血糖 0.586 0.153 14.721 <0.001 1.797(1.332~2.423)
    尿酸 0.494 0.133 13.809 <0.001 1.639(1.263~2.126)
    糖化血红蛋白 0.551 0.274 4.059 0.044 1.735(1.015~2.967)
    hs-CRP 27.394 <0.001 1
      Q2 vs. Q1 0.416 0.177 5.547 0.019 1.516(1.072~2.143)
      Q3 vs. Q1 0.730 0.166 19.425 <0.001 2.075(1.500~2.871)
      Q4 vs. Q1 0.790 0.166 22.556 <0.001 2.203(1.590~3.053)
    下载: 导出CSV

    表  5  不同hs-CRP浓度对老年人NAFLD的患病影响的logistic回归分析

    Table  5.   Logistic regression analysis of the influence of different hs-CRP concentrations on the incidence of NAFLD in the elderly

    组别 例数 模型1 模型2
    P OR(95% CI) P OR(95% CI)
    Q2 437 <0.001 2.133(1.560~2.917) 0.016 1.554(1.086~2.223)
    Q3 515 <0.001 3.185(2.383~4.258) 0.001 1.828(1.298~2.574)
    Q4 505 <0.001 3.804(2.851~5.074) <0.001 1.895(1.335~2.692)
    注:以Q1为参照。模型1为未校正; 模型2为调整年龄、性别、BMI、腰围、收缩压、舒张压、空腹血糖、TC、TG、HDL-C、ALT、AST、GGT、尿酸、HbA1c。
    下载: 导出CSV
  • [1] AVAN A, TAVAKOLY SANY S B, GHAYOUR-MOBARHAN M, et al. Serum C-reactive protein in the prediction of cardiovascular diseases: overview of the latest clinical studies and public health practice[J]. J Cell Physiol, 2018, 233(11): 8508-8525. doi: 10.1002/jcp.26791
    [2] 孙慧文, 占伊扬, 陈敏敏, 等. 南京地区事业单位老年人群非酒精性脂肪肝相关代谢指标分析[J]. 中华全科医学, 2021, 19(6): 1035-1038. doi: 10.16766/j.cnki.issn.1674-4152.001978

    SUN H W, ZHAN Y Y, CHEN M M, et al. Analysis of related metabolic indexes of non-alcoholic fatty liver disease in the elderly popluation of public institutions in Nanjing[J]. Chinese Journal of General Practice, 2021, 19(6): 1035-1038. doi: 10.16766/j.cnki.issn.1674-4152.001978
    [3] ZHENG X, ZENG N, WANG A, et al. Elevated C-reactive protein and depressed high-density lipoprotein cholesterol are associated with poor function outcome after ischemic stroke[J]. Curr Neurovasc Res, 2018, 15(3): 226-233. doi: 10.2174/1567202615666180712100440
    [4] TAN C H, AL-KALIFAH N, LEE W J, et al. HSCRP as surrogate marker in predicting long term effect of bariatric surgery on resolution of non-alcoholic steatohepatitis[J]. Asian J Surg, 2019, 42(1): 203-208. doi: 10.1016/j.asjsur.2018.04.010
    [5] JIA M, SHI Y X, WANG Y M, et al. High-sensitivity C-reactive protein and ischemic stroke in patients with nonalcoholic fatty liver disease: a prospective study[J]. J Healthc Eng, 2022: 9711712. DOI: 10.1155/2022/9711712.
    [6] 中华医学会肝病学分会脂肪肝和酒精性肝病学组, 范建高. 非酒精性脂肪性肝病诊疗指南(2010年修订版)[J]. 中华肝脏病杂志, 2010(3): 163-166. doi: 10.3760/cma.j.issn.1007-3418.2010.03.002

    Fatty liver and alcoholic liver Disease Group, Chinese Society of Hepatology. Guidelines for Diagnosis and Treatment of non-alcoholic Fatty Liver Disease (Revised 2010)[J]. Chin J Hepatol, 2010(3): 163-166. doi: 10.3760/cma.j.issn.1007-3418.2010.03.002
    [7] 嵇龙飞, 蔡云祥, 强鑫华. 非酒精性脂肪肝现状与糖化血红蛋白的关系[J]. 浙江临床医学, 2022, 24(12): 1798-1800. https://www.cnki.com.cn/Article/CJFDTOTAL-TJYZ201812012.htm

    JI L F, Cai YUN X, QIANG X H. The relationship between the current status of non-alcoholic fatty liver disease and glycated hemoglobin[J]. Zhejiang Clinical Medical Journal, 2022, 24(12): 1798-1800. https://www.cnki.com.cn/Article/CJFDTOTAL-TJYZ201812012.htm
    [8] 王程成, 刘怀磊, 龚卫红. 社区老年高血压人群中血细胞参数与非酒精性脂肪肝的关系[J]. 中华全科医学, 2021, 19(6): 979-981, 1007. doi: 10.16766/j.cnki.issn.1674-4152.001965

    WANG C C, LIU H L, GONG W H. Association of blood cell parameters with non-alcoholic fatty liver disease in the elderly with hypertension[J]. Chinese Journal of General Practice, 2021, 19(6): 979-981, 1007. doi: 10.16766/j.cnki.issn.1674-4152.001965
    [9] ESLAM M, SANYAL A J, GEORGE J, et al. MAFLD: a consensus driven proposed nomenclature for metabolic associated fatty liver disease[J]. Gastroenterology, 2020, 158(7): 1999-2014. doi: 10.1053/j.gastro.2019.11.312
    [10] 王思超, 孙卫霞, 成艺坪, 等. 非酒精性脂肪肝合并2型糖尿病患者的肝脏脂肪含量与各代谢指标的相关性[J]. 医学临床研究, 2020, 37(2): 189-192. doi: 10.3969/j.issn.1671-7171.2020.02.009

    WANG S C, SUN W X, CHENG Y P, et al. Correlation between Liver Fat Content and Metabolic Indexes in Patients with Non-alcoholic Fatty Liver Complicated with Type 2 Diabetes[J]. J Clin Res, 2020, 37(2): 189-192. doi: 10.3969/j.issn.1671-7171.2020.02.009
    [11] BENNOUAR S, CHERIF A B, KESSIRA A, et al. Association and interaction between vitamin D level and metabolic syndrome for non-alcoholic fatty liver disease[J]. J Diabetes Metab Disord, 2021, 20(2): 1309-1317. doi: 10.1007/s40200-021-00857-5
    [12] 李婧, 李小凤, 闫妮, 等. 评估肥胖相关指标对非酒精性脂肪肝的筛查价值[J]. 中华全科医学, 2023, 21(2): 195-198. doi: 10.16766/j.cnki.issn.1674-4152.002843

    LI J, LI X F, YAN N, et al. Evaluation the screening value of obesity-related indices for non-alcoholic fatty liver disease[J]. Chinese Journal of General Practice, 2023, 21(2): 195-198. doi: 10.16766/j.cnki.issn.1674-4152.002843
    [13] COlCA J R, SCHERER P E. The metabolic syndrome, thiazolidinediones, and implications for intersection of chronic and inflammatory disease[J]. Mol Metab, 2022: 101409. DOI: 10.1016/j.molmet.2021.101409.
    [14] ZAHARI SHAM S Y, HANIF E, THAMBIAH S C, et al. High sensitivity C-reactive protein(hsCRP): its relationship with metabolic syndrome and Framingham risk score[J]. Malay J Pathol, 2021, 43(1): 33-40.
    [15] KUMAR R, PORWAL YC, DEV N, et al. Association of high-sensitivity C-reactive pro-tein (hs-CRP) with non-alcoholic fatty liver disease (NAFLD) in Asian Indians: a cross-sectional study[J]. J Family Med Prim Care, 2020, 9(1): 390-394.
    [16] ZIEMIAŃSKI P, DOMIENIK-KARLOWICZ J, CYLKE R, et al. High-sensitivity C-reactive protein as a new predictor of the course of nonalcoholic fatty liver disease in patients after bariatric surgery[J]. Pol Arch Intern Med, 2019, 129(7-8): 556-558.
    [17] 刘思甫, 谢正元, 汤胜兰, 等. 高敏C反应蛋白与非酒精性脂肪性肝病相关性的Meta分析[J]. 中国循证医学杂志, 2020, 20(7): 769-775. https://www.cnki.com.cn/Article/CJFDTOTAL-ZZXZ202007006.htm

    LIU S P, XIE Z Y, TANG S L, et al. Association between high sensitivity C-reactive protein and nonalcoholic fatty liver disease: a meta-analysis[J]. Chinese Journal of Evidence-based Medicine, 2020, 20(7): 769-775. https://www.cnki.com.cn/Article/CJFDTOTAL-ZZXZ202007006.htm
    [18] BIAN F, YANG X Y, XU G, et al. CRP-Induced NLRP3 Inflammasome Activation Increases LDL Transcytosis Across Endothelial CellsCRP-Induced NLRP3 Inflammasome activation increases LDL transcytosis across endothelial cells[J]. Front Pharmacol, 2019, 10: 40. DOI: 10.3389/fphar.2019.00040.
    [19] 陈明, 谭强. 非酒精性脂肪肝对急性心肌梗死患者预后的影响[J]. 中华实用诊断与治疗杂志, 2020, 34(1): 33-36. https://www.cnki.com.cn/Article/CJFDTOTAL-HNZD202001009.htm

    CHEN M, TANG Q. Influence of non-alcoholic fatty liver disease on acute myocardial infarction[J]. J Chin Pract Diagn Ther, 2020, 34(1): 33-36. https://www.cnki.com.cn/Article/CJFDTOTAL-HNZD202001009.htm
    [20] 董桂芳, 陈杰, 李雪梅. 自主神经调控参与非酒精性脂肪肝发生发展的相关机制研究进展[J]. 北京医学, 2022, 44(10): 920-922. https://www.cnki.com.cn/Article/CJFDTOTAL-BJYX202210011.htm

    DONG G F, CHEN J, LI X M. Research progress on the mechanism of autonomic nervous regulation involved in the occurrence and development of non-alcoholic fatty liver disease[J]. Beijing Medical Journal, 2022, 44(10): 920-922. https://www.cnki.com.cn/Article/CJFDTOTAL-BJYX202210011.htm
  • 加载中
表(5)
计量
  • 文章访问数:  157
  • HTML全文浏览量:  36
  • PDF下载量:  13
  • 被引次数: 0
出版历程
  • 收稿日期:  2023-02-03
  • 网络出版日期:  2023-10-19

目录

    /

    返回文章
    返回