自身免疫性疾病对胰腺内分泌和外分泌疾病风险的影响: 基于英国生物样本库的前瞻性队列研究

张晶晶, 袁晨晨, 路国涛, 肖炜明, 龚卫娟, 冯学兵

张晶晶, 袁晨晨, 路国涛, 肖炜明, 龚卫娟, 冯学兵. 自身免疫性疾病对胰腺内分泌和外分泌疾病风险的影响: 基于英国生物样本库的前瞻性队列研究[J]. 实用临床医药杂志, 2025, 29(7): 1-7, 12. DOI: 10.7619/jcmp.20245503
引用本文: 张晶晶, 袁晨晨, 路国涛, 肖炜明, 龚卫娟, 冯学兵. 自身免疫性疾病对胰腺内分泌和外分泌疾病风险的影响: 基于英国生物样本库的前瞻性队列研究[J]. 实用临床医药杂志, 2025, 29(7): 1-7, 12. DOI: 10.7619/jcmp.20245503
ZHANG Jingjing, YUAN Chenchen, LU Guotao, XIAO Weiming, GONG Weijuan, FENG Xuebing. Impact of autoimmune diseases on risk of pancreatic endocrine and exocrine diseases: a prospective cohort study based on the UK Biobank[J]. Journal of Clinical Medicine in Practice, 2025, 29(7): 1-7, 12. DOI: 10.7619/jcmp.20245503
Citation: ZHANG Jingjing, YUAN Chenchen, LU Guotao, XIAO Weiming, GONG Weijuan, FENG Xuebing. Impact of autoimmune diseases on risk of pancreatic endocrine and exocrine diseases: a prospective cohort study based on the UK Biobank[J]. Journal of Clinical Medicine in Practice, 2025, 29(7): 1-7, 12. DOI: 10.7619/jcmp.20245503

自身免疫性疾病对胰腺内分泌和外分泌疾病风险的影响: 基于英国生物样本库的前瞻性队列研究

基金项目: 

国家自然科学基金面上项目 82270680

国家自然科学基金面上项目 82241043

江苏省扬州市重点学科重症医学实验室 YZYXZDXK-11

详细信息
    通讯作者:

    冯学兵

  • 中图分类号: R593.2;R576;R181.3

Impact of autoimmune diseases on risk of pancreatic endocrine and exocrine diseases: a prospective cohort study based on the UK Biobank

  • 摘要:
    目的 

    分析自身免疫性疾病(AIDs)与胰腺内分泌和外分泌疾病发生风险的相关性。

    方法 

    纳入来自英国生物样本库中的451 497名参与者, 主要结局为胰腺内分泌和外分泌疾病。使用国际疾病分类9/10(ICD9/10)代码定义各个AIDs以及胰腺内分泌和外分泌疾病。采用多变量Cox风险模型对年龄、性别、种族、汤森剥夺指数、吸烟、饮酒、体质量指数、腰围、臀围、合并高血压、血脂异常和胆结石进行校正,评估AIDs与胰腺内分泌和外分泌疾病的关系。

    结果 

    共纳入415 497名参与者,其中37 482例在随访期间出现胰腺相关疾病。AIDs患者中,胰腺外分泌疾病、内分泌疾病的患者比率增高,差异有统计学意义(P < 0.05)。类风湿关节炎[HR (95% CI)=1.438(1.161~1.781)]、强直性脊柱炎[HR (95% CI)=1.675(1.009~2.780)]、溃疡性结肠炎[HR (95% CI)=1.335(1.037~1.719)]和克罗恩病[HR (95% CI)=1.530(1.154~2.028)]均与胰腺外分泌疾病发生风险增加相关(P均 < 0.05);类风湿关节炎[HR (95% CI)=1.119(1.004~1.248)]、溃疡性结肠炎[HR (95% CI)=1.324(1.175~1.491)]、系统性硬化症[HR (95% CI)=2.08(1.355~3.191)]和克罗恩病[HR (95% CI)=1.394(1.197~1.624)]均与胰腺内分泌疾病发生风险增加有关(P均 < 0.05)。

    结论 

    总体的AIDs以及部分特定的AIDs与胰腺内分泌和外分泌疾病风险增加相关,临床上应重视AIDs患者并发胰腺疾病的早期预防。

    Abstract:
    Objective 

    To analyze the correlations of autoimmune diseases (AIDs) with the risk of developing pancreatic endocrine and exocrine diseases.

    Methods 

    A total of 451, 497 participants from the UK Biobank were recruited, with the primary outcomes being pancreatic endocrine and exocrine diseases. International Classification of Diseases 9/10 (ICD9/10) codes were used to define each AIDs, the pancreatic endocrine and exocrine diseases. Multivariable Cox proportional hazards models were employed to assess the relationships between AIDs and pancreatic endocrine and exocrine diseases, with adjustments for age, gender, ethnicity, Townsend deprivation index, smoking, alcohol consumption, body mass index, waist circumference, hip circumference, hypertension, dyslipidemia, and gallstones.

    Results 

    A total of 415, 497 participants were included, among which 37, 482 developed pancreas-related diseases during follow-up. Among patients with AIDs, the proportions of those with pancreatic exocrine and endocrine diseases were significantly increased (P < 0.05). Rheumatoid arthritis [HR(95%CI): 1.438(1.161 to 1.781)], ankylosing spondylitis [HR(95%CI): 1.675(1.009 to 2.780)], ulcerative colitis [HR(95%CI): 1.335(1.037 to 1.719)], and Crohn's disease [HR(95%CI): 1.530(1.154 to 2.028)] were all associated with an increased risk of developing pancreatic exocrine diseases (all P < 0.05); additionally, rheumatoid arthritis [HR(95%CI): 1.119(1.004 to 1.248)], ulcerative colitis [HR(95%CI): 1.324(1.175 to 1.491)], systemic sclerosis [HR(95%CI): 2.08(1.355 to 3.191)], and Crohn's disease[HR(95%CI): 1.394(1.197 to 1.624)] were also associated with an increased risk of developing pancreatic endocrine diseases (all P < 0.05).

    Conclusion 

    Overall AIDs and some specific AIDs are associated with an increased risk of developing pancreatic endocrine and exocrine diseases, and early prevention of pancreatic diseases in patients with AIDs should be emphasized in clinical practice.

  • 图  1   筛选流程图

    图  2   伴有AIDs组与无AIDs组发生胰腺疾病的累积概率

    A: 总体发生胰腺疾病的风险; B: 发生胰腺外分泌疾病的风险; C: 发生胰腺内分泌疾病的风险。

    表  1   伴有AIDs与无AIDs的参与者基线特征比较[n(%)][M(P25, P75)]

       基线特征 分类 无AIDs组(n=443 271) 伴有AIDs组(n=8 226) P
    年龄/岁 58.0(50.0, 63.0) 59.0(52.0, 64.0) < 0.001
    人种(白种人) 420 846(94.9) 7 863(95.6) 0.008
    性别(女性) 239 902(54.1) 5 032(61.2) < 0.001
    吸烟 从不 245 702(55.4) 3 854(46.9) < 0.001
    既往 151 652(34.2) 3 388(41.2)
    现在 45 917(10.4) 984(12.0)
    饮酒 从不 18 440(4.2) 520(6.3) < 0.001
    既往 14 661(3.3) 584(7.1)
    现在 410 170(92.5) 7 122(86.6)
    体质量指数/(kg/m2) 26.6(24.1, 29.7) 26.9(24.1, 30.3) < 0.001
    腰围/cm 89.0(80.0, 98.0) 90.0(80.0, 99.0) < 0.001
    臀围/cm 102.0(97.0, 108.0) 102.0(97.0, 109.0) 0.076
    汤森剥夺指数 -2.2(-3.7, 0.4) -1.9(-3.5, 1.0) < 0.001
    高血压 133 728(30.2) 3 800(46.2) < 0.001
    血脂异常 68 120(15.4) 1 784(21.7) < 0.001
    胆结石 23 012(5.2) 908(11.0) < 0.001
    总胰腺疾病 36 364(8.2) 1 118(13.6) < 0.001
    胰腺外分泌疾病 7 432(1.6) 280(3.4) < 0.001
    急性胰腺炎 2 849(0.6) 111(1.3) < 0.001
    胰腺癌 1 749(0.4) 33(0.4) 0.925
    其他胰腺外分泌疾病 2 834(0.6) 136(1.7) < 0.001
    胰腺内分泌疾病 34 259(7.7) 1 078(13.1) < 0.001
    糖尿病 31 438(7.1) 911(11.1) < 0.001
    其他胰腺内分泌疾病 2 821(0.6) 167(2.0) < 0.001
    下载: 导出CSV

    表  2   AIDs与总体胰腺疾病发生风险的相关性

    变量 模型1 模型2
    P HR 95%CI P HR 95%CI
    系统性红斑狼疮 0.005 1.605 1.157~2.225 0.895 0.978 0.705~1.357
    类风湿关节炎 < 0.001 1.792 1.624~1.977 < 0.001 1.199 1.087~1.323
    干燥综合征 < 0.001 1.720 1.296~2.283 0.359 1.142 0.860~1.516
    系统性硬化症 < 0.001 2.645 1.772~3.946 < 0.001 2.062 1.381~3.077
    肌炎 0.034 2.025 1.054~3.893 0.132 1.652 0.859~3.175
    血管炎 < 0.001 1.929 1.503~2.474 0.110 1.225 0.955~1.572
    强直性脊柱炎 0.007 1.446 1.107~1.888 0.838 0.973 0.745~1.270
    银屑病和肠性关节炎 < 0.001 1.861 1.467~2.361 0.503 1.085 0.855~1.376
    多发性硬化症 < 0.001 1.671 1.369~2.040 0.071 1.202 0.985~1.467
    重症肌无力 < 0.001 2.504 1.705~3.677 0.030 1.529 1.041~2.246
    自身免疫性肝炎 0.013 2.055 1.167~3.619 0.315 1.337 0.759~2.354
    溃疡性结肠炎 < 0.001 1.499 1.345~1.672 < 0.001 1.347 1.208~1.502
    克罗恩病 < 0.001 1.744 1.522~1.999 < 0.001 1.477 1.289~1.693
    Graves病 < 0.001 1.928 1.409~2.640 0.060 1.351 0.987~1.850
    自身免疫性甲状腺炎 0.479 1.127 0.707~2.096 0.929 0.976 0.566~1.681
    自身免疫性溶血 0.028 2.680 1.115~6.439 0.536 1.318 0.549~3.168
    特发性血小板减少 0.001 1.697 1.235~2.333 0.167 1.252 0.910~1.720
    模型1: 根据招募时的年龄、性别、种族及汤森剥夺指数进行调整; 模型2: 进一步调整了吸烟、饮酒、BMI、腰围、臀围、合并高血压、血脂异常、胆结石。
    下载: 导出CSV

    表  3   AIDs与胰腺外分泌疾病发生风险的相关性

    变量 模型1 模型2
    P HR 95%CI P HR 95%CI
    系统性红斑狼疮 0.003 2.545 1.368~4.734 0.175 1.536 0.826~2.859
    类风湿关节炎 < 0.001 2.151 1.738~2.662 < 0.001 1.438 1.161~1.781
    干燥综合征 0.102 1.726 0.897~3.319 0.783 1.096 0.570~2.109
    系统性硬化症 0.104 2.253 0.845~6.006 0.409 1.512 0.567~4.030
    肌炎 0.184 2.560 0.640~10.237 0.695 1.319 0.330~5.276
    血管炎 0.011 2.086 1.184~3.675 0.312 1.339 0.760~2.361
    强直性脊柱炎 < 0.001 2.503 1.508~4.155 0.046 1.675 1.009~2.780
    银屑病和肠性关节炎 0.050 1.805 0.999~3.260 0.682 1.132 0.626~2.046
    多发性硬化症 0.004 1.897 1.223~2.943 0.317 1.251 0.806~1.942
    重症肌无力 0.003 3.363 1.511~7.488 0.151 1.799 0.808~4.007
    自身免疫性肝炎 0.394 1.826 0.457~7.302 0.986 1.012 0.253~4.051
    溃疡性结肠炎 < 0.001 1.687 1.311~2.171 0.025 1.335 1.037~1.719
    克罗恩病 < 0.001 2.418 1.833~3.216 0.003 1.530 1.154~2.028
    Graves病 0.066 2.004 0.955~4.205 0.328 1.447 0.690~3.038
    自身免疫性甲状腺炎 0.496 1.482 0.478~4.597 0.907 0.935 0.301~2.900
    自身免疫性溶血
    特发性血小板减少 0.551 1.306 0.543~3.138 0.841 0.914 0.380~2.197
    模型1: 根据招募时的年龄、性别、种族及汤森剥夺指数进行调整; 模型2: 进一步调整了吸烟、饮酒、BMI、腰围、臀围、合并高血压、血脂异常、胆结石。在自身免疫性溶血基础上患有胰腺外分泌疾病参与者过少,因此未纳入分析。
    下载: 导出CSV

    表  4   AIDs与胰腺内分泌疾病发生风险的相关性

    变量 模型1 模型2
    P HR 95%CI P HR 95%CI
    系统性红斑狼疮 0.053 1.443 0.996~2.090 0.530 0.888 0.613~1.286
    类风湿关节炎 < 0.001 1.688 1.514~1.881 0.043 1.119 1.004~1.248
    干燥综合征 0.002 1.635 1.194~2.239 0.853 1.030 0.752~1.411
    系统性硬化症 < 0.001 2.675 1.744~4.103 < 0.001 2.080 1.355~3.191
    肌炎 0.105 1.845 0.880~3.871 0.142 1.742 0.830~3.655
    血管炎 < 0.001 1.871 1.426~2.456 0.237 1.178 0.898~1.547
    强直性脊柱炎 0.117 1.274 0.941~1.724 0.319 0.857 0.633~1.161
    银屑病和肠性关节炎 < 0.001 1.804 1.394~2.334 0.973 0.996 0.769~1.288
    多发性硬化症 < 0.001 1.686 1.361~2.089 0.076 1.214 0.980~1.504
    重症肌无力 < 0.001 2.249 1.466~3.449 0.083 1.460 0.951~2.239
    自身免疫性肝炎 0.012 2.128 1.178~3.843 0.192 1.482 0.820~2.677
    溃疡性结肠炎 < 0.001 1.441 1.279~1.622 < 0.001 1.324 1.175~1.491
    克罗恩病 < 0.001 1.578 1.355~1.838 < 0.001 1.394 1.197~1.624
    Graves病 < 0.001 1.958 1.399~2.741 0.055 1.389 0.992~1.945
    自身免疫性甲状腺炎 0.713 1.123 0.604~2.088 0.936 0.975 0.525~1.813
    自身免疫性溶血 0.010 3.156 1.314~7.582 0.332 1.543 0.642~3.707
    特发性血小板减少 0.003 1.679 1.194~2.363 0.235 1.230 0.874~1.731
    模型1: 根据招募时的年龄、性别、种族及汤森剥夺指数进行调整; 模型2: 进一步调整了吸烟、饮酒、BMI、腰围、臀围、合并高血压、血脂异常、胆结石。
    下载: 导出CSV
  • [1] 张佳旭, 杨婷, 李燃. 中老年重症急性胰腺炎患者住院期间死亡预测模型的构建与验证[J]. 实用临床医药杂志, 2024, 28(17): 51-55. doi: 10.7619/jcmp.20241933
    [2]

    HOQUE R, MALIK A F, GORELICK F, et al. Sterile inflammatory response in acute pancreatitis[J]. Pancreas, 2012, 41(3): 353-357. doi: 10.1097/MPA.0b013e3182321500

    [3]

    WATANABE T, KUDO M, STROBER W. Immunopathogenesis of pancreatitis[J]. Mucosal Immunol, 2016, 10(2): 283-298.

    [4]

    GUKOVSKY I, LI N, TODORIC J, et al. Inflammation, autophagy, and obesity: common features in the pathogenesis of pancreatitis and pancreatic cancer[J]. Gastroenterology, 2013, 144(6): 1199-1209. e4. doi: 10.1053/j.gastro.2013.02.007

    [5]

    HAYTER S M, COOK M C. Updated assessment of the prevalence, spectrum and case definition of autoimmune disease[J]. Autoimmun Rev, 2012, 11(10): 754-765. doi: 10.1016/j.autrev.2012.02.001

    [6]

    XIANG Y, ZHANG M X, JIANG D, et al. The role of inflammation in autoimmune disease: a therapeutic target[J]. Front Immunol, 2023, 14: 1267091. doi: 10.3389/fimmu.2023.1267091

    [7]

    GOBELET C, GERSTER J C, RAPPOPORT G, et al. A controlled study of the exocrine pancreatic function in Sj?gren's syndrome and rheumatoid arthritis[J]. Clin Rheumatol, 1983, 2(2): 139-143. doi: 10.1007/BF02032170

    [8]

    TÉL B, STUBNYA B, GEDE N, et al. Inflammatory bowel diseases elevate the risk of developing acute pancreatitis: a meta-analysis[J]. Pancreas, 2020, 49(9): 1174-1181. doi: 10.1097/MPA.0000000000001650

    [9]

    DESSEIN P H, JOFFE B I. Insulin resistance and impaired beta cell function in rheumatoid arthritis[J]. Arthritis Rheum, 2006, 54(9): 2765-2775. doi: 10.1002/art.22053

    [10]

    GARCÍA-CARRASCO M, MENDOZA-PINTO C, MUNGUÍA-REALPOZO P, et al. Insulin resistance and diabetes mellitus in patients with systemic lupus erythematosus[J]. Endocr Metab Immune Disord Drug Targets, 2023, 23(4): 503-514. doi: 10.2174/1871530322666220908154253

    [11]

    DONG X W, ZHU Q T, YUAN C C, et al. Associations of intrapancreatic fat deposition with incident diseases of the exocrine and endocrine pancreas: a UK biobank prospective cohort study[J]. Am J Gastroenterol, 2024, 119(6): 1158-1166. doi: 10.14309/ajg.0000000000002792

    [12]

    GUKOVSKAYA A S, GUKOVSKY I, ALGVL H, et al. Autophagy, inflammation, and immune dysfunction in the pathogenesis of pancreatitis[J]. Gastroenterology, 2017, 153(5): 1212-1226. doi: 10.1053/j.gastro.2017.08.071

    [13]

    REN W X, ZHAO L, SUN Y, et al. HMGB1 and toll-like receptors: potential therapeutic targets in autoimmune diseases[J]. Mol Med, 2023, 29(1): 117. doi: 10.1186/s10020-023-00717-3

    [14]

    CHANG C C, CHIOU C S, LIN H L, et al. Increased risk of acute pancreatitis in patients with rheumatoid arthritis: a population-based cohort study[J]. PLoS One, 2015, 10(8): e0135187. doi: 10.1371/journal.pone.0135187

    [15]

    ALKHAYYAT M, ABOU SALEH M, GREWAL M K, et al. Pancreatic manifestations in rheumatoid arthritis: a national population-based study[J]. Rheumatology: Oxford, 2021, 60(5): 2366-2374. doi: 10.1093/rheumatology/keaa616

    [16]

    MONTENEGRO M L, CORRAL J E, LUKENS F J, et al. Pancreatic disorders in patients with inflammatory bowel disease[J]. Dig Dis Sci, 2022, 67(2): 423-436. doi: 10.1007/s10620-021-06899-2

    [17]

    MASSIRONI S, FANETTI I, VIGANÒ C, et al. Systematic review-pancreatic involvement in inflammatory bowel disease[J]. Aliment Pharmacol Ther, 2022, 55(12): 1478-1491. doi: 10.1111/apt.16949

    [18]

    PEDERSEN J E, ÄNGQUIST L H, JENSEN C B, et al. Risk of pancreatitis in patients with inflammatory bowel disease - a meta-analysis[J]. Dan Med J, 2020, 67(3): A08190427.

    [19] 李金强, 惠亮亮. 急性胰腺炎患者肠道菌群的研究进展[J]. 中国微生态学杂志, 2024, 36(12): 1480-1484.
    [20]

    NAVARRO J F, MORA C. Role of inflammation in diabetic complications[J]. Nephrol Dial Transplant, 2005, 20(12): 2601-2604. doi: 10.1093/ndt/gfi155

    [21]

    ROHM T V, MEIER D T, OLEFSKY J M, et al. Inflammation in obesity, diabetes, and related disorders[J]. Immunity, 2022, 55(1): 31-55. doi: 10.1016/j.immuni.2021.12.013

    [22]

    NIE Y Q, ZHOU H T, WANG J, et al. Association between systemic immune-inflammation index and diabetes: a population-based study from the NHANES[J]. Front Endocrinol (Lausanne), 2023, 14: 1245199. doi: 10.3389/fendo.2023.1245199

    [23]

    WU D, LAN Y L, CHEN S H, et al. Combined effect of adiposity and elevated inflammation on incident type 2 diabetes: a prospective cohort study[J]. Cardiovasc Diabetol, 2023, 22(1): 351. doi: 10.1186/s12933-023-02067-0

    [24]

    MA X L, CHEN Z J, WANG L, et al. The pathogenesis of diabetes mellitus by oxidative stress and inflammation: its inhibition by berberine[J]. Front Pharmacol, 2018, 9: 782. doi: 10.3389/fphar.2018.00782

    [25]

    DUBREUIL M, RHO Y H, MAN A D, et al. Diabetes incidence in psoriatic arthritis, psoriasis and rheumatoid arthritis: a UK population-based cohort study[J]. Rheumatology (Oxford), 2014, 53(2): 346-352. doi: 10.1093/rheumatology/ket343

    [26]

    TIAN Z X, MCLAUGHLIN J, VERMA A, et al. The relationship between rheumatoid arthritis and diabetes mellitus: a systematic review and meta-analysis[J]. Cardiovasc Endocrinol Metab, 2021, 10(2): 125-131. doi: 10.1097/XCE.0000000000000244

    [27]

    SANG M M, SUN Z L, WU T Z. Inflammatory bowel disease and diabetes: is there a link between them[J]. World J Diabetes, 2022, 13(2): 126-128. doi: 10.4239/wjd.v13.i2.126

    [28]

    JESS T, JENSEN B W, ANDERSSON M, et al. Inflammatory bowel diseases increase risk of type 2 diabetes in a nationwide cohort study[J]. Clin Gastroenterol Hepatol, 2020, 18(4): 881-888. e1. doi: 10.1016/j.cgh.2019.07.052

    [29]

    JASSER-NITSCHE H, BECHTOLD-DALLA POZZA S, BINDER E, et al. Comorbidity of inflammatory bowel disease in children and adolescents with type 1 diabetes[J]. Acta Paediatr, 2021, 110(4): 1353-1358. doi: 10.1111/apa.15643

图(2)  /  表(4)
计量
  • 文章访问数:  75
  • HTML全文浏览量:  20
  • PDF下载量:  26
  • 被引次数: 0
出版历程
  • 收稿日期:  2024-11-11
  • 修回日期:  2025-02-15
  • 刊出日期:  2025-04-14

目录

    /

    返回文章
    返回