血清生物标志物在溃疡性结肠炎诊治应用中的研究进展
The Latest Research Progress on the Application of Serum Biomarkers in the Diagnosis and Treatment of Ulcerative Colitis
DOI: 10.12677/acm.2026.1682771, PDF,   
作者: 杨 佳, 艾克鹏, 杨伊琪:延安大学延安医学院,陕西 延安;古巧燕*:延安大学附属医院消化内科,陕西 延安
关键词: 溃疡性结肠炎;血清生物标志物;白细胞介素;MicroRNA;Ulcerative Colitis; Serum Biomarker; Interleukins; MicroRNA
摘要: 溃疡性结肠炎(ulcerative colitis, UC)是一种慢性、非特异性的肠道炎症性疾病,其诊断和疗效监测长期依赖内镜与组织病理学检查,这些“金标准”虽准确但具有侵入性、费用高昂且患者依从性差。因此,开发便捷、无创且能反映疾病活动度的血清生物标志物成为临床迫切需求。传统血清指标如C反应蛋白(CRP)和红细胞沉降率(ESR)虽临床应用广泛,但敏感性与特异性有限,部分活动期患者可表现为正常水平。近年来,随着对UC免疫病理机制的深入认识,包括肠上皮屏障功能障碍、固有免疫与适应性免疫的异常激活、以及肠道微生态紊乱,一系列新型血清生物标志物相继涌现,如肠道微生态标志物、肠道屏障损伤相关标志物、基因组学相关标志物。本文系统梳理该领域的研究进展,为实现UC的精准诊疗提供新的思路和手段。
Abstract: Ulcerative colitis (UC) is a chronic, non-specific inflammatory bowel disease whose diagnosis and therapeutic monitoring have long relied on endoscopic and histopathological examinations. Although these ‘gold standards’ are accurate, they are invasive, costly, and associated with poor patient compliance. Therefore, there is an urgent clinical need to develop convenient, non-invasive serum biomarkers that can reflect disease activity. Although traditional serum markers such as C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) are widely used in clinical practice, their sensitivity and specificity are limited, and some patients with active disease may present with normal levels. In recent years, with a deeper understanding of the immunopathological mechanisms of UC—including intestinal epithelial barrier dysfunction, aberrant activation of innate and adaptive immunity, and gut microbiota dysbiosis—a range of novel serum biomarkers have emerged, such as gut microbiome-related markers, intestinal barrier injury-associated markers, and genomics-related markers. This article systematically reviews the research progress in this field, aiming to provide new ideas and approaches for achieving precision diagnosis and treatment of UC.
文章引用:杨佳, 艾克鹏, 杨伊琪, 古巧燕. 血清生物标志物在溃疡性结肠炎诊治应用中的研究进展[J]. 临床医学进展, 2026, 16(8): 55-61. https://doi.org/10.12677/acm.2026.1682771

参考文献

[1] Li, W., Zhao, T., Wu, D., Li, J., Wang, M., Sun, Y., et al. (2022) Colorectal Cancer in Ulcerative Colitis: Mechanisms, Surveillance and Chemoprevention. Current Oncology, 29, 6091-6114.
https://doi.org/10.3390/curroncol29090479
[2] Neubauer, K., Woźniak-Stolarska, B. and Krzystek-Korpacka, M. (2018) Peripheral Lymphocytes of Patients with Inflammatory Bowel Disease Have Altered Concentrations of Key Apoptosis Players: Preliminary Results. BioMed Research International, 2018, Article ID: 4961753.
https://doi.org/10.1155/2018/4961753
[3] Bakkaloglu, O.K., Sen, G., Kepil, N., Eskazan, T., Kurt, E.A., Onal, U., et al. (2024) Comparative Value of CRP and FCP for Endoscopic and Histologic Remissions in Ulcerative Colitis. Diagnostics, 14, Article No. 2283.
https://doi.org/10.3390/diagnostics14202283
[4] Zhu, P., Wu, Y., Sun, Y., Yan, Y., Wang, Y., Yu, Y., et al. (2025) SAA1 Promotes Ulcerative Colitis and Activating Colonic TLR4/NF-κB/NLRP3 Signaling Pathway. Inflammation, 48, 3898-3911.
https://doi.org/10.1007/s10753-025-02299-0
[5] 胡玲珍, 陈志芬. 血清淀粉样蛋白A在炎症性肠病中的价值[J]. 胃肠病学和肝病学杂志, 2018, 27(9): 1031-1034.
[6] Isaac, A., Keddeas, M.W., Abd Elhady, A.A., Khatab, S.M., Elgohary, S.A. and El Baz, H.S. (2024) Serum Amyloid a as a Non-Invasive Predictive Biomarker of Mucosal Healing in Ulcerative Colitis Patients. Egyptian Journal of Immunology, 31, 130-144.
https://doi.org/10.55133/eji.310214
[7] Liu, C., Gong, Q., Liu, W., Zhao, Y., Yan, X. and Yang, T. (2024) Berberine-Loaded PLGA Nanoparticles Alleviate Ulcerative Colitis by Targeting IL-6/IL-6R Axis. Journal of Translational Medicine, 22, Article No. 963.
https://doi.org/10.1186/s12967-024-05682-x
[8] Mirica, R.E., Coman, A., State, M. and Popp, C. (2025) Targeting Molecular Dysregulation in Ulcerative Colitis: A Paired Cellular Perspective on CD4+, CD8+, and IL-6 Immunohistochemistry. International Journal of Molecular Sciences, 26, Article No. 11773.
https://doi.org/10.3390/ijms262411773
[9] Caviglia, G., Rosso, C., Stalla, F., Rizzo, M., Massano, A., Abate, M., et al. (2020) On-Treatment Decrease of Serum Interleukin-6 as a Predictor of Clinical Response to Biologic Therapy in Patients with Inflammatory Bowel Diseases. Journal of Clinical Medicine, 9, Article No. 800.
https://doi.org/10.3390/jcm9030800
[10] Vasylieva, I., Nakonechna, O., Popova, L., Yarmysh, N., Bezrodna, A. and Pustova, N. (2024) Blood Serum Interleukins Levels and Their Relationship with Colon Tissue Prostanoids in Experimental Ulcerative Colitis. Wiadomości Lekarskie, 77, 1712-1717.
https://doi.org/10.36740/wlek/192139
[11] 周传波, 刘立坤, 史晓斌, 等. 溃疡性结肠炎患者肠黏膜组织IL-23、IL-10、TLR2表达与Baron分级和肠道菌群的关系[J]. 现代消化及介入诊疗, 2024, 29(5): 610-613.
[12] 顾烨飞, 陈彦君, 叶玉兰, 等. 血浆IL-17A、IFN-γ、TNF-α在炎症性肠病中的变化及临床意义研究[J]. 新医学, 2026, 57(5): 547-554.
[13] Fousekis, F., Siebler, J., Rath, T., Hartmann, A., Neurath, M.F., Vieth, M., et al. (2026) Case Report: Successful Anti-TNF Antibody Therapy in Steroid-Dependent Segmental Colitis Associated with Diverticulosis and Concomitant Ulcerative Colitis. Frontiers in Immunology, 17, Article ID: 1764305.
https://doi.org/10.3389/fimmu.2026.1764305
[14] Lin, H., Bai, Z., Wu, Q., Chu, G., Zhang, Y., Guo, X., et al. (2022) Inflammatory Indexes for Assessing the Severity and Disease Progression of Ulcerative Colitis: A Single-Center Retrospective Study. Frontiers in Public Health, 10, Article ID: 851295.
https://doi.org/10.3389/fpubh.2022.851295
[15] Wen, C., Hu, H., Yang, W., Zhao, Y., Zheng, L., Jiang, X., et al. (2022) Targeted Inhibition of FcRn Reduces NET Formation to Ameliorate Experimental Ulcerative Colitis by Accelerating ANCA Clearance. International Immunopharmacology, 113, Article ID: 109474.
https://doi.org/10.1016/j.intimp.2022.109474
[16] 钟选芳, 周潇, 张丽科. 血清学抗中性粒细胞胞浆抗体在炎症性肠病中的表达及其诊断价值[J]. 中国当代医药, 2022, 29(28): 19-23.
[17] Angyal, D., Balogh, F., Gonczi, L., Lontai, L., Kosa, J.P., Garam, N., et al. (2026) Clinical Value of Anti-Integrin αvβ6 Antibody Serum-Level Measurement in Inflammatory Bowel Diseases. Journal of Clinical Medicine, 15, Article No. 948.
https://doi.org/10.3390/jcm15030948
[18] Yamada, Y., Ishida, N., Takebe, T., Takahashi, K., Asai, Y., Yamade, M., et al. (2026) Comparison of Changes in Biomarkers with Changes in Endoscopic Scores in Patients with Ulcerative Colitis: A Single‐Center, Retrospective, Observational Study. JGH Open, 10, e70405.
https://doi.org/10.1002/jgh3.70405
[19] Parihar, S., Yadav, D.P., Verma, A., Shukla, S.K., Tiwari, A.K., Kumar, V., et al. (2026) Evaluating the Correlation of Intestinal Ultrasound and Fecal Calprotectin with Endoscopic Severity Scores in Assessing Disease Activity in Ulcerative Colitis Patients. Journal of Ultrasound, 29, 325-335.
https://doi.org/10.1007/s40477-026-01127-x
[20] 王淑芳, 赵昌东, 李雪, 等. 溃疡性结肠炎患者血清NGAL、I-FABP和NLRP3 mRNA水平变化及其意义[J]. 国际消化病杂志, 2024, 44(3): 200-205.
[21] Varvarynets, A.V. (2024) Specifics of Barrier Function Impairment of the Large Intestine in Patients with Ulcerative Collitis and Joint Damage. Wiadomości Lekarskie, 77, 1989-1995.
https://doi.org/10.36740/wlek/195166
[22] AlRasheed, H.A., El-Haggar, S.M., Hegazy, S.K., Maher, M.M., Bahgat, M.M. and Bahaa, M.M. (2025) Repurposing Atorvastatin, HMGCO-A Reductase Inhibitor, in Patients with Ulcerative Colitis: A Randomized Controlled Study. Journal of Clinical Medicine, 14, Article No. 3077.
https://doi.org/10.3390/jcm14093077
[23] Ding, H., Zhang, H., Li, D., Hu, Z., Xiang, G., Nie, Q., et al. (2026) miR-9394b from Lactobacillus paracasei Extracellular Vesicles Targets iNOS to Reprogram Host NO-Ornithine Metabolism and Ameliorate DSS-Induced Murine Colitis. NPJ Biofilms and Microbiomes.
https://doi.org/10.1038/s41522-026-01023-6
[24] 陈国雁, 尚精娟, 李敏虹, 等. 血清miR-31、miR-155和CCL26在溃疡性结肠炎中预后不良的诊断价值[J]. 西部医学, 2024, 36(4): 544-548.