切换至 "中华医学电子期刊资源库"

中华关节外科杂志(电子版) ›› 2023, Vol. 17 ›› Issue (01) : 29 -34. doi: 10.3877/cma.j.issn.1674-134X.2023.01.004

临床论著

两种微小RNA表达与痛风性关节炎免疫指标的相关性
安丽欣1,(), 张倩1, 李昆1, 刘耔序1, 刘健1, 石蕊1   
  1. 1. 066000 秦皇岛市第一医院风湿免疫科
  • 收稿日期:2021-08-13 出版日期:2023-02-01
  • 通信作者: 安丽欣
  • 基金资助:
    秦皇岛市市级自筹项目(202101A087)

Correlation between miRNA22-3p and miRNA223-3p expression and immune markers in gouty arthritis

Lixin An1,(), Qian Zhang1, Kun Li1, Zixu Liu1, Jian Liu1, Rui Shi1   

  1. 1. The First Hospital of Qinhuangdao Rheumatology and immunology, Qinhuangdao 066000, China
  • Received:2021-08-13 Published:2023-02-01
  • Corresponding author: Lixin An
引用本文:

安丽欣, 张倩, 李昆, 刘耔序, 刘健, 石蕊. 两种微小RNA表达与痛风性关节炎免疫指标的相关性[J/OL]. 中华关节外科杂志(电子版), 2023, 17(01): 29-34.

Lixin An, Qian Zhang, Kun Li, Zixu Liu, Jian Liu, Rui Shi. Correlation between miRNA22-3p and miRNA223-3p expression and immune markers in gouty arthritis[J/OL]. Chinese Journal of Joint Surgery(Electronic Edition), 2023, 17(01): 29-34.

目的

研究miRNA22-3p、miRNA223-3p在痛风性关节炎患者中的表达水平及其炎症免疫反应调节机制。

方法

2020年1月到2021年1月在秦皇岛市第一医院诊治且符合痛风诊断标准的80例痛风患者资料纳入研究作为观察组进行回顾性分析。同期行健康体检且临床指标无明显异常,身体健康的80例患者作为对照组。排除标准:合并重要脏器系统严重疾病者;近3个月使用过激素类药物者;其他疾病所致继发性痛风性关节炎;药物诱发痛风性关节炎发作者;精神障碍疾病者等。采用独立样本t检验比较两组的miRNA22-3p、miRNA223-3p、炎性反应以及免疫指标之间的差异;Pearson相关性分析miRNA22-3p和miRNA223-3p与炎性因子的关系。

结果

观察组患者的miRNA22-3p、miRNA223-3p水平分别为(4.0±1.0)、(1.51±0.12),显著高于对照组的(1.12±0.26)、(0.62±0.20)(t=24.333、34.130,均为P<0.05)。观察组患者的白介素(IL)-1β、肿瘤坏死因子(TNF)-α及IL-6水平分别为(57.77±7.24)、(24.04±4.24)、(49.27±3.72)均显著高于对照组的(42.27±3.31)、(18.07±4.17)、(39.75±3.73)(t=17.415、8.979、16.164,均为P<0.05);观察组的单核细胞趋化因子(MCP)-1、胸腺调节趋化因子(TARC)、嗜酸性粒细胞趋化因子(eotaxin)-2水平分别为(106±12)、(215±13)、(347±11)均显著高于对照组(72±12)、(159±12)、(317±12)(t=18.095、29.356、16.713,均为P<0.05)。Pearson相关性分析显示患者的miRNA22-3p、miRNA223-3p与MCP-1、TARC、eotaxin-2、IL-1β、TNF-α以及IL-6呈现显著正相关(r=0.609、0.659、0.545、0.610、0.551、0.571、0.684、0.668、0.671、0.542、0.534、0.458,均为P<0.05)。

结论

miRNA22-3p、miRNA223-3p在痛风性关节炎患者中的表达水平显著升高,与炎症以及免疫反应呈现正相关。

Objective

To investigate the expression levels of miRNA22-3p and miRNA223-3p in gouty arthritis patients and the regulatory mechanism of inflammatory immune response.

Methods

The data of 80 gout patients who met the gouty diagnosis creteria and treated in the First Hospital of Qinhuangdao from January 2020 to January 2021 were retrospectively analyzed. Other 80 healthy patients who underwent rountine health check-up during the same period without obvious abnormality in clinical indicators were enrolled as the control group. Exclusion criteria: the patients with severe diseases of the vital organs and systems; patients who used hormone drugs in the past three months; secondary gouty arthritis caused by other diseases; dryg induced gouty arthritis attacks; mental disorders. The observation group met the diagnostic criteria of gout. Independent sample t test was used to compare the differences in miRNA22-3p, miRNA223-3p, infla-mmatory response and immune indicators between the two groups. Pearson correlation analysis was applied for the relationship between inflammatory indicators and miRNA22-3p as well as miRNA223-3p.

Results

Expression levels of miRNA22-3p and miRNA223-3p in the observation group were (4.01±1.03) and (1.51±0.12), respectively, which were significantly higher than those in the control group [(1.12±0.26) and (0.62±0.20)] (t=24.333, 34.130, both P<0.05). The levels of IL-1β, TNF-α and IL-6 in the observation group were (57.77±7.24), (24.04±4.24) and (49.27±3.72), respectively, which were significantly higher than those in the control group. (42.27±3.31), (18.07±4.17), (39.75±3.73), respectively (t=17.415, 8.979, 16.164, all P<0.05). The levels of monocyte chemoattractant protein (MCP)-1, thymus and activation regulated chemokine (TARC), eotaxin-2 in the observation group were(106±12), (215±13), (347±11) which were higher than those in the control group [(72±11), (159±12), (317±12)](t=18.095, 29.356, 16.713, all P<0.05). Pearson correlation analysis showed the expressions of miRNA22-3p and miRNA223-3p were positively correlated with MCP-1, TARC, eotaxin-2, IL-1β, TNF-α and IL-6 (r=0.609, 0.659, 0.545, 0.610, 0.551, 0.571, 0.684, 0.668, 0.671, 0.542, 0.534, 0.458, all P<0.05).

Conclusion

The expression levels of mirNA22-3p and mirNA223-3p in gouty arthritis patients are significantly increased, which are positively correlated with inflammation and immune response.

表1 两组患者一般资料比较
Table 1 Comparison of general information between two groups of patients
表2 两组患者miRNA22-3p、miRNA223-3p水平比较(±s)
Table 2 Comparison of miRNA22-3p and miRNA223-3p levels between two groups of patients
表3 不同状态患者的miRNA22-3p、miRNA223-3p水平比较(±s)
Table 3 Comparison of miRNA22-3p and miRNA223-3p levels in patients with different states
表4 两组患者的炎性指标比较(±s)
Table 4 Comparison of inflammatory indicators between two groups of patients
表5 两组患者的变态反应指标比较(±s)
Table 5 Comparison of allergic index between two groups of patients
表6 miRNA22-3p、miRNA223-3p与炎性反应及变态反应指标的相关性分析
Table 6 Correlation analysis of miRNA22-3p, miRNA223-3p with inflammatory and allergic response indicators
[1]
朱丹,李玲琴,张全波,等. 原发性痛风中微小RNA-223表达变化及其临床意义[J]. 中华风湿病学杂志201721(3):167-171.
[2]
陈刚,李梦兰,彭春梅,等. 微RNA-21在原发性痛风患者中的变化及意义[J]. 中华风湿病学杂志201923(3):165-169.
[3]
杨彬,黄俊卿,孟庆良,等. 秦艽醇提物对痛风性关节炎大鼠氧化应激损伤及miR-34a/sirt1轴的影响研究[J]. 中药药理与临床201935(5):64-69.
[4]
柳涛红,朱丹,青玉凤,等. 微RNA-146a通过Toll样受体信号途径在RAW264.7细胞痛风性关节炎模型炎症反应中的研究[J]. 中华风湿病学杂志202024(8):522-529.
[5]
殷春明,潘晓华.膝骨关节炎患者关节液中miR-140-3p表达可反映骨关节炎进程[J].中国组织工程研究201620(35):2095-4344.
[6]
徐阳洋,青玉凤,张全波,等.微小RNA-146a在原发性痛风性关节炎患者的变化及其临床意义[J].中华风湿病学杂志201620(12):1007-7480.
[7]
Liu YF, Xing GL, Chen Z, et al. Long non-coding RNA HOTAIR knockdown alleviates gouty arthritis through miR-20b upregulation and NLRP3 downregulation[J]. Cell Cycle202120(3):332-344.
[8]
张羽,钟晓鸣,杨静,等. 葛根素对痛风性关节炎小鼠炎性相关细胞因子表达的影响[J]. 免疫学杂志202036(10):903-907,913.
[9]
Torres RJ. Toll-like receptor 4(TLR4)polymorphism rs2149356 and risk of gout in a Spanish cohort[J]. Nucleosides Nucleotides Nucleic Acids, 2020, 39(10/12): 1424-1431.
[10]
Mishra R, Panigrahi VP, Adsul N, et al. Tophaceous gout in thoracic spine mimicking meningioma: a case report and literature review[J]. Surg Neurol Int, 2020, 11(364): 10-12.
[11]
Doucet V, Mcleod GJ, Petropolis CJ. Gouty stenosing tenosynovitis: trigger finger as a first presentation of tophaceous gout[J]. Plast Reconstr Surg Glob Open20208(8):15-19.
[12]
Otani N, Ouchi M, Kudo H, et al. Recent approaches to gout drug discovery:an update[J]. Expert Opin Drug Discov202015(8):943-954.
[13]
Misra A, Kumar B, Shukla P, et al. Simultaneous HPTLC-UV quantification of colchicine and gloriosine alkaloids in the natural population of Gloriosa superba L.,collected from Eastern Ghats of India for the identification of elite chemotypes[J]. J Liq Chromatogr Relat Technol, 2020, 43(9/10): 351-360.
[14]
AbdullGaffar B, Abdul Hameed B, Fodeh Set, et al. Concomitant gouty and tuberculous granulomatous arthritis[J]. Int J Surg Pathol202028(3):288-289.
[15]
Azab N, Elhelbawy R, Abdelaal G, et al. Antioxidant and gouty arthritis in chronic obstructive pulmonary disease: the perplexing uric acid molecule[J]. Egypt J Chest Dis Tuberc202069(2):331-338.
[16]
Murayama M, Nishida M, Kudo Y, et al. Case with long-standing gout showing various ultrasonographic features caused by monosodium urate monohydrate crystal deposition[J]. Mod Rheumatol Case Rep20204(1):110-115.
[17]
Cui R, Li M, Tuerxun G, et al. Research on the role of toll-like receptor 2 and toll-like receptor 4 and its signal pathway in the pathogenesis of primary gout arthritis[J]. MSP20204(1):1-3.
[18]
Ma Q, Honarpisheh M, Li C, et al. Soluble uric acid is an intrinsic negative regulator of monocyte activation in monosodium urate crystal-induced tissue inflammation[J]. J Immunol2020205(3):789-800.
[19]
Han J, Shi G, Li W, et al. Preventive effect of dioscin against monosodium urate-mediated gouty arthritis through inhibiting inflammasome NLRP3 and TLR4/NF-kappa B signaling pathway activation: an in vivo and in vitro study[J]. J Nat Med202175(1):37-47.
[20]
Ren S, Meng F, Liu Y, et al. Effects of external application of compound Qingbi granules on acute gouty arthritis with dampness-heat syndrome: a randomized controlled trial[J]. Chin Med202015(1):12-15.
[21]
Towiwat P, Phungoen P, Tantrawiwat K, et al. Quality of gout care in the emergency departments: a multicentre study[J]. BMC Emerg Med, 2020, 20(1):112-114.
[1] 李文金, 薛庆云. 白细胞介素家族炎性细胞因子在骨关节炎中的研究进展[J/OL]. 中华关节外科杂志(电子版), 2023, 17(03): 348-353.
[2] 钱雅君, 虞竹溪, 徐颖, 董丹江, 顾勤. 危重型新型冠状病毒感染合并侵袭性肺曲霉病的临床特征和高危因素分析[J/OL]. 中华危重症医学杂志(电子版), 2024, 17(01): 3-9.
[3] 陈腊青, 林佳佳, 毛洪刚, 童冠海, 汪梦娜, 夏红波, 刘卓, 徐海霞, 赵玉华, 张传领. 血清细胞因子及呼出气一氧化氮在哮喘-慢性阻塞性肺疾病重叠综合征中的临床意义[J/OL]. 中华危重症医学杂志(电子版), 2023, 16(04): 316-320.
[4] 李永浩, 高雪菲, 郭田田, 张进, 张彩针, 刘静. 肥胖合并甲状腺癌相关机制的研究进展[J/OL]. 中华普通外科学文献(电子版), 2023, 17(04): 311-315.
[5] 张燕, 杨跃青, 邱峥. IgG 联合血清细胞因子对肺结核并发慢性肺曲霉菌病的诊断意义[J/OL]. 中华肺部疾病杂志(电子版), 2024, 17(05): 809-812.
[6] 蒋丽芳, 林冰. 桑菊清解汤联合左氧氟沙星治疗社区获得性肺炎的临床分析[J/OL]. 中华肺部疾病杂志(电子版), 2024, 17(03): 458-461.
[7] 傅红兴, 王植楷, 谢贵林, 蔡娟娟, 杨威, 严盛. 间充质干细胞促进胰岛移植效果的研究进展[J/OL]. 中华细胞与干细胞杂志(电子版), 2024, 14(06): 351-360.
[8] 徐嘉愉, 张复华, 牛国敏, 梁家宝, 潘焕玉, 麦秀蕖, 杨国雷, 徐嘉良, 黄佑勇. Th1/Th2细胞因子谱在恶性血液肿瘤患者化疗后中性粒细胞缺乏伴感染的应用价值[J/OL]. 中华细胞与干细胞杂志(电子版), 2024, 14(03): 143-150.
[9] 阿卜杜萨拉木·图尔荪麦麦提, 吐尔洪江·吐逊, 温浩. 肝脏缺血-再灌注损伤与cGAS-STING信号通路[J/OL]. 中华肝脏外科手术学电子杂志, 2024, 13(03): 394-397.
[10] 杨金涓, 夏建平. 糖尿病性黄斑水肿患者基线房水细胞因子水平评估血管内皮生长因子疗效的临床研究[J/OL]. 中华眼科医学杂志(电子版), 2023, 13(06): 350-355.
[11] 杨智钧, 谷佳, 丁聿贤, 张正奎, 于如同. 脑胶质瘤患者血清炎性因子水平与病理分级及预后的相关性[J/OL]. 中华神经创伤外科电子杂志, 2024, 10(04): 238-242.
[12] 丛黎, 马林, 陈旭, 李文文, 张亮亮, 周华亭. 改良CT严重指数联合炎症指标在重症急性胰腺炎患者胰腺感染预测及预后评估中的研究[J/OL]. 中华消化病与影像杂志(电子版), 2024, 14(05): 432-436.
[13] 刘立业, 赵德芳. 非酒精性脂肪肝患者血清细胞因子信号转导抑制因子3、肝X受体α水平与CT影像学特征的相关性[J/OL]. 中华消化病与影像杂志(电子版), 2023, 13(04): 211-215.
[14] 李益军, 梁兴森, 方细霞, 肖文良, 李湘, 高彦平, 李嘉, 李玲. 温针灸治疗早中期寒湿痹阻型膝骨关节炎的疗效观察[J/OL]. 中华针灸电子杂志, 2024, 13(01): 7-12.
[15] 南朝涛, 陈建, 王书鸿, 李刚, 郝俊杰. 血清细胞因子预测急性脑梗死后肺炎的价值[J/OL]. 中华卫生应急电子杂志, 2024, 10(01): 16-20.
阅读次数
全文


摘要


AI


AI小编
你好!我是《中华医学电子期刊资源库》AI小编,有什么可以帮您的吗?