胃炎通络颗粒治疗脾虚瘀阻型慢性萎缩性胃炎的多中心随机双盲双模拟临床对照研究

Efficacy of Weiyan Tongluo Granules in Patients with Chronic Atrophic Gastritis of Spleen Deficiency and Blood Stasis Type: A Multi-Center, Double-Blind, Double-Dummy, Randomized Controlled Trial

  • 摘要:
    目的 评价胃炎通络颗粒治疗慢性萎缩性胃炎(CAG)的有效性与安全性并探讨其可能机制。
    方法 于2020年6月至2022年12月纳入100例脾虚瘀阻型CAG受试者,采用随机数表法随机分为试验组、对照组各50例。试验组服用胃炎通络颗粒联合叶酸模拟剂,对照组服用叶酸片联合中药颗粒模拟剂,2组疗程均为24周,研究过程中试验组脱落8例、对照组脱落10例。治疗前后比较可操作的与胃癌风险联系的胃炎评估(OLGA)、可操作的与胃癌风险联系的肠化生评估(OLGIM)分期和胃黏膜低级别上皮内瘤变逆转率;治疗前后评估脾胃系疾病之慢性胃炎患者报告结局量表(SSDPRO-CG)评分、中医证候积分和安全性指标变化;ELISA法比较血清胃蛋白酶原(PG)Ⅰ、PGⅡ、PGⅠ/PGⅡ比值(PGR)、胃泌素17(G-17)含量;Western blot检测胃黏膜磷酸化的核因子κB(p-NF-κB)、尾型同源框转录因子2(CDX2)蛋白水平,qPCR法比较白介素-1β(IL-1β)、白介素-6(IL-6)、绒毛蛋白1(VIL1)、黏蛋白2(MUC2) mRNA表达水平变化。
    结果 治疗后,试验组OLGA分期逆转率和OLGIM分期逆转率均显著高于对照组(P < 0.05,P < 0.01),但2组胃黏膜低级别上皮内瘤变逆转率未见显著差异; 2组生理领域得分和总分较治疗前均显著提升(P < 0.01);试验组生理领域、独立性、心理得分和总分均优于对照组(P < 0.05,P < 0.01);2组中医证候总积分和胃脘痞满、胃脘疼痛、食少纳呆、腹胀积分均较治疗前显著降低(P < 0.01),试验组便溏和面色暗滞积分较治疗前显著降低(P < 0.01),而对照组并未观察到此效应,试验组中医证候总积分和各证候条目积分均显著低于对照组(P < 0.05,P < 0.01)。治疗后,试验组血清PGⅠ、PGⅡ、PGR、G-17含量,胃黏膜p-NF-κB、CDX2蛋白和IL-1β、IL-6、VIL1、MUC2 mRNA表达水平均显著改善(P < 0.05, P < 0.01),而对照组除PGⅡ外,其他指标均显著改善(P < 0.05, P < 0.01),试验组上述指标改善均优于对照组(P < 0.05, P < 0.01)。2组均无治疗相关不良事件发生。
    结论 胃炎通络颗粒能一定程度改善CAG患者胃黏膜病理情况,改善患者临床症状、心理状态和生存质量,且未见明显不良反应,其作用机制可能与抑制NF-κB炎症通路降低IL-1β、IL-6表达、下调CDX2抑制VIL1、MUC2肠化标志物转录,进而逆转炎症-肠化恶性循环有关。

     

    Abstract:
    OBJECTIVE To evaluate the efficacy and safety of Weiyan Tongluo Granules in treating chronic atrophic gastritis (CAG) and explore its potential mechanisms.
    METHODS From June 2020 to December 2022, 100 CAG patients with spleen deficiency and blood stasis syndrome were enrolled and randomly divided into a trial group (n=50) and a control group (n=50) using a random number table. The trial group received Weiyan Tongluo Granules plus a folic acid placebo, while the control group received folic acid tablets plus a traditional Chinese medicine granule placebo. The treatment course for both groups was 24 weeks, with 8 and 10 dropouts in the trial and control groups, respectively. Post-treatment comparisons included OLGA/OLGIM staging reversal rates, low-grade intraepithelial neoplasia regression rate, SSDPRO-CG (Patient-Reported Outcome Scale for Chronic Gastritis in Spleen-Stomach Diseases) scores, TCM syndrome scores, and safety indicators. Serum levels of PG Ⅰ, PGⅡ, PGR, and G-17 were measured via ELISA before and after treatment. Gastric mucosal p-NF-κB and CDX2 protein expression levels were analyzed by Western blot, while mRNA levels of IL-1β, IL-6, VIL1, and MUC2 were quantified via qPCR.
    RESULTS After treatment, the trial group showed significantly higher OLGA and OLGIM stage reversal rates than the control group (P < 0.05, P < 0.01), though no significant difference was observed in low-grade intraepithelial neoplasia regression. Both groups exhibited significant improvements in physiological domain scores and total SSDPRO-CG scores (P < 0.01), with the trial group outperforming the control group in physiological, independence, psychological domains, and total scores (P < 0.05, P < 0.01). TCM syndrome scores (total and sub-items: gastric distension, pain, poor appetite, bloating) decreased significantly in both groups (P < 0.01), while the trial group showed greater reductions in loose stools and dull complexion (P < 0.01). After-treatment, the trial group had significantly lower TCM syndrome scores than the control group (P < 0.05, P < 0.01). Serum PG Ⅰ, PGⅡ, PGR, G-17, gastric mucosal p-NF-κB, CDX2, and IL-1β, IL-6, VIL1, MUC2 mRNA levels improved significantly in the trial group (P < 0.05, P < 0.01), while the control group improved only in PGⅡ (P < 0.05, P < 0.01). The trial group's improvements in these biomarkers surpassed the control group's (P < 0.05, P < 0.01). No treatment-related adverse events occurred in either group.
    CONCLUSION Weiyan Tongluo Granules ameliorate gastric mucosal pathology, clinical symptoms, psychological state, and quality of life in CAG patients without significant adverse effects. Its mechanism may involve suppressing the NF-κB pathway to reduce IL-1β and IL-6 expression, downregulating CDX2 to inhibit VIL1 and MUC2 transcription, thereby reversing the vicious cycle of inflammation-intestinal metaplasia.

     

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