5-氨基水杨酸与印尼灵芝菌丝体提取物多糖肽联合治疗溃疡性结肠炎

M. Simadibrata, Aditya Rachman, F. Budimutiar, Paulus Simadibrata, M. Abdullah, Raja Mangatur Haloho, A. Wijaya, Batara Bisuk, Shabrina Maharani, Dewi Mustikarani, D. M. Simadibrata, P. Sugita
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引用次数: 0

摘要

背景:炎症性肠病(IBD)是一种以胃肠道慢性炎症为特征的特发性疾病。灵芝菌丝体提取物(PPGL)是一种很好的辅助治疗IBD的方法。本研究旨在评估PPGL在5-ASA治疗患者中的益处。方法:对124例溃疡性结肠炎患者的病历资料进行回顾性观察队列研究。干预组80例患者采用5-ASA联合PPGL治疗,对照组44例患者仅采用5-ASA治疗。在基线和30、60和90天后观察临床和实验室终点。临床终点包括腹痛、带血腹泻、口疮性口炎和多发性关节炎;同时,实验室终点包括血红蛋白水平、ESR、CRP、粪便钙保护蛋白、m2 -丙酮酸激酶(MP2K)、粪便培养、艰难梭菌培养、结肠镜检查结果。患者入组后进行的临床试验,注册号为ClinicalTrials.gov NCT04029649。结果:第30天,干预组腹痛主诉45.6%,对照组2.3%,差异有统计学意义(p < 0.001)。此外,干预组在第30天的粪便钙保护蛋白(p 0.001)、粪便MP2K (p = 0.015)和血红蛋白(p 0.001)的实验室参数均明显改善。这些差异在第60天和第90天一直存在。结论:该研究提示PPGL给药与90天临床和实验室终点的改善之间存在潜在的相关性。需要一项更大的随机、盲法、前瞻性研究来证实溃疡性结肠炎的这些作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combination Treatment in Ulcerative Colitis using 5-Aminosalysilic Acid (5-ASA) and Polysaccharide Peptide of Indonesian Ganoderma lucidum Mycelium Extract
Background:  Inflammatory bowel disease (IBD) is idiopathic disease characterized by chronic inflammation of the gastrointestinal tract. Polysaccharide peptide of Ganoderma lucidum mycelium extract (PPGL) is considerably a good option for adjunctive therapy of IBD. This study aims to evaluate the benefit of PPGL in patients treated with 5-ASA.Method: A retrospective observational cohort study was conducted to examine the medical records of 124 ulcerative colitis patients. There were 80 patients in intervention group who were treated with a combination of 5-ASA and PPGL, and there were 44 patients in the control group who were treated with 5-ASA only. Clinical and laboratory endpoints were observed at the baseline and after 30, 60, and 90 days. Clinical endpoints included abdominal pain, bloody diarrhea, aphthous stomatitis, and polyarthritis; meanwhile, laboratory endpoints included hemoglobin level, ESR, CRP, fecal calprotectin, M2-pyruvate kinase (MP2K), fecal culture, C. difficile culture, and colonoscopy results. Clinical trials conducted after patient enrollment with registry number ClinicalTrials.gov NCT04029649.Results: On day-30 there was a significant difference between intervention group 45.6%  and control group 2.3% in abdominal pain complaints (p 0.001). Moreover, laboratory parameters of fecal calprotectin (p 0.001), fecal MP2K (p = 0.015), and hemoglobin (p 0.001) were considerably better in intervention group on day-30. These differences were consistently found on day 60 and 90.Conclusion: The study implies potential correlation between PPGL administration and improvement of clinical and laboratory endpoints up to 90 days. A larger randomized, blinded, prospective study is required to confirm these effects in ulcerative colitis.
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