Combination Treatment in Ulcerative Colitis using 5-Aminosalysilic Acid (5-ASA) and Polysaccharide Peptide of Indonesian Ganoderma lucidum Mycelium Extract

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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Abstract

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.
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
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。
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