Henrotin Yves, Pap Thomas, Lieten Siddhartha, Badot Valérie, Dubuc Jean-Emile, Urbin-Choffray Didier, von Eynatten Maximilian, Johansen Odd Erik, Rau Stefanie, Brabants Karl
musculoSKeletal Innovative Research Lab (mSKIL), Université de Liège, Liège, Belgium
Institute of Musculoskeletal Medicine, University Hospital Münster, Münster, Germany.
RMD Open. 2025 Aug 12;11(3):e005433. doi: 10.1136/rmdopen-2025-005433.
Oral enzyme combination (OEC) therapy with bromelain, trypsin and rutoside reduces pain and improves function in patients with knee osteoarthritis (OA). Here, we investigated several potential biological mechanisms underlying the clinical effects of OEC therapy in patients with established knee OA with respect to innate immunity, systemic inflammation and cartilage turnover (EudraCT 2020-003154-80, NCT05038410).
Patients (age ≥40 years, body mass index (BMI) ≤35 kg/m) with symptomatic knee OA were randomised to either placebo or OEC, administered 2×3 tablets/day, for 8 weeks before crossing over after a 4-week washout period. Different markers exploring innate immunity, inflammation and cartilage matrix degradation have been measured in the blood using immunoassays or cytometric methods. Data from the modified intention-to-treat population (mITT) were analysed using a generalised linear mixed model. No correction for multiple comparisons was made due to the exploratory nature of the study.
Altogether, 45 patients were randomised; 43 completed both treatment sequences (mITT; mean age: 63.3 years; mean BMI: 27.4 kg/m; mean global Knee injury and Osteoarthritis Outcome Score (KOOS): 48.7). OEC significantly increased levels of α2-macroglobulin (p=0.038) and interleukin-10 (p<0.0001) while decreasing urinary carboxyl-terminal cross-linked telopeptide of type II collagen (p=0.038). Patients administered OEC exhibited significant improvements in KOOS Pain (p=0.0464) and Symptoms (p=0.026) subdomains but not globally. OEC was well tolerated, with no serious related adverse events reported in either group.
One of the key findings of this proof-of-mechanism study is that OEC modulates IL-10 production, suggesting an anti-inflammatory effect in patients with knee OA. This main finding contributes to explaining the effects of OEC on pain and function in these patients.
NCT05038410.
菠萝蛋白酶、胰蛋白酶和芦丁的口服酶组合(OEC)疗法可减轻膝关节骨关节炎(OA)患者的疼痛并改善其功能。在此,我们研究了OEC疗法对已确诊膝关节OA患者临床疗效的几种潜在生物学机制,涉及先天免疫、全身炎症和软骨更新(欧盟临床试验数据库编号:2020-003154-80,美国国立医学图书馆临床试验注册号:NCT05038410)。
将有症状的膝关节OA患者(年龄≥40岁,体重指数(BMI)≤35kg/m²)随机分为安慰剂组或OEC组,每天服用2×3片,持续8周,之后经过4周的洗脱期再交叉治疗。使用免疫测定法或细胞计数法检测血液中探索先天免疫、炎症和软骨基质降解的不同标志物。采用广义线性混合模型对改良意向性治疗人群(mITT)的数据进行分析。由于本研究具有探索性,因此未对多重比较进行校正。
共有45例患者被随机分组;43例完成了两个治疗阶段(mITT;平均年龄:63.3岁;平均BMI:27.4kg/m²;平均膝关节损伤和骨关节炎结局评分(KOOS)总分:48.7)。OEC显著提高了α2-巨球蛋白水平(p=0.038)和白细胞介素-10水平(p<0.0001),同时降低了尿II型胶原羧基末端交联肽水平(p=0.038)。接受OEC治疗的患者在KOOS疼痛(p=0.0464)和症状(p=0.026)子领域有显著改善,但总体上没有。OEC耐受性良好,两组均未报告严重的相关不良事件。
这项机制验证研究的主要发现之一是,OEC可调节白细胞介素-10的产生,提示其对膝关节OA患者具有抗炎作用。这一主要发现有助于解释OEC对这些患者疼痛和功能的影响。
NCT05038410。