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KC3 与提取物联合应用对呼吸不适的影响:一项随机、双盲、安慰剂对照试验。

Effect of a Combination of KC3 and Extracts in Respiratory Discomfort: A Randomized, Double-Blind, Placebo-Controlled Trial.

机构信息

College of Korean Medicine, Woosuk University, Jeonju-si 54986, Jeollabuk-do, Republic of Korea.

CKD BiO Research Institute, 8 Chungjeong-ro, Seodaemun-gu, Seoul 03742, Republic of Korea.

出版信息

Nutrients. 2024 Jul 3;16(13):2128. doi: 10.3390/nu16132128.

Abstract

The increased global prevalence of chronic respiratory diseases in recent years has caused a substantial public health burden. KC3 and Houtt. (LJH) extracts can alleviate respiratory symptoms and improve lung function in vitro and in vivo. However, the clinical efficacy and safety profile of this combination in patients with respiratory diseases remain unclear. Therefore, this multicenter, randomized, double-blind, placebo-controlled clinical trial aimed to evaluate the efficacy and safety of KC3 and LJH extracts in adults with respiratory discomfort. This mixture was termed 'CKDB-315'. Participants, randomly assigned to the CKDB-315 or placebo groups, were treated for 12 weeks. Assessments included the St. George's Respiratory Questionnaire (SGRQ) and the Chronic Obstructive Pulmonary Disease Assessment Test (CAT). The CKDB-315 group showed considerably improved SGRQ and CAT scores compared with the placebo group. Secondary outcomes, including dyspnea, pulmonary function, total antioxidant status, and inflammatory cytokine levels, were consistent with the primary outcomes. Exploratory analyses of the gut microbiota and short-chain fatty acid contents revealed the potential mechanisms underlying the effects of CKDB-315. Finally, safety analysis indicated that CKDB-315 was well tolerated and caused few adverse events. Our findings indicate that CKDB-315 is a promising therapeutic option for respiratory discomfort in adults.

摘要

近年来,慢性呼吸道疾病在全球的患病率不断上升,给公共卫生带来了巨大负担。KC3 和 Houtt.(LJH)提取物可缓解呼吸道症状,并改善体外和体内的肺功能。然而,这种组合在呼吸道疾病患者中的临床疗效和安全性尚不清楚。因此,本项多中心、随机、双盲、安慰剂对照临床试验旨在评估 KC3 和 LJH 提取物在有呼吸道不适的成年人中的疗效和安全性。该混合物被命名为“CKDB-315”。参与者随机分配至 CKDB-315 或安慰剂组,接受为期 12 周的治疗。评估包括圣乔治呼吸问卷(SGRQ)和慢性阻塞性肺疾病评估测试(CAT)。与安慰剂组相比,CKDB-315 组的 SGRQ 和 CAT 评分明显改善。次要结局,包括呼吸困难、肺功能、总抗氧化状态和炎症细胞因子水平,与主要结局一致。对肠道微生物群和短链脂肪酸含量的探索性分析揭示了 CKDB-315 作用的潜在机制。最后,安全性分析表明 CKDB-315 耐受良好,引起的不良事件很少。我们的研究结果表明,CKDB-315 是治疗成人呼吸道不适的一种有前途的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e86/11243513/b9f6493927ca/nutrients-16-02128-g001.jpg

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