Center for Traditional Medicine, Taipei Veterans General Hospital, Taipei, Taiwan; Institute of Traditional Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan; School of Chinese Medicine, Colledge of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Department of Neurology, Kuang Tien General Hospital, Taichung, Taiwan; Program in Translational Medicine, National Chung Hsing University, Taichung, Taiwan; Management Office for Health Data, China Medical University Hospital, Taichung, Taiwan.
Clin Nutr. 2024 Dec;43(12):275-284. doi: 10.1016/j.clnu.2024.10.039. Epub 2024 Nov 6.
Alpha-s1 casein hydrolysate (ACH; Lactium®) is recognized as a supplementary treatment to enhance sleep quality. However, limited studies utilizing objective sleep assessment tools have resulted in a lack of substantial validation. This study aimed to assess the effects of ACH on both subjective sleep assessments and objective polysomnography (PSG) recordings in a hospital-based cohort of Taiwanese individuals with chronic insomnia.
In this 4-week randomized, double-blind, placebo-controlled trial, 36 participants diagnosed with chronic insomnia were enrolled and randomly assigned to either the ACH or placebo groups. Initially, participants in the ACH group received 600 mg of ACH daily, which was reduced to 300 mg for the latter two weeks; the placebo group received maltodextrin capsules throughout the study. The study utilized polysomnography (PSG), along with detailed sleep questionnaires including the Insomnia Severity Index (ISI), Global Sleep Disorders Score (GSDS), Pittsburgh Sleep Quality Index (PSQI), Epworth Sleepiness Scale (ESS), and Hospital Anxiety and Depression Scale (HADS), to assess improvements in sleep quality and related health markers. The efficacy of the intervention was assessed through measures of sleep efficiency, stage distribution, and psychological well-being, comparing results from before to after the treatment phase.
The study demonstrated that ACH treatment notably enhanced sleep quality, evidenced by significant improvements in ISI, GSDS, PSQI, ESS, and HADS scores at both week 2 and 4 (all p-values <0.05) compared with baseline scores. When compared to the placebo group, the ACH group experienced a marked reduction in GSDS scores over time (p = 0.045). Furthermore, PSG data revealed a significant decrease in sleep onset latency from baseline in the ACH group compared to the placebo group (p = 0.012; -7.7 ± 16.0 min vs. 6.1 ± 17.7 min for ACH and placebo groups, respectively). These results indicate that ACH treatment effectively improved sleep initiation and overall sleep quality.
ACH Supplementation significantly improved sleep quality, particularly by reducing GSDS scores and sleep onset latency, demonstrating its potential as an effective intervention for chronic insomnia. Future studies with larger samples and exploration of long-term effects are needed to confirm these results.
α-乳白蛋白水解物(ACH;Lactium®)被认为是一种辅助治疗方法,可改善睡眠质量。然而,利用客观睡眠评估工具进行的有限研究缺乏实质性验证。本研究旨在评估 ACH 对台湾慢性失眠患者的主观睡眠评估和客观多导睡眠图(PSG)记录的影响。
在这项为期 4 周的随机、双盲、安慰剂对照试验中,招募了 36 名被诊断为慢性失眠的参与者,并将其随机分配到 ACH 或安慰剂组。在初始阶段,ACH 组的参与者每天接受 600mg 的 ACH,后两周减少至 300mg;安慰剂组在整个研究期间接受麦芽糊精胶囊。该研究使用多导睡眠图(PSG)以及详细的睡眠问卷,包括失眠严重程度指数(ISI)、全球睡眠障碍评分(GSDS)、匹兹堡睡眠质量指数(PSQI)、Epworth 嗜睡量表(ESS)和医院焦虑和抑郁量表(HADS),评估睡眠质量和相关健康指标的改善。通过睡眠效率、阶段分布和心理健康的测量来评估干预的疗效,比较治疗前后的结果。
研究表明,ACH 治疗显著改善了睡眠质量,ISI、GSDS、PSQI、ESS 和 HADS 评分在第 2 周和第 4 周(均 p 值<0.05)均显著改善,与基线评分相比。与安慰剂组相比,ACH 组的 GSDS 评分随时间的推移明显降低(p=0.045)。此外,PSG 数据显示,与安慰剂组相比,ACH 组的睡眠潜伏期从基线开始显著缩短(p=0.012;ACH 组和安慰剂组分别为-7.7±16.0min 和 6.1±17.7min)。这些结果表明,ACH 治疗可有效改善睡眠起始和整体睡眠质量。
ACH 补充剂显著改善了睡眠质量,特别是通过降低 GSDS 评分和睡眠潜伏期来改善睡眠质量,表明其作为慢性失眠的有效干预措施具有潜力。需要更大样本量的研究和对长期效果的探索来证实这些结果。