Impact of probiotic supplementation on exercise endurance among nonelite athletes: a randomized, placebo-controlled, double-blind, clinical trial.

Caitlin E McDermott, Taylor C Judkins, Heather K Vincent, Tyler Culpepper, James Colee, Carmelo Nieves, Anne E Mathews, Bobbi Langkamp-Henken
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Abstract

This randomized, placebo-controlled, double-blind, parallel trial investigated whether generally healthy adult, nonelite runners would have a greater time-to-exhaustion during submaximal treadmill running with probiotic versus placebo supplementation. It was hypothesized that the probiotic would impact training progression by reducing gastrointestinal (GI) and cold/flu symptoms. Participants who typically ran ≥24 km/week, ran or cross-trained 3-5 days per week, and had a maximal oxygen intake (V̇O2 max) in the 60-85th percentile were enrolled. V̇O2 max was used to establish individualized workload settings (85% of V̇O2 max) for the submaximal endurance tests at baseline and following 6 weeks of supplementation with a probiotic (Lactobacillus helveticus Lafti L10, 5×109 CFU/capsule/day) or placebo. Participants self-reported GI and cold/flu symptoms and physical activity via daily and weekly questionnaires. Outcomes were tested using a linear model to determine if mean response values adjusted for baseline differed between groups. Twenty-eight participants (n = 14/group), aged 25 ± 5 years (mean ± SD) with a body mass index of 23 ± 3 kg/m2, completed the study. At the final visit the probiotic group had a lower time-to-exhaustion versus the placebo group (P = 0.01) due to an increase in time-to-exhaustion with the placebo (1344 ± 188 to 1565 ± 219 s, P = 0.01) with no change with the probiotic (1655 ± 230 to 1547 ± 215 s, P = 0.23). During the intervention, the probiotic group completed fewer aerobic training sessions per week (P = 0.02) and trained at a lower intensity (P = 0.007) versus the placebo group. Few GI and cold/flu symptoms were reported with no differences between groups. Time-to-exhaustion increased in the placebo group, possibly due to differences in training habits.

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补充益生菌对非精英运动员运动耐力的影响:随机、安慰剂对照、双盲临床试验。
这项随机、安慰剂对照、双盲、平行试验研究了一般健康的成年非精英跑步者在补充益生菌和安慰剂的情况下,在亚极限跑步过程中的耗竭时间是否会更长。试验假设益生菌将通过减轻胃肠道(GI)和感冒/流感症状来影响训练进度。参与者通常每周跑步≥24公里,每周跑步或交叉训练3-5天,最大摄氧量(VO2 max)在60-85百分位数之间。在基线和补充益生菌(螺旋乳杆菌 Lafti L10,5x109 CFU/胶囊/天)或安慰剂 6 周后,最大氧饱和度被用来为次最大耐力测试设定个性化的工作量(最大氧饱和度的 85%)。受试者通过每日和每周的问卷自我报告消化道症状、感冒/流感症状和体育锻炼情况。结果采用线性模型进行检验,以确定调整基线后的平均反应值在组间是否存在差异。28名参与者(n=14/组)完成了研究,他们的年龄为255(平均SD),体重指数为233 kg/m2。在最后一次检查中,益生菌组的耗竭时间低于安慰剂组(P=0.01),原因是安慰剂组的耗竭时间增加(从1344±188秒到1565±219秒,P=0.01),而益生菌组没有变化(从1655±230秒到1547±215秒,P=0.23)。在干预期间,与安慰剂组相比,益生菌组每周完成的有氧训练次数较少(P=0.02),训练强度较低(P=0.007)。据报告,益生菌组很少出现消化道症状和感冒/流感症状,组间无差异。可能由于训练习惯的不同,安慰剂组的耗竭时间有所增加。
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