Laparoscopy Research Center, School of medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Department of Nutrition, School of Nutrition and Food Sciences, Shiraz University of Medical Sciences, Shiraz, Iran.
Nutr Neurosci. 2021 Jun;24(6):490-499. doi: 10.1080/1028415X.2019.1646975. Epub 2019 Aug 4.
The aim of this study was to investigate the effects of probiotic and synbiotic supplementation on the depression and anxiety symptoms and serum brain-derived neurotrophic factor (BDNF) level.
Seventy-five HD patients were randomly assigned to receive the synbiotic (15 g of prebiotics, 5 g of probiotic containing T16, BIA-6, BIA-7, and BIA-8 (2.7 × 10 CFU/g each)) or probiotics (5 g probiotics as in synbiotic group with 15 g of maltodextrin as placebo) or placebo (20 g of maltodextrin) for 12 weeks. Serum BDNF was measured by ELISA kit. Hospital Anxiety and Depression Scale (HADS) was used to assess symptoms of depression (HADS-DEP) and anxiety (HADS-ANX).
From baseline to 12 weeks, synbiotic supplementation resulted in a significant decrease in HADS-DEP score in a subgroup of patients with depressive symptom (HADS-DEP ≥ 8) compared to the placebo and probiotic supplementation ( = .001, = .002, respectively) and in all patients compared to the placebo ( = .004). There was no significant difference among the groups in terms of HADS-ANX scores. However, the HADS-ANX scores decreased significantly in the synbiotic group compared to the baseline in all patients ( = .047) and also patients with depressive symptom ( = .03). In addition, in a subgroup of HD patients with depressive symptom, the serum BDNF increased significantly in the synbiotic group when compared to the placebo ( < .001) and probiotic group ( = .011).
Overall, 12 weeks of synbiotic supplementation resulted in greater improvement in depression symptoms and serum BDNF level compared to the probiotic supplementation in HD patients especially in the subgroup of patients with depression symptoms.
本研究旨在探讨益生菌和合生剂补充对抑郁和焦虑症状及血清脑源性神经营养因子(BDNF)水平的影响。
75 例 HD 患者随机分为接受合生剂(15g 益生元、5g 益生菌,含 T16、BIA-6、BIA-7 和 BIA-8(每种 2.7×10 CFU/g))、益生菌(与合生剂相同的 5g 益生菌,用 15g 麦芽糊精作为安慰剂)或安慰剂(20g 麦芽糊精)治疗 12 周。通过 ELISA 试剂盒测定血清 BDNF。采用医院焦虑抑郁量表(HADS)评估抑郁症状(HADS-DEP)和焦虑症状(HADS-ANX)。
从基线到 12 周,与安慰剂和益生菌组相比,合生剂组中存在抑郁症状(HADS-DEP≥8)的患者 HADS-DEP 评分显著下降( = .001, = .002),与所有患者相比,合生剂组 HADS-DEP 评分也显著下降( = .004)。各组间 HADS-ANX 评分无显著差异。然而,与基线相比,所有患者( = .047)和存在抑郁症状的患者( = .03)中,合生剂组 HADS-ANX 评分显著下降。此外,在存在抑郁症状的 HD 患者亚组中,与安慰剂组( < .001)和益生菌组( = .011)相比,合生剂组血清 BDNF 显著增加。
总之,与益生菌组相比,12 周合生剂补充可显著改善 HD 患者的抑郁症状和血清 BDNF 水平,尤其是在存在抑郁症状的患者亚组中。