Introduction:
The purpose of this double-blind clinical trial, was to examine the effect of supplementation with the synbiotic and probiotic on the mental health, quality of life, and anemia in HD patients.
Methods:
Seventy-five HD patients were randomly assigned to receive the synbiotic (
n
= 23) as 15 g of prebiotics, 5 g of probiotic powder containing
Lactobacillus acidophilus, Bifidobacterium bifidum, Bifidobacterium lactis
, and
Bifidobacterium longum
(2.7 × 107 CFU/g each); probiotics (
n
= 23) as 5 g probiotics similar to the synbiotic group with 15 g of maltodextrin as placebo; and placebo (
n
= 19) as 20 g of maltodextrin. Serum hemoglobin (Hb) and albumin (Alb) were measured. Beck depression and anxiety index (BDI/BAI) was used to assess symptoms of depression and anxiety. The health-related quality of life (HRQoL) was assessed using the questionnaire SF-36.
Results:
From baseline to 12 weeks, synbiotic and probiotic supplementation resulted in a significant decrease in BDI and BAI score in comparison to the placebo (
P
< 0.05). Between and intergroup comparison showed no significant changes between the groups in terms of HRQoL. However, the serum Hb level increased significantly in the synbiotic and probiotic group compared to the placebo group (
P
< 0.001).
Conclusion:
Overall, 12 weeks of synbiotic and probiotic supplementation resulted in an improvement in mental health and anemia compared with the placebo, whereas they failed to enhance the quality of life in HD patients.