The effects of saffron supplementation on inflammation and hematological parameters in patients with sepsis: a randomized controlled trial.
- 2025-05-09
- Nutrition journal 24(1)
- Shirin Hassanizadeh
- Babak Alikiaii
- Mohammad Hossein Rouhani
- Shokoofeh Talebi
- Zeinab Mokhtari
- Manoj Sharma
- Mohammad Bagherniya
- PubMed: 40346613
- DOI: 10.1186/s12937-025-01148-y
Study Design
- Type
- Randomized Controlled Trial (RCT)
- Population
- 90 ICU sepsis patients with GCS lower than 13
- Methods
- double-blind clinical trial, 90 ICU sepsis patients randomized to receive either an intervention tablet containing 100 mg of saffron or a placebo tablet containing 100 mg of corn starch for seven days
- Blinding
- Double-blind
- Duration
- seven days
- Funding
- Unclear
Background
Critically ill patients suffering from sepsis are at an increased risk of morbidity and mortality due to its serious complications. Saffron as an herbal medicine has been proven to have anti-inflammatory and anti-oxidative stress effects previously. Hence, this study aimed to determine how saffron supplementation affected inflammatory and hematological factors in patients admitted to the intensive care unit (ICU) with sepsis.Methods
In this double-blind clinical trial, 90 ICU sepsis patients with GCS lower than 13 were randomized to receive either an intervention tablet containing 100 mg of saffron or a placebo tablet containing 100 mg of corn starch for seven days. Before and after the intervention, clinical, inflammatory, hematological, and mortality parameters were assessed.Results
After seven days, the saffron group showed a significantly decline from baseline compared to the placebo group in inflammatory markers, including CRP (-24.58 ± 22.16 vs. -2.42 ± 30.86; P < 0.001), ESR (-5.36 ± 28.75 vs. 24.29 ± 28.24; P < 0.001), IL-6 (-22.09 ± 25.22 vs. -4.02 ± 20.04; P < 0.001), IL-18 (-9.56 ± 9.31 vs. -0.89 ± 3.38; P < 0.001), and TNF-α (-2.52 ± 3.79 vs. -0.035 ± 2.35; P < 0.001). Regarding clinical outcomes, significant improvements were observed in APACHE II (-2.55 ± 5.47 vs. 0.78 ± 3.37; P = 0.003), SOFA (-1 ± 1.07 vs. -0.05 ± 1.53; P < 0.001), NUTRIC score (-1.2 ± 1.01 vs. 0.2 ± 0.87; P < 0.001), and WBC count (-4176.34 ± 4063.01 vs. 61.57 ± 4118.97; P < 0.001). Moreover, the effect sizes (Cohen's d) for these factors ranged from moderate to large, except for IL-6, which had a small effect size (d = -0.38). However, no significant differences were found between the groups in the Glasgow Coma Scale, FOUR Score, 28-day and 90-day mortality rates, or other hematological parameters (P > 0.05).Conclusions
Saffron administration in sepsis patients admitted to the ICU led to significant improvements in inflammatory markers and some clinical parameters. However, the clinical significance of these findings remains to be fully established.Trial registration
Iranian Registry of Clinical Trials: IRCT20201129049534N8. It was registered on 17 March 2024.Research Insights
no significant differences were found between the groups in the ... FOUR Score
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg/day
no significant differences were found between the groups in the Glasgow Coma Scale
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg/day
significant improvements were observed in APACHE II (-2.55 ± 5.47 vs. 0.78 ± 3.37; P = 0.003)
- Effect
- Beneficial
- Effect size
- Moderate
- Dose
- 100 mg/day
the saffron group showed a significantly decline from baseline compared to the placebo group in inflammatory markers, including CRP (-24.58 ± 22.16 vs. -2.42 ± 30.86; P < 0.001)
- Effect
- Beneficial
- Effect size
- Moderate
- Dose
- 100 mg/day
ESR (-5.36 ± 28.75 vs. 24.29 ± 28.24; P < 0.001)
- Effect
- Beneficial
- Effect size
- Moderate
- Dose
- 100 mg/day
IL-18 (-9.56 ± 9.31 vs. -0.89 ± 3.38; P < 0.001)
- Effect
- Beneficial
- Effect size
- Moderate
- Dose
- 100 mg/day
no significant differences were found between the groups in the ... 90-day mortality rates
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg/day
no significant differences were found between the groups in the 28-day ... mortality rates
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg/day
NUTRIC score (-1.2 ± 1.01 vs. 0.2 ± 0.87; P < 0.001)
- Effect
- Beneficial
- Effect size
- Moderate
- Dose
- 100 mg/day
SOFA (-1 ± 1.07 vs. -0.05 ± 1.53; P < 0.001)
- Effect
- Beneficial
- Effect size
- Moderate
- Dose
- 100 mg/day
TNF-α (-2.52 ± 3.79 vs. -0.035 ± 2.35; P < 0.001)
- Effect
- Beneficial
- Effect size
- Moderate
- Dose
- 100 mg/day
WBC count (-4176.34 ± 4063.01 vs. 61.57 ± 4118.97; P < 0.001)
- Effect
- Beneficial
- Effect size
- Large
- Dose
- 100 mg/day