The effects of L-carnitine supplementation on inflammation, oxidative stress, and clinical outcomes in critically Ill patients with sepsis: a randomized, double-blind, controlled trial.
- 2024-03-06
- Nutrition journal 23(1)
- Mahdi Keshani
- Babak Alikiaii
- Zahra Babaei
- Gholamreza Askari
- Zahra Heidari
- Manoj Sharma
- Mohammad Bagherniya
- PubMed: 38444016
- DOI: 10.1186/s12937-024-00934-4
Study Design
- Type
- Randomized Controlled Trial (RCT)
- Sample size
- n = 60
- Population
- 60 critically ill septic patients
- Methods
- randomized double-blinded controlled trial, 3 g/day L-carnitine or placebo for 7 days
- Blinding
- Double-blind
- Duration
- 7 days
Background
Sepsis, a life-threatening organ dysfunction caused by a host's dysregulated response to infection with an inflammatory process, becomes a real challenge for the healthcare systems. L-carnitine (LC) has antioxidant and anti-inflammatory properties as in previous studies. Thus, we aimed to determine the effects of LC on inflammation, oxidative stress, and clinical parameters in critically ill septic patients.Methods
A randomized double-blinded controlled trial was conducted. A total of 60 patients were randomized to receive LC (3 g/day, n = 30) or placebo (n = 30) for 7 days. Inflammatory and oxidative stress parameters (C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), superoxide dismutase (SOD), malondialdehyde (MDA), total antioxidant capacity (TAC), 28-day mortality rate, and some monitoring variables were evaluated.Results
There was no statistically significant difference between study arms in baseline characteristics and disease severity scores. CRP (p < 0.001) and ESR (p: 0.004) significantly reduced, and SOD (p < 0.001) and TAC (p < 0.001) significantly improved in the LC group after 7 days. Between-group analysis revealed a significant reduction in CRP (p: 0.001) and serum chloride (p: 0.032), an increase in serum albumin (p: 0.036) and platelet (p: 0.004) significantly, and an increase in SOD marginally (p: 0.073). The 28-day mortality rate was also lower in the LC group compared with placebo (7 persons vs. 15 persons) significantly (odds ratio: 0.233, p: 0.010).Conclusions
L-carnitine ameliorated inflammation, enhanced antioxidant defense, reduced mortality, and improved some clinical outcomes in critically ill patients with sepsis.Trial registration
IRCT20201129049534N1; May 2021.Research Insights
SOD (p < 0.001) significantly improved in the LC group after 7 days.
- Effect
- Beneficial
- Effect size
- Small
- Dose
- 3 g/day
increase in platelet (p: 0.004) significantly
- Effect
- Beneficial
- Effect size
- Small
- Dose
- 3 g/day
increase in serum albumin (p: 0.036) significantly
- Effect
- Beneficial
- Effect size
- Small
- Dose
- 3 g/day
TAC (p < 0.001) significantly improved in the LC group after 7 days.
- Effect
- Beneficial
- Effect size
- Small
- Dose
- 3 g/day
CRP (p < 0.001) significantly reduced in the LC group after 7 days.
- Effect
- Beneficial
- Effect size
- Moderate
- Dose
- 3 g/day
Between-group analysis revealed a significant reduction in serum chloride (p: 0.032)
- Effect
- Beneficial
- Effect size
- Small
- Dose
- 3 g/day
ESR (p: 0.004) significantly reduced in the LC group after 7 days.
- Effect
- Beneficial
- Effect size
- Small
- Dose
- 3 g/day
No significant between-group difference for MDA is reported; baseline and within-group changes are not detailed for MDA in the abstract results.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 3 g/day
The 28-day mortality rate was also lower in the LC group compared with placebo (7 persons vs. 15 persons) significantly (odds ratio: 0.233, p: 0.010).
- Effect
- Beneficial
- Effect size
- Large
- Dose
- 3 g/day