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The effects of Taurine supplementation on inflammatory markers and clinical outcomes in patients with traumatic brain injury: a double-blind randomized controlled trial

Abstract

Background

Traumatic brain injury is a public health concern and is the main cause of death among various types of trauma. The inflammatory conditions due to TBI are associated with unfavorable clinical outcomes. Taurine has been reported to have immune-modulatory effects. Thus, the aim of this study was to survey the effect of taurine supplementation in TBI patients.

Methods

In this study, 32 patients with TBI were randomized into two groups. The treatment group received 30 mg/kg/day of taurine in addition to the Standard Entera Meal and the control group received Standard Entera Meal for 14 days. Prior to and following the intervention, the patients were investigated in terms of serum levels of IL-6, IL-10, hs-CRP and TNF-α as well as APACHEII, SOFA and NUTRIC scores, Glasgow coma scale and weight. In addition, the length of Intensive Care Unit stay, days of dependence on ventilator and 30-day mortality were studied. SPSS software (version 13.0) was used for data analysis.

Results

Taurine significantly decreased the serum levels of IL-6 (p = 0.04) and marginally APACHEII score (p = 0.05). In addition, weight loss was significantly lower in taurine group (p = 0.03). Furthermore, taurine significantly increased the GCS (p = 0.03). The groups were not different significantly in terms of levels of IL-10, hs-CRP, and TNF-α, SOFA and NUTRIC scores, 30-day mortality, length of ICU stay and days of dependence on ventilator.

Conclusion

According to the results of the present study, taurine supplementation can reduce the IL-6 levels as one of the important inflammatory markers in these patients; and enhances the clinical outcomes too.

Trial registration

IRCT, IRCT20180514039657N1. Registered 22 June 2018.

Peer Review reports

Background

Traumatic brain injury (TBI) is defined as the change in the brain function or other brain pathologic evidence caused by an external force [1]. It is one of the most common types of trauma and the main cause of death among various types of trauma [2,3,4]. Despite tangible developments in trauma management, the disease remains a great cause of mortality and is a serious problem for any society [5]. TBI occurs under two phases. Primary injury, which is the main determinant of outcomes, occurs at the time of the incident and is resistant to treatment. After that, physiological and pathophysiological reactions including the activation of inflammatory response involved in delayed cell death leading to a secondary injury and providing a chance for clinical interventions. The activation of inflammatory pathways in response to TBI leads to the release of pro- and anti-inflammatory cytokines and chemokines [6, 7]. Secondary injuries lead to inflammation in the nervous system and this process increases the nervous system damages [8]. TBI illustrates the pathophysiology of inflammation including brain edema and functional deficits in the nervous system [9]. If the inflammation is controlled for a specific period of time; it can be beneficial. While persistent or excessive inflammation is one of the main cause of nervous defects [10]. TBI is associated with increased levels of cytokines such as IL-6, IL-10, and TNF-α [11,12,13], which worsen the TBI condition and delay the improvement by generating oxidative stress and metalloproteinases [14, 15].

Taurine (2-aminoethane sulfonic acid) is a beta amino acid that is not involved in the structure of proteins and is found in the free form in the body. This is one of the most abundant free amino acids in the brain of mammals, which is essential to proper functioning of it [16, 17]. The synthesis of Taurine under stress can be reduced [18]. Taurine is influential in terms of detoxification, membrane stabilization, osmoregulation, nervous system, calcium homeostasis, inflammatory reactions, conjugation of bile acids, glucose metabolism, and anti-oxidant activity [16, 18,19,20,21].

Several studies have reported that taurine concentration decreases in response to trauma [22,23,24,25]. On the other hand, some studies have suggested the modification of inflammatory response by taurine supplementation [26,27,28].

To date, no investigation has focused on the efficacy of supplementation with taurine in TBI patients. Therefore, we carried out this study to assay the influence of taurine on this specific patient. The primary aims were to determine whether taurine affects the serum levels of IL-6, IL-10, TNF-α, and hs-CRP. Our secondary aim was specifying the effect of taurine on disease progression, length of ICU stay, duration of mechanical ventilation, 30-day mortality rate, weight, and nutritional risk.

Material and methods

This double-blind randomized controlled trial (RCT) was performed on TBI patients, who were admitted to the ICU of Golestan Hospital in Ahvaz, the largest city in southwest of Iran. On the first day of ICU admission, the patients were assessed based on the inclusion and exclusion criteria and enrolled in the study if they were eligible. The study protocol was approved by the Ethics Committee of Ahvaz Jundishapour University of Medical Sciences. This study was also registered in the Iranian Registry of Clinical Trials (code: IRCT20180514039657N1). Because of the patients’ unconsciousness, informed consent was obtained from their families for inclusion in the study.

The patients (n = 22) were divided into two groups via randomization (ratio, 1:1). To assign the patients into each group, a randomized block method was applied with a block size of six patients. Randomization was carried out based on a computer-generated random sequence of numbers. The sealed envelopes containing the numbers were kept by an independent third party, who was not involved in the clinical conduct of this study until all data were collected and verified. The patients, as well as individuals who were engaged in recruiting the participants, assigning the interventions, and evaluating the results, were blind to the group assignments.

The inclusion criteria were TBI patients over the age of 18 years, receiving enteral nutrition, with a Glasgow Coma Scale (GCS) score of 6–12. The GCS score was determined based on the patient’s condition and the intensivist’s opinion. On the other hand, patients were excluded if they were pregnant or lactating; taking anti-inflammatory medications or corticosteroids before admission; or had liver disorders, kidney diseases, or congenital disorders affecting amino acid metabolism. Also, patients were excluded if more than 60% of their energy requirements were not provided by enteral nutrition in the first week.

The enteral nutrition was initiated on the first day of ICU admission. The control group received an Standard Entera Meal (Karen Pharma and Food Supplement Co., Iran), and the taurine group received 30 mg/kg/day of taurine powder (Nutricost, USA) at a maximum dose of 3 g/day for 14 days, in addition to the Standard Entera Meal. This dosage of taurine was selected based on previous studies on the safe and effective dose of taurine [29, 30]. Taurine powder was given to the patients in two divided doses. The third person, who was given the randomization sequence, prepared the patient’s gavage for each meal and delivered it to the nurse in a solution form. The appearance, taste, color, odor, and containers of the gavage solution were similar. The gavages were coded by the third person, and only he was aware of their contents.

The weight of the patients was measured upon entering the study, using Seca 984 bed and dialysis scale. The patients’ energy requirements were calculated to be 25 kcal/kg/day, based on the formula. The patient’s feeding started at 30 ml/h, and then, 30 ml/h was added every three hours to reach the calculated energy requirements within 48–72 h. For determining the nutritional risk, the Nutrition Risk in Critically Ill (NUTRIC) score was measured. The NUTRIC score is the first nutrition risk instrument that is specifically validated for ICU patients and can identify patients at risk of malnutrition [31].

The clinical history and demographic characteristics of the patients were determined upon admission to the ICU. To evaluate the disease progression (response to treatment), the Sequential Organ Failure Assessment (SOFA) and Acute Physiology and Chronic Health Evaluation II (APACHE II) scores, along with the GCS score, were computed for all patients on the 1st and 14th days of the study. Generally, the GCS score is the most commonly used clinical tool for evaluating the severity of neurological injury in adults [32] due to its acceptable inter-observer reliability and predictive validity [33]. Moreover, the APACHE II score is a tool to measure disease severity in patients hospitalized in ICU [34]. The SOFA score is an objective and simple score that allows measuring the number and severity of organ dysfunction; it is a suitable prognostic index within the first days of hospitalization in ICU [35].

To measure the serum levels of IL-6, IL-10, TNF-α, and hs-CRP on the 1st and 14th days, 10 mL of venous blood was taken from each patient, and after centrifugation and serum detachment, the serum was kept at − 70 °C until further analysis. The IL-6, IL-10, TNF-α, and hs-CRP levels were measured using the ELISA kits. Changes were calculated based on the difference in each variable on day 14 vs. day 1. The length of ICU stay, duration of mechanical ventilation, and 30-day mortality rates were also investigated.

Statistical analysis

As specified by the preceding study on the serum levels of IL-6 variable [29], the total sample size of 30 patients was calculated by the averages comparison formula based on α = 0.01 and β = 0.1.

$$\mathrm{n}=\left\{{\left({\mathrm{Z}}_{1-\frac{\upalpha}{2}}+{\mathrm{Z}}_{1-\upbeta}\right)}^2\left({\mathrm{S}}_1^2+{\mathrm{S}}_2^2\right)\right\}/{\left({\upmu}_1-{\upmu}_2\right)}^2$$

Considering the probability of 30% dropout of patients during the study, the final sample size was considered 44 patients.

The data were analyzed using the statistical software program SPSS 13.0 (SPSS Inc., Chicago, IL, USA).

The Kolmogorov-Smirnov test was used to determine the distribution of quantitative data. Comparisons between mean of the groups were made by Independent Samples t-test if data distribution was normal. The comparisons of non-normally distributed data were performed using Mann-Whitney U test to compare the differences between the two groups. Comparisons of qualitative data were done by chi-squared test or Fisher’s exact test. Within-group comparisons were made using Paired-Samples t-test or its nonparametric equivalent (Wilcoxon). Outcomes were reported at 95% confidence intervals. The significance level was considered two-sided p < 0.05.

Results

From April to November 2018, 97 patients with TBI were assessed for eligibility and 44 were enrolled (Fig. 1); 32 patients completed the study, and others were excluded due to the reasons mentioned in Fig. 1.

Fig. 1
figure 1

Flow diagram of the trial

Baseline characteristics of patients are shown in Table 1. No significant difference existed between the groups. It should be noted that according to the set criteria, all patients who entered the study had GCS = 6–9.

Table 1 Baseline characteristics of the study participants

Nutrition variables were assessed in each group and are presented in Table 2. Mean energy intake was compared with the energy requirement calculated by the formula. No significant difference existed between the groups for energy intake. Weight loss in the taurine group was significantly lower than the control group (p = 0.03). The changes of NUTRIC score showed no significant difference between the groups (p = 0.40), but it was decreased significantly in taurine group (p = 0.01).

Table 2 Nutritional variables of the study participants

Figure 2 shows the levels of inflammatory markers. At the beginning of the study, no significant difference excited between the groups for any of the inflammatory markers. The mean changes of serum IL-6 between the groups were significantly different (− 70.75 ± 71.89 vs. -20.09 ± 59.51, p = 0.04). There were no significant differences between the groups in levels of IL-10, hs-CRP, and TNF-α (p = 0.81, p = 0.24 and p = 0.07, respectively). However, the increase in TNF-α in the control group and the decrease in hs-CRP in the taurine group was significant after 14 days (p = 0.004 and p = 0.02, respectively).

Fig. 2
figure 2

Serum levels of inflammatory markers. IL-6 shown as Mean ± SD, others as median (IQR). Independent Samples t-test was used for IL-6, and Mann-Whitney U test for others. A group comparison was made using a paired-samples t-test for IL-6; this was made by Wilcoxon for the others. * P < 0.05, # P < 0.01

Clinical outcomes are presented in Table 3. On the 1st day, no significant difference existed between the groups in GCS, APACHEll, and SOFA scores. The mean changes of GCS significantly increased by taurine supplementation (p = 0.03). The changes of APACHEll score showed marginal differences between two groups (p = 0.05). In other words, taurine decreased it. The SOFA score, mortality rate, duration on mechanical ventilation, and length of ICU stay were not different considerably between the groups (p = 0.06, p = 0.33, p = 0.26 and p = 0.96, respectively). However the SOFA score decreased significantly in Taurine group (p = 0.003).

Table 3 The clinical outcomes of study participants

Discussion

The present study evaluated the effects of taurine on the clinical outcomes of patients with sustained TBI. The results revealed the beneficial effect of taurine supplementation on the serum concentration of IL-6, APACHE II score, and GCS score.

One of the most important ways to increase immunity and reduce the likelihood of adverse outcomes in patients admitted to the ICU is to use enteral immunonutrition [36]. Over the years, researchers have studied the effects of various nutrients, such as omega-3 and glutamine, which can boost the immune system in critically ill patients. Taurine is a sulfur-containing amino acid, which has been evaluated as an immunomodulator [37, 38]. However, to the best of our knowledge, it has not been evaluated in patients with TBI. Previous studies indicated that the plasma taurine levels declined in critically ill patients. In this regard, Vermeulen et al., in an observational study, found that in patients admitted to the ICU, the plasma concentration of taurine decreased by more than 50% in the first 5 days of admission, which was associated with a high lactate level and a longer duration of mechanical ventilation and ICU stay [25].

Evidence suggests that the overexpression of inflammatory cytokines, such as IL-6, TNF-α, and hs-CRP, plays an important role in the pathogenesis of TBI [39]. In these patients, the acute inflammatory response varies in the early and late stages [40]. Also, within a short time after brain injury, abundant production of pro-inflammatory cytokines, such as IL-6 and CRP, occurs [41]. The role of inflammatory cytokines, especially TNF-α, IL-1β, IL-6, and IL-8, is well-established in neurodegeneration and cognitive deficits. Recently, Su et al. reported that the level of hs-CRP was associated with cognitive impairments following TBI [42].

The addition of taurine to a nutritional formula may reduce neuroinflammation and improve the clinical and nutritional status of TBI patients. The use of inexpensive, safe, and natural supplements is considered as an adjuvant therapy to inflammation control in these patients. As mentioned earlier, taurine is a beta-amino acid with anti-inflammatory and antioxidant activities in the central nervous system [43, 44]. However, no clinical trial has been conducted on taurine in patients with TBI so far. Our findings demonstrated that supplementation with taurine caused a significant decrease in the serum levels of IL-6 and hs-CRP and also prevented a further increase in the level of TNF-α; nevertheless, it exerted no effects on the IL-10 level.

In line with our findings, in a RCT, the administration of taurine, in addition to enteral nutrition, resulted in a decrease in the levels of IL-6 and CRP in critically ill septic patients [29]. Also, in a study on rats with TBI, 200 mg/kg/day of taurine for 1 week reduced the levels of IL-6, IL-10, and TNF-α [45]. Similar findings have been also reported in some animal studies [46,47,48,49]. However, contrary to our findings, a previous study on burn patients showed that the enteral administration of taurine significantly reduced the IL-10 levels, but did not affect the serum levels of hs-CRP and TNF-α [50]. Besides, in another study on elderly people with hip fractures, supplementation with 6 g/day of taurine had no effects on inflammatory markers, length of hospital stay, and mortality [51]. One of the reasons for the discrepancy between the results of different studies is the difference in the study population and the type of disease.

The mechanisms through which taurine acts as an anti-inflammatory agent have not been clearly defined. It is known that activated inflammatory cascades damage the blood-brain barrier (BBB) after TBI, which leads to the entry of circulating immune cells to the injured site and directly affects neuronal survival and death [52,53,54,55,56]. It has been shown that these activated cells release mediators, such as free radicals and pro-inflammatory cytokines [14]. Also, some studies have suggested the ability of taurine to suppress the NF-κB signaling pathway. It seems that taurine supplementation can exert inhibitory effects on NF-κB by oxidation of IĸB-α as an inhibitory protein [57].

Moreover, the anti-inflammatory activity of taurine may be attributed to its antioxidant ability to neutralize hypochlorous acids, which are reactive molecules in mammalian neutrophils, as well as monocytes, produced through the myeloperoxidase pathway [58], by forming taurine chloramine, as a relatively more stable and less toxic compound. Taurine chloramine can be generated at the inflammation site and control the expression and release of cytokines, such as nitric oxide, IL-6, IL-8, and TNF-α [59]. Since cytokines are mostly secreted by reactive astrocytes, inhibition of astrocytes may be another mechanism that regulates the cytokine levels [45].

Our findings related to the clinical outcomes of the patients showed that taurine supplementation decreased weight loss, APACHE II score, and SOFA score, while increasing the GCS score; however, it had no effects on the length of ICU stay, duration of mechanical ventilation, and 30-day mortality. Since APACHE II and SOFA scores represent the performance of different organs, a reduction in these scores (even if classifications for mortality prediction do not change) can indicate progress in recovery through reduction and control of organ dysfunction. Similar to our findings, an experimental model of head injury showed that taurine supplementation at 15 and 50 mg/kg/day decreased weight loss [60]. Since limited studies have been carried out in this area, the mechanism of action is not clear, and further studies are needed in the future to investigate the mechanisms of its effect. Nevertheless, the observed effect may be related to the reduction of inflammation and oxidative stress in these patients, leading to reduced weight loss in the intervention group.

According to our literature review, there was no study evaluating the effects of taurine supplementation on the GCS, APACHE II, and SOFA scores. Although differences in the length of ICU stay, duration of mechanical ventilation, and 30-day mortality were not statistically significant, they might be clinically important and reduce the imposed costs on the healthcare system. Also, changes in these clinical data are usually statistically significant in studies with a large sample size. Therefore, future studies with a larger sample size are needed to determine the effects of taurine on the clinical improvement of patients with TBI.

The present study had several strengths, which made the results more reliable. First, this study was the first trial evaluating the effects of taurine supplementation on patients with TBI. Second, the dosage of taurine used in this study was well-tolerated by the patients, and no side effects were reported.

On the other hand, the limitations of this study were its small sample size, short duration of supplementation, lack of measurement of the plasma taurine concentration due to limited finances, and lack of resting energy expenditure (REE) measurements due to the absence of necessary equipment. Since this study is the first clinical trial evaluating the effects of taurine supplementation on TBI patients, there was no similar study in the literature to review and compare the clinical outcomes. Therefore, it is necessary to conduct further studies with a larger sample size and longer supplementation periods while measuring the plasma concentration of taurine to confirm the use of this agent for TBI patients to improve inflammation and clinical outcomes.

Conclusion

According to the findings of this study, taurine supplementation in TBI patients was followed by clinical benefits, because it is reduced the levels of IL-6, APACHEII score, and weight loss.

Furthermore, GCS of patients in the taurine group improved significantly. Therefore, taurine can reduce the inflammation of patients with TBI and may be considered as an adjunctive treatment for these patients. However, more studies with larger sample size are needed to highlight the taurine advantages for this group of patients.

Availability of data and materials

The materials of this study are available at https://en.irct.ir/trial/31173.

Abbreviations

TBI:

Traumatic brain injury

ICU:

Intensive Care Unit

BBB:

Blood Brain Barrier

GCS:

Glasgow coma scale

SOFA:

Sequential Organ Failure Assessment

APACHEII:

Acute Physiology and Chronic Health Evaluation II

NUTRIC:

Nutrition risk in critically ill

IL-6:

Interleukin 6

IL-10:

Interleukin 10

hs-CRP:

High sensitive C-Reactive Protein

TNF-α:

Tumor Necrosis Factor-alpha

IQR:

Interquartile range

SD:

Standard deviation

NF-κB:

Nuclear factor kappa B

IĸB-α:

Inhibitory kappa B alpha

References

  1. Menon DK, Schwab K, Wright DW, Maas AI. Position statement: definition of traumatic brain injury. Arch Phys Med Rehabil. 2010;91(11):1637–40.

    Article  PubMed  Google Scholar 

  2. Jones N, Fear NT, Rona R, Fertout M, Thandi G, Wessely S, et al. Mild traumatic brain injury (mTBI) among UK military personnel whilst deployed in Afghanistan in 2011. Brain Inj. 2014;28(7):896–9.

    Article  PubMed  Google Scholar 

  3. Anderson V, Godfrey C, Rosenfeld JV, Catroppa C. 10 years outcome from childhood traumatic brain injury. Int J Dev Neurosci. 2012;30(3):217–24.

    Article  PubMed  Google Scholar 

  4. Halbauer JD, Lew HL, Yesavage JA. Neuropsychiatric diagnosis and management of chronic sequelae of war-related mild to moderate traumatic brain injury. J Rehabil Res Dev. 2009;46(6):757.

    Article  PubMed  Google Scholar 

  5. Gad MA, Saber A, Farrag S, Shams ME, Ellabban GM. Incidence, patterns, and factors predicting mortality of abdominal injuries in trauma patients. N Am J Med Sci. 2012;4(3):129.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Kumar A, Loane DJ. Neuroinflammation after traumatic brain injury: opportunities for therapeutic intervention. Brain Behav Immun. 2012;26(8):1191–201.

    Article  PubMed  Google Scholar 

  7. Schmidt OI, Infanger M, Heyde CE, Ertel W, Stahel PF. The role of neuroinflammation in traumatic brain injury. Eur J Trauma. 2004;30(3):135–49.

    Article  Google Scholar 

  8. Sherwood ER, Prough DS. Interleukin-8, neuroinflammation, and secondary brain injury. Crit Care Med. 2000;28(4):1221–3.

    Article  CAS  PubMed  Google Scholar 

  9. Laird MD, Vender JR, Dhandapani KM. Opposing roles for reactive astrocytes following traumatic brain injury. Neurosignals. 2008;16(2–3):154–64.

    Article  CAS  PubMed  Google Scholar 

  10. Correale J, Villa A. The neuroprotective role of inflammation in nervous system injuries. J Neurol. 2004;251(11):1304–16.

    Article  PubMed  Google Scholar 

  11. Ziebell JM, Morganti-Kossmann MC. Involvement of pro-and anti-inflammatory cytokines and chemokines in the pathophysiology of traumatic brain injury. Neurotherapeutics. 2010;7(1):22–30.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Maier B, Schwerdtfeger K, Mautes A, Holanda M, Müller M, Steudel WI, et al. Differential release of interleukines 6, 8, and 10 in cerebrospinal fluid and plasma after traumatic brain injury. Shock (Augusta, Ga). 2001;15(6):421–6.

    Article  CAS  Google Scholar 

  13. Morganti-Kossman MC, Lenzlinger PM, Hans V, Stahel P, Csuka E, Ammann E, et al. Production of cytokines following brain injury: beneficial and deleterious for the damaged tissue. Mol Psychiatry. 1997;2(2):133.

    Article  CAS  PubMed  Google Scholar 

  14. Werner C, Engelhard K. Pathophysiology of traumatic brain injury. BJA. 2007;99(1):4–9.

    Article  CAS  PubMed  Google Scholar 

  15. Lucas SM, Rothwell NJ, Gibson RM. The role of inflammation in CNS injury and disease. Br J Pharmacol. 2006;147(S1):S232–40.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Huxtable RJ. Physiological actions of taurine. Physiol Rev. 1992;72(1):101–63.

    Article  CAS  PubMed  Google Scholar 

  17. Huxtable RJ. Taurine in the central nervous system and the mammalian actions of taurine. Prog Neurobiol. 1989;32(6):471–533.

    Article  CAS  PubMed  Google Scholar 

  18. Vanitha MK, Baskaran K, Periyasamy K, Saravanan D, Ilakkia A, Selvaraj S, et al. A review on the biomedical importance of taurine. Int J Pharm Res Health Sci. 2015;3(3):680–6.

    CAS  Google Scholar 

  19. Schaffer S, Takahashi K, Azuma J. Role of osmoregulation in the actions of taurine. Amino Acids. 2000;19(3–4):527–46.

    Article  CAS  PubMed  Google Scholar 

  20. Schuller-Levis GB, Park E. Taurine: new implications for an old amino acid. FEMS Microbiol Lett. 2003;226(2):195–202.

    Article  CAS  PubMed  Google Scholar 

  21. El Idrissi A. Taurine increases mitochondrial buffering of calcium: role in neuroprotection. Amino Acids. 2008;34(2):321–8.

    Article  PubMed  CAS  Google Scholar 

  22. Engel JM, Mühling J, Weiss S, Kärcher B, Löhr T, Menges T, et al. Relationship of taurine and other amino acids in plasma and in neutrophils of septic trauma patients. Amino Acids. 2006;30(1):87–94.

    Article  CAS  PubMed  Google Scholar 

  23. Paauw JD, Davis AT. Taurine concentrations in serum of critically injured patients and age-and sex-matched healthy control subjects. Am J Clin Nutr. 1990;52(4):657–60.

    Article  CAS  PubMed  Google Scholar 

  24. Boelens PG, Houdijk AP, de Thouars HN, Teerlink T, van Engeland MI, Haarman HJ, et al. Plasma taurine concentrations increase after enteral glutamine supplementation in trauma patients and stressed rats. Am J Clin Nutr. 2003;77(1):250–6.

    Article  CAS  PubMed  Google Scholar 

  25. Vermeulen MA, van Stijn MF, Visser M, Lemmens SM, Houdijk AP, van Leeuwen PA, et al. Taurine concentrations decrease in critically ill patients with shock given enteral nutrition. J Parenter Enter Nutr. 2016;40(2):264–72.

    Article  CAS  Google Scholar 

  26. Cruzat VF, Krause M, Newsholme P. Amino acid supplementation and impact on immune function in the context of exercise. J Int Soc Sports Nutr. 2014;11(1):61.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  27. Chen X, Sebastian BM, Tang H, McMullen MM, Axhemi A, Jacobsen DW, et al. Taurine supplementation prevents ethanol-induced decrease in serum adiponectin and reduces hepatic steatosis in rats. Hepatology. 2009;49(5):1554–62.

    Article  CAS  PubMed  Google Scholar 

  28. Fürst P, Kuhn KS. Amino-acid substrates in new bottles: implications for clinical nutrition in the 21st century. Nutrition. 2000;16(7):603–6.

    Article  PubMed  Google Scholar 

  29. Elmokadem EM, Sabri NA, Roshdy TA, Hasanin AM. Clinical outcome study of critically-ill septic patients given taurine supplemented enteral nutrition. Int J Pharm Sci Res. 2015;6(8):3544.

    CAS  Google Scholar 

  30. Aguilar F, Charrondiere UR, Dusemund B, Galtier P, Gilbert J, Gott DM, et al. The use of taurine and d-glucurono-gamma-lactone as constituents of the so-called" energy" drinks. EFSA J. 2009;935:1–31.

    Google Scholar 

  31. Heyland DK, Dhaliwal R, Jiang X, Day AG. Identifying critically ill patients who benefit the most from nutrition therapy: the development and initial validation of a novel risk assessment tool. Crit Care. 2011;15(6):R268.

    Article  PubMed  PubMed Central  Google Scholar 

  32. American Association of Neurological Surgeons. The Brain Trauma Foundation. The Joint Section on Neurotrauma and Critical Care. Glasgow Coma Scale score. J Neurotrauma. 2000;17:563–71.

    Article  Google Scholar 

  33. Narayan RK, Michel ME, Ansell B, Baethmann A, Biegon A, Bracken MB, et al. Clinical trials in head injury. J Neurotrauma. 2002;19(5):503–57.

    Article  PubMed  Google Scholar 

  34. Knaus WA, Draper EA, Wagner DP, Zimmerman JE. APACHE II: A severity of disease classification system. Crit Care Med. 1985;13:818–29.

    Article  CAS  PubMed  Google Scholar 

  35. Vincent JL, Moreno R, Takala J, Willatts S, De Mendonça A, Bruining H, et al. The SOFA (sepsis-related organ failure assessment) score to describe organ dysfunction/failure. Intensive Care Med. 1996;22(7):707–10.

    Article  CAS  PubMed  Google Scholar 

  36. Slotwinski R, Olszewski WL, Slotkowski M, Lech G, Zaleska M, Slotwinska SM, et al. Can the interleukin-1 receptor antagonist (IL-1ra) be a marker of anti-inflammatory response to enteral immunonutrition in malnourished patients after pancreaticoduodenectomy. JOP. 2007;8(6):759–69.

    PubMed  Google Scholar 

  37. Wu GH, Zhang YW, Wu ZH. Modulation of postoperative immune and inflammatory response by immune-enhancing enteral diet in gastrointestinal cancer patients. World J Gastroenterol. 2001;7(3):357.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Bouckenooghe T, Remacle C, Reusens B. Is taurine a functional nutrient? Curr Opin Clin Nutr Metab Care. 2006;9(6):728–33.

    Article  CAS  PubMed  Google Scholar 

  39. Woodcock T, Morganti-Kossmann C. The role of markers of inflammation in traumatic brain injury. Front Neurol. 2013;4:18.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. McGuire MF, Savarraj JP, Kitagawa RS, Choi HA. Acute inflammation after traumatic brain injury. In: Translational Inflammation. Academic Press; 2019. p. 221–39.

    Google Scholar 

  41. Vaughan LE, Ranganathan PR, Kumar RG, Wagner AK, Rubin JE. A mathematical model of neuroinflammation in severe clinical traumatic brain injury. J Neuroinflammation. 2018;15(1):345.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Su SH, Xu W, Li M, Zhang L, Wu YF, Yu F, et al. Elevated C-reactive protein levels may be a predictor of persistent unfavourable symptoms in patients with mild traumatic brain injury: a preliminary study. Brain Behav Immun. 2014;38:111–7.

    Article  CAS  PubMed  Google Scholar 

  43. Redmond HP, Stapleton PP, Neary P, Bouchier-Hayes D. Immunonutrition: the role of taurine. Nutrition. 1998;14(7–8):599–604.

    Article  CAS  PubMed  Google Scholar 

  44. Wu JY, Prentice H. Role of taurine in the central nervous system. J Biomed Sci. 2010;17(1):S1.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  45. Su Y, Fan W, Ma Z, Wen X, Wang W, Wu Q, et al. Taurine improves functional and histological outcomes and reduces inflammation in traumatic brain injury. Neuroscience. 2014;266:56–65.

    Article  CAS  PubMed  Google Scholar 

  46. Lin S, Hirai S, Yamaguchi Y, Goto T, Takahashi N, Tani F, et al. Taurine improves obesity-induced inflammatory responses and modulates the unbalanced phenotype of adipose tissue macrophages. Mol Nutr Food Res. 2013;57(12):2155–65.

    Article  CAS  PubMed  Google Scholar 

  47. Das J, Vasan V, Sil PC. Taurine exerts hypoglycemic effect in alloxan-induced diabetic rats, improves insulin-mediated glucose transport signaling pathway in heart and ameliorates cardiac oxidative stress and apoptosis. Toxicol Appl Pharmacol. 2012;258(2):296–308.

    Article  CAS  PubMed  Google Scholar 

  48. Pei P, Yao X, Jiang L, Qiu T, Wang N, Yang L, et al. Inorganic arsenic induces pyroptosis and pancreatic β cells dysfunction through stimulating the IRE1α/TNF-α pathway and protective effect of taurine. Food Chem Toxicol. 2019;125:392–402.

    Article  CAS  PubMed  Google Scholar 

  49. Abd El-Twab SM, Mohamed HM, Mahmoud AM. Taurine and pioglitazone attenuate diabetes-induced testicular damage by abrogation of oxidative stress and up-regulation of the pituitary–gonadal axis. Can J Physiol Pharmacol. 2016;94(6):651–61.

    Article  CAS  PubMed  Google Scholar 

  50. Lak S, Ostadrahimi A, Nagili B, Asghari-Jafarabadi M, Beigzali S, Salehi F, et al. Anti-inflammatory effect of taurine in burned patients. Adv Pharm Bull. 2015;5(4):531.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. Van Stijn M, Bruins A, Vermeulen M, Witlox J, Teerlink T, Schoorl M, et al. Effect of oral taurine on morbidity and mortality in elderly hip fracture patients: a randomized trial. Int J Mol Sci. 2015;16(6):12288–306.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  52. Bye N, Habgood MD, Callaway JK, Malakooti N, Potter A, Kossmann T, et al. Transient neuroprotection by minocycline following traumatic brain injury is associated with attenuated microglial activation but no changes in cell apoptosis or neutrophil infiltration. Exp Neurol. 2007;204(1):220–33.

    Article  CAS  PubMed  Google Scholar 

  53. McIntosh TK, Saatman KE, Raghupathi R, Graham DI, Smith DH, Lee VM, et al. The Dorothy Russell memorial lecture. The molecular and cellular sequelae of experimental traumatic brain injury: pathogenetic mechanisms. Neuropathol Appl Neurobiol. 1998;24(4):251–67.

    Article  CAS  PubMed  Google Scholar 

  54. Clark RS, SCHIDING JK, KACZOROWSKI SL, MARION DW, KOCHANEK PM. Neutrophil accumulation after traumatic brain injury in rats: comparison of weight drop and controlled cortical impact models. J Neurotrauma. 1994;11(5):499–506.

    Article  CAS  PubMed  Google Scholar 

  55. Kato H, Walz W. The initiation of the microglial response. Brain Pathol. 2000;10(1):137–43.

    Article  CAS  PubMed  Google Scholar 

  56. Kubes P, Ward PA. Leukocyte recruitment and the acute inflammatory response. Brain Pathol. 2000;10(1):127–35.

    Article  CAS  PubMed  Google Scholar 

  57. Barua M, Liu Y, Quinn MR. Taurine chloramine inhibits inducible nitric oxide synthase and TNF-α gene expression in activated alveolar macrophages: decreased NF-κB activation and IκB kinase activity. J Immunol. 2001;167(4):2275–81.

    Article  CAS  PubMed  Google Scholar 

  58. Schuller-Levis GB, Park E. Taurine and its chloramine: modulators of immunity. Neurochem Res. 2004;29(1):117–26.

    Article  CAS  PubMed  Google Scholar 

  59. Marcinkiewicz J, Grabowska A, Bereta J, Stelmaszynska T. Taurine chloramine, a product of activated neutrophils, inhibits in vitro the generation of nitric oxide and other macrophage inflammatory mediators. J Leukoc Biol. 1995;58(6):667–74.

    Article  CAS  PubMed  Google Scholar 

  60. Sun M, Zhao Y, Gu Y, Zhang Y. Protective effects of taurine against closed head injury in rats. J Neurotrauma. 2015;32(1):66–74.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

The reported results were a part of the MSc thesis of Mahsa Vahdat (NRC-9630). That is registered in the Nutrition and Metabolic Diseases Research Center, Ahvaz Jundishapur University of Medical Sciences.

Funding

This study was supported by the Vice Chancellor for research affairs of Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran (NRC-9630).

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Authors and Affiliations

Authors

Contributions

Mahsa Vahdat: Conceptualization, Methodology, Investigation and Writing-original draft; Seyed Ahmad Hosseini: Conceptualization, Project administration, Supervision and Writing-review & editing; Farhad Soltani: Clinical supervisor, Help in selecting samples and Clinical evaluator; Bahman Cheraghian: Formal Analysis; Masih Namjoonia: Investigation. The authors(s) read and approved the final manuscript.

Corresponding author

Correspondence to Seyed Ahmad Hosseini.

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Ethics approval and consent to participate

Our study protocol was approved by the Ethics Committee of Ahvaz Jundishapour University of Medical Sciences with a code number of (IR.AJUMS.REC.1396.919). Because of the unconsciousness of patients, informed consent was taken from their family for their inclusion in the study.

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Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Vahdat, M., Hosseini, S.A., Soltani, F. et al. The effects of Taurine supplementation on inflammatory markers and clinical outcomes in patients with traumatic brain injury: a double-blind randomized controlled trial. Nutr J 20, 53 (2021). https://doi.org/10.1186/s12937-021-00712-6

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