Methods: T hirty-five p atients w ith c ongenital h eart diseases undergoing surgical treatment were divided into two groups: 20 patients were operated with using cardiopulmonary bypass (group 1, on-pump) and 15 patients were operated without cardiopulmonary bypass (group 2, off-pump). Blood samples were collected before surgery and at 1, 24 and 72 hours following surgery.
Results: Total antioxidant response was prompt and drew a peak within the first hour following surgery in group 1. After 24 hours, it showed a sustained increase (p=0.009). In the group 2, total antioxidant response decreased significantly within the first hour, and then increased to a peak level within the 24 hours (p=0.04). Thereafter, it was gradually reduced. Total antioxidant response, albumin, bilirubin and hsCRP levels remained high in group 1, after 24 hours. Total antioxidant response levels were positively associated with the albumin levels at 24 hours following surgery in group 2 (r=0.669, p=0.01).
Conclusion: The plasma levels of albumin may be considered in the assessment of global antioxidant response in patients treated with CPB technique.
The purpose of this prospective study was to analyze the operative and early postoperative changes of the TAR, high-sensitivity C-reactive protein (hs-CRP) and activated and/or generated antioxidants, including endogenous antioxidants, in infants who undergoing cardiac surgery using both on-pump and off-pump techniques.
Table 1: Patient characteristics and operative data
Surgical technique
Standard general anesthesia was applied to all patients
in the same manner, and the surgery consisted of either a median sternotomy or thoracotomy. In group 1, the CPB
circuit was composed of a Sarns roller pump (Terumo
Cardiovascular Systems, Ann Arbor, Michigan, USA)
and a membrane oxygenator (Bentley Oxygenation
System CM50, Baxter-Bentley Laboratories, Irvine,
California, USA) with an incorporated cardiotomy
reservoir. The pump was primed with Ringer’s solution,
20% mannitol (3 ml/kg), and 8.4% sodium bicarbonate
(1 mmol/kg). The flow rate was 2.4 L/min per square
meter (m2) body surface area. Heparin (Liquemine,
La Roche Ltd., Basel, Switzerland) 3 mg/kg was
given before cannulation. The activated clotting time
(ACT) was monitored and kept at >480 seconds.
Cardiopulmonary bypass was established by cannulation
of the ascending aorta and the right atrium. Moderate
hemodilution (down to a hematocrit of 15-34%) and
moderate systemic hypothermia (a nasopharyngeal
temperature of 28-30 °C) were employed. A blood
cardioplegic solution was infused into the aortic root at
sequences as warm induction, cold maintenance, and
hot-shot, respectively. After discontinuation of CPB,
the heparin was neutralized with an equipotent dose of
protamine chloride (La Roche Ltd., Brussels, Belgium).
Blood sampling
The measured biochemical parameters were the plasma
levels of TAR, albumin, total bilirubin, uric acid, and
hs-CRP levels in both groups. Venous blood samples
were collected before surgery (after an overnight fast)
and at one, 24, and 72 hours afterwards. The times of
the blood sampling were chosen based on both literature
data and our own opinion, which both pointed to the fact
that the most intense alterations occur at those times.
The samples were withdrawn from a cubital vein into
vacutainer tubes and immediately stored at 4 °C. The
sera were then separated from the cells by centrifugation
at 1500 x g for 10 minutes and stored at -20 °C until the
day of analysis.
Measurement of the total antioxidant response
The TAS of the sera was measured using an automated
colorimetric measurement method developed by Erel.[4]
In this method, the hydroxyl radical, which is the most potent biological radical, is produced by the Fenton reaction and reacts with the colorless substrate o-dianisidine. This produces the dianisidyl radical that is bright yellow-brown in color. Next, the rate of the reaction is monitored by following the absorbance of this radical. The antioxidants of the sample suppress the oxidative reactions and prevent the color change. The assay results are expressed as millimoles of trolox equivalent per liter. Within- and between-batch precisions were lower than 3%.
Measurement of the individual antioxidants and
hs-CRP
The serum albumin, uric acid, and total bilirubin levels
were measured by commercial kits using an Abbott
Aeroset auto analyzer (Abbot Laboratories, Abbott Park,
Illinois, USA), and the serum hs-CRP was measured by
a Delta nephelometer (Radim Diagnostics, Italy).
Statistical analysis
Statistical analysis of data was performed using the
Statistical Package for the Social Sciences (SPSS Inc,
Chicago, Illinois, USA) version 14.0 for Windows
software program. Values were given as means ±
standard deviation (SD) of in vitro samples that
were analyzed four times. The equality of means
of the independent samples were compared using
Student’s t-test. All p values <0.05 were considered
to be significant. Relationships among variables were
obtained using Pearson’s correlation coefficient.
The preoperative levels of bilirubin and uric acid were slightly higher (p=NS) in group 2. There was a significant increase (p=0.009) in the TAR the first hour after surgery in group 1 as it was slightly decreased during the first 24 hours but increased again after that. In contrast to group 1, the TAR was significantly decreased (p=0.04) at the first hour and increased within the first 24 hours in group 2. After 24 hours, the TAR decreased in this group. The TAS was positively related to the albumin levels at 24 hours (r=0.669, p=0.01) in group 2, and the albumin, bilirubin, and hs-CRP had similar curves within the first 24 hours in both groups. After that time, the TAR, albumin, and hs-CRP increased in group 1 and decreased in group 2 (Figure 1-5).
Since the antioxidative effects of the antioxidant components of plasma are additive, the measurement of the TAR reflects the antioxidative status of plasma. In the present study, as previously mentioned, the total antioxidant status of the plasma was measured using an automated colorimetric measurement method developed by Erel.[4] In this method, the total antioxidant response of plasma, especially against potent free radical reactions, which strongly lead to oxidative damage of biomolecules such as lipids, proteins and DNA, is measured. In addition, hydrogen peroxide and other derivatives of peroxides, which produce physiologically and increase under some conditions, diffuse into the plasma. Here, the antioxidant components of plasma overcome them, and they are simultaneously consumed.[9] We evaluated the oxidative status of plasma by measuring the TAR.
There are only a few studies which have compared the degree of OS for patients undergoing on-pump versus off-pump techniques. In general, it has been demonstrated that the on-pump procedure gives rise to a more pronounced systemic inflammation and OS than the off-pump procedure.[10,11] The extracorporeal circulation apparatus, ischemia-reperfusion, and changes in body temperature are some of the sources of ROS production, and these lead to a depletion of the endogenous antioxidant response. There seem to be significant differences between the susceptibility of pediatric patients and adults to CPB surgery regarding OS. Similar to Christensen’s pediatric population study,[12] Ballmer et al.[13] found that individual antioxidant levels in adult patients were significantly depleted following surgery performed with CPB. However, the antioxidant decline immediately after CPB (<20%) was much less extensive than in pediatric study patients, and the maximum decline (>50%) was not observed until 24 hours after CPB.
Oxidative stress occurs when the free radical generation exceeds the human antioxidant defense mechanisms. In the present study, both groups of patients had visible changes in antioxidant response. As metioned previously, the most intense alterations occur before surgery and at one, 24, and 72 hours after the operation. In group 1, the TAR increase was prompt and peaked within the first hour. After that, it slightly decreased during the first 24 hours. This occurrence is closely linked to CPB. After the first 24 hours, it showed a slow and sustained increase. In group 2, the TAR decreased to a minimum within the first hour and then slowly increased to a peak level within the first 24 hours, which is nearly the same as in the first hour level of group 1. Thereafter, it slowly decreased, which is in contrast to group 1. These changes indicate that severe OS in off-pump surgery is limited within the first 24 hours, but it remains constantly in on-pump surgery.
Albumin, the most abundant protein in serum, bilirubin, and uric acid work in the antioxidant defense mechanism against OS. Recent evidence indicates that albumin may provide antioxidant protection by functioning as a serum peroxidase in the presence of reduced glutathione, an intracellular antioxidant. Various epidemiological and clinical data consistently has shown that a reduced level of serum albumin is associated with an increased event and mortality risk.[14] A decreased albumin level might act as a marker for other pathogenic processes or factors, such as infection, inflammation, loss of lean mass associated with illness, undernutrition, or lack of activity, and it also reflects a serum antioxidant deficit. In our study, the albumin levels and the TAR were correlated in group 2 within the first 24 hours. In group 1, the TAR and albumin levels were not correlated during this period of time because of many factors such as hemodilution, which possibly affected the albumin level with CPB. After 24 hours, the albumin levels and the TAR had similar curves in group 1.
As early as 1959, it was suggested that bilirubin might be an antioxidant, and it can suppress the oxidation of lysosomes at physiologically relevant oxygen concentrations. Bilirubin can scavenge the chain-carrying peroxyl radical, which is the primary proposed mechanism of the antioxidant effect.[15] It can act as an important cytroprotector of tissues that are poorly equipped with antioxidant defense systems, including the myocardium and nervous tissue,[16] and it provides important protection against postoperative complications and inflammation.[17] Although the baseline level of bilirubin was slightly higher (but not significant) in group 1, the bilirubin curve was similar in both groups in the 24 hours. However, after 24 hours, the levels were decreased in group 2. The bilirubin levels stayed high in group 1 like other antioxidants.
Uric acid, a metabolic breakdown product of nucleic acids in DNA (purines), is found in the serum at concentrations ten times higher than those of vitamin C and has recently been shown to offer significant antioxidant activity and a potential protecting role against oxidative injury.[18] In contrast to the other antioxidants, the uric acid levels were decreased after 24 hours in group 1. Uric acid, like vitamin C, is known as a low molecular weight antioxidant (LMWA). Decreased levels of uric acid might be related to possible consumption by the myocardium within the period of reperfusion and removal from the circulation.[19]
In both groups, the hs-CRP increase was prompt and peaked within the first 24 hours. After 24 hours, these levels decreased in group 2. In group 1, after the first 24 hours, it showed a slow, sustained increase. These changes may be associated with limited, severe OS in off-pump surgery and were constant in group 1. The higher increase in group 2 versus group 1 may indicate that substantial OS arose after conventional CPB, but this was mainly induced by the surgical trauma.
We think that variations in plasma levels of single antioxidants are not good markers of OS involvement. Indeed, the TAR measurement is a global marker of the antioxidant capacity of plasma. In this prospective clinical study, we tried to point out that the TAR is affected by on-pump and off-pump surgery, and supplementation of antioxidant agents a short time after surgery may lead to desired and beneficial changes in postoperative complications.
To the best of our knowledge, there is no study about changes in serum TAR and its comparison to serum albumin, uric acid, bilirubin, and hs-CRP levels in patients who underwent congenital heart surgery with on-pump or off-pump techniques. One of the limitations of our study was the relatively small sample size of the groups. Another limitation of this study was that the oxidative status of the cyanotic and acyanotic patients did not compare. In a recent study of children with cyanotic or acyanotic congenital heart disease, the level of OS was more evident in the cyanotic group.[20] However, in our study population, the two groups had a fairly homogeneous composition and did not present significant differences concerning the cardiac pathology itself. However, it should be noted that these patients were operated with different surgical techniques. This consideration could affect the patient’s response to similar OS. This study showed that there is a strong antioxidant response that occurs after pediatric cardiac surgery in both the off-pump and on-pump techniques, and this response was sustained after the first 24 hours in patients operated with CPB. We think that this result demonstrates the protracted effect of CPB on antioxidant status on the postoperative period. It may be speculated that the hemodilution associated with CPB could be partially responsible for the significant reduction in plasma antioxidative capacity. Finally, it should be noted that the contact between the blood and the CPB circuit is very complex and is related to a number of OS sources. Further studies are necessary to establish whether early and late OS is indeed a cause of CPB-associated postoperative complications in pediatric patients.
Declaration of conflicting interests
The authors declared no conflicts of interest with respect
to the authorship and/or publication of this article.
Funding
The authors received no financial support for the
research and/or authorship of this article.
1) Clermont G, Vergely C, Jazayeri S, Lahet JJ, Goudeau JJ,
Lecour S, et al. Systemic free radical activation is a major
event involved in myocardial oxidative stress related to
cardiopulmonary bypass. Anesthesiology 2002;96:80-7.
2) Matata BM, Sosnowski AW, Galiñanes M. Off-pump bypass
graft operation significantly reduces oxidative stress and
inflammation. Ann Thorac Surg 2000;69:785-91.
3) Pyles LA, Fortney JE, Kudlak JJ, Gustafson RA, Einzig
S. Plasma antioxidant depletion after cardiopulmonary
bypass in operations for congenital heart disease. J Thorac
Cardiovasc Surg 1995;110:165-71.
4) Erel O. A novel automated method to measure total
antioxidant response against potent free radical reactions.
Clin Biochem 2004;37:112-9.
5) Elmoselhi AB, Lukas A, Ostadal P, Dhalla NS.
Preconditioning attenuates ischemia-reperfusion-induced
remodeling of Na+-K+-ATPase in hearts. Am J Physiol Heart
Circ Physiol 2003;285:H1055-63.
6) Suzuki S, Kaneko M, Chapman DC, Dhalla NS. Alterations
in cardiac contractile proteins due to oxygen free radicals.
Biochim Biophys Acta 1991;1074:95-100.
7) Biglioli P, Cannata A, Alamanni F, Naliato M, Porqueddu M,
Zanobini M, et al. Biological effects of off-pump vs. on-pump
coronary artery surgery: focus on inflammation, hemostasis
and oxidative stress. Eur J Cardiothorac Surg 2003;24:260-9.
8) Tarpey MM, Wink DA, Grisham MB. Methods for detection
of reactive metabolites of oxygen and nitrogen: in vitro and in
vivo considerations. Am J Physiol Regul Integr Comp Physiol
2004;286:R431-44.
9) Koracevic D, Koracevic G, Djordjevic V, Andrejevic S, Cosic
V. Method for the measurement of antioxidant activity in
human fluids. J Clin Pathol 2001;54:356-61.
10) Gerritsen WB, van Boven WJ, Driessen AH, Haas FJ,
Aarts LP. Off-pump versus on-pump coronary artery
bypass grafting: oxidative stress and renal function. Eur J
Cardiothorac Surg 2001;20:923-9.
11) Akila, D’souza B, Vishwanath P, D’souza V. Oxidative injury
and antioxidants in coronary artery bypass graft surgery:
off-pump CABG significantly reduces oxidative stress. Clin
Chim Acta 2007;375:147-52.
12) Christen S, Finckh B, Lykkesfeldt J, Gessler P, Frese-Schaper
M, Nielsen P, et al. Oxidative stress precedes peak systemic
inflammatory response in pediatric patients undergoing
cardiopulmonary bypass operation. Free Radic Biol Med
2005;38:1323-32.
13) Ballmer PE, Reinhart WH, Jordan P, Bühler E, Moser UK,
Gey KF. Depletion of plasma vitamin C but not of vitamin E in response to cardiac operations. J Thorac Cardiovasc Surg
1994;108:311-20.
14) Malatino LS, Benedetto FA, Mallamaci F, Tripepi G, Zoccali
C, Parlongo S, et al. Smoking, blood pressure and serum
albumin are major determinants of carotid atherosclerosis
in dialysis patients. CREED Investigators. Cardiovascular
Risk Extended Evaluation in Dialysis patients. J Nephrol
1999;12:256-60.
15) Stocker R, Yamamoto Y, McDonagh AF, Glazer AN, Ames
BN. Bilirubin is an antioxidant of possible physiological
importance. Science 1987;235:1043-6.
16) Temme EH, Zhang J, Schouten EG, Kesteloot H. Serum
bilirubin and 10-year mortality risk in a Belgian population.
Cancer Causes Control 2001;12:887-94.
17) Mayer M. Association of serum bilirubin concentration with
risk of coronary artery disease. Clin Chem 2000;46:1723-7.
18) Becker BF. Towards the physiological function of uric acid.
Free Radic Biol Med 1993;14:615-31.