Total antioxidant concentrations of breastmilk--an eye-opener to the negligent.
Abstract: The balance between free radical production and antioxidant defenses in the body has important systemic and oral health implications. There is convincing evidence that breastmilk containing antioxidants is important in the prevention of diseases in infancy. This study compared the total antioxidant concentration of human breastmilk expressed at different stages of lactation, stored at various temperatures and durations. Expressed breastmilk (EBM) samples of the third, seventh and 30th day were collected from women who had term and preterm deliveries (n=20). Another cohort of women (n=20) was also assessed; these women were more than five months postpartum and lactating. The total antioxidant capacity (TAC) of EBM was assessed at zero hours at room temperature, at 48 hours, one week post-refrigeration (4[degrees]C), and freezing (-8[degrees]C) respectively using the phosphomolybdenum method. The highest antioxidant levels were found in colostrum. The TAC of EBM reduced with time and at post-refrigeration and after freezing (p<0.0005). No significant difference in the mean TAC was observed between the EBM samples obtained from women with either term or preterm deliveries. The progressive loss of antioxidant content of EBM emphasizes the need of awareness and curtailment of the practice of storing and later use of EBM.

Key words: Antioxidants; Breastfeeding; Breastmilk; Milk, Human; Total antioxidant capacity; India
Article Type: Report
Subject: Breast milk (Health aspects)
Breast milk (Chemical properties)
Antioxidants (Usage)
Antioxidants (Health aspects)
Authors: Xavier, Arun Mamachan
Rai, Kavita
Hegde, Amitha M.
Pub Date: 12/01/2011
Publication: Name: Journal of Health Population and Nutrition Publisher: International Centre for Diarrhoeal Disease Research Bangladesh Audience: Academic Format: Magazine/Journal Subject: Health Copyright: COPYRIGHT 2011 International Centre for Diarrhoeal Disease Research Bangladesh ISSN: 1606-0997
Issue: Date: Dec, 2011 Source Volume: 29 Source Issue: 6
Accession Number: 280004943
Full Text: INTRODUCTION

The period from birth to two years of age is a 'crucial window' for the promotion of optimal growth, health, and cognitive development of a child. Adequate nutrition through appropriate infant and young child-feeding (IYCF) practices is fundamental to the development of each child's full human potential (1). Human milk is species-specific, and all substitute feeding preparations differ remarkably from it, making human milk uniquely superior for infant feeding. It contains, on average, 1.1% protein, 4.2% fat, and 7.0% carbohydrate and supplies 72 kcal of energy per 100 g (2).

Premature infants (<37 weeks gestation) are a very vulnerable group. They are at a high risk of medical and surgical complications that are costly to the healthcare system and compromise the quality of their lives (3). There is strong evidence that feeding of human breastmilk decreases the incidence and/ or severity of various infectious diseases, including bacterial meningitis (4), bacteraemia (5), diarrhoea (6), respiratory tract infection (7), otitis media (8), and late-onset sepsis in preterm infants (9).

Saugstadt suggests that all the factors, conditions, and problems affecting infants, especially those born prematurely, are the outcomes of one unifying disease--oxygen radical disease (10). If there are too many free radicals produced and too few antioxidants, a condition of oxidative stress develops, which may cause serious damage in infancy. A need to reduce oxidative stress and/or boost antioxidant defenses in these vulnerable infants is essential.

Human milk has antioxidant properties. It contains vitamin C and E and enzymes, including superoxide dismutase, catalase, and glutathione peroxidase. These are known to protect against the potentially-harmful effects of oxidative stress (3). Apart from its role in maintaining the viability and texture of human tissue cells, it also modulates immune-mediated mechanisms in the body for a healthy survival. The role of antioxidants has also been depicted in the first window of infectivity, gingival and periodontal diseases, oral infections, and tissue morphogenesis. Hence, antioxidants form an important part of diet and, together with intracellular antioxidant enzyme systems, prevent various diseases (11).

The storage of expressed breastmilk (EBM) for later use by working mothers is well on the rise. Feeding-bottle systems are used for delivering stored EBM to infants (12). Evidence shows that storage of human milk and infant formula leads to a loss of ascorbic acid (12). The purpose of this study was to evaluate the influence of storage temperature and duration on the total antioxidant capacity (TAC) of human EBM.

MATERIALS AND METHODS

The study was carried out at Justice K S Hegde Charitable Hospital, Mangalore and at the Department of Pediatric Dentistry of A.B. Shetty Memorial Institute of Dental Sciences, Mangalore, India.

Study subjects and samples

The study women included inmates from the Gynecology Ward of Justice K S Hegde Charitable Hospital and the local residents. They were healthy women aged less than 30 years and belonged to the middle socioeconomic strata. The categorization of economic backgrounds was made based on a standard annual income chart. Mothers belonging to the middle-class families and of similar ages were selected for the study, assuming that wide discrepancies among their lifestyles and dietary patterns would not exist.

Based on a pilot study for a pooled standard deviation of 8 [micro]g/dL in the TAC and the clinical difference of 10 [micro]g/dL, for a power of 80%, the sample-size calculated was 14 in each experimental group. Although the research initiated with 14 mothers in a group, four mothers had to be excluded as three failed to report on the mentioned day for the collection of samples and one fell ill. To standardize the total number of samples in each group, 10 term and preterm mothers each were selected for the respective analyses. The clinical and demographic data of the selected mothers are summarized in Table 1.

Study design

Two mL of breastmilk was collected on the third day (colostrum), seventh day (transitional milk), and 30th day (mature milk) postpartum from 10 mothers each who delivered at term (n=10) and preterm (n=10). EBM samples were also collected from randomly-selected mothers who delivered at term (n=10) and preterm (n=10) and who were five months to one year postpartum.

Breastmilk for the measurement of TAC was expressed into sterile plastic containers. The sample was then divided into five aliquots. The fresh samples were immediately tested, and the remaining aliquots were stored at 4[degrees]C and at -8[degrees]C for analysis at 48 hours and one week (Fig.).

Estimation of total antioxidant capacity

The phosphomolybdenum method was used for assessing the TAC of the milk samples (13). An aliquot of 0.1 mL of the sample solution containing a reducing species (ethanol) was combined in an Eppendorf tube. To this, 1 mL of reagent solution, containing 28 mM of sodium monophosphate, 0.6 mM of sulphuric acid, and 4 mM of ammonium heptamolybdate, was added. The Eppendorf tubes were capped and incubated in a thermal block (Rotek Co., Ernakulam, India) at 95[degrees]C for 90 minutes. The samples were then allowed to cool at room temperature. The absorbance of the aqueous solution for each sample was measured at 695 nm against a blank solution using a spectrophotometer (Spectrophotometer 106, Systronics Co., Ahmedabad). The typical blank solution contained 1 mL of reagent alone without the test solution and was incubated under the same conditions as the remaining samples.

Analysis of data

Data were analyzed using Student's f-test and repeated measures (analysis of variance-ANOVA), with Bonferroni multiple comparison test. The paired f-test compared the variations in the TAC between two storage periods within a group while the unpaired f-tests compared the TAC inter-group following a particular storage period. The repeated measures ANOVA was used for statistically assessing the variations in the TAC through all the phases of lactation. The differences at the 5% level of probability were considered significant. The SPSS soft ware (version 15.0) (SPSS Inc., Chicago, IL, USA) was used for all analyses.

[FIGURE OMITTED]

Ethical aspects

The institutional committee for ethics and research approved the study protocol. A written informed consent was taken from the participants of the study.

RESULTS

A significant difference (p<0.05) in the level of antioxidants was observed in colostrum, transitional milk, and mature milk assessed immediately following expression at room temperature (Table 2). However, Bonferroni pair-wise comparison test showed no significant difference (p>0.05) between transitional and mature breastmilk at room temperature. The TAC of colostrums in full-term and preterm pregnancies was compared. There was a significant difference (p<0.001) and higher TAC in full-term pregnancies. However, no significant difference was observed between the TAC of transitional and mature milk.

There was a significant decrease in the TAC of EBM after refrigeration and freezing for 48 hours and one week when compared with the TAC at zero hour (p<0.0005) (Table 3). This suggests that subjecting EBM to low temperatures for a prolonged time causes a significant loss of antioxidant levels.

No difference was found in the TAC between transitional and mature milk refrigerated at 48 hours and one week (p>0.05).

Mature milk from the cohort of women who were more than five months postpartum showed a similar pattern of variations in the TAC following storage at different temperatures compared to room temperature (p<0.0005) (Table 4). No statistical difference was observed between the TAC of breastmilk samples at room temperature, obtained from the full-term and preterm mothers. Table 4 illustrates the TAC levels of maternal milk following the fifth month postpartum subjected to various temperature treatments.

DISCUSSION

Low levels of antioxidants, or inhibition of the antioxidant enzymes, cause oxidative stress and may damage or kill viable cells (14).

Breastmilk appears to be beneficial in providing antioxidative protection. The complete list of active antioxidant components in breastmilk is still unknown. Compared to infants born full-term, preterm infants are more vulnerable to oxidative stress caused by infections, mechanical ventilation, intravenous nutrition, and deficiency in alphatocopherol which accumulates mainly during the third trimester of pregnancy (15). The antioxidant enzyme systems contained in maternal milk help the premature infant cope with reactive oxygen species (ROS)-mediated diseases (3,16,17). Lactoferrin, abundant in human milk, is a member of the iron-binding transferrin protein family that inhibits the formation of ROS by binding iron, thereby attenuating the conversion of hydrogen peroxide into hydroxyl radical via the Fenton type reaction (18).

The ROS and antioxidant systems act in concert rather than alone (19). Hence, investigations of any individual antioxidant activity may be misleading, and the measurement of any individual antioxidant may be less representative of the whole antioxidant status. Moreover, the number of different antioxidants makes it difficult, and also expensive, to measure each antioxidant separately, especially during daily clinical treatments. For these reasons, research is now being directed towards assays that evaluate the TAC of biological fluids (20). Hence, the present study aimed at estimating the TAC of breastmilk.

In the present study, a significant difference in the TAC was observed over the three phases of milk transition (Table 2). The variations observed in the mean TAC values may be attributed to the discrepancy in the dietary patterns of the participants, the immune capacity of their bodies, and ethnic or racial differences (21,22). Thus, these values cannot be deemed universal. The TAC in colostrum from term pregnancies was higher compared to preterm pregnancies, which could probably be attributed to the increased oxidative stress; this would, however, require further investigations.

Expression and storage of breastmilk are a way to maintain breastfeeding when the mother and the infant are separated, provided its nutritional value can be conserved. The effect of storage on various components of human milk has been studied. Most of these studies have focused, however, on the bacteriological, nutritional and immunological effects of storage (23-26). Refrigeration and freezing of breastmilk cause a significant decline in the levels of individual antioxidants, including vitamin C, A, and E. Nevertheless, the values of all nutrients were still within the international reference ranges for mature breastmilk (12). The paucity of research-based data documenting the TAC of maternal milk subjected to storage for longer durations at reduced temperatures prompted us to conduct this work.

The TAC of transitional and mature milk from both full-term and preterm mothers was subjected to refrigeration and freezing for 48 hours and one week in the present study. It was found to deplete the TAC of milk by 10-20% and 15-30% following a 48-hour and one-week storage period respectively (p<0.0005) when compared with the TAC at zero hour at room temperature (Table 3). The values obtained were similar to those found by Hanna et al., which compared the antioxidant capacity of breastmilk stored at lower temperatures using ABTS assay and showing the rapid decline over time, more gravely observed with the f1rozen samples over a seven-day period (27). Miranda et al. found an increase of malondialdehyde, a marker of oxidative stress, in refrigerated milk but not in frozen samples and a decrease of glutathione peroxidase activity in both refrigerated and frozen samples of human milk (28). Results of a study on the glutathione status of stored human breastmilk by Ankrah et al. showed a substantial loss of glutathione when breastmilk was kept at -20[degrees]C, 4[degrees]C, or at room temperature for two hours when compared with fresh breastmilk (29). Our study proved that subjecting EBM to reduced temperatures for prolonged duration significantly reduces the TAC. With the increasing number of working mothers, it is essential that they are educated by sharing with them pertinent information on the safe-handling procedures of breastmilk and its potential influence on its TAC.

Many components of milk change with storage, including immune cells, which get inactivated by freezing (24,30). A conspicuous formation of lipid peroxides in human milk stored at lower temperature is documented, probably caused by an increased presence of free fatty acids due to lipoprotein lipase activity during storage (3,31). This could be ascribed to the higher susceptibility of human milk to degradation in the current analysis, resulting in a loss of TAC over a longer storage time at reduced temperatures.

Further, long-term research can be directed towards analyzing the health effects upon feeding infants with stored milk at reduced temperatures. These scientific facts should evoke responsibility among paediatric health professionals in providing prenatal and postnatal counselling to mothers through effective strategies. With the growing concerns in today's society over maintaining a healthy lifestyle, one of the keys to protection against oxygen radical disease could be rethinking what the infant should be fed each day. Paediatric health specialists should include in their preventive strategies provision for giving antioxidants to infants through breastfeeding, emphasizing its role in health and disease.

ACKNOWLEDGEMENTS

The authors extend their deepest gratitude to Prof. (Dr.) Suchetha Shetty, Department of Biochemistry, K S Hegde Medical Academy, Mangalore, for her sincere contributions to this research. They gratefully acknowledge the valuable assistance received from Ms Ramitha for laboratory service and Ms Neevan D'Souza for her sincere help in analyzing the study data.

REFERENCES

(1.) Srivastava N, Sandhu A. Infant and child feeding index. Indian J Paediatr 2006;73:767-70.

(2.) Hambraeus L, Forsum E, Lonnerdal B. Nutritional aspects of breast milk versus cow's milk formulas. In: Hambraeus L, Hanson L, MacFarlane H, editors. Symposium on food and immunology. Stockholm: Almqvist and Wiksell, 1975:116-24.

(3.) Tsopmo A, Friel JK. Human milk has antioxidant properties to protect premature infants. Curr Paediatr Rev 2007;3:45-51.

(4.) Cochi SL, Fleming DW, Hightower AW, Limpakarnjanarat K, Facklam RR, Smith JD et al. Primary invasive Haemophilus influenzae type b disease: a population-based assessment of risk factors. J Paediatr 1986;108:887-96.

(5.) Takala AK, Eskola J, Palmgren J, Ronnberg PR, Kela E, Rekola P et al. Risk factors of invasive Haemophilus influenzae type b disease among children in Finland. J Paediatr 1989;115:694-701.

(6.) Dewey KG, Heinig MJ, Nommsen-Rivers LA. Differences in morbidity between breast-fed and formulated infants. J Paediatr 1995;126:696-702.

(7.) Blaymore Bier JA, Oliver T, Ferguson A, Vohr BR. Human milk reduces outpatient upper respiratory symptoms in premature infants during their first year of life. J Perinafol 2002;22:354-9.

(8.) Saarinen UM. Prolonged breast feeding as prophylaxis for recurrent otitis media. Acta Paediatr Scand 1982;71:567-71.

(9.) Schanler RJ, Shulman RJ, Lau C. Feeding strategies for premature infants: beneficial outcomes of feeding fortified human milk versus preterm formula. Pediatrics 1999;103:1150-7.

(10.) Saugstad OD. Oxygen toxicity in the neonatal period. Acta Paediatr Scand 1990;79:881-92.

(11.) Sardesai VM. Role of antioxidants in health maintenance. Nutr Clin Pract 1995;10:19-25.

(12.) Francis J, Rogers K, Brewer P, Dickton D, Pardini R. Comparative analysis of ascorbic acid in human milk and infant formula using varied milk delivery systems. Int Breastfeed J 2008;3:19.

(13.) Priedo P, Prinda M, Aguilar M. Spectrophotometric quantitation of antioxidant capacity through the formation of phosphomolybdenum complex: specific application to the determination of vitamin E. Anal Biochem 1999;269:337-41.

(14.) Blokhina O, Virolainen E, Fagerstedt KV. Antioxidants, oxidative damage and oxygen deprivation stress: a review. Ann Bot 2003;91:179-94.

(15.) Saugstadt OD. Oxygen radical disease in neonatology. Semin Neonatol 1998;3:239-44.

(16.) Goldman AS, Goldblum RM, Hanson KA. Anti-inflammatory systems in human milk. Adv Exp Med Biol 1990;262:69-76.

(17.) Friel JK, Martin SM, Langdon M, Herzberg GR, Buettner GR. Milk from mothers of both premature and full-term infants provides better antioxidant protection than does infant formula. Paediatr Res 2002; 51:612-8.

(18.) Raghuveer TS, McGuire EM, Martin SM, Wagner BA, Rebouche CJ, Buettner GR et al. Lactoferrin in the preterm infants' diet attenuates iron-induced oxidation products. Paediatr Res 2002;52:964-72.

(19.) Lindmark-Mansson H, Akesson B. Antioxidative factors in milk. Br J Nutr 2000;84:S103-10.

(20.) Battino M, Ferreiro MS, Gallardo I, Newman HN, Bullon P. The antioxidant capacity of saliva. J Clin Periodontol 2002;29:189-94.

(21.) Emmett PM, Rogers IS. Properties of human milk and their relationship with maternal nutrition. Early Hum Dev 1997;49(Suppl):S7-28.

(22.) House JS, Williams DR. Understanding and reducing socioeconomic and racial/ethnic disparities in health. In: Smedley BD, Syme SL, editors. Promoting health: interventions strategies from social and behavioral research. Washington, DC: National Academy Press, 2000:81-124.

(23.) Igumbor EO, Mukura RD, Makandiramba B, Chihota V. Storage of breast milk: effect of temperature and storage duration on microbial growth. Cent Atr J Med 2000;46:247-51.

(24.) Lawrence RA. Storage of human milk and the influence of procedures on immunological components of human milk. Acta Paediatr Suppl 1999;88:14-8.

(25.) Ogundele MO. Effects of storage on the physicochemical and antibacterial properties of human milk. Br J Biomed Sci 2002;59:205-11.

(26.) Williamson MT, Murti PK. Effects of storage, time, temperature, and composition of containers on biologic components of human milk. J Hum Lact 1996; 12:31-5.

(27.) Hanna N, Ahmed K, Anwar A, Petrova A, Hiatt T, Hegyi T. Effect of storage on breast milk antioxidant activity. Arch Dis Child Fetal Neonatal Ed 2004;89:F518 20.

(28.) Miranda M, Muriach M, Almansa I, Jareno E, Bosch-Morell F, Romero FJ et al. Oxidative status of human milk and its variations during cold storage. Biofactors 2004;20:129-37.

(29.) Ankrah NA, Appiah-Opong R, Dzokoto C. Human breast milk storage and the glutathione content. J Trop Paediatr 2000;46:111-3.

(30.) Lawrence RA. Milk banking: the influence of storage procedures and subsequent processing on immunological components of human milk. Adv Nutr Res 2001;10:389-404.

(31.) Berkow SE, Freed LM, Hamosh M, Bitman J, Wood DL, Happ B et al. Lipases and lipids in human milk: effect of freeze-thawing and storage. Paediatr Res 1984; 18:1257-62.

Arun Mamachan Xavier [1], Kavita Rai [2], and Amitha M. Hegde [2]

[1] Department of Pediatric Dentistry, Amrita School of Dentistry, AIMS Ponekkara PO, Cochin, India and [2] Department of Pedodontics and Preventive Children Dentistry, A.B. Shetty Memorial Institute of Dental Sciences, Mangalore, India

Correspondence and reprint requests should be addressed to:

Dr. Arun Mamachan Xavier

Clinical Assistant Professor

Department of Pediatric Dentistry

Amrita School of Dentistry

AIMS Ponekkara PO, Cochin

India

Email: arunmamachan@yahoo.co.in
Table 1. Clinical and demographic data of milk
donors (n=40)

Parameter                     No.

Age (years)
  Median                       27
  Range                      20-30
Gestation (weeks)
  Preterm (<37 weeks)
  Median                       36
  Range                      34-37
Term (>37 weeks)
  Median                     39.75
  Range                      38-41
Weight (kg)
  Median                      64.5
  Range                      55-72
Geographic location
  Rural                        37
  Semi-urban                   3
  Urban                        --

Table 2. Total antioxidant capacity of breastmilk assessed
immediately following expression at room temperature

                                Mean TAC (SD) ([micro]g dL)

Lactating             Colostrum       Transitional     Mature milk
mothers                                   milk

Mothers delivered    112.9 (8.38)    103.93 (7.13)    101.82 (6.73)
full-term

Mothers delivered    104.6 (6.02)     98.47 (6.49)     97.45 (6.71)
preterm

                                 Statistical significance

Lactating            Colostrum vs     Colostrum vs      T. milk vs
mothers                T. milk          T. milk          T. milk

Mothers delivered       8.97 *          11.08 **           2.11
full-term

Mothers delivered       6.13 *           7.15 *            1.02
preterm

The repeated measures ANOVA and Bonferroni multiple comparison
analyses were the statistical tests applied. * p<0.05; ** p<0.005;
ANOVA=Analysis of variance; M=Mature; SD=Standard deviation;
T=Transitional; TAC=Total antioxidant capacity

Table 3. Total antioxidant capacity of breastmilk of the 7th day
(transitional milk) and 30th day (mature milk) stored at various
temperatures and durations

                                 Mean TAC (SD) ([micro]g/dL)

Type of milk              Room        Refrigeration   Refrigeration
                       temperature      48 hours         1 week
                      37[degrees]C     4[degrees]C     4[degrees]C

Transitional milk

  Mothers delivered   103.93 (7.13)   98.27 (7.71)    89.17 (7.41)
  full-term

  95% CI                98.83-109      92.7-103.7       83.9-94.5

  Mothers delivered   100.77 (6.78)    93.94 (6.3)    86.31 (5.23)
  preterm

  95% CI               95.9-105.6       89.4-98.4        82.5-90

Mature milk

  Mothers delivered
  full-term           101.82 (6.73)   95.99 (6.51)    89.53 (7.07)

  95% CI                97-106.6       91.3-100.6       84.4-94.5

  Mothers delivered
  preterm             97.45 (7.53)    90.12 (5.65)    89.32 (4.68)

  95% CI               92.1-102.8       86.1-94.2       85.9-92.6

                        Mean TAC (SD) ([micro]g/dL)

Type of milk            Freezing       Freezing
                        48 hours        1 week
                      -8[degrees]C   -8[degrees]C

Transitional milk

  Mothers delivered   83.98 (6.12)   78.02 (5.23)
  full-term

  95% CI               79.6-88.3      74.2-81.7

  Mothers delivered   81.56 (5.67)   75.45 (4.34)
  preterm

  95% CI               77.5-85.6      72.3-78.5

Mature milk

  Mothers delivered
  full-term           80.89 (6.45)   76.87 (5.86)

  95% CI               76.2-85.5       72.6-81

  Mothers delivered
  preterm             84.45 (5.76)   74.27 (6.23)

  95% CI               80.3-88.5      69.8-78.7

The paired and unpaired f-test analyses were applied. The TAC at all
storage temperatures showed a difference from room temperature
(baseline), which was highly significant (p<0.005). CI=Confidence
interval; SD=Standard deviation; TAC=Total antioxidant capacity

Table 4. Total antioxidant capacity of breastmilk from mothers
following the 5th month post-conception stored at various
temperatures and durations (baseline to different storage
temperatures and durations)

                               Mean TAC (SD) ([micro]g/dL)

Mature milk               Room        Refrigeration    Refrigeration
(>5 months)           temperature        48 hours          1 week
                      37[degrees]C     4[degrees]C      4[degrees]C

Mothers delivered    109.34 (11.4)    101.9 (12.03)     94.78 (11.1)
full-term

95% CI                101.2-117.5       93.3-110.5        87-102.7

Mothers delivered    106.36 (4.23)    100.03 (5.12)     93.31 (7.16)
preterm

95% CI                103.3-109.4       96.4-103.6       88.2-98.4

                      Mean TAC (SD) ([micro]g/dL)

Mature milk             Freezing         Freezing
(>5 months)             48 hours          1 week
                      -8[degrees]C     -8[degrees]C

Mothers delivered     81.2 (4.76)      75.02 (5.2)
full-term

95% CI                 77.8-84.6        71.3-78.7

Mothers delivered     82.72 (4.9)      73.55 (6.39)
preterm

95% CI                 79.2-86.2        68.9-78.1

The paired and unpaired f-test analyses were applied. The TAC at all
storage temperatures showed a difference from room temperature
(baseline), which was highly significant (p<0.005). CI=Confidence
interval; SD=Standard deviation; TAC=Total antioxidant capacity
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