Pakistan Journal of Medical Sciences

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ORIGINAL ARTICLE

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Volume 25

October - December 2009 (Part-I)

Number  5


 

Abstract
PDF of this Article

Effects of Socio demographic factors on plasma ascorbic
acid and alpha tocopherol anti oxidants during pregnancy

Idogun E Sylvester1, Aikoriogie Paul2

ABSTRACT

Objectives: To assess the plasma levels of vitamins C and E at the various stages of pregnancy and to correlate their plasma levels with the socio-demographic factors of pregnant Nigerians.

Methodology: The pregnant cases (n=180) were randomly selected according to gestational ages. And the controls (n=20) were non-pregnant women of the same age. Plasma levels of both vitamins were assayed with well established laboratory methods.

Results: The mean plasma vitamins C and E in the pregnant cases was lower (by 17-23%) than controls across the three trimesters, p<0.0001. The correlation of vitamin C versus maternal age was significant; r = - 0.59, p<0.05; the mean plasma level of vitamin C declined by 57% as the maternal age increases from 22-37 years.

Conclusion: The mean plasma Ascorbic acid and Alpha-tocopherol are reduced during pregnancy and socio-demographic factors have mild effects on the plasma levels of these vitamins.

KEY WORDS: Antioxidants, Vitamins C and E, Pregnancy, Socio-demographic factors.

Pak J Med Sci    October - December 2009 (Part-I)    Vol. 25 No. 5    755-759

How to cite this article:

Sylvester IE, Paul A. Effects of Socio demographic factors on plasma ascorbic acid and alpha tocopherol anti oxidants during pregnancy. Pak J Med Sci 2009;25(5):755-759.


1. Dr. Idogun E. Sylvester, MB.CHB., MSC., MPH, Fmc Path,
2. Aikoriogie paul, BMLS, MSC,
1,2: Department of Chemical Pathology,
University of Benin Teaching Hospital,
Benin City, Nigeria.

Correspondence

Dr. Idogun E. Sylvester
Department of Chemical Pathology
University of teaching Hospital
P.M.B 1111, Benin City,
Nigeria.
E-mail: Sylvesteridogun@yahoo.co.uk 

* Received for Publication: March 16, 2009

* Revision Received: July 20, 2009

* Accepted: July 24,2009


INTRODUCTION

Pregnancy is the state of carrying a developing embryo or fetus within the female body. It is a physiological process that alters the physiology of the female body with changes ranging from increased hormonal secretions to elevated basal metabolic rate and increased muscular activity.1 During pregnancy, mostly because of the mitochondria-rich placenta, it favors oxidative stress. Oxidative stress occurs as a consequence of imbalance between the formation of oxygen free radicals and inactivation of these species by antioxidant defense system.2 Many diseases occur for the first time during pregnancy probably as a result of oxidative stress. Total anti oxidant capacity represents the balance between oxidative stress (oxidants) and the neutralizing systems such as Ascorbic acid (vitamin C), Alpha tocopherol (vitamin E), Catalase, ceruloplasmin, betacarotene, super oxide dismutase, glutathione peroxidase and transferin.3

Ascorbic acid is regarded as the major aqueous phase antioxidant.4 By reacting with activated oxygen more readily than other aqueous component, ascorbic acid protect critical macromolecules from oxidative damage thus it act as an effective stabilizer of free radical minimizing the damage caused by oxidative stress.

Alpha tocopherol (vitamin E) is a membrane bound antioxidant employed by cells.5 Research has shown it to be a membrane stabilizer and a multifaceted antioxidant that scavenges oxygen free radicals and lipid peroxy radicals and singlet oxygen.5 Ascorbic acid and alpha tocopherol may function together in a cycle type of reaction.5

It has been reported that antioxidants such as vitamin C may be reduced during pregnancy but in Nigeria there is dearth of literature about the stage of pregnancy that these antioxidants begin to decline. The objective of this study was to assess the plasma levels of vitamins C and E at the various stages of pregnancy as well as correlate the plasma levels with some socio-demographic factors of pregnant Nigerians.

METHODOLOGY

The cases were selected from the antenatal clinic attendees, according to the gestational period calculated from their last menstrual periods (LMP) and confirmed by uterine ultrasound investigation. Sixty cases each were recruited from first, second and third trimester (total=180).The controls were non-pregnant women of the same age range attending the gynecology clinic for routine medical check-ups. The inclusion criteria were age 18-40 years, confirmed pregnancy either in the first, second, or third trimester without any pregnancy complication. Excluded from the study were pregnant women with medical complications such as diabetes mellitus, hypertension, eclampsia, heart failure or ischemic heart diseases as well as those on vitamins C and E supplements.

Ethical Consideration: Ethical approval was obtained from the hospital research ethical committee. All the participants gave approval after due explanation by the researchers.

Sample Collection: Ten milliliters of venous blood was obtained from each of the participant into heparinized specimen bottles; they were separated after centrifugation at 3000rpm for ten minutes and the plasma stored frozen and the analysis of the vitamins done within 12 hours after blood collection to prevent vitamin C deterioration.

Laboratory assay: Ascorbic acid assay was analyzed using the 2,4 Dinitrophenyl hydrazine methodology6 and Alpa tocopherol assay was done using the Hexane extraction method.7 All samples were assayed in duplicate and the interassay and intraassay CVs were less than 5% for all procedures.

Statistics: Statistical analysis was performed using Instat graph pad soft ware version 3.0. Means and standard deviations were determined for quantitative data and frequency determined for categorical variables. Student-t test was used to test for significant association and analysis of variance was used to compare multiple means. P value < 0.05 was considered statistically significant.

RESULTS

A total of 180 pregnant cases (1st trimester n=60, 2nd trimester n=60 and 3rd trimester n=60) were studied, the controls were twenty (n=20).Among the cases; the civil servants were 56 (31.1%), traders 80 (44.4%), full time housewives were 28 (15.6%) and farmers 16 (8.9%), primiparous women (para 0) were 56(25.6%), para one, 71 (39.4%), para two, 49 (27.2%), para three, 13(7.2%) and para four , one(0.6%).

The mean plasma vitamins C and E at the three trimesters are shown in Table 1. The mean plasma vitamin C in controls 2.1±0.41µg/ml is significantly different from the pregnant cases (1.75±0.36, 1.76±0.38, 1.67±0.37µg/ml for 1st, 2nd and 3rd trimester respectively), p=0.001. Also the mean plasma vitamin C is significantly different across the three trimesters. The mean plasma vitamin E is significantly higher in the controls when compared with pregnant cases p<0.0001.

The mean plasma levels of the vitamins and parity, occupation and age are shown in Table-II. The mean plasma level of vitamin C is highest 1.660±0.461µg/ml, in the farmers and lowest 1.396 ±0.524µ/ml in the house wives, it is highest 1.973±0.252µg/ml, in the age group 22-25 years and lowest 1.418±0.375µg/ml, in the age group 34-37 years. Also mean plasma vitamin E levels are highest 1.317±0.780mg/ml in age group 22-25 years and lowest 1.307±0.780mg/ml in the age group 30-33 years. The correlation of parity and plasma levels of vitamins C and E showed positive correlations but not statistically significant, r=0.0134, P>05; r=0.05, P>0.05, for vitamins C and E respectively. The correlation of vitamin C versus the maternal age showed a negative significant relationship; r = -0.59, p<0.05, (the plasma level decreases with increase in maternal age) but that of vitamin E was not significant r = 0.08, P>0.05.

DISCUSSION

We found low (17-23% reduction) in plasma vitamin C level which was significant across the three trimesters. Uchenna etal similarly found significant reduction in serum vitamin C in pregnant Nigerians.8 Plasma vitamin C decline during pregnancy have been shown elsewhere to follow a linear trend with time 9. Our findings are similar as the decline was gradual and became more significant in the last trimester. It has been found that this decline of vitamin C during pregnancy is progressive even with vitamin C supplementation.9 This decrease most likely reflects the effects of hemodilution and of active transport of the vitamin to the fetus, which increases throughout pregnancy.10 We found significantly reduced level of vitamin E through the three trimester of pregnancy. This is contrary to the findings of Roes etal, who reported a linear increase of vitamin E during pregnancy.11 The differences in finding may have been due to differences in socioeconomic and nutritional factors of the studied populations.

At the beginning of this study, we hypothesized that occupation which determine to a large extent the social status of people, may impact significantly on the plasma levels of vitamins C and E during pregnancy, since humans and primates lack L-gulonolactone oxidase, rendering them incapable of synthesizing ascorbate and thus make them completely dependent on dietary sources of the vitamin.12 But curiously, we found plasma vitamin C to be higher in the farmers than even the civil servants probably because the farmers in our community have more access to green vegetables and different kind of fruits that are rich in vitamin C than the civil servants. On the other hand, occupation had no effect on plasma level of Vitamin E, probably because vitamin E unlike vitamin C can be stored to a reasonable extent in the liver and other storage depot of the body.

Another revelation from this study is the inverse relationship between plasma level of vitamin C and the maternal age, the vitamin level decreases with increase in maternal age. We are unable to explain this relationship but we hypothesized that it may have been due to environmental stress which is likely to be more on older women in our community than on the younger women. This hypothesis will require further investigation.

The low antioxidant vitamin C and E reported in this study may appear to support the use of these vitamins supplementation during pregnancy but there are conflicting reports on the benefits of these vitamins’ supplementation on the outcome of pregnancy. Whereas, many studies have shown that low antioxidants status in pregnancy may lead to pregnancy complications such as preeclampsia, threatened abortion, placenta calcification.13-15 Some interventional studies have shown that the use of vitamins C and E supplementations during pregnancy did not yield better pregnancy outcome,16-18 other studies contradict this, by reporting that the use of vitamin C and E supplementation during pregnancy are beneficial.19-21 Even in the face of conflicting reports on the benefits of antioxidant supplementations during pregnancy, it is generally agreed that although pregnancy is a physiological process, it promotes oxidative stress and antioxidants are used as defense mechanism against oxidative stress.22,23

CONCLUSIONS

Plasma levels of vitamins C and E decline during pregnancy. The plasma level of vitamin C decreases with increase in the maternal age. These findings are important when considering supplementation with these vitamins during pregnancy.

ACKNOWLEDGEMENT

We express our sincere gratitude to Prof Onyeneke for his useful advice during the work. We also want to thank all members of staff of Chemical Pathology of the University of Benin Teaching Hospital for their co-operation while carrying out this study.

REFERENCES

1. Warth M, Ark RA, Knoop RH. Lipid metabolism in pregnancy: altered lipid Composition in intermediate, very low, low and high density lipoprotein fraction. J Clin Endocrinol Metab 1975;14:649-65.

2. Frank. TM, Hoibrook NJ. Oxidants, oxidative stress and biology of ageing. AMJ Clin Nutr 2000;40:239-47.

3. Darley-Usmar V, Halliwel B. Blood radicals: Reactive nitrogen species, reactive oxygen species, transitional metal ions and vascular system. Pharm Res 1997;649-62.

4. Halliwell B. How to characterize a biological antioxidant radicals. Research Comm 1990;9:1-30.

5. Packerland Fuchs J. Vitamin E in Health and Disease; Marcel and Dekker Inc. New York 1992;289-94.

6. Donald B, Mc Cormick, Henry LG. Photometric method for the determination of Ascorbic acid In: Tietz Textbook of clinical chemistry 3rd Ed. Car LAB, Edward RE (Edi) Philadelphia, W.B Saunders company, 1999;1024-5.

7. Henry J, Donal C, James N. Clinical chemistry principles and Techniques. Harpers and Rows Publishers, New York 1974;1401.

8. Uchenna IN, Fedilis EE. Serum ascorbic acid level during pregnancy in Enugu, Nigeria. J Col Med 2005;10(1):43-5.

9. Choi JL, Rose RC. Transport and metabolism of ascorbic acid in human placenta. Am J Physiol 1989;257:110-3.

10. Food and Nutrition Board. Institute of medicine. Dietary reference intakes for vitamin C, E, Selenium and carotenoids. Washington DC; National Academy Press, 2000;95-185.

11. Roes EM, Hendriks JC, Ranjmarkers MT, Steegers- Theu-nissen RP, Groenen P, Peters WH, et al. A longitudinal study of antioxidant status during uncomplicated and hypertensive pregnancies. Acta Obstet Gynecol Scand 2006;85(2):148-55.

12. Kawai T, Nishikimi M, Ozawa T, Yagi K. A missense mutation of L-gulono- gamma-lactone oxidase causes the inability of scurvy-prone osteogenic disorder rats to synthesize L-ascorbic acid. J Biol Chem 1992;267:21973-76.

13. Kaja RJ, Greer LA. Manifestations of chronic disease during pregnancy. JAMA 2005;294(21):2751-7.

14. Klesgee LM, Murray DM, Brow JE, Cliver SP, Goldberg RL. Reactions of cigarette smoking and dietary antioxidants with placenta calcification. Amer J Epidemiology 1998;147:127-35.

15. Stark JM. Inadequate reducing system in pre-eclampsia: a complementary role for vitamin C and E with thioredoxin-related activities. British J Obs Gyn 2001;108:339-43.

16. Kontic-Vucinic O, Terzic M, Radunovic N. The role of antioxidant vitamins in hypertensive disorders of pregnancy. J Perinat Med 2008;36(4):282-90.

17. Spinnato JA 2nd, Freires S, Pinto E Silva JL, Rudge WV, Martins Costa S, Kech MA et al. Antioxidant therapy to prevent Preeclampsia: A randomized controlled trial. Obstet Gynecol 2007;110(6):1311-8.

18. Rumboid AR, Crowther CA, Hasiam RR, Dekker GA, Robinson JS. Acts study group. Vitamin C and E and the risks of Pre-eclampsia and perinatal complications. N Engl J Med 2006;354 (17):1796-806.

19. Holmes VA, McCance DR. Could antioxidant supplementation prevent pre - eclampsia? Proc Nutr Soc 2005;64(4):491-501.

20. Esther C, Camina R, Maricruz T, Rosa MM, Frania P, Paslo V, et al. Vitamin C supplementation to prevent premature rupture of the chorioamniotic membranes: a randomized trial. AMJ Clin Nutr 2005;81:859-63.

21. Ochoa-Brust GJ, Fernandez AR, Villanueva-Ruiz GJ, Velasco R, Trujillo - Hernandez B, Vasquez C. Daily intake of 100mg ascorbic acid as urinary tract infection prophylactic agent during pregnancy. Act Obstet Gynecol Scand 2007;86(7):783-7.

22. Idogun ES, Odiegwu ME, Momoh SM. Effect of pregnancy on total antioxidant Capacity in Nigerian women. Pak J Med Sci 2008;24(2):292-95.

23. Sharma JB, Sharma A, Bahadur A, Vimala N, Satyam A, Mittal S. Oxidative stress markers and antioxidant levels in normal pregnancy and pre-eclampsia. Int J Gynaecol Obstet 2006;94(1):23-7.


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