Miscarriage and Oxidative Stress of Iron Supplementation during Pregnancy
Keywords:
iron; oxidative stress; miscarriage; free radicals
Abstract
Background: Iron supplementations to the pregnant women in Iraq mostly considered as obligatory routine health care additive treatment without real assessing to the iron status in these people, therefore the acceptable range of iron must be estimated and the relationship between iron status and miscarriage should be explored. Objective: In miscarriage and pregnant women that supplemented with iron tablets the levels of oxidative stress should be assessed and compared to the iron status to show the type and the strength of correlation between them. Patients and methods: 96 pregnant women were participate in this study and categorized into. First group: Pregnant iron supplemented group (PIS group) includes 35 pregnant women (36.46%) during their 1st trimester or middle of 2nd trimester of pregnancy (18-36 year) and they were received an oral iron supplementation as 250 mg of ferrous gluconate tablet, three times a day. Second group: Pregnant iron non- supplemented group (PINS group) includes 31 pregnant women (32.29%) during their 1st trimester or middle of 2nd trimester of pregnancy (19-37 year) and they were non supplemented with iron and they considered as control group. Third group: Miscarriage iron supplemented group (MIS group) includes 30 miscarriage pregnant women(31.3%) during their 1st trimester or middle of 2nd trimester (19-40 year) taken an oral iron supplementation as 250 mg of ferrous gluconate tablet, three times a day. Results: The study at first assess the iron status by measuring Hb, serum ferritin and serum iron in the three groups of women and shows that there is a significant differences p< 0.005 between oxidative stress parameters of the miscarriage women and the pregnant women that taken oral supplements of iron tablets. The MDA and PC were higher in miscarriage in comparison to pregnant. The decrement in GSH level in miscarriage was also significant (P value< 0.025). The correlations between serum iron concentration and oxidative stress parameters MDA, PC and GSH were plotted using the regression line analysis where the r2 values were obtained respectively r2 = 0.63, r2 = 0.55 and r2 = 0.70. It is obvious that there is a high correlation between the level of iron in the circulation and the oxidative stress of the reactive oxygen species that generated by the catalytic effect of this transition metal. Conclusion: The high level of iron that obligatory supplemented to the pregnant women in Iraq should be restricted and early careful investigation should be performed to assess the status of iron before any iron supplements prescribed. The spontaneous abortion or miscarriage is highly correlated to the oxidative stress that induced by the flood of iron in the circulation.
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References
Andrews NC (1999) Disorders of iron metabolism. 341, 1986-95.
K. Lao, L. Chan (2000) Third trimester iron status and pregnancy outcome in non-anemic women. pregnancy unfavourably affected by maternal iron excess. 15(8), 1843-1848.
Katsuya Yutaka Kohgo (2008) Body iron metabolism and pathophysiology of iron overload. 88, 7-15.
Beard JL (2001) Iron biology in immune function, muscle metabolism and neural functioning. 131, 568S-580S.
(2015) What is pregnancy loss/miscarriage?. http://www.nichd.nih.gov/.2013-07-15
(2015) What are the symptoms of pregnancy loss/miscarriage?. http://www.nichd.nih.gov/
Buss JL, Torti FM, Toriti SV (2003) The role of iron chelating in the cancer therapy. 10, 1021_34.
Institute of Medicine, Food and Nutrition Board (2001) Iron in Dietary Reference Intakes for Vitamin A, Vitamin K, Arsenic, Boron, Chromium, Copper, Iodine, Iron, Manganese, Molybdenum, Nickel, Silicon. Vanadium and Zinc. 290-393. https://doi.org/10.17226/10026
Luis Valerio, G. Luis (2007) Mammalian Iron Metabolism. 17(9), 497-517. https://doi.org/10.1080/15376510701556690
P. Brissot, Y. Deugnier (1999) Oxford Textbook of Clinical Hepatology. 1999, 133-136.
L. Hallberg, L. Rossander-Hultén (1991) Iron requirements in menstruating women .Am J Clin Nutr. 54(6), 1047-1058. https://doi.org/10.1093/ajcn/54.6.1047
Bothwell TH (2000) Iron requirements in pregnancy and strategies to meet them. 72, 257S-264S.
Mashaal AL-Toub (2006) Study of serum ferritin and other hematological parameter in pregnancy. 108, 18-p21.
Casanueva E, Viteri FE (2003) Iron and oxidative stress in pregnancy. 133, 1700S₈S.
Lund EK, Fairweather-Tait SJ, Warf SG (2001) Chonic exposure to high levels of dietary iron fortification increases lipid peroxidation in the mucosa of the rat large intestine. 131, 2928_31.
A. Ashok, A. Anamar, Mellado, J. Beena, Premkumar (2012) The effects of oxidative stress on female reproduction: a review biomedical central. 10-49.
(1999) Assessment of iron status in US pregnant women from the National Health and Nutrition Examination Survey (NHANES).
Cogswell Mei Z, Pfeiffer Looker AC, Lacher Cusick SE (2011) 2011 Jun. 93(6), 1312-20.
C. Savona-Ventura, E. Grech (1991) Pregnancy complications in homozygous thalassaemia patients. 11, 175-6.
S. Tuck, C. Jensen, B. Wonke, A. Yardumian (1998) Pregnancy management and outcomes in women with thalassaemia major J Pediatr Endocrinol Metab. 11, 923-928.
Cunningham MJ, Macklin EA, Neufeld EJ, Cohen AR (2004) Thalassemia Clinical Research Network Complications of β- thalassemia major in North America Blood. 104(1), 34-39.
Toumba M, Sergis A, Kanaris C, Skordis N (2007) Endocrine complications in patients with thalassaemia major. 5(2), 642-8.
B. Halliwell, C. Gutteridge (1992) Free radicals, antioxidants and human disease: Where are we now?. 119, 598-260.
Wardman P, Candeias PL (1996) Fenton centennial symposium Radiat Res. 145, 523.
Imlay AJ, Linn S (1988) DNA damage and oxygen radical toxicity Science. 240, 1302-1309.
B. Halliwell, Jmc Gutteridge (1989) Halliwell B and Gutteridge JMC. Free Radicals in Biology and Medicine, 2nd ed. 333, 56.
Perry G, Nunomura A, Raina AK (2003) A metabolic basis for Alzheimer disease. 28, 1549_52.
Dalle-Donne I, Giustarini D, Colombo R (2003) Protein carbonylation in human diseases. 9, 169_76.
Dalle-Donne I, Rossi R, Giustarini D (2003) Protein carbonyl groups as biomarkers of oxidative stress. 329, 23_38.
Cighetti G, Bortone L, Sala S (2001) Mechanisms of Action of Malondialdehyde and 4-Hydroxynonenal on Xanthine Oxidoreductase. 389(2), 195-200. https://doi.org/10.1006/abbi.2001.2328
Kose K, Yazici C, Assioglu O (2001) The evaluation of lipid peroxidation and adensine Deaminase activity in patient with Behcehs disease. 34(2), 125-9.
Daniele Del Rio, Amanda Stewart, Nicoletta Pellegrini (2005) A review of recent studies on malondialdehyde as toxic molecule and biological marker of oxidative stress Nutr Metab Cardiovasc Dis. 15(4), 316-328. https://doi.org/10.1016/j.numecd.2005.05.003
C. White, H. Viernes, C. Krejsa, D. Botta, T. Kavanagh (2003) Fluorescence-based microtiter plate assay for glutamate-cysteine ligase activity. 318(2), 175-180. https://doi.org/10.1016/S00032697(03)00143-X
Yonghong Li, Pamela Maher, David Schubert (1997) A Role for 12-lipoxygenase in Nerve Cell Death Caused by Glutathione Depletion. 19(2), 453-463. https://doi.org/10.1016/s0896-6273(00)80953-8
U. WuÈllner, J. Seyfried, P. Groscurth, S. Beinroth, S. Winter, M. Gleichmann, M. Heneka, P. LoÈschmann, J. Schulz, M. Weller, T. Klockgether (1999) Glutathione depletion and neuronal cell death: the role of reactive oxygen intermediates and mitochondrial function. 826(1), 53-62. https://doi.org/10.1016/s0006-8993(99)01228-7
WHO/CDC 2005 (2005) World Health Organization Centers for Disease Control and Prevention Assessing the iron status of populations Report of a joint World Health Organization/Centers for Disease Control and Prevention technical consultation on the assessment of iron status at the population level. 2005, 1-30.
A. Makarem (1974) Clinical chemistry - principles and techniques. 1128-1135.
N. TIETZ (1995) Clinical Guide to laboratory test. 3 rd Ed. 374-375.
Jouanolle AM, David Legall jy (1997) Genetic emochromatosis. 55, 189-193.
B. Guidet, S. Shah (1989) 257(26), 440.
Levine RL, Garland D, Oliver CN Determination of carbonyl content in oxidatively modified proteins. 186, 464-78.
C. Burtis, E. Ashwood (1999) Text Book of Clinical Chemistry.
Gitto E., Reiter R.J., Karbownik M. (2002) Causes of oxidative stress in the perinatal period.
J. Clapp (1988) Maternal physiological adaptation during early human pregnancy. 224-236.
Pernoll M.L., Metcalfe J, Kovacl P.A. (1975) Ventilation during rest and exercise in pregnancy & Post partum. 295. 25.
John West (1991) Best in Taylor's Physiological Basis of Medical Practice. 894.
U. Adiga, Mns Adiga (2009) Adiga U and Adiga MNS. Total Antioxidant Activity in Normal Pregnancy. 8(2), 8.
Robert Hillman, Perry Henderson (1969) Control of marrow production by the level of iron supply. 48(3), 454-460. https://doi.org/10.1172/jci106002
Minic -Oka (2005) Evaluation of oxidative stress after intravenous iron supplementation renal failure. 27, 345-351.
P. Starkee-Reed (1989) E and Oliver, C N., Arch Biochem. 275, 559-567.
M. Fisher, E. Stadtman (1992) T and Stadtman, E R., J Biol Chem. 267, 1872-1880.
Thomas MC, Maclsaac RJ, Tsalamandris C (2004) Elevated Iron Indices in Patients with Diabetes Diabet Med. 21(7), 798-802. https://doi.org/10.1111/j.1464-5491.2004.01196.x
Carmen Sarah M king, Donangelo (2008) daily supplementation with iron increase lipid peroxidation in young women with iron store. 233, 701-707.
Michael Davies, Shanlin Fu, Hongjie Wang, Roger Dean (1999) Stable markers of oxidant damage to proteins and their application in the study of human disease. 27(11-12), 1151-1163. https://doi.org/10.1016/s0891-5849(99)00206-3
Rajdl D, Racek J, Steiherova A (2005) Markers of oxidative stress in diabetic mothers and their infants during delivery. 54(4), 429-36.
Farshad Amirkhizi, Fereydoun Siassi, Sara Minaie (2008) the relation of body iron stores and oxidative stress markers related toatherosclerosis in women of reproductive ARYA Atherosclerosis Journal. 4(4), 159-165.
Paik- Lim, Yau- Wei, nephrol Transplant (1999) Enhanced oxidative stress in haemodialysis patients receiving intravenous iron therapy. 14(11), 2680-2687. https://doi.org/10.1093/ndt/14.11.2680
M. Mustafa, Rahul Pathak, Tanzeel Ahmed, Rafat Ahmed, A. Tripathi, Kiran Guleria, B. Banerjee (2010) Association of glutathione S transferase M1 and T1 gene polymorphisms and oxidative stress markers in preterm labor Clin Biochem. 43(13-14), 1124-1128. https://doi.org/10.1016/j.clinbiochem.2010.06.018
Watson Jauniaux E, Bao Hempstock J, Burton Skepper JN (2000) Onset of maternal arterial blood flow and placental oxidative stress: a possible factor in human early pregnancy failure. 157, 2111-2122.
Graham Burton, Joanne Hempstock, Eric Jauniaux (2003) Oxygen, early embryonic metabolism and free radical-mediated embryopathies. 6(1), 84-96. https://doi.org/10.1016/s1472-6483(10)62060-3
Jawerbaum A, Gonzales E (2005) The Role of Alterations in Arachidonic Acid Metabolism and Nitric Oxide Homeostasis in Rat Models of Diabetes During Early Pregnancy. 11(10), 1327-1342. https://doi.org/10.2174/1381612053507503
E. Ruder, T. Hartman, J. Blumberg, M. Goldman (2008) Oxidative stress and antioxidants: exposure and impact on female fertility. 14, 345-357.
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