Abstract
Background
Preterm premature rupture of membranes (PPROM) is one of the most important complications of the pregnancy and cause perinatal morbidity and mortality. History of PPROM is a risk factor of recurrent PPROM. Vitamin C plays an important role in collagen metabolism and increases resistance maintenance of the chorioamniotic membranes.
Objectives
The aim of this study is to evaluate the role of vitamin C supplementation in prevention of PPROM in women with a positive history of PPROM.
Patients and Methods
This clinical trial study was performed on 170 pregnant women with the history of PPROM, with singleton pregnancy and gestational age 14 weeks in Imam-Reza Hospital, Mashhad University of Medical Sciences during 2008 to 2010. They were randomly divided into two groups. The case patients received 100 mg vitamin C daily from 14th weeks of gestation. PPROM occurrence was compared between two groups as an indicator of the protective effect of vitamin C supplements.
Results
PPROM occurred in 44.7% of controls and 31.8% of cases (P < 0.05). PROM occurred in 34.1% of controls and 18.8% of cases (P < 0.05). Pregnancy was terminated at term gestation in 21.2% of controls and 49.4% of cases (P < 0.05). Rupture of membranes was significantly decreased in the case group.
Conclusions
Vitamin C supplementations after 14th weeks of gestation can prevent from PPROM in women with the history of PPROM.
Keywords: Ascorbic Acid; Pregnancy; Fetal Membranes, Premature Rupture; Prevention and Control
1. Background
Premature rupture of membranes (1) defined as leakage of amniotic fluid through rupturedchorioamnioticmembranes that occur before starting the labor pain at any gestational age. It is one of the most common problems in obstetrics and affects 10-20% of all pregnancies. (2,3) If PROMoccurrbefore term pregnancy (37 gestational weeks), it is named as preterm premature rupture of membranes (PPROM). Although PPROM involves 3% of pregnancies, it is the cause of one third of all preterm births with increased rates of neonatal and maternal morbidity and mortality (4). Its pathophysiologic mechanism is little known. It has been reported that premature ruptured membranes have less collagen content, which is necessary to provide mechanical strength to fetal membranes and therefore tension resistance is decreased (5). However, PPROM should be considered important because of intrauterine infection risk (6). Smoking, previous PPROM, intrauterine infection, bacterialvaginosis,multifetalgestations, cervical shortening,hydramniosis, and inadequate availability of some nutrients during pregnancy such as copper, zinc, magnesium, β-carotenes, vitamin E, and vitamin C have been identified as risk factors for PPROM and low birth-weight (7-9). Vitamin C is involved in collagen synthesis, collagen secretion, andcollagenolysisprocesses (10). Occurrence of PPROM has been associated with changed patterns of collagen synthesis and decreased concentration of vitamin C at 28th weeks of gestation (11). It is reported that PROM could be used as a functional test of vitamin C status during pregnancy (12). Some studies have shown that there were lower levels of ascorbic acid (vitamin C) in serum, leucocytes, and amniotic fluid of cases with PPROM as compared to the control group (13). But they have provided little information about the relationship between vitamin C intake and its role in PPROM. The aim of this study is to evaluate the role of vitamin C in prevention of PPROM.
2. Objectives
The aim of this study is to evaluate the role of vitamin C supplementation in prevention of PPROM in women with a positive history of PPROM.
3. Patients and Methods
One hundred and seventy pregnant women with 14 weeks gestational age and the history of at least one PPROM with singleton pregnancy were enrolled in this clinical trial, after being completely explained about study conditions and signing informed consent. The study was approved by the Ethics Committee of Mashhad University of Medical sciences, and was performed in Imam-Reza University Hospital during a time period of 2008 to 2010. Inclusion criteria was the history of at least one PPROM in previous pregnancies, body mass index (BMI) of 18.5-30 kg/m2, singleton pregnancy, normal fetus and normal amniotic fluid insonography, mother age of 18-35yrs, normal cervix length (more than 25mm), no Tobacco usage, and no consumption of vitamin C supplements. Patients were randomly divided into two groups:
For 85 women in the case group, 400µg folic acid daily was prescribed in the first trimester, then iron tablet containing 30 mg elemental iron and chewing tablet of 100 mg vitamin C (Iran-Darufactory) daily were added from 14th weeks of gestation (2) and was continued up to 37th weeks.
In control group,85patientsweretreated similar except for chewing tablet of placebo insist of same shape of vitamin C tablets. A questionnaire was completed for each woman including age, weight, history of previous disease, history of previous pregnancies, and gestational age of PPROM at previous pregnancy. The patients were evaluated for bacterialvaginosisin the first visit, moreover anytime during the survey whenever the patient has been complaining ofvaginosissigns, and if discovered it was treated medially.Sonographywas performed for all of the cases during 12-14 weeks to evaluate the length of cervix and number of fetuses. All of thepatients were evaluated monthly during the second trimester. At the end of second trimester, they were evaluated withsonographyfor the volume of amniotic fluid and fetal anomalies. The fetal membrane rupture was obtained by sterile speculum and observing amniotic fluid existing from the cervix, fern test orNitrazintest. After delivery, the questionnaire was completed by data such as the date and cause of referring to the hospital, date and time of rupture of membranes, gestational age, neonate’s sex, birth-weight, and five minute Apgar score. Data was analyzed by SPSS software (version 11). For quantitative variables, T test, and variance analysis were used if the variables were parametric inKolmograv-Smironovtest. Otherwise, Mann-Whitney and Cross-Calvaistests were used. Chi-square test was used for qualitative variables. P ≤ 0.05 wasconsidered statistically significant.
4. Results
There was no significant difference between case and control groups in basic interventional factors (Table 1). Rupture of membranes was significantly decreased in the case group in the shape of PPROM, PROM and during term labor. Mean latency period was significantly (P = 0.002) higher in case group (19.02 ± 6.1 hours) vs. control group (13.42 ± 6.3 hours). Both groups were statistically different in the view of gestational age, birth-weight, and neonatal Apgar score (Table 2). In the case group, 61 patients (71.8%) had vaginal delivery and 24 patients (28.2%) underwent cesarean section. it was similar in the control group, (60 women (70.6%) underwent vaginal delivery and 25 women (29.4%) cesarean section). (P = 1.007). In the next step we compared neonatal outcomes between case and control groups in specific patient who were involved PPROM or PROM. The mean birth-weight of women with PROM was significantly higher in the case group (3068 gram) compared to the control (2968 gram) (P = 0.002). The mean neonatal Apgar score in patients with PROM was 9.0 in the case group and 8.3in the control group (P = 0.03). The mean gestational age at delivery was 38.1 weeks in case group and 37.7 weeks in control group (P = 0.02). Mean of latency period was 3.6 ± 2.9 hours in case group and 3.3 ± 3.6 hours in control group (P ≤ 0.001). The mean birth-weight of women with PPROM was 2370 grams in case and 2102 grams in control group (P ≤ 0.001). The mean neonatal Apgar score was 8 in patients with PPROM in case group and 7.3 in control group (P ≤ 0.001). The mean of latency period was 59.2 ± 38.1 hours in case group and 27.5 ± 14.6 hours in control group. (P ≤ 0.001) The mean gestational age at the time of delivery was 34.7 ± 1.2 weeks in case group and 33.3 ± 1.4 weeks in control group (P ≤ 0.001). All the mentioned differences were statistically significant.
Table 1. Comparison of Interventional Factors Between Case and Control Groups Interventional.
Interventional Factors, Mean | Case Group | Control Group | P value |
---|---|---|---|
Age, y | 29.8 | 29 | 0.132 |
Number of Pregnancy | 2.5 | 2.6 | 0.99 |
BMI, Kg/ m2 | 21.4 | 20.8 | 0.4 |
Gestational age at PPROM in previous pregnancy | 31.05 | 31.4 | 1.70 |
Number of Dead neonates | 0.3 | 0.6 | 1.88 |
Number of Abortion | 0.14 | 0.05 | 0.62 |
Table 2. Comparison of Pregnancy and Neonatal OutcomesBetween Case and Control Groups.
Outcome | Case Group | Control Group | P value |
---|---|---|---|
Pregnancy, No. (%) | |||
PPROM | 27 (31.8) | 38 (44.7) | 0.000 |
PROM | 16 (18.8) | 29 (34.1) | 0.000 |
Normal a | 42 (49.4) | 18 (21.2) | 0.000 |
Neonatal, Mean ± SD | |||
Mean gestational age at delivery (week) | 37.1 ± 1.9 | 35.9 ± 2.8 | 0.000 |
Mean birth weight, gram | 2840 ± 382 | 2630 ± 529 | 0.000 |
Neonatal Apgar score | 8.4 ± 0.7 | 7.83 ± 0.7 | 0.000 |
aRupture of membrane during term delivery
5. Discussion
PPROM has been known as the main cause of preterm delivery and associated with increased rates of neonatal and maternal morbidity and mortality (14-16).Although it has different causes, collagen metabolism is considered as the main factor in premature rupture of membranes. Vitamin C usage during pregnancy can modulate the collagen metabolism and cause the strength ofamniochorionmembranes. There are many factors that affect the availability of vitamin C during pregnancy.15Simhanet al. reported decreased level of vitamin C in women with premature rupture of membranes (17). The results of this study showed that vitamin C usage incase group significantly increased the gestational age at delivery, neonatal Apgar score, birth-weight, and latency period. This finding was confirmed by the study ofBarretet al. He concluded that the administration of 100mg of vitamin C in pregnant women after 20th weeks of gestation can significantly decrease the incidence of PROM and PPROM (18). Siegaet al. showed that the rates of membranes rupture before 37 weeks is increased with decrease of vitaminC supplements, although the relation was not statistically significant (1). In addition, Hajifoghahaet al. reported that the usage of vitamin C supplements after 20th weeks of gestation prevents of PPROM (19). Vermilion et al. performed a study that one group of pregnant women with the history of PPROM received vitamin C along with ferrous sulfate. Although the incidence of iron shortage anemia was decreased, no difference was observed in term of PPROM between case and control group (20). Also, Casaneuvaet al. reported no significant difference between two groups in the view of vitamin C intake and PPROM (21). These different results from the results of the present study may be due to the lower volume sample in their study. In Borna et al. study no statistically significant difference was reported between vitamin C supplements and placebo groups in terms of sepsis incidence, but resemble to our study, neonatal Apgar score and birth-weight was different between two groups (22). Vitamin C is an essential nutrient, involved in several biochemical functions. It is an antioxidant that blocks the damaging effects of oxidative stress in vitro (23). Therefore, vitamin C can prevent premature rupture of membranes through its role as an antioxidant or in collagen synthesis and maintenance (24,25). The present study had some limitations, we aimed to study the independent effect of vitamin C, but because the serum level of vitamin C was not assayed, isolation of the effect of a single nutrient is difficult. We propose a relationship between low vitamin C intake and an increased risk of preterm premature rupture of membranes. Vitamin C supplement is recommended to beadministered for pregnant women with the history of PPROM during pregnancy to prevent PPROM. Nevertheless, further studies with larger sample size and fewer limitations are needed to best clarify the role of vitamin C in prevention of PPROM especially in women with other risk factors of PPROM.
Acknowledgments
None declared.
Footnotes
Implication for health policy/practice/research/medical education: Premature rupture of membranes defined as amniotic fluid leakage before starting the labor pain. If PROM occurred before term pregnancy it is named as preterm premature rupture of membranes (PPROM). PPROM is associated with neonatal and maternal morbidity and mortality. It has been reported that premature ruptured membranes have less collagen content. Vitamin C is involved in collagen synthesis, secretion, and collagenolysis processes. Some studies have shown that there were lower levels of vitamin C in serum and amniotic fluid of cases with PPROM. The aim of this study is to evaluate the role of vitamin C in prevention of PPROM.
Please cite this paper as: Hafizi Lotfabadi L. The Role of Vitamin C in Prevention of Preterm Premature Rupture of Membranes. Iran Red Cres Med J.2013;15(2):113-6. DOI: 10.5812/ircmj.5138
Financial Disclosure: None declared.
Funding Support: None declared.
References
- 1.Siega-Riz Anna Maria, Promislow Joanne HE, Savitz David A, Thorp John M, McDonald Thad. Vitamin C intake and the risk of preterm delivery. American journal of obstetrics and gynecology. 2003;189(2):519–525. doi: 10.1067/s0002-9378(03)00363-6. [DOI] [PubMed] [Google Scholar]
- 2.Cunningham FG, Leveno KJ, Bloom SL, Hauth JC, Rouse DJ, Spong CY. Management of preterm labor. Williams obstetrics. 23th ed. New york: MC Graw Hill; 2010. pp. 232–47. [Google Scholar]
- 3.Mercer BM. Premature rupture of the membrane. In: Petraglia F, StrauSS GF, Gabbe SG, Wises G, editors. Complicated Pregnancy. 4th ed. London: Informa health care; 2007. pp. 713–27. [Google Scholar]
- 4.Parry S, Strauss JF, 3rd. Premature rupture of the fetal membranes. N Engl J Med. 1998;338(10):663–70. doi: 10.1056/NEJM199803053381006. [DOI] [PubMed] [Google Scholar]
- 5.Malak TM, Ockleford CD, Bell SC, Dalgleish R, Bright N, Macvicar J. Confocal immunofluorescence localization of collagen types I, III, IV, V and VI and their ultrastructural organization in term human fetal membranes. Placenta. 1993;14(4):385–406. doi: 10.1016/s0143-4004(05)80460-6. [DOI] [PubMed] [Google Scholar]
- 6.Pasquier JC, Picaud JC, Rabilloud M, Claris O, Ecochard R, Moret S, et al. Neonatal outcomes after elective delivery management of preterm premature rupture of the membranes before 34 weeks' gestation (DOMINOS study). Eur J Obstet Gynecol Reprod Biol. 2009;143(1):18–23. doi: 10.1016/j.ejogrb.2008.10.017. [DOI] [PubMed] [Google Scholar]
- 7.Institute of Medicine Food and Nutrition Board. Dietary reference intakes for vitamin C, vitamin E, selenium, and carotenoids. Washington DC: National Academy Press; 2000. [PubMed] [Google Scholar]
- 8.Khadem N, Mohammadzadeh A, Farhat AS, Valaee L, Khajedaluee M, Parizadeh SM. Relationship between Low Birth Weight Neonate and Maternal Serum Zinc Concentration. Iran Red Crescent Med J. 2012;14(4):240–4. [PMC free article] [PubMed] [Google Scholar]
- 9.Tejero E, Perichart O, Pfeffer F, Casanueva E, Vadillo-Ortega F. Collagen synthesis during pregnancy, vitamin C availability, and risk of premature rupture of fetal membranes. Int J Gynaecol Obstet. 2003;81(1):29–34. doi: 10.1016/s0020-7292(02)00400-9. [DOI] [PubMed] [Google Scholar]
- 10.Pfeffer F, Casanueva E, Kamar J, Guerra A, Perichart O, Vadillo-Ortega F. Modulation of 72-kilodalton type IV collagenase (Matrix metalloproteinase-2) by ascorbic acid in cultured human amnion-derived cells. Biol Reprod. 1998;59(2):326–9. doi: 10.1095/biolreprod59.2.326. [DOI] [PubMed] [Google Scholar]
- 11.Bryant-Greenwood GD. The extracellular matrix of the human fetal membranes: Structure and function. Placenta. 1998;19(1):1–11. doi: 10.1016/s0143-4004(98)90092-3. [DOI] [PubMed] [Google Scholar]
- 12.Casanueva E, Ripoll C, Tolentino M, Morales RM, Pfeffer F, Vilchis P, et al. Vitamin C supplementation to prevent premature rupture of the chorioamniotic membranes: a randomized trial. Am J Clin Nutr. 2005;81(4):859–63. doi: 10.1093/ajcn/81.4.859. [DOI] [PubMed] [Google Scholar]
- 13.Hadley CB, Main DM, Gabbe SG. Risk factors for preterm premature rupture of the fetal membranes. Am J Perinatol. 1990;7(4):374–9. doi: 10.1055/s-2007-999527. [DOI] [PubMed] [Google Scholar]
- 14.Mercer BM, Rabello YA, Thurnau GR, Miodovnik M, Goldenberg RL, Das AF, et al. The NICHD-MFMU antibiotic treatment of preterm PROM study: impact of initial amniotic fluid volume on pregnancy outcome. Am J Obstet Gynecol. 2006;194(2):438–45. doi: 10.1016/j.ajog.2005.07.097. [DOI] [PubMed] [Google Scholar]
- 15.Martin RJ, Fanaroff AA, Walsh ME. Fanaroff and Martins neonatal perinatal medicine. 8th ed. Philadelphia: Frank Polizzano; 2006. p. 1097. [Google Scholar]
- 16.Petralia GF, Strauss GF, Gabbe SG, Wises G. Complicated pregnancy. 4th ed. London: In forma heath care; 2007. pp. 852–85. [Google Scholar]
- 17.Simhan HN, Canavan TP. Preterm premature rupture of membranes: diagnosis, evaluation and management strategies. BJOG. 2005;112 Suppl 1:32–7. doi: 10.1111/j.1471-0528.2005.00582.x. [DOI] [PubMed] [Google Scholar]
- 18.Barrett BM, Sowell A, Gunter E, Wang M. Potential role of ascorbic acid and beta-carotene in the prevention of preterm rupture of fetal membranes. Int J Vitam Nutr Res. 1994;64(3):192–7. [PubMed] [Google Scholar]
- 19.Hajifoghaha M, Keshavarz T. Vitamin C supplementation and PROM. Iran J Obstet Gynecol Infertil. 2008;11(2):33–9. [Google Scholar]
- 20.Vermillion ST, Kooba AM, Soper DE. Amniotic fluid index values after preterm premature rupture of the membranes and subsequent perinatal infection. Am J Obstet Gynecol. 2000;183(2):271–6. doi: 10.1067/mob.2000.107653. [DOI] [PubMed] [Google Scholar]
- 21.Casanueva E, Magana L, Pfeffer F, Baez A. Incidence of premature rupture of membranes in pregnant women with low leukocyte levels of vitamin C. Eur J Clin Nutr. 1991;45(8):401–5. [PubMed] [Google Scholar]
- 22.Borna S, Borna H, Khazardoost S, Hantoushzadeh S. 'Perinatal outcome in preterm premature rupture of membranes with Amniotic fluid index < 5 (AFI < 5). BMC Pregnancy Childbirth. 2004;4(1):15. doi: 10.1186/1471-2393-4-15. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Gopalani S, Krohn M, Meyn L, Hitti J, Crombleholme WR. Contemporary management of preterm premature rupture of membranes: determinants of latency and neonatal outcome. Am J Perinatol. 2004;21(4):183–90. doi: 10.1055/s-2004-828609. [DOI] [PubMed] [Google Scholar]
- 24.Fortunato SJ, Menon R. Distinct molecular events suggest different pathways for preterm labor and premature rupture of membranes. Am J Obstet Gynecol. 2001;184(7):1399–405. doi: 10.1067/mob.2001.115122. [DOI] [PubMed] [Google Scholar]
- 25.Plessinger MA, Woods JR, Jr, Miller RK. Pretreatment of human amnion-chorion with vitamins C and E prevents hypochlorous acid-induced damage. Am J Obstet Gynecol. 2000;183(4):979–85. doi: 10.1067/mob.2000.106676. [DOI] [PubMed] [Google Scholar]