Abstract
Methods
A population-based case-control study was conducted including 48 women having preterm delivery (case group) and 100 women having term delivery (control group) between March 2007 and March 2012 in the maternity hospitals of the Selseleh County, Lorestan province, Iran. Information regarding maternal risk factors was collected by structured interview and reviewing the medical records. The maternal risk factors associated with preterm delivery were identified using univariate and multivariable logistic regression analysis after adjusting the sparse data bias. The area under the receiver operating characteristic (ROC) curves was estimated to evaluate the discrimination power of the statistical models.
Results
Multivariable analysis demonstrated that multiparty (odds ratio [OR], 14.23; 95% confidence interval [CI], 1.60–127.05), history of gestational diabetes (OR, 0.10; 95% CI, 0.01–0.99), thyroid dysfunction (OR, 97.32; 95% CI, 5.78–1,637.80), urinary tract infection (OR, 16.60; 95% CI, 3.20–85.92), and taking care during pregnancy (OR, 0.12; 95% CI, 0.03–0.50) had significant impact on preterm delivery after adjusting the potential confounders. The area under the ROC curve for the aforementioned maternal risk factors was 0.86 (95% CI, 0.80–0.92).
Preterm delivery takes place before the 37th week of pregnancy [1]. This type of delivery is one of the most important causes of mortality and morbidity in infants around the world [23]. Even, in the most developed countries, the preterm delivery rate has increased. For example, in the United States, it has risen from 9.5% in 1981 to 12.7% in 2005 [4]. In Europe and other developed countries, the estimated preterm delivery rate is about 5–9% [56]. Preterm delivery is also responsible for 17–34% of deaths in infants in the first year of life in the United States [7]. However, almost 90% of the preterm deliveries occur in the developing countries of which 85% take place in Asia and Africa [8]. In Iran, as a developing country, the preterm delivery rate was estimated between 5.6% and 13.4% based on the geographical regions under study [9]. Preterm birth causes 75% of perinatal deaths and over 50% of the preterm babies have long-term morbidities. Many preterm infants are at increased risk of death, different diseases, and disabilities, such as developmental disorders of the nervous and respiratory system, defect in sense, learning disability, digestive complications, and many other health problems [1011].
Given the worrying trend of preterm delivery throughout the world and its related outcomes, it seems that studying the causes and risks of these factors is very important [812]. Factors causing preterm birth have not been fully identified yet, however, various studies have considered different factors in the etiology of this outcome [13]. Some studies in this regard have mentioned the following factors as possible causes of preterm birth: genetic factors, rupture of membranes, hypertension, diabetes, multiparity, multiple births, techniques of infertility treatment, elective Caesarean section during previous pregnancies, smoking and alcohol consumption during pregnancy, mental disorders, and environmental exposures [8]. However, identifying the precise cause of preterm delivery still requires further studies, especially in developing countries where few studies have been conducted in this area [14].
Hence, given the importance of preterm delivery and its consequences as a major global health problem and the few studies conducted so far in Iran, the present study was designed to determine the maternal risk factors of preterm delivery in Iran. Identifying the risk factors can be an effective step in preventing and controlling the consequences and complications of preterm delivery.
This study was a population-based case-control study. Cases included all pregnant mothers referred to the maternity wards of the Selseleh County hospitals (Lorestan province, Iran) who had preterm delivery between March 21, 2007 and March 21, 2012. The preterm delivery was defined as delivery before 37 weeks of gestation. Preterm delivery cases were identified by daily monitoring of all the new deliveries in all the maternity wards of the County hospitals. On the other hands, the preterm delivery cases were considered as incident cases. Then, for each case, two controls were selected. The controls were a selected by random sampling from all the pregnant mothers referred to the same maternity wards of the County hospitals who had term delivery (≥37 weeks of gestation) during the same period (±2 weeks). In this study, mothers with premature infants due to congenital or chromosomal anomalies were excluded.
The data collection tool was a standard questionnaire. However, some information was obtained through interviews with the pregnant mothers and some were gathered from the medical records. The questionnaire included information, such as demographic characteristics of the mother (age, occupation, body mass index, education, etc.), past obstetric history (gestational age at delivery, history of caesarian delivery, unwanted pregnancy, gravidity, multiparity, childbirth, etc.), complications of pregnancy and delivery (such as history of gestational diabetes, hypertension, abortion, eclampsia, placenta previa, uterine prolapse, stillbirth and etc.). The data were collected by a trained research doctor.
For analysis, the relevant data were entered into Stata 14. Descriptive analyses, such as mean and standard deviation were used for the continuous variables; and number and relative frequency were used for the categorical variables. For determination of the most important risk factors of preterm delivery, univariate and multivariable logistic regression analyses were performed. Then, the crude and adjusted odds ratio (OR) with 95% confidence interval (CI) were calculated. A large number of risk factors were evaluated, and hence, inadequate data for the combination of the maternal risk factors and preterm delivery (2×2 contingency table) are expected. It is argued that when there are inadequate data for the combination of the risk factors and outcomes, the estimates, such as OR and its CI, could be biased [15]. As a result, the OR tends to be inflated and its CI tends to be inappropriately wide. Such bias is known as sparse data bias and it can exaggerate the results of the multivariable analysis [15]. Penalization via data augmentation and firth bias adjustment was performed to offset the impact of sparse data bias on the results. Firth bias adjustment is a common traditional technique for reducing sparse data bias in which ½ is added to each cell of a contingency table. In penalization by data augmentation method, a very weakly informative prior [log-F(2, 2)] was considered for the effect of the maternal risk factors (βi in logistic regression model or ORs) on the preterm delivery. It is argued that very weakly informative prior provides a plausible range for the relative estimates with 95% certainty and the OR of the effect of maternal risk factors on preterm delivery falls between 1/40 and 40 [16]. The area under the receiver operating characteristic (ROC) curve was used for assessing the discriminative ability of the multivariable logistic regression analysis. A P-value of <0.05 was considered as statistically significant.
The maternal characteristics of the cases and controls, as well as the results of the univariate logistic regression analysis, are shown in Table 1. A total of 48 cases with preterm delivery and 100 controls were enrolled in the study. The mean (standard deviation) age of the cases was 32.25 (6.81) years and that of the controls was 29.33 (6.56) years (P=0.02). A majority of the cases and controls had a school or lower level of education (65% vs. 70%, respectively). A majority of the cases and controls had a gravida of ≤3, history of ≤2 childbirths, and no history of abortion.
A significant difference was found between the cases and the controls regarding the multiparty, history of coronary heart disease (CHD), gestational diabetes, blood pressure, thyroid dysfunction, hemorrhage, urinary tract infection, taking care during pregnancy, and FBS level (all P≤0.05). The highest significant crude OR was found for multiparity (OR, 31.60; 95% CI, 3.99–250.09). The odds of preterm delivery was 5.40 times higher in those having a history of urinary tract infection than those without (95% CI, 2.24–12.97). Similarly, the odds of the outcome was 2.73 times lower in the women who received ≥6 care during pregnancy from rural or urban health centers than those who received <6 care during pregnancy (OR, 0.37; 95% CI, 0.15–0.88).
The results of the multivariable logistic regression analysis are presented in Table 2. After selecting the variables with a P-value of ≤0.20 in the univariate analysis for the multivariable analysis, only multiparity, history of gestational diabetes, thyroid dysfunction, urinary tract infection, and taking care during pregnancy were statistically significant (P≤0.05). The highest adjusted OR was determined for a history of thyroid dysfunction (OR, 97.32; 95% CI, 5.78–1,637.80).
The ROC curves for model 1 with all 13 maternal characteristics included in the multivariable logistic regression analysis and for model 2 with only the significant maternal characteristics included in the multivariable logistic regression analysis are shown in Fig. 1. In analyses that compared the ability of the models to discriminate preterm labor, the ROC for model 1 was significantly greater than that of model 2 (0.93 vs. 0.86, P=0.002).
The present study aimed to determine the maternal risk factors for preterm delivery in Iran, which was achieved by a population-based case-control study. The results of the multivariable logistic regression analysis showed that variables, such as multiparity, history of gestational diabetes, thyroid dysfunction, urinary tract infection, and taking care during pregnancy had significant statistical associations with preterm delivery (P<0.05). Besides, the area under the ROC curve for the significant maternal variables in the multivariable logistic regression analysis was 0.86 (95% CI, 0.80–0.92)
In the present study, mothers who received prenatal care for ≥6 times during pregnancy had a lower risk of preterm delivery as compared to those who received care for <6 times (OR, 0.12; 95% CI, 0.03–0.50). This finding has been supported by various other studies in this regard [1314171819]. For example, the study by Jiang et al. [13] showed that lack of prenatal care is related to an increased risk of preterm birth, so that the mothers without prenatal care during pregnancy had 5.19 times increased risk of preterm birth (OR, 5.19; 95% CI, 3.77, −7.14); and mothers with irregular prenatal care had 2.87 times of increased risk of preterm birth (OR, 2.87; 95% CI, 2.16–3.80). Another study performed in Iran showed that mothers of premature infants received less perinatal care; while with more care, the risk of premature delivery was reduced [18]. Perhaps more attention to risk symptoms is paid during prenatal care along with appropriate health and treatment advice by the health care personnel. Hence, improving prenatal care and increasing the number of care can be effective in reducing the risk of premature birth. However, this interpretation about the number of prenatal care in the present study should be done with caution, because the low number of perinatal care in the mothers with premature infants might be due to premature birth and consequently shorter gestational age.
In agreement with other previous studies, the results of this study showed that there was a significant statistical association between multiparity and preterm delivery after adjusting the confounding variables (OR, 14.23; 95% CI, 1.60–127.05) [1320212223]. The study by Shoja et al. [23] indicated that the odds of preterm delivery in mothers with multiparity pregnancy was more than those without multiparity pregnancy (OR, 3.09; 95% CI, 1.01–9.6). This problem may be because multiparity limits the uterine space for the fetus and also causes secretion of hormones inducing delivery, and therefore, preterm labor was more in this group.
In this study, we found a significant negative association between preterm delivery and maternal medical disorders, such as gestational diabetes (OR, 0.10; 95% CI, 0.01–1.01) after adjustment of the confounding variables. This finding was inconsistent with studies conducted in this field [3141824252627]. The study by Namakin et al. [18] in Iran showed that mothers with a history of gestational diabetes and hypertension had a higher risk of preterm delivery (OR, 2.99; 95% CI, 1.6–5.5). Zhang et al. [14] in China reported that women with a history of gestational diabetes have 3.44-fold increased risk of preterm birth (OR, 3.44; 95% CI, 1.69–6.99). On the other hand, several studies have shown that there no association between preterm delivery and gestational diabetes [132829]. For example, a case-control study in China showed no relationship between gestational diabetes and preterm delivery [13]. Perhaps one of the reasons for the negative relationship in this study was the low sample size involved. However, it can be said that gestational diabetes can affect the growth and development of the fetus during pregnancy. Particularly, during the second and third trimesters of pregnancy, maternal diabetes can lead to a high level of nutrition and fetal growth. Subsequently, a large fetus with increased bodyweight may also increase the risk of preterm delivery. Therefore, regular monitoring of blood glucose during pregnancy should be given special attention.
In the present study, there was a significant statistical association between thyroid dysfunction (OR, 97.32; 95% CI, 5.78–1,637.80) and preterm delivery in the multivariable logistic regression analysis, and this is in agreement with other previous studies [33031323334]. A review by Nazarpour et al. [32] showed that thyroid dysfunction has adverse effects on pregnancy outcomes especially on the preterm delivery. Another review by Stagnaro-Green [30] also suggested that hypothyroidism and autoimmune thyroid disease are associated with preterm delivery in women. Given the high prevalence of thyroid disorders in women on one hand and the hormonal changes and multiple metabolic needs occurring during pregnancy affecting the mother's thyroid function on the other, it is recommended that all pregnant women check their thyroid gland function before trying for pregnancy to prevent adverse consequences of thyroid disorders.
Finally, in agreement with other previous studies [2335363738], the results of our study indicated that there is a significant statistical association between the history of urinary tract infection and preterm delivery after adjusting the confounding variables (OR, 16.60; 95% CI, 3.20–85.92). A study by Shoja et al. [23] demonstrated that there was a significant statistical relationship between pregnancy infection and preterm delivery (OR, 2.78; 95% CI, 1.07–7.20). Another study in this field showed that mothers with a history of urinary tract infection had a 1.59-fold increased risk of preterm delivery (OR, 1.59; 95% CI, 1.14–2.21) [38]. Different studies indicate that microorganisms in the membranes are associated with increased prostaglandin production, which is one of the important factors associated with the prevalence of preterm labor. Prostaglandin is produced by the invasion of microorganisms, coagulase protease, and elastase and the endotoxin directly induces preterm delivery. One of the most common microorganisms is β-hemolytic streptococcus, which may be present in the natural vaginal flora in 50% of women and causes 20% of preterm labor [3839]. Therefore, treatment of infections in pregnancy is one of the factors that reduce the prevalence of preterm labor and its recurrence.
One of the limitations of this study that can be noted is the retrospective nature and low sample size. Therefore, it is recommended that cohort studies be carried out in larger geographic units and with a larger sample size to determine the precise causes of preterm delivery. Additionally, some information was extracted from the mother's medical records which may not be accurately recorded and associated with information bias. Also, the last limitation of this study, which should be mentioned, is selection bias. For some of the variables, such as multiparity, unwanted pregnancy, stillbirth, CHD, etc., there were no women in the control group, therefore, these risk factors might be have been affected by selection bias rather than by the actual risks.
In summary, the results of this study suggest that multiparity, history of gestational diabetes, thyroid dysfunction, urinary tract infection, and taking care during pregnancy have a significant statistical association with preterm delivery. The area under the ROC curve for these variables was 0.86. Therefore, performing perinatal care and identifying pregnant mothers with the above risk factors can reduce the preterm delivery rate, and subsequently reduce the consequences of preterm delivery in the infants and the mothers.
Acknowledgements
The study was supported by the Deputy of Research of the Iran University of Medical Sciences, Tehran, Iran.
Notes
References
1. Obstetrics Subgroup, Chinese Society of Obstetrics and Gynecology, Chinese Medical Association. Diagnosis and therapy guideline of preterm birth (2014). Zhonghua Fu Chan Ke Za Zhi. 2014; 49:481. PMID: 25327726.
2. Simmons LE, Rubens CE, Darmstadt GL, Gravett MG. Preventing preterm birth and neonatal mortality: exploring the epidemiology, causes, and interventions. Semin Perinatol. 2010; 34:408–415. PMID: 21094415.
3. Goldenberg RL, Culhane JF, Iams JD, Romero R. Epidemiology and causes of preterm birth. Lancet. 2008; 371:75–84. PMID: 18177778.
4. Hamilton BE, Martin JA, Ventura SJ. Births: preliminary data for 2006. Natl Vital Stat Rep. 2007; 56:1–18.
6. Hamilton BE, Ventura SJ. Births: preliminary data for 2005. Health E-Stats [Internet]. Hyattsville (MD): Centers for Disease Control and Prevention;2006. cited 2007 Jul 15. Available from: http://www.cdc.gov/nchs/products/pubs/pubd/hestats/prelimbirths05/prelimbirths05.htm.
7. Hamilton BE, Kirmeyer SE. Trends and Variations in reproduction and intrinsic rates: United States, 1990-2014. Natl Vital Stat Rep. 2017; 66:1–14.
8. Beck S, Wojdyla D, Say L, Betran AP, Merialdi M, Requejo JH, et al. The worldwide incidence of preterm birth: a systematic review of maternal mortality and morbidity. Bull World Health Organ. 2010; 88:31–38. PMID: 20428351.
9. Kamali Fard M, Alizadeh R, Sehati Shafaei F. The effect of lifestyle on the rate of preterm birth. J Ardabil Univ Med Sci. 2010; 10:55–63.
10. Honest H, Bachmann LM, Sundaram R, Gupta JK, Kleijnen J, Khan KS. The accuracy of risk scores in predicting preterm birth--a systematic review. J Obstet Gynaecol. 2004; 24:343–359. PMID: 15203570.
11. Selling KE, Carstensen J, Finnström O, Sydsjö G. Intergenerational effects of preterm birth and reduced intrauterine growth: a population-based study of Swedish mother-offspring pairs. BJOG. 2006; 113:430–440. PMID: 16553655.
12. Langhoff-Roos J, Kesmodel U, Jacobsson B, Rasmussen S, Vogel I. Spontaneous preterm delivery in primiparous women at low risk in Denmark: population based study. BMJ. 2006; 332:937–939. PMID: 16497733.
13. Jiang M, Mishu MM, Lu D, Yin X. A case control study of risk factors and neonatal outcomes of preterm birth. Taiwan J Obstet Gynecol. 2018; 57:814–818. PMID: 30545533.
14. Zhang YP, Liu XH, Gao SH, Wang JM, Gu YS, Zhang JY, et al. Risk factors for preterm birth in five maternal and child health hospitals in Beijing. PLoS One. 2012; 7:e52780. PMID: 23300774.
15. Greenland S, Mansournia MA, Altman DG. Sparse data bias: a problem hiding in plain sight. BMJ. 2016; 352:i1981. PMID: 27121591.
16. Greenland S, Mansournia MA. Penalization, bias reduction, and default priors in logistic and related categorical and survival regressions. Stat Med. 2015; 34:3133–3143. PMID: 26011599.
17. Mohammadian S, Vakili M, Tabandeh A. Survey of related factors in prematurity birth. J Guilan Univ Med Sci. 2000; 9:117–122.
18. Namakin K, Sharifzadeh G, Malekizadeh AJ. To identify the risk factors in prematurity birth in Birjand, Iran: a case-control study. Iran J Edpidemiol. 2011; 7:1–5.
19. Heman ML, Albini M. Risk factors for spontaneous preterm birth among aboriginal and nonaboriginal women in Manitoba. J Obstet Gynecol. 2000; 90:43–49.
20. Lotfalizadeh M, Mohammadzadeh A, Kamandi S, Bagheri S. Incidence and risk factors of preterm birth in Imam Reza hospital-2000-2001. J North Khorasan Univ Med Sci. 2005; 8:93–100.
21. Zafarghandi N, Zafarghandi AS, Torkestani F, Fallah N, Jadidi F. Prevalence of risk factors for preterm birth. J Shahed Univ. 2004; 12:25–29.
22. Rajaeefard A, Mohammadbeigi A, Mohammadi M, Jolaee H, Alipour H. Evaluation of risk factors in preterm delivery and impact of education in its prevention. Daneshvar Med. 2010; 17:11–18.
23. Shoja M, Shoja E, Gharaei M. Prevalence and affecting factors on preterm birth in pregnant women Referred to Bentolhoda hospital-Bojnurd. J North Khorasan Univ Med Sci. 2016; 7:855–863.
24. Jakobsson M, Gissler M, Sainio S, Paavonen J, Tapper AM. Preterm delivery after surgical treatment for cervical intraepithelial neoplasia. Obstet Gynecol. 2007; 109:309–313. PMID: 17267829.
25. Hedderson MM, Ferrara A, Sacks DA. Gestational diabetes mellitus and lesser degrees of pregnancy hyperglycemia: association with increased risk of spontaneous preterm birth. Obstet Gynecol. 2003; 102:850–856. PMID: 14551018.
26. Derakhshi B, Esmailnasab N, Ghaderi E, Hemmatpour S. Risk factor of preterm labor in the west of Iran: a case-control study. Iran J Public Health. 2014; 43:499–506. PMID: 26005661.
27. Nabavizadeh SH, Malekzadeh M, Mousavizadeh A, Shirazi HR, Ghaffari P, Karshenas N, et al. Retrospective study of factors related to preterm labor in Yasuj, Iran. Int J Gen Med. 2012; 5:1013–1017. PMID: 23271920.
28. Magee MS, Walden CE, Benedetti TJ, Knopp RH. Influence of diagnostic criteria on the incidence of gestational diabetes and perinatal morbidity. JAMA. 1993; 269:609–615. PMID: 8421365.
29. Tallarigo L, Giampietro O, Penno G, Miccoli R, Gregori G, Navalesi R. Relation of glucose tolerance to complications of pregnancy in nondiabetic women. N Engl J Med. 1986; 315:989–992. PMID: 3762619.
30. Stagnaro-Green A. Maternal thyroid disease and preterm delivery. J Clin Endocrinol Metab. 2009; 94:21–25. PMID: 18984665.
31. Casey BM, Dashe JS, Wells CE, McIntire DD, Byrd W, Leveno KJ, et al. Subclinical hypothyroidism and pregnancy outcomes. Obstet Gynecol. 2005; 105:239–245. PMID: 15684146.
32. Nazarpour S, Ramezani Tehrani F, Simbar M, Azizi F. Thyroid dysfunction and pregnancy outcomes. Iran J Reprod Med. 2015; 13:387–396. PMID: 26494985.
33. Idris I, Srinivasan R, Simm A, Page RC. Maternal hypothyroidism in early and late gestation: effects on neonatal and obstetric outcome. Clin Endocrinol (Oxf). 2005; 63:560–565. PMID: 16268809.
34. Blazer S, Moreh-Waterman Y, Miller-Lotan R, Tamir A, Hochberg Z. Maternal hypothyroidism may affect fetal growth and neonatal thyroid function. Obstet Gynecol. 2003; 102:232–241. PMID: 12907094.
35. Romero R, Espinoza J, Kusanovic JP, Gotsch F, Hassan S, Erez O, et al. The preterm parturition syndrome. BJOG. 2006; 113(Suppl 3):17–42.
36. Goldenberg RL, Hauth JC, Andrews WW. Intrauterine infection and preterm delivery. N Engl J Med. 2000; 342:1500–1507. PMID: 10816189.
37. Srinivas SK, Ma Y, Sammel MD, Chou D, McGrath C, Parry S, et al. Placental inflammation and viral infection are implicated in second trimester pregnancy loss. Am J Obstet Gynecol. 2006; 195:797–802. PMID: 16949414.
38. Yadani S, Bouzari Z, Akhondi S. The comparison of the risk factors in the term and preterm delivery. J Babol Univ Med Sci. 2015; 17:7–12.
39. Valadan M, Kaveh M, Bagherzadeh S, Hasanzade M. Risk factors for recurrent preterm delivery in three university hospitals. Tehran Univ Med J. 2008; 65:24–29.