- Research article
- Open Access
- Open Peer Review
Preeclampsia complicated by advanced maternal age: a registry-based study on primiparous women in Finland 1997–2008
© Lamminpää et al.; licensee BioMed Central Ltd. 2012
- Received: 20 October 2011
- Accepted: 22 May 2012
- Published: 11 June 2012
Preeclampsia is a frequent syndrome and its cause has been linked to multiple factors, making prevention of the syndrome a continuous challenge. One of the suggested risk factors for preeclampsia is advanced maternal age. In the Western countries, maternal age at first delivery has been steadily increasing, yet few studies have examined women of advanced maternal age with preeclampsia. The purpose of this registry-based study was to compare the obstetric outcomes in primiparous and preeclamptic women younger and older than 35 years.
The registry-based study used data from three Finnish health registries: Finnish Medical Birth Register, Finnish Hospital Discharge Register and Register of Congenital Malformations. The sample contained women under 35 years of age (N = 15,437) compared with those 35 and over (N = 2,387) who were diagnosed with preeclampsia and had their first singleton birth in Finland between 1997 and 2008. In multivariate modeling, the main outcome measures were Preterm delivery (before 34 and 37 weeks), low Apgar score (5 min.), small-for-gestational-age, fetal death, asphyxia, Cesarean delivery, induction, blood transfusion and admission to a Neonatal Intensive Care Unit.
Women of advanced maternal age (AMA) exhibited more preeclampsia (9.4%) than younger women (6.4%). They had more prior terminations (<0.001), were more likely to have a body mass index (BMI) >25 (<0.001), had more in vitro fertilization (IVF) (<0.001) and other fertility treatments (<0.001) and a higher incidence of maternal diabetes (<0.001) and chronic hypertension (<0.001). Multivariate logistic regression indicated that women of AMA had higher rates of: preterm delivery before 37 weeks 19.2% (OR 1.39 CI 1.24 to 1.56) and before 34 weeks 8.7% (OR 1.68 CI 1.43 to 2.00) low Apgar scores at 5 min. 7.1% (OR 1.37 CI 1.00 to 1.88), Small-for-Gestational Age (SGA) 26.5% (OR 1.42 CI 1.28 to 1.57), Asphyxia 12.1% (OR 1.54 CI 1.34 to 1.77), Caesarean delivery 50% (OR 2.02 CI 1.84 to 2.20) and admission to a Neonatal Intensive Care Unit (NICU) 31.6% (OR 1.45 CI 1.32 to 1.60).
Preeclampsia is more common in women with advanced maternal age. Advanced maternal age is an independent risk factor for adverse outcomes in first-time mothers with preeclampsia.
- Neonatal Intensive Care Unit
- Preterm Delivery
- Fertility Treatment
- Placenta Previa
Maternal age at the time of first delivery has increased in many Western countries . A woman who is 35 years or older at the time of delivery has been defined as being of “advanced maternal age (AMA)” . In Finland, the mean age of women giving birth has, for a long time, been around 30 years, and the average age in 2009 was 28 years among primigravidas. However, the proportion of parturients aged over 35 in 2009 was 18.7%, and this percentage has been consistently increasing .
Several studies have shown an association between AMA and adverse perinatal outcomes as well as an increased risk of certain pregnancy complications. Specifically, women of AMA have an increased risk of gestational diabetes, placenta previa [4–6], preeclampsia [5, 7], miscarriage , pregnancy-induced hypertension  and the need for Caesarean deliveries . Induction of labor [5, 9, 10], augmentation with oxytocin and assisted deliveries are also known to be associated with women of AMA . Furthermore, increasing maternal age contributes to fetal, perinatal and neonatal death . Women of AMA are also more likely to have been diagnosed with chronic diseases, such as hypertensive disorders and diabetes mellitus, thus further complicating their pregnancies [4, 5, 7, 9, 10].
Preeclampsia is a frequent and potentially severe disease that affects about 3-8% of all pregnancies and increases the mothers risk for morbidity [11–13]. Risks associated with preeclampsia include nulliparity, pre-existing medical conditions (e.g. hypertension, diabetes mellitus and anti-phospholipid syndrome), plurality, older maternal age and obesity [11, 12]. The aim of this study was to compare pregnancy outcomes in women with preeclampsia aged 35 and over to those with preeclampsia under 35 years of age to examine differences in obstetric outcomes.
Data and variables
The original dataset contained information on 690,555 women and their newborns, for births between the years 1997 and 2008. Eligibility criteria for this analysis included primiparous women with singleton pregnancies diagnosed with preeclampsia without malformations (N = 17,824).
Approval for the study was obtained from the National Institute for Health and Welfare (THL). The data used in this study consisted of information from the Finnish Medical Birth Register (MBR), Hospital Discharge Register (HDR) and The Register of Congenital Malformations. The THL stores information from each of these registers and was responsible for providing all of the data.
The Finnish Medical Birth Register is a population-based registry established in 1987 and is currently compiled by the THL. The MBR includes information on maternal and neonatal birth characteristics and perinatal outcomes for all women giving birth in Finland and all newborns up to seven days of age. The form is filled in by the hospital and sent, typically in electronic format, to the THL .
The Hospital Discharge Register was established in 1967 and contains information on all aspects of inpatient care in public and private hospitals and outpatient visits to public hospitals (since 1996) in Finland. The data are sent electronically to the THL by each setting .
The Register of Congenital Malformations is controlled by THL and contains data on congenital chromosomal and structural anomalies detected in stillborn and live born infants and terminated fetuses from all healthcare settings in Finland. The Register was established in 1962 and registration of anomaly data began in 1963 .
Preeclampsia was defined as repeated periods of blood pressure > 140/90 mmHg accompanied by proteinuria (>0.3 g/day). Participants were identified in two ways. First, we included eligible women based on diagnoses recorded using ICD-10 codes (preeclampsia: ICD-10 codes O11, O14 and with seizures O15). All identified cases of preeclamptic and eclamptic pregnancies were used in the analysis. Second, we identified participants who were hospitalized during pregnancy because of hypertension. This was necessary because, in the MBR, ICD-10 coding of diagnoses during pregnancy did not start until 2004. Some of the women with preeclampsia were hospitalized during pregnancy, but they were not allocated ICD-codes and were recorded as being hospitalized because of hypertension; however, this diagnosis generally identifies those with preeclampsia.
The following definitions were used to record pregnancy outcomes: preterm delivery, before 34 and 37 weeks of gestation; Apgar score <7 at 5 minutes; and small for gestational age (SGA), infants whose sex- and age-adjusted birth weight was below the tenth percentile according to the normal tables for our population .
Statistical analysis was conducted using SPSS for Windows, version 17. Statistical differences between the study and control groups were evaluated using chi square-tests for dichotomous variables; continuous variables were analyzed using independent sample t-tests.
Results of binary logistic regression analysis of women aged under 35 and 35 and over with preeclampsia (* BMI included)
Preterm delivery (before <34 wk)
<0.000 (* < 0.000)
Preterm delivery (before 37 wk)
Low Apgar score (<7) at 5 min
SGA (<90th percentile)
<0.001 (* < 0.001)
<0.001 (* < 0.001)
Admission to a neonatal unit
<0.001 (* < 0.001)
Background information about women aged under 35 and 35 and over who had preeclampsia
(n = 15 437)
(n = 2387)
Pregravid BMI >25 kg/m2
Late pregnancy bleeding
Fertility treatment other than IVF
The mean weight before pregnancy in the control group was 69.6 ± 16.3 kg versus 73.9 ± 16.3 kg (<0.001) in the study group. In the control group the mean birth weight was 3179 ± 730.4 g versus 3037 ± 788.3 g (<0.001) in the study group. Pregnancy outcomes for the two groups are compared in Table 1.
Cesarean delivery was found to be twice as likely in women of AMA. The rate of preterm delivery before 34 and 37 weeks’ gestation, low Apgar score at 5 min., SGA, asphyxia and admission to a NICU were also significantly higher in women of AMA. No significant differences between groups were found in rates of fetal death, eclampsia and blood transfusion to mothers.
Women of AMA were 1.5 times more likely to have preeclampsia compared to women under 35 years of age. The main finding of the present study, however, was that among preeclamptic women, adverse pregnancy outcomes were more common in women of AMA.
First, women of AMA were significantly more likely to have preterm deliveries before 34 and 37 weeks and to have SGA- infants the risk increase being 70% in preterm delivery before 34 weeks and 40% in both preterm delivery before 37 weeks and SGA. Second, women of AMA had a twofold increased risk of requiring Cesarean deliveries. Finally, these obstetric risks led to approximately 50% higher frequencies of neonatal asphyxia and 40% of admission of the infant in the neonatal intensive care unit.
Similar to other studies, the women of AMA in this sample experienced more prior terminations and IVF and other fertility treatments [18–20]. On the other hand, they smoked less often than younger women, but they were more often obese and had higher rates of gestational diabetes. Obesity is known to be a risk factor for preeclampsia , whereas smoking is a protective factor . The net effect of maternal obstetric history and health behavior is likely to play a minor or moderate role in the entire picture, since some of the effects are beneficial while others are harmful depending on whether the outcome under consideration is the frequency of preeclampsia, premature delivery, fetal growth or neonatal outcome [8, 18, 22–25]. In other words, maternal age appeared to be an independent obstetric risk factor for early onset of preeclampsia and impaired fetal growth. It has also been stated that chronic and pregnancy-related hypertension increase risk for low birthweight and preterm birth as well as older maternal age was resulting in shorter gestations .
The mechanism behind this risk is beyond the scope of the present study but may be related to aging of the uterine blood vessels .
The strength of the current study was that it used a population-based cohort including data from three national Finnish health registries. The data stored in these registries have demonstrated both high quality and validity , affirming that the registries are a valuable resource for studying maternal and obstetric health outcomes as the identification of preeclampsia is shown to be accurate in such databases . Weaknesses of the study were that there may have been some error in the data collection, such as coding errors; however, considering the size of the data set, the impact of this factor was probably minor. It is also possible that picking out preeclamptic and eclamptic women from the data on the basis of diagnoses and hospital stay may have slightly increased the number in the sample. However, the data was recorded using a standard format among the registries and therefore, any inconsistency in reporting would have been a random event independent of maternal age.
In this study, women of AMA had preeclampsia more often than younger women, and their pregnancies were more likely to be complicated by preterm deliveries and impaired fetal growth. As a consequence, the need for neonatal intensive care was significantly higher for women of AMA, suggesting a substantial increase in the use of healthcare resources. Premature infants are at higher risk of neonatal mortality and morbidity as well as neurodevelopmental impairments; these tend to be inversely proportional to gestational age . The preventive measures, such as taking supplements of vitamins C and E, do not reduce the occurrence of preeclampsia  but it has been demonstrated that low-dose aspirin started in early pregnancy may reduce the incidence of preeclampsia and intrauterine growth restriction . However, postponing pregnancy to an older age is an obvious risk and the implications for the timing of assisted reproduction and family planning policies are relevant.
This study was supported by the University of Eastern Finland, Department of Nursing Science, The Finnish Doctoral Programme in Nursing Science and Emil Aaltonen foundation. The funding sources were not involved in the study design, interpretation of results, manuscript preparation, or the decision to submit the article for publication.
- Benzies KM: Advanced maternal age: are decisions about the timing of child-bearing a failure to understand the risks?. Can Med Assoc J. 2008, 178 (2): 183-184. 10.1503/cmaj.071577.View ArticleGoogle Scholar
- Bayrambour H, Heaman M: Advanced maternal age and the risk of Cesarean birth: a systematic review. Birth. 2010, 37 (3): 219-226. 10.1111/j.1523-536X.2010.00409.x.View ArticleGoogle Scholar
- The National Institute for Health and Welfare. 2010, Available at: http://www.stakes.fi/tilastot/tilastotiedotteet/2010/Tr26_10.pdf (retrieved April 14, 2011),
- Cleary-Goldman J: Impact of maternal age on obstetric outcome. Obstet Gynecol. 2005, 105 (5): 983-990. 10.1097/01.AOG.0000158118.75532.51.View ArticlePubMedGoogle Scholar
- Jacobsson B: Advanced Maternal age and adverse perinatal outcome. Obstet Gynecol. 2004, 104 (4): 727-733. 10.1097/01.AOG.0000140682.63746.be.View ArticlePubMedGoogle Scholar
- Jolly M, Sebire N, Harris J, Robinson S, Regan L: The risks associated with pregnancy in women aged 35 years or older. Hum Reproduction. 2000, 15: 2433-2437. 10.1093/humrep/15.11.2433.View ArticleGoogle Scholar
- Ozalp S, Tanir HM, Sener T, Yaza S, Keskin AE: Health risks for early (or =35) childbearing. Arch Gynecol Obstet. 2003, 268 (3): 172-174. 10.1007/s00404-002-0359-7.View ArticlePubMedGoogle Scholar
- Hsieh TT, Liou JD, Hsu JJ, Lo LM, Chen SF, Hung TH: Advanced maternal age and adverse perinatal outcomes in an Asian population. Eur J Obstet Gynecol Reprod Biol. 2010, 148: 21-26. 10.1016/j.ejogrb.2009.08.022.View ArticlePubMedGoogle Scholar
- Joseph KS, Allen AC, Dodds L, Turner LA, Scott H, Liston R: The Perinatal effects of delayed childbearing. Obstet Gynecol. 2005, 105 (6): 1410-1418. 10.1097/01.AOG.0000163256.83313.36.View ArticlePubMedGoogle Scholar
- Bell JS: Can obstetric complications explain the high levels of obstetric interventions and maternity service use among older women? A retrospective analysis of routinely collected data. BJOG. An International Journal of Obstetrics and Gynaecology. 2001, 108 (9): 910-918. 10.1111/j.1471-0528.2001.00214.x.View ArticleGoogle Scholar
- Hutcheon JA, Lisonkiva S, Joseph KS: Epidemiology of pre-eclampsia and the other hypertensive disorder of pregnancy. Best Pract Res Clin Obstet Gynaecol. 2011, 25: 391-403. 10.1016/j.bpobgyn.2011.01.006.View ArticlePubMedGoogle Scholar
- Turner JA: Diagnosis and management of preeclampsia: an update. International Journal of Women’s Health. 2010, 2: 327-337.View ArticlePubMedPubMed CentralGoogle Scholar
- Villar J, Carroli G, Wojdyla D, Abalos E, Giordano D, Ba’aqeel H, Farnot U, Bergsjo P, Bakketeig L, Lumbiganon P, Campodonico L, Al-Mazrou Y, Lindheimer M, Kramer M: Preeclampsia, gestational hypertension and intrauterine growth restriction, related or independent conditions?. Am J Obstet Gynecol. 2006, 194: 921-931. 10.1016/j.ajog.2005.10.813.View ArticlePubMedGoogle Scholar
- The National Institute for Health and Welfare: 2010, Available at: http://www.stakes.fi/FI/tilastot/tausta/Laatuselosteet/syntymarekisteri.htm (retrieved April 14, 2011),
- The National Institute for Health and Welfare: 2011, Available at: http://www.stakes.fi/FI/tilastot/tausta/Laatuselosteet/hilmoraportit.htm (retrieved April 14, 2011),
- The National Institute for Health and Welfare: 2011, Available at: http://www.stakes.fi/FI/tilastot/tausta/Laatuselosteet/epamuodostumarekisteri.htm (retrieved April 14, 2011),
- Heinonen S, Taipale P, Saarikoski S: Weights for placentae from small-for-gestational age infants revisited. Placenta. 2001, 22: 399-404. 10.1053/plac.2001.0630.View ArticlePubMedGoogle Scholar
- Hoffman NC, Jeffers S, Carter J, Duthely L, Cotter A, González-Quintero VH: Pregnancy at or beyond age 40 years is associated with an increased risk of fetal death and other adverse outcomes. Am J Obstet Gynecol. 2007, 196 (5): e11-e13. 10.1016/j.ajog.2006.10.862.View ArticlePubMedGoogle Scholar
- Nybo Andersen AM, Wohlfahrt J, Christens P, Olsen J, Melbye M: Maternal age and fetal loss: population-based register linkage study. Br Med J. 2000, 320: 1708-10.1136/bmj.320.7251.1708.View ArticleGoogle Scholar
- Segev Y, Riskin-Mashiah S, Lavie S, Auslender R: Assisted reproductive technologies: medical safety issues in the older woman. J Womens Health. 2011, 20 (6): 853-861. 10.1089/jwh.2010.2603.View ArticleGoogle Scholar
- Ness RB, Zhang J, Bass D, Klebanoff MA: Interactions between smoking and weight in pregnancies complicated by preeclampsia and small-for-gestational-age birth. Am J Epidemiol. 2008, 168 (4): 427-433. 10.1093/aje/kwn140.View ArticlePubMedPubMed CentralGoogle Scholar
- Luke B, Brown M: Elevated risks of pregnancy complications and adverse outcomes with increasing maternal age. Hum Reprod. 2007, 22 (5): 1264-1272. 10.1093/humrep/del522.View ArticlePubMedGoogle Scholar
- Zeitlin JA, Ancel PY, Saurel-Cubizolles MJ, Papiernik E: Are risk factors the same for small for gestational age versus other preterm births?. Am J Obstet Gynecol. 2001, 185 (1): 208-215. 10.1067/mob.2001.114869.View ArticlePubMedGoogle Scholar
- McIntyre SF, Newburn-Cook CV, O’Brien B, Demianczuk NN: Effect of older maternal age on the risk of spontaneous preterm labor: a population based study. Health Care Women Int. 2009, 30: 670-689. 10.1080/07399330802596473.View ArticlePubMedGoogle Scholar
- Newburn-Cook CV, Onyskiw JE: Is older maternal age a risk factor for preterm birth and fetal growth restriction? A systematic review. Health Care Women Int. 2005, 26: 852-875. 10.1080/07399330500230912.View ArticlePubMedGoogle Scholar
- Miranda M, Swamy G, Edwards S, Maxson P, Gelfand A, James S: Disparities in maternal hypertension and pregnancy outcomes: evidence from North Carolina, 1994–2003. Public Health Rep. 2010, 125: 579-587.PubMedPubMed CentralGoogle Scholar
- Cunningham FG, Leveno KJ: N Engl J Med. 1995, 333 (15): 1002-1003. 10.1056/NEJM199510123331511.View ArticlePubMedGoogle Scholar
- Gissler M, Haukka J: Finnish health and social welfare registers in epidemiological research. Norsk Epidemiologi. 2004, 14 (1): 113-120.Google Scholar
- Lain S, Hadfield R, Raynes-Greenow C, Ford J, Mealing N, Algert C, Roberts C: Quality of data in perinatal population health databases: a systematic review. Medical Care. 2012, 50 (4): 7-20. 10.1097/MLR.0b013e31821d2b1d.View ArticleGoogle Scholar
- Gruslin A, Lemyre B: Pre-eclampsia: Fetal assessment and neonatal outcomes. Best Pract Res Clin Obstet Gynaecol. 2011, 25: 491-507. 10.1016/j.bpobgyn.2011.02.004.View ArticlePubMedGoogle Scholar
- Conde-Agudelo A: Supplementation with vitamins C and E during pregnancy for the prevention of preeclampsia and other adverse maternal and perinatal outcomes: a systematic review and meta-analysis. Am J Obstet Gynecol. 2011, 204 (6): 503-512.View ArticlePubMedPubMed CentralGoogle Scholar
- Bujold E, Roberge S, Lacasse Y, Bureau M, Audibert F, Marcoux S, Forest J, Giquére Y: Prevention of preeclampsia and intrauterine growth restriction with aspirin started in early pregnancy: a meta-analysis. Obstet Gynecol. 2010, 116 (1): 402-414.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2393/12/47/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.