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The aim of this prospective study was to investigate whether selective serotonin reuptake inhibitors (SSRIs) utilized by pregnant women influence fetal neurobehavioral development. In this observational study we investigated developmental milestones of fetal behavior during the pregnancy of women with psychiatric disorders who took SSRIs throughout gestation (medicated group; n=96) or who had discontinued medication early in gestation or before conception (unmedicated group; n=37). Healthy unexposed fetuses of women without mental disorders comprised the control group (n=130). Ultrasonographic observations of fetal behavior were made three times in pregnancy (T1–T3). Effects of SSRIs were studied over a wide range of dosages (low, standard, or high) and for different drug types. Fetuses exposed to standard or high SSRI dosages compared with control, unmedicated, or low-medicated fetuses showed significantly increased motor activity at the beginning (T1) and end of the second trimester (T2). They particularly exhibited disrupted emergence of non-rapid eye movement (non-REM; quiet) sleep during the third trimester, characterized by continual bodily activity and, thus, poor inhibitory motor control during this sleep state near term (T3). The SSRI effects on the fetus were dose related, but independent of SSRI type. The results demonstrate changes in fetal neurobehavioral development associated with standard and high SSRI dosages that are observable throughout gestation. A first-choice SSRI type was not apparent. Bodily activity at high rate during non-REM sleep in SSRI-exposed fetuses is an abnormal phenomenon, but its significance for postnatal development is unclear.
Selective serotonin reuptake inhibitors (SSRIs) are increasingly utilized in pregnancy to treat major affective (anxiety, depression) and other psychiatric disorders (Andrade et al, 2008; Vaswani et al, 2003; Ververs et al, 2006). Although SSRIs are currently believed to carry no risk of major fetal malformations (Louik et al, 2007), there are still concerns that relate to increased risks of preterm birth, low birth weight, and pulmonary hypertension (Rahimi et al, 2006; Chambers et al, 2006). In addition, neonatal symptoms (‘poor adaptation'), involving altered motor activity (restlessness, jitteriness) and sleep disturbance, are abundant after prenatal exposure to SSRIs (Sanz et al, 2005; Zeskind and Stephens, 2004). It is unknown whether the neonatal problems result from acute cessation of SSRI exposure at birth (withdrawal), or result from alterations in fetal neurobehavioral development secondary to sustained prenatal exposure (ie, an in utero effect; Lattimore et al, 2005).
SSRIs taken by the mother might directly affect the fetus. They readily cross the placenta and enter the fetal brain where serotonin and its neurons and receptors are present from early in life onward (Kinney et al, 2007). The inability of the fetus to metabolize SSRIs and the second pass of SSRIs through reuptake from the amniotic fluid may render the fetus also indirectly but continually exposed to raised drug levels. In sheep, maternal infusion of fluoxetine for 8 days has been shown to alter fetal rapid eye movement (REM) sleep and electrical brain activity (Morrison et al, 2005). In rodents, long-term neurobehavioral effects have been described in offspring after perinatal exposure to SSRIs (Maciag et al, 2006; Noorlander et al, 2008).
In normal human pregnancy, fetal generalized body movements occur randomly during the first half of gestation. They become progressively clustered to appear as phases of rest and activity around 28 weeks of gestation, which are fairly associated with patterns of low and high heart rate variability, respectively. As the fetuses grow older, episodes of rest and activity and their heart rate patterns become increasingly linked to absence and presence of eye movements, respectively. Eventually, stable non-REM (quiet) and REM (active) sleep states with sharp transitions are present near term (Nijhuis et al, 1982; Visser et al, 1992). Fetal sleep regulation is a well-controlled behavior reflecting the primary brain activity at this stage of development.
Previous ultrasound studies of fetal behavior have proven to be a powerful means of detecting variations in antenatal CNS functioning under normal and abnormal conditions (Mulder et al, 1987, 1998, 2009; Nijhuis et al, 1999). However, no data have been collected regarding the possible effect of SSRI exposure on neurobehavioral development in the human fetus.
The aim of this study was to compare behavioral development in a group of fetuses exposed to SSRIs throughout pregnancy with a control group of healthy unexposed fetuses. To separate potential effects of SSRIs on fetal behavior from those of depression and other mental disorders per se, we included a third group of fetuses of women who suffered from psychiatric problems but were unmedicated. In this prospective observational study, fetal motor behavior, heart rate, and the emergence of behavioral (sleep–wake) states were examined with special emphasis on SSRI type and dosage.
This study was part of a larger prospective project on the impact of SSRI antidepressant medication use during pregnancy. Potentially eligible participants were identified by physicians or midwives at participating sites and were approached by the study coordinator (FFTV). Exclusion criteria were fetal abnormality, multiple pregnancy, pre-existent maternal disease, psychosis or bipolar disorder, and use of benzodiazepines or medications classified as category D or X according to the FDA guidelines (Lo and Friedman, 2002). The study population comprised a total of 262 pregnant women with mood disorders and other psychiatric illnesses. Of these, 133 (51%) women agreed to participate in the present study involving additional ultrasound sessions for the study of fetal behavior in our research unit. Maternal and neonatal demographic differences between those who participated and those who declined were not statistically significant. The 133 women were recruited from the antenatal clinic at Utrecht Medical Centre (tertiary hospital) or were self-referrals or physician referrals for research purpose only from first- and second-line obstetric practices in the surrounding area. All participants (continuers and discontinuers, see below) had been taking SSRI therapy for at least 6 months. Psychiatric diagnosis, SSRI assignment, dose management, and drug discontinuation were at the discretion of the treating physician. Clinical diagnoses comprised major depression (n=51), panic disorder (n=12), a combination of both (n=62), generalized anxiety disorder (n=4), obsessive–compulsive disorder (n=2), and bulimia (n=2).
All pregnancies were dated by the last menstrual period and an ultrasound scan before 12 weeks of gestational age (wGA). The study was approved by the Dutch Central Committee on Research Involving Human Subjects (CCMO) and the local ethics committee. Subjects were enrolled on a voluntary basis after written informed consent had been obtained.
At study entry (15–19 wGA), 96 women (72%) were receiving SSRIs. They had conceived during treatment and remained on medication throughout pregnancy with no change of drug type (medicated study group). In addition, 37 (28%) women were not receiving SSRI therapy at study entry and did not resume taking SSRIs during the remainder of their pregnancy. They had discontinued medication before conception or before 12 wGA (unmedicated study group). The comparison group comprised 130 healthy women with no history of psychiatric or other illnesses. These were unexposed pregnancies that remained uncomplicated throughout the entire gestation. All fetuses of the comparison group were born healthy at full term (37 wGA) and of appropriate weight for gestation.
A longitudinal design with three times of assessment aimed to collect data for the mother and her fetus at 15–19 wGA at time 1 (T1), 27–29 wGA at time 2 (T2), and 37–39 wGA at time 3 (T3). A questionnaire booklet was mailed to the participant ~1 week before each appointment. Upon completion, they were returned directly to the study coordinator. The principal investigator (EJHM) remained blind to the mental health and drug status of the women until all fetal data had been collected and analyzed.
Data were collected on sociodemographic status, lifestyle, and medical and obstetric history. The information gathered related to maternal age, socioeconomic status (SES; highest achieved educational level), marital status, parity, psychiatric diagnosis, duration of therapy, time at discontinuation as appropriate, type and dosage of SSRI, cigarette smoking, and alcohol consumption.
The defined daily dose (DDD) of SSRIs used in this study was 20mg for paroxetine, fluoxetine, and citalopram; 50mg for sertraline; and 100mg for fluvoxamine and venlafaxine, according to the ATC−DDD index (WHO, 2008). These values were set to 1 to indicate standard exposure. For each woman, the prescribed total daily dose was expressed as a multiple of the standard, the mDDD. For example, mDDD was 3 for a woman who was daily using 60mg of paroxetine. Participants were categorized as having low intake (0 < mDDD <1), standard intake (mDDD=1), or high intake (mDDD >1). Absolute mDDD values were also used to compare drug effects across the different SSRI types.
The following self-administered questionnaires were applied. Anxiety was assessed with the State−Trait Anxiety Inventory (STAI) (Spielberger et al, 1970). The STAI comprises two scales, each containing 20 items to be rated on a four-point scale (range of possible scores 20−80). This standardized questionnaire differentiates between state anxiety (how respondents currently feel) and trait anxiety that reflects anxiety proneness (how respondents generally feel). The state anxiety scale was completed in 10min before ultrasound recording. Pregnancy-specific fears and worries were rated using a 10-item version of the Pregnancy-Related Anxieties Questionnaire (PRAQ). This instrument deals with the components, ‘fear of child integrity', ‘fear of giving birth', and ‘concern about bodily appearance', in a five-point response format; range of possible scores 0–40 (Huizink et al, 2004). Depression was measured using the Edinburgh Depression Scale (EDS), a 10-item scale that has satisfactory sensitivity and specificity for assessing prepartum depression; range of possible scores 0–30 (Cox et al, 1996).
One maternal saliva sample was collected halfway the fetal ultrasound session on each occasion and stored at −70°C until assay. Cortisol content was determined according to standard procedure (Huizink et al, 2002).
Fetal recordings were made following established procedures with the women semi-recumbent, slightly tilted to the left, in a quiet environment (Mulder et al, 1987). Real-time ultrasound observations of fetal generalized body movements (GMs) were made for 1h (T1, T2) or 2h (T3) between 1000 and 1600h, starting at least 1.5h after the last meal. The images were stored for off-line analysis; the presence of GM was marked during full image replay. The number and duration (in seconds) of GM bursts were subsequently determined for each recording (ten Hof et al, 1999). Fetal heart rate (FHR) was monitored with a cardiotocograph using Doppler ultrasound (Hewlett Packard, Böblingen, Germany). Continuous FHR monitoring occurred simultaneously with fetal visualization at T2 and T3, but is technically not possible at T1. Off-line, all FHR tracings were judged visually and divided into episodes of heart rate pattern (HRP) A through D (see below). Fetal REMs were observed and marked online at T3 by a second investigator using another ultrasound device.
Behavioral (sleep–wake) states are present in healthy fetuses after 36 wGA (Visser et al, 1992). Figure 1 shows an example of normal state organization in a near-term fetus. States are characterized by stable concordant association of the parameters of three variables (HRP, GM, and EM) for long periods of time and the simultaneous change of parameters at transitions (<3min). The 3-min moving window technique, a smoothing procedure, was used to draw up profiles for each T3 recording, indicating the on and off time of GM and EM combined with the presence of a particular HRP rounded off to the nearest 0.5min (Mulder et al, 1987; Nijhuis et al, 1982). The temporal association between parameters of the state variables was assessed by two complementary procedures. First, the presence of each of four distinct behavioral states was identified based on all three variables (Mulder et al, 1987; Nijhuis et al, 1982). Episodes of state 1F (S1F; quiet, non-REM sleep) are defined by the absence of both general and eye movements and a stable heart rate with a small oscillation bandwidth (HRPA); FHR accelerations may incidentally occur but must be disregarded when evaluating this pattern (Mulder et al, 1987). State 2F (S2F; active, REM sleep): general and eye movements are present and heart rate has a wide oscillation bandwidth between the frequent accelerations (HRPB). State 3F (S3F; quiet awake): general movements are absent and eye movements present; heart rate is stable without accelerations (HRPC). State 4F (S4F; active awake): frequent vigorous general movements in the presence of eye movements; unstable heart rate with large and prolonged accelerations (HRPD). No-state identified (NoS) was considered if none of the S1F–S4F combinations was valid. The presence of S1F–S4F and NoS was expressed as the percentage of recording time. Behavioral state organization reflects the degree of neurophysiologic integrity and maturity, with %NoS being an overall measure of disorganization (Visser et al, 1992). However, when increased, the %NoS does not tell which parameter(s) specifically underlie(s) state dissociation. Therefore, based on our results, the association between pairs of state parameters was also analyzed (Nijhuis et al, 1999). For each recording, we calculated the time that one of the three variables was absent (−) or present (+) during the time that another variable was absent or present. With HRPA denoted as (−) and HRPB as (+), 12 possible combinations were obtained (EM± vs HRP± EM± vs GM± and GM ± vs HRP ±). The degree of association between pairs was expressed as percent linkage.
For episodes of HRPA and HRPB lasting 10min identified at T2 and T3, computerized numerical FHR analysis yielded information about basal FHR (in b.p.m.) and long-term FHR variability (in ms) as described previously (Nijhuis et al, 1998a, 1998b). The sum duration of GM bursts (in seconds) was expressed as percentage of time (incidence) and calculated for total recording (T1) and for episodes of HRPA and HRPB lasting 10min (T2, T3) (ten Hof et al, 2002). Note that GMs were treated differently between macro- and micro-analyses. With the former, GM was considered continuously present if bursts occurred at <3min apart, whereas with the latter method, GMs were considered for the time they had been actually observed.
SPSS for Windows (version 16; SPSS, Chicago, IL) was used for data management and statistical analysis. Results were summarized with the use of standard descriptive statistics: counts and percentages for categorical variables, and means and SD or SE for continuous variables. Main study groups were evaluated for equivalence in patient characteristics using the χ2 or Fisher's exact test for categorical measures and one-way ANOVA for continuous variables. Analyses of the fetal outcome measures were performed in two steps using multivariable analysis of variance (GLM) with Sidak post hoc comparisons. First, possible differences in fetal behavior between the three main groups were evaluated. Second, we studied differences in fetal behavior between the unmedicated group and the medicated subgroups (low, standard, and high mDDD) and also examined linear relationships between fetal variables and the absolute mDDD values by regression analysis (GLM). With all tests, significance was assumed at the level of α=0.05 (two sided).
At study entry (T1), the unmedicated and medicated groups did not differ with regard to psychiatric diagnoses (χ2=0.82, P=0.84), history of admission to a psychiatric clinic (χ2=1.70, P=0.19), and SSRI dosage before T1 (median mDDD was 1; range 0.2–3.0 mDDD for both groups; P=0.44).
Women in the medicated group compared with control women were older, more often multiparous, and had shorter gestation and infants with lower Apgar scores (Table 1). There were no significant differences in the use of alcohol or tobacco, (adjusted) birth weight, mode of delivery, SES, or marital status across the main groups (Table 1 or data not shown).
Of the 133 women in the study groups, 28 women attended once, 45 twice, and 60 completed all three sessions. For the comparison group (n=130), these numbers were 2, 16, and 112, respectively. Several factors account for the difference in participation rate. Study group participants compared with control subjects were allowed to enter the study at any stage of pregnancy and they were more likely to drop out because of loss of interest, physical or mental discomfort, or delivery before the last session. The numbers of participants (recordings) at T1–T3 were distributed as shown in Table 2. For fetal recordings, there were modest differences in gestational age and time of day at recording (ie, before or after 1200h). Hours of fetal observation obtained from the study and comparison groups were 482 and 393, respectively.
All medicated women were on SSRI monotherapy. The majority of these (44%) used paroxetine (type 1), 21% used fluoxetine (type 2), 20% used citalopram (type 3), 7% used venlafaxine, 4% used fluvoxamine, and 4% took sertraline (the latter three combined; type 4). The median mDDD was 1 (range 0.2–3.0 mDDD) on each occasion.
The women in the unmedicated and medicated groups had similar scores on the STAI, PRAQ, and EDS questionnaires. Both study groups had higher stress/anxiety and depression scores compared with control women (Table 2). Maternal cortisol content did not differ across the main groups at T1 and T2, but was higher in the unmedicated and medicated groups at T3 compared with control women (Table 2).
The clinical and psychological factors presented in Tables 1 and and22 were examined as potential confounders. Gestational age and time of the day at recording, state/trait anxiety, pregnancy-specific fears, and depression were modestly associated with some fetal movement and heart rate parameters, notably at T3, in bivariate analyses (Pearson's r between 0.144 and 0.257; 0.0001<P<0.05). Gestational age at T1 and T3 continued to demonstrate a significant association on occasions in multivariable analyses (see Tables 3 and and4).4). Maternal age, parity, SES, smoking, alcohol use, cortisol, and fetal sex were unrelated to any of the fetal outcome measures at T1–T3.
One or more episodes of HRPB were present during each recording made at T2. However, recordings with episodes of HRPA were less frequently seen in the medicated group (69%) when compared with the unmedicated (94%) and comparison (96%) groups (χ2=25.52, P<0.0001). Episodes of HRPs C and D were excluded from analysis because of their low occurrence. Fetuses in the total medicated group spent less time in episodes of HRPA and more time in HRPB than did fetuses in the comparison and unmedicated groups (Table 3). Compared with the unmedicated group, the effect of SSRIs on the distribution of HRPs was largest for the standard- and high-exposure subgroups and was dose dependent (Table 4), with no significant effect of drug type (types 1–4) or other covariates.
Episodes (at least one) of HRPs A and B were present among all recordings made at T3. The proportions of recordings with the presence of HRPC or HRPD as well as their percent incidences were similar across the main groups. Therefore, episodes of HRPs C and D were not considered further. The percent incidences of HRPs A and B showed similar distributions across the main groups (Table 3) and medicated subgroups (Table 4). However, analysis of the temporal association between the parameters of the three state variables (HRP, GM, and EM) demonstrated altered fetal state distribution across the main groups (Table 3). Fetuses in the total medicated group compared with the control and unmedicated groups showed less %S1F, increased no-state identified (%NoS), and unaffected %S2F (Table 3). Although not different between the unmedicated group and low-exposure subgroup, the %NoS was increased in the standard- and high-exposure subgroups at the cost of %S1F (Table 4). The effect of SSRIs on the %NoS occurred in a dose-dependent manner, but was not related to drug type or other covariates. Examples of normal well-organized fetal behavioral states and of disrupted state organization are shown in Figures 1 and and2,2, respectively.
The reason for the SSRI-related increase in %NoS was revealed by 2 × 2 analysis of the linkage between state 1F parameters, that is, episodes of HRPA, episodes of GM absent (GM–), and episodes of EM absent (EM–). All fetuses, irrespective of (sub)group, showed excellent linkage of HRPA and EM–, indicating that EMs were generally absent when the heart rate of the fetus showed an A-pattern (Figure 3). Control fetuses and fetuses of the unmedicated group and low-exposure subgroup also showed excellent linkage of HRPA and GM– and that of EM– and GM–. However, in fetuses exposed to standard or high SSRI doses, the linkage of HRPA/GM– and the linkage of EM–/GM– were highly disturbed. This demonstrates that poor linkage in these fetuses was solely because of GM bursts that continued to be present for an average of 40–60% of time during the presumed 1F state (Figures 2 and and3).3). For 2F combinations, linkage of the state parameters was unremarkable (not shown).
The time fetuses spent making GMs was similar in the comparison and unmedicated groups on each occasion, but was increased in the total medicated group (Table 3). Analysis of the medicated subgroups showed no differences in %GM between the low-exposure subgroup and unmedicated group (Table 4). However, the %GM was increased in the subgroups with standard and high exposure. These fetuses were more active at T1, during episodes of HRPB at T2 (but not T3), and notably during episodes of HRPA both at T2 and T3. The observed increases in %GM at T2 and T3 were generally associated with increases in FHR variability (Tables 3 and and4).4). Basal FHR did not differ across the main groups (Table 3) or medicated subgroups (not shown in Table 4). There were significant linear relationships between the absolute mDDD values and %GM or FHR variability (Table 4). Drug type was not significantly associated with %GM or FHR variability on any occasion.
The present findings demonstrate that neurobehavioral development in fetuses of low-medicated and unmedicated women with psychiatric problems is indistinguishable from development in healthy control fetuses. However, fetuses exposed to standard or supra-standard SSRI doses developed differently irrespective of SSRI type. Characteristics were increased motor activity at the beginning (T1) and end of the second trimester (T2), and most strikingly lack of inhibitory control of motor output at times the fetuses are supposed to be ‘at rest' (T2) or in ‘quiet' or non-REM sleep (T3). Thus, fetal effects of standard to high SSRI doses were observable throughout pregnancy, but effects were most prominent on the architecture of non-REM sleep near term.
We observed increased bodily activity in SSRI-exposed fetuses already at 16–19 weeks (T1). These fetuses also spent more time in the activity phase at 27–29 weeks (T2) and showed more general movements during episodes of both HRPA and HRPB. At term (T3), SSRI-exposed fetuses showed good association between episodes of HRPA and absence of eye movements, and parameters changed in concert on either side of the ‘1F-state' as expected. However, frequent GM bursts disrupted this state's stability, and led to lack of synchronized transitions (Figure 2). The building up and maintenance of REM sleep and awake states were not influenced by SSRIs.
Clinical characteristics and depression scores of women were similar between the unmedicated and medicated groups. Other factors, including SSRI type, also did not essentially confound alterations in fetal performance. The observed fetal effects may be because of the shared mechanism of action of SSRIs (raising of CNS serotonin), but not to chemical variations among different SSRI types. Our findings in fetuses of medicated women were not explained by factors other than SSRI dosage. The SSRI-induced effect on fetal non-REM sleep seems to be specific, as it has not been described with other fetal exposures (Mulder et al, 1998, 2009, 2010; Van den Bergh et al, 2005). Our unprecedented results show an in utero effect of SSRIs on fetal functioning and challenge the view that adaptation problems in the neonate are solely because of acute cessation of SSRI exposure at birth (withdrawal). The findings also do not lend support to the hypothesis of in utero overstimulation of the serotonergic system or SSRI-induced intoxication (Laine et al, 2003).
Serotonergic neurons in the raphe nuclei project extensively to other brain nuclei that regulate motor activity and sleep–wake cycling (Lu et al, 2006; Fuller et al, 2007). The serotonergic system also interacts with other neurotransmitter systems that regulate autonomic control (Bairy et al, 2007), and has an important role in the functional organization of developing neural networks in the brain and spinal cord (Branchereau et al, 2002). Both serotonin neurons and receptors undergo quantitative ontogenetic changes. Therefore, modulation of fetal serotonin by SSRI exposure at different stages of pregnancy may affect structural and functional processes, leading to varied behavioral effects.
Increased activity in SSRI-exposed fetuses supports the view that serotonergic neurons can increase motor output and facilitate execution of repetitive movements in particular (Lucki, 1998; Branchereau et al, 2002). Ontogenetic changes in fetal neurobehavior in the medicated group may also underlie dysregulation of motor control during both non-REM sleep at term and its precursor ‘state' at T2 (episode of HRPA). It is puzzling why general movements occur frequently in non-REM sleep and withdraw selectively from inhibitory control after prolonged SSRI exposure. This phenomenon resembles adult sleepwalking occasionally described with the use of SSRIs (Healy et al, 2006). Fetal behavior studies are labor intensive and time consuming. However, fetal observations like ours are of importance for studying the young nervous system and for revealing basic and pathophysiological mechanisms underlying sleep–wake ontogeny and organization (Lu et al, 2006; Fuller et al, 2007).
Neonatal problems often seen after prenatal exposure to SSRIs are time limited and usually resolve within a couple of weeks (Sanz et al, 2005), although exposed infants appear to have increased health utilization during the first year of life (Ververs et al, 2009). Follow-up studies up to 5 years of age are presently reassuring as to the safety of SSRIs. Apart from subtle motor deficits in prenatally exposed infants (Casper et al, 2003), no major effects have been found on cognition, temperament, or internalizing and externalizing behaviors (Nulman et al, 2002; Misri et al, 2006; Oberlander et al, 2007).
From a neurodevelopmental view, however, the signs of non-REM sleep disruption may pose the SSRI-exposed fetus to future risks. In rodents, long-term neurobehavioral effects have been described after perinatal exposure to some individual SSRIs. Noorlander et al (2008) demonstrated in mice that pups exposed to maternally administered daily injections of fluoxetine (but not fluvoxamine) from embryonic days 8–18 exhibit increased anxiety and depression-like behaviors in adulthood (3 months). Similar deficits in adult behavior were found after daily administration of fluoxetine or citalopram over postnatal days (PNDs) 4–21 and PNDs 5–19, respectively (Ansorge et al, 2008; Popa et al, 2008). An early postnatal regimen using citalopram (PNDs 5–19) also resulted in increased total REM sleep (more episodes and shorter latency to sleep onset) in adult mice with no effect on non-REM sleep (Popa et al, 2008), and resulted in reduced sexual activity in male adult rats treated as pups at PNDs 8–21 (Maciag et al, 2006). These alterations have been found to be developmentally specific, as they cannot be produced by SSRI treatment at adult age (Ansorge et al, 2008; Popa et al, 2008).
The present study has a number of strengths, including its prospective design, the relatively large sample of human fetuses exposed to SSRIs, and blinded assessments with the use of standardized and comprehensive measures of fetal sleep. In addition, we controlled for multiple potential confounding factors.
Several limitations must be considered. Although the study was longitudinal in character, 45% of participants in the study groups as opposed to 86% in the control group did not attend all three antenatal sessions for reasons outlined in the Results section. Therefore, developmental trajectories for individual fetuses could not be assessed with the use of longitudinal data analysis.
There was a difference in parity between the studied groups. However, parity was used as a confounder in the analyses and had no effect on the measures of fetal behavior.
The unmedicated group comprised both women who discontinued taking SSRIs before conception (n=22) and women who were using these drugs at the outset of pregnancy but stopped at first notion of pregnancy (<8 weeks; n=11) or stopped at 8–12 wGA (n=4). In the latter subgroups, a potential effect of early SSRI exposure on the developing nervous system cannot be excluded. However, the behavior measures obtained at T1 (18 wGA) and on subsequent occasions did not differ statistically between fetuses exposed for some time during embryogenesis and fetuses of discontinuers before conception. Note that the term ‘unmedicated' refers to maternal drug status at first fetal observation (T1).
Another limitation of the study is that its findings cannot be compared with fetal sleep study data from animal experiments on the same subject, as these are not available.
The programming hypothesis suggests that altering key developmental processes in utero can predispose the offspring to late-onset disorders (Gluckman et al, 2008). There is some evidence that poor sleep in children may have prenatal origins (Pesonen et al, 2009). Our results may predict sleep problems in children prenatally exposed to SSRIs. Child sleep problems, in turn, are linked to later behavioral difficulties, anxiety, depression, poor attention, and aggression (Gregory et al, 2008; Pesonen et al, 2009). Hence, future follow-up studies should focus on sleep development and neurophysiological and neuropsychological tests that challenge autonomic control and regulatory/inhibition mechanisms in prenatally SSRI-exposed individuals.
Treatment decisions for women with psychiatric problems when pregnant or with intention to be are difficult because of conflicting risks (Hampton, 2006). The present study provides data showing that fetal performance varies as a function of different SSRI dosages, not drug type. To stay free of drugs appears to be the optimal choice with respect to potential fetal and obstetrical complications, but relapse of mental disorders is imminent (Cohen et al, 2006). For women who continue SSRI medications in pregnancy, the use of above-standard dosage for a particular SSRI type may be discouraged, if possible and safe.
A financial contribution in laboratory costs by The Netherlands Brain Foundation is gratefully acknowledged. We thank the participants of the ongoing Study of Antidepressants in Pregnancy (OAZE) project for their cooperation. We thank gratefully Judie Hulsbosch and Hetty Rijksen for help with patient recruitment and data management, and Mieke Helman for assistance during recording sessions.
The authors declare no conflict of interest.