Literature DB >> 35053633

Consequences of Prematurity on Cortisol Regulation and Adjustment Difficulties: A 9-Year Longitudinal Study.

Auriana Urfer1, Hélène Turpin1, Nevena Dimitrova1, Ayala Borghini1, Kerstin Jessica Plessen1, Mathilde Morisod Harari1, Sébastien Urben1.   

Abstract

A preterm birth represents a stressful event having potentially negative long-term consequences. Thirty-three children born preterm (<33 weeks gestational age) and eleven full-term children participated in a nine-year longitudinal study. Perinatal Risk Inventory (PERI) was used at birth to assess the perinatal stress. Salivary cortisol, collected four times a day over two consecutive days, was measured with radioimmunoassay technique at six months and nine years to assess the hypothalamic-pituitary-adrenal (HPA) axis. Mothers reported post-traumatic symptoms on a self-report questionnaire 12 months after their child's birth and children's adjustment problems at 9 years of child age on the Child Behavior Checklist. Results showed a significant difference in cortisol regulation at nine years between preterm and full-term children but no differences in adjustment problems. Whereas biological factors (i.e., PERI, cortisol regulation at six months) explained cortisol at nine years, maternal post-traumatic symptoms were predictive of adjustment problems in their child. In conclusion, very preterm birth has some long-term consequences on the HPA-axis regulation at nine years. Although cortisol regulation is mostly influenced by biological factors, the presence of maternal post-traumatic symptoms predicts the manifestation of adjustment problems in both groups. This shows the importance of maternal psychological well-being for child development. Further research is needed to understand the exact consequences of premature birth on cortisol regulation and the implication for the child's development and health.

Entities:  

Keywords:  HPA axis regulation; child’s behaviors problems; child’s emotional problems; follow-up; prematurity

Year:  2021        PMID: 35053633      PMCID: PMC8774148          DOI: 10.3390/children9010009

Source DB:  PubMed          Journal:  Children (Basel)        ISSN: 2227-9067


1. Introduction

1.1. Prematurity

Preterm birth is defined [1] by birth before 37 weeks of gestation (with sub-categories: moderate preterm—32 to 37 weeks, very preterm—28 to 32 weeks, and extremely preterm—less than 28 weeks). It represented 10% of all living births worldwide [1] and 6.4% in Switzerland, in 2020 [2]. Recent progress in medical techniques and care instructions of preterm infants has enabled to increase the survival rate of premature infants [3,4,5]. However, it is nowadays well established that premature birth has an important impact on the infant and the family not only at birth but also on long-term [6,7]. Indeed, preterm children are at higher risk for long-term medical and developmental difficulties [6,8,9]. In particular, it has been recognized that preterm-born children are more at risk of presenting maladaptive self-regulation skills including stress response system regulation such as the hypothalamic-pituitary-adrenal (HPA) axis [10], as well as the development of behavioral (or externalizing) and emotional (or internalizing) problems [11]. Although some studies have shown that preterm children were more at risk to develop internalizing and externalizing problems [6,7,12], other studies did not observe any difference between preterm and full-term children [13,14]. Internalizing and externalizing problems are often co-morbid and closely related to each other in children and adolescents [15,16,17]. They differ in the way of expressing the distress, either inwardly (i.e., internalizing: depression, anxiety) or outwardly directed (i.e., externalizing: conduct disorder, substance abuse) [18,19]. In our study, we will consider both internalizing and/or externalizing problems and examine them together to define the presence of adjustment problems [20,21].

1.2. Preterm Birth: A Stressful Event

Preterm birth can be a particularly stressful event for the newborn and their parents. More specifically, in the context of prematurity, two types of stress might be articulated: perinatal stress (newborn’s stress such as neonatal complications, painful medical procedures) and parental stress (e.g., post-traumatic stress disorder, depression). Early exposure to repeated stress put the preterm-born children at risk for developing behavioral and emotional problems or in other terms, adjustment difficulties [6,11,22]. These difficulties [20,21] often persist into adolescence and early adulthood [23] and can have an important negative impact on their quality of life and their family [24].

1.2.1. Stress Regulation: Hypothalamic-Pituitary-Adrenal (HPA) Axis

From a biological point of view, a stressful event activates the neuro-endocrinologic pathways and more specifically the HPA axis, which results in the release of cortisol [25,26,27]. Beyond the reactivity to a stressful event, the HPA axis also has a circadian rhythm with a high cortisol level in the morning, a gradual decline throughout the day, and the lowest level in the evening [28]. This rhythm is established between three to nine months [29]. However, the exposure to extreme or chronic stress, such as prematurity, can lead to a long-term elevation of cortisol [30,31]. Persistent higher cortisol has been shown to have a toxic effect on neuronal cells, altering the function of different neuronal system, and even affecting brain structures that are essential for self-regulation skills [32,33].

1.2.2. Perinatal Stress

Premature birth is undeniably a stressful event for the newborn. The organism of preterm children is immature and not physiologically ready for an extra-uterine environment [34]. They will spend their first days of life in the neonatal unit, where they might be exposed to several painful and invasive procedures, as well as to sensory dystimulation (i.e., intensive light and noise), in other terms to a highly stressful environment [7,35] which is significantly different from the maternal womb [36]. Moreover, during the neonatal period, neuronal pathways are immature and are therefore particularly vulnerable [37]. Exposition to stress and multisensory dystimulation during this period can induce long term impacts on developmental outcomes, including brain development, stress regulation system and adjustment problems [29,38,39].

1.2.3. Parental Stress

Premature birth is often associated with important parental, and especially maternal stress. Mothers are rapidly separated from their newborn child, and they might have lots of concerns regarding its survival and its medical complications [40,41]. Moreover, preterm birth can be traumatic for mothers and may induce post-traumatic stress disorder (PTSD), depressive symptoms, anxiety, and worry symptoms [42,43]. The presence of maternal stress and PTSD symptoms can affect their emotional and psychological availability for the care of their child and negatively impact the quality of mother-child interactions [44,45].

1.2.4. Impact of Perinatal and Maternal Stress on Child Development

Chronic exposition to stress has been shown to have a detrimental impact on the neuroendocrinological system, as well as on behaviors regulation [46]. Regarding the HPA axis, it is known that early life experience, perinatal stress, and maternal stress can affect the programming of the HPA axis [47,48,49]. Some studies have demonstrated that premature children showed alterations at different levels of the HPA axis. For instance, a study from Grunau et al. has shown that preterm children had a lower level of cortisol at 3 months but a higher level at 8 and 18 months compared to full-term children [50]. Over time, a high level of cortisol may have a detrimental effect on the brain due to the toxic effect on neurons and their myelinization [26,50]. These alterations can influence the development of health problems later in life, such as cardiovascular, metabolic, and psychological problems [48,51]. Moreover, perinatal stress influences the development of brain areas which are important for the regulation of emotions and behaviors [38,52]. Maternal stress has an impact on the mother-child attachment and interactions, which is known to have an important influence on children’s social, cognitive, and emotional development and might later lead to adjustment problems [53,54,55,56].

1.3. The Current Study

In summary, a preterm birth is a stressful event for both the child and the parents. It may lead to the development of adjustment problems and dysfunctional HPA axis regulation [27,35,37,47,50]. Although several studies have suggested that children’s development of emotional and behavioral problems and HPA axis regulation were modulated by factors such as perinatal stress and parental attitudes [57,58], the interaction of these factors as a whole is not yet fully understood. To the best of our knowledge, no longitudinal study examines the influence of perinatal stress and maternal stress on child’s psychophysiological self-regulation skills (i.e., HPA axis regulation and adjustment problems) in the context of intense early stress, namely prematurity. The purpose of the study was to understand the consequences of the stress, induced by prematurity, on the HPA axis regulation and the development of adjustment problems at nine years. In particular, our primary objective was to examine the interplay between prematurity and HPA axis’ regulation at nine years alongside the presence of adjustment problems. To do so, we will compare preterm to full-term regarding the HPA axis regulation, as well as on adjustment problems. The secondary objective was to specify the risk factors (i.e., perinatal risk, the cortisol level at six months, and the maternal PTSD of the parents) of the HPA axis dysregulation and adjustment problems (i.e., internalizing and/or externalizing symptoms) at nine years. Identifying the risk factors could help to identify risk groups of preterm children that would benefit the most from early intervention.

2. Materials and Methods

2.1. Participants

All infants (n = 242) born before 33 weeks of gestation (very preterm infants -VPT), in the University Hospital of Lausanne between 2005 and 2009 were eligible to participate in the first part of the study. Twenty-nine infants were excluded due to death and an additional eighty-seven parents did not want to participate in the study. The exclusion criteria were parents who were not fluent in French, parental mental illness, infant malformation, periventricular leuko-malacia with a grade > 2 or intraventricular hemorrhage with a grade > 2 and neonatal abstinence syndrome. If an infant was found to have severe mental or psychomotor delays at their six months corrected age (defined as 6 months after 40 weeks of gestational age) pediatric appointment, then the infant was also excluded from the study. Moreover, twenty-five families with an infant born at full-term (gestational age over 37 weeks) were also recruited between 2008 and 2009 in the University Hospital of Lausanne. The exclusion criteria were parents who were not fluent in French, somatic problems, complications during pregnancy or delivery, and parental mental illness. At the 9-year follow-up, 33 mothers and their preterm children as well as 11 mothers and their full-term children participated in the study. Dropouts were due to non-reachable families or refusal to participate in the follow-up. Moreover, one subsample of preterm children (n = 21) did not have the assessment at six months, excluding them from the current study. The Figure 1 illustrates the flow chart.
Figure 1

Flow chart.

The data was drawn from an intervention study, where the group of preterm infants were separated into two sub-groups, one with a brief intervention and the other without an intervention. The focus of the intervention was the early relationships between mothers and their child [59]. Since there was no significant difference in terms of cortisol regulation, development of adjustment problems and socio-demographic data, the present study will treat both groups as one sample. Descriptive statistics are reported in the Table 1.
Table 1

Socio-demographic variables and dropout analysis.

Included (N = 44)Dropout (N = 38) p 1 p 2 p 3
1. Preterm2. Full-Term3. Preterm4. Full-Term
n = 33n = 11n = 24n = 14
GA30.11 (1.84)40.18 (0.90)30.15 (2.00)39.34 (1.49)0.001nsns
Gender (F/M) 54.5/45.536.4/63.637.5/62.535.7/64.3nsnsns
SES2.71 (0.61)2.55 (0.47)2.54 (0.88)2.56 (0.93)nsnsns
Mat. Age (yrs)32.73 (4.30)31.64 (5.08)33.75 (4.19)30.86 (5.17)nsnsns
PERI7.73 (2.38)0.00 (0.00)8.08 (3.45)0.00 (0.00)<0.001nsns
BW (gr)1369.24 (373.63)3383.00 (425.02)1406.46 (418.73)3256.43 (365.36)<0.001nsns
PPQ2.73 (2.67)1.22 (1.64)3.56 (3.31)0.90 (1.45)nsnsns

Data expressed in Mean (SD) except for gender. 1 p-value of the results of t-tests comparison between the preterm and full-term included in the follow-up. 2 p-value of the results of t-tests comparison between the 2 group of preterm (drop out vs. included). 3 p-value of the results of t-tests comparison between the 2 groups of full-term (drop out vs. included). Notes. GA, gestational age; F, female; M, male; SES, socio-economic status; Mat., maternal; PERI, perinatal risk inventory score; BW, birth weight; PPQ, Perinatal Posttraumatic stress Questionnaire score.

There was no significant difference between the group of preterm and full-term children in terms of gender (p = 0.598), maternal age (p = 0.607), and socio-economic status (SES; p = 0.418). As expected, the preterm children had a significantly (p < 0.001) higher perinatal risk inventory (PERI, see below for details) and a significantly (p < 0.001) lower birthweight compared to the full-term children. Dropout analysis showed that there was no significant difference between the group who remained in the study and the participants who dropped out of the study at nine years in terms of gender, parent’s age, socioeconomic status and neonatal data (PERI, birth weight, gestational age). We observed a significant age differences at the follow-up (Preterm: M = 8.99 SD = 0.73, Full-term: M = 9.51, SD = 0.38, t(41) = 2.22, p = 0.032).

2.2. Procedure

The design of the study was a longitudinal cohort study (see Figure 2). The study was approved by the Ethics Committee for Clinical Research of the Vaud state (#256/14). Parental written consent was obtained after an exhaustive explanation of the research procedure.
Figure 2

Procedure. Notes. PERI, perinatal risk inventory, PPQ, Perinatal Posttraumatic stress Questionnaire score, CBCL, child behavior checklist.

At the birth of the child, various data was collected (e.g., APGAR score, gestational age, birth weight, head growth) to score the PERI [60] and estimate the perinatal risk of the infant. When the child was six months old (corrected age for premature children), eight “Salivettes” were sent to the parents. The parents were asked to collect the infant’s saliva four times per day over two consecutive days to collect information on the diurnal cortisol profile. Parents also received a leaflet with instructions for the infant’s saliva collection and a diary to write down the time of the collection. When children were 12 months old, the mothers were asked to rate a PTSD self-questionnaire, the PPQ [61], to evaluate the presence of post-traumatic symptoms linked with the premature birth of their child. When children were nine years old, families were seen again. They were asked, again, to collect their infant’s saliva four times per over two consecutive days the same way as at six months. Mothers were also asked to fill the child behavior checklist [62], to screen for possible internalizing and externalizing symptoms or in other terms adjustment problems.

2.3. Measures

2.3.1. Socio-Economic Status

Socio-economic status (SES) was assessed by the use of an adaptation of the Hollingshead index [63]. This index measures the social status of an individual (SES) and is based on the average of four scores: the maternal and paternal education level and professional occupation rated each on a four-point scale (i.e., degree: 1 = compulsory school, 4 = university grade completed; occupation: 1 = no job/unqualified employee, 4 = senior banker or physician in a private practice). A higher score means higher SES.

2.3.2. Perinatal Risk Inventory: PERI

The perinatal risk inventory (PERI) [60] is an 18-item inventory used to describe the severity of the infant’s perinatal problems. Each item is scored from zero to three and includes the APGAR score, the gestational age, birth weight, head circumference, the presence or absence of congenital infection, the absence or presence of seizures, the nature of the electroencephalogram, cranial computed tomographic, ultrasound, presence of sepsis and/or meningitis, the duration of ventilation, presence of polycythemia, hypoglycemia, hyperbilirubinemia, and long-term physical disabilities. The total score is obtained by adding up all of the items. The PERI was used to estimate the perinatal risk of each infant, with a higher score reflecting higher perinatal risk [60]. It is also correlated with the duration of the hospital stay and intensive procedures, giving an indication of the stress experienced by the preterm child.

2.3.3. Cortisol Regulation

The diurnal cortisol measure was collected over two consecutive days at home totaling four saliva samples per day: just after waking up (08:00), before mealtime at noon (12:00), in the afternoon (17:00), and in the evening (20:00). In cases of infection, fever or antibiotic treatment, the procedure was delayed. Cotton rolls containing saliva were sent by post to the lab of Prof. Kirschbaum [64] from the Technical University of Dresden (Germany) for cortisol concentration measurements by enzyme immunoassay. Cortisol concentrations were expressed as nanomoles per liter (nmol/L). As a standard procedure [59], the raw cortisol levels received from the lab were transformed into logarithms (log10) allowing the approximation of the Gaussian-like distribution. We computed the area under the curve with respect to the ground (AUCG) with our cortisol measures to estimate ultradian and circadian changes of hormones and to assess the overall secretion over the day. The AUCG represents the total hormonal output. We used one deriving formula for computation of the AUCG: With t denoting the individual time distance between measurements, m the individual measurements, and n the total amount of measurement [65].

2.3.4. Maternal Post-Traumatic Stress Symptoms

Mothers were asked to fill out a self-report questionnaire about post-traumatic stress symptoms, the Perinatal Post-Traumatic Stress Disorders Questionnaire (PPQ) [61], when their child was 12 months old. The PPQ is a 14 questions questionnaire based on the Diagnostic and Statistical Manual of Mental Disorders IV criteria which assesses maternal symptoms of PTSD related to the infant’s perinatal period. Questions are retrospective, mothers are asked to answer about situations they have experienced since and during the six months following their childbirth, and which lasted more than one month. Higher scores mean higher PTSD symptoms.

2.3.5. Adjustment Problems

The Child Behavior Checklist (CBCL) [62] was used to detect behavioral and emotional problems in children and adolescents from 6 to 18 years of age. It consists of 113 questions answered by the parents and scored on a three-point Likert scale (0 = absent, 1 = occurs sometimes, 2 = occurs often). These scales have good internal reliability (αs > 0.80), with relatively high 1-week test–retest reliability (r > 0.85) reported [62,66]. Adjustment problems were computed by averaging externalizing and internalizing T-scores [20,21]. Higher scores refer to more adjustment problems.

2.4. Data Analysis

The data were analyzed with SPSS version 27. As a first step, we examined the differences between preterm and full-term infants on neuroendocrine regulation by computing a repeated-measures (four measures a day) analysis of covariance (RM-ANCOVA) by groups (full-term vs. preterm) controlling for age differences whereas ANCOVAs was computed to assess the between-group differences in adjustment problems and AUCG. Then, we computed Bravais-Pearson coefficients of correlations between PERI, cortisol regulation (i.e., AUCG, maternal PTSD and adjustment problems). Finally, we used two separate regression models to identify possible predictors (i.e., PERI, early cortisol regulation, maternal PTSD) of children adjustment problems (i.e., externalizing and/or internalizing symptoms) or cortisol regulation (i.e., AUCG) at nine years. Regarding the important collinearity between group and PERI, we used only PERI scores in the regression models. Age was also introduced in the model as covariate.

3. Results

3.1. Between Group Differences on Neuroendocrine Regulation and Adjustment Problems

Descriptive data are reported in Table 2.
Table 2

Descriptive data on cortisol regulation and adjustment problems in VPT and FT children.

Preterm (n = 33)Full-Term (n = 11)p 1ɳ2p
AUCG106.51 (42.14)35.39 (17.94)<0.0010.34
Adjustment problems 52.63 (7.04)53.09 (6.93) ns -

Data expressed in Mean (SD). 1 p-value of the results of ANCOVA between the two groups and controlling for age differences. Notes. AUCG, area under the curve with respect to the ground.

Preterm showed higher AUCG at nine years of age compared to full-term children. By contrast, the ANCOVA comparing the group on adjustment problems revealed no difference. Figure 3 shows the diurnal cortisol evolution by groups.
Figure 3

Mean cortisol levels over two days at nine years. Notes. Reference population, reference range values from the CIRCORT database meta-analysis [67].

The RM-ANCOVA on the cortisol data revealed no main effect of time, a main effect of group, (F(1, 30) = 9.44, p = 0.004 ɳ2 = 0.239). A significant interaction effect between time and group (F(3, 90) = 4.91, p < 0.01, ɳ2 = 0.141) was also observed. In particular, post hoc pairwise comparisons indicated that morning and midday results showed that preterm children had significantly higher cortisol levels than full-term children (morning: p = 0.001; midday: p = 0.004). In the afternoon and at night, cortisol levels did not differ between preterm and full-term. In the preterm group, morning cortisol levels were significantly higher than other measures (ps < 0.001). There was a significant difference between levels at midday and in the evening (p < 0.001). At night, cortisol levels were significantly lower than in the afternoon (p = 0.012). In the full-term group, there was no significant differences between the daytime. Finally, we compared our results to reference values from a meta-analysis from Miller et al. [68]. Our group control was small (n = 11) and we wanted to enforce our results by comparing with reference values. We observed that our full-term children did not differ significantly from reference values, except for the afternoon data (p = 0.005). However, preterm values were significantly higher than reference values for all of the values throughout the day (ps < 0.002).

3.2. Association between Neuro-Endocrine Regulation, Adjustment Problems and Stress

Table 3 describes the correlations analysis. We can observe that a higher PERI is related to a higher AUCG at nine years. Moreover, maternal PTSD is linked to a lower AUCG at six months, and higher adjustment problems.
Table 3

Bravais-Pearson coefficient of correlations.

PERIMaternal PPQAUCG at 9yAUCG at 6m
Maternal PTSD0.29
AUCG at 9y0.53 **0.22
AUCG at 6m−0.26−0.37 *−0.17
Adjustment problems0.050.41 **−0.250.04

* p < 0.05, ** p < 0.01. Notes. AUCG, area under the curve with respect to the ground; PERI: perinatal risk inventory; PPQ, Perinatal Posttraumatic Stress Questionnaire score.

The regression analysis conducted on AUCG at nine years revealed that predictors (i.e., PERI, maternal PTSD, AUCG at six months) explain a significant part of the variance, F(5, 29) = 5.46, p = 0.002, R2 = 0.532. In particular, higher AUCG at nine years is predicted by a higher PERI and lower adjustment problems. In addition, the regression analysis on adjustment problems revealed that the predictors explain a significant part of the variance, F(5, 29) = 2.94, p = 0.033, R2 = 0.380. In particular, higher adjustment problems are related to higher maternal PTSD and a lower AUCG at nine years (Table 4).
Table 4

Regression analysis explaining cortisol regulation (AUCG) or adjustment problems at nine years.

CriterionVariables β p
AUCG at 9yAge−0.3640.022
PERI0.4180.012
Maternal PPQ0.2710.137
Adjustment problems −0.4140.014
AUCG at 6m0.1360.403
Adjustment problemsAge−0.2220.245
PERI0.2360.243
Maternal PPQ0.5220.009
AUCG 9y −0.5490.014
AUCG at 6m0.2320.212

Notes. AUCG, area under the curve with respect to the ground; PERI: perinatal risk inventory; PPQ, Perinatal Posttraumatic Stress Questionnaire score.

4. Discussion

The purpose of the present study was to analyze the consequences of stress related to a preterm birth on the child’s HPA axis regulation, as well as on the development of adjustment problems at nine years. We also examined which factors predict the self-regulatory outcomes at nine years (i.e., HPA regulation and adjustment problems) to identify high risk populations where preventive intervention could play an important role. In particular, this study highlighted a significant difference in cortisol regulation at nine years between preterm and full-term children, and showed that the biological stress (i.e., PERI and cortisol at six months) explains the diurnal cortisol concentration at nine years. Age is related to AUCG. We did not find any significant differences in adjustment problems in general between the two groups. However, we could show that maternal PTSD’s symptoms at 12 months (i.e., maternal stress) were predictive of adjustment problems in their child at 9 years. We did also show that higher adjustment problems were related to lower AUCG at nine years, which is in line with previous studies [68,69,70].

4.1. Cortisol Regulation

The main between-group difference lay in the morning cortisol levels. Indeed, preterm children had a higher cortisol level in the morning compared to full-term ones, as well as a higher AUCG. Likewise, De Graaf et al. [71] showed that at five years, preterm children had higher cortisol levels in comparison to full-term children. Grunau et al. [50] also reported greater levels of cortisol at 8 months and 18 months in preterm children. A possible explanation for these high levels is that premature birth impacts the early programming of the HPA axis, which was shown in the animal model [48,72,73], leading to long-term consequences. In humans, the development of the neuroendocrine regulation occurs in the postnatal period. This period is characterized by elevated synaptic plasticity, making the brain particularly vulnerable and sensitive [74]. Adverse events such as a premature birth can have an impact on the development and the “programming” of the HPA axis. This study is the first one identifying consequences on the HPA regulation nine years later. Moreover, we have shown that the level of stress endured by the preterm infants (i.e., PERI) was related to higher cortisol release at nine years (i.e., AUCG). This suggests that more stress during the neonatal period contributes to more alteration of the HPA axis regulation up to nine years. This might be related to the impact of stress on several brain structures (i.e., cortex, thalamus, basal ganglia) following a premature birth [38,75,76]. These brains areas are responsible for the neuroendocrine regulation systems such as the HPA axis [38].

4.2. Adjustment Problems

We did not find between-group differences regarding adjustment problems. Although some previous studies have demonstrated that preterm children were more at risk to develop adjustment problems [6,7,24,77,78], others have found no differences between late preterm and full-term infants at a young age [13,14]. Our findings can be explained by the fact that the children with biomedical complications (i.e., leukomalacia, intraventricular hemorrhage, mental or psychomotor delay at 6six months) were excluded from our study, whereas various other studies included preterm children with neurological damage [7,79]. Our sample may therefore be considered as low risk of developing adjustment problems and our results seem to indicate that children without biomedical complications are not more at risk to develop adjustment problems. The level of stress at birth (i.e., PERI) was not associated with the presence of adjustment problems in the child, which is in line with a previous studies [80]. This emphasizes the fact that other factors play a key role in the development of these problems later in childhood. Indeed, the quality of the postnatal environment (i.e., parental interaction, parental stress) has been proved to have a higher impact on the development of adjustment problems than the somatic risk (i.e., neonatal variables: low birth weight, gestational age) [7,81]. Our results further emphasize that the presence of maternal PTSD symptoms was associated with adjustment problems in the child. There are many ways in which PTSD might affect a child’s development. The presence of PTSD might have an impact on the capacity of mothers to understand their infant’s needs and signals [82], and thus tend to be less sensitive towards their infant [43,44,80,83]. PTSD therefore has an impact both on the mother’s role and the mother-child interaction. The mother-infant attachment, which is the relationship that develops between an infant and its caregiver early in infancy [84], is also important to understand how maternal stress and PTSD can influence the child’s development. Indeed, a secure attachment is essential for optimal child development. The presence of mother PTSD symptoms may lead to an insecure attachment, which has been shown to be associated with greater mental health problems [84,85]. Therefore, symptoms of maternal PTSD, by affecting attachment relationships, can explain the risk of children developing adjustment problems [86].

4.3. Clinical Implications

One of our objectives was to identify a high-risk population that would benefit the most from early interventions. We have shown that the presence of postnatal PTSD symptomatology in the mother was a risk factor for the child to develop adjustment problems. This result emphasizes the importance of considering the mother’s mental well-being in the child development. More attention should be given to children whose mothers experience PTSD symptoms following premature birth. The development of preventive intervention concerning specifically maternal PTSD symptoms due to preterm birth could be beneficial for the child’s development and health. Early interventions enhancing the mother-child relationship seem to have a positive effect on child development [87]. It would be also important to develop interventions focusing specifically on maternal PTSD symptoms. Since PTSD symptoms have been shown to affect the quality of the mother-child interaction [83], reducing these symptoms may be a way to improve the quality of this relationship and have a positive impact on the preterm development [88,89]. However, studies focusing on PTSD are limited [90], and future research is needed to develop interventions and evaluate their impact. In the neonatal unit, mental health professionals could offer the possibility to parents to talk about their experience and express their intense emotions, as well as joint observation to help understand and interpret their child’s behavior. This could reinforce their investment in their child and mother-child interaction, which might have a positive effect on child outcomes [44,83,91]. Another important finding was the presence of persistent alterations of the HPA axis regulation even after nine years, which seems related to the severity of the perinatal stress. Early intervention could focus on the reduction of infant’s stress, for instance through skin-to-skin contact (kangaroo care), which has been shown to reduce stress reactivity [92,93], cortisol level at short term [94,95], and improve brain development [96] in preterm children. However, it is not known if this method has a long-term effect on cortisol regulation. Kangaroo care also has positive effects on attachment and on parental stress levels. This might, in turn, have positive effects on the preterm development of the stress regulation system [92,97]. Interventions in the neonatal unit environment could also be offered, for instance by limiting the exposure to deleterious stimulations (i.e., painful procedures, noise) or by adapting the different sensorial stimulations (i.e., auditory, tactile, visual and vestibular) to support the neonate’s brain development and stress regulation [91,98,99].

4.4. Limitations and Strengths

The present study has some limitations. First, the size of our sample was relatively small. Although we had access to longitudinal information from the birth to nine years, no information was available on events between six months and nine years (i.e., traumatic event, parental separation). Additionally, the study relied only on the mother’s perspective for the assessment of the children’s behavioral problems (CBCL). Results could be influenced by the mental health of the mother. The teacher’s and father’s perspectives for instance would have been beneficial for a more comprehensive view of the children’s adjustment problems, as well as using other questionnaires. Finally, although the PPQ has good reliability [61], it was retrospective rated and self-reported. The strengths of this study are, first, to have a longitudinal information from birth to nine years. Moreover, we articulated the biological and psychological aspects of stress due to prematurity on the long-term outcomes of the children.

5. Conclusions

This study highlights that very preterm birth has long-term consequences on the cortisol regulation at nine years and that it is mostly influenced by perinatal stress (i.e., PERI). We show that the presence of maternal PSTSD’s symptoms contrary to biological factors is a predictor of the development of adjustment problems, underlying the importance of maternal psychological well-being and the negative impact of maternal PTSD symptoms on the child’s adjustment development. The most important clinical implications should be to develop preventive intervention dealing with postnatal stress and maternal PTSD symptoms, which would be beneficial for the child development and health. Finally, the association between cortisol regulation and adjustment problems is complex. The question of whether dysregulation of cortisol is one of the mechanisms putting preterm children more at risk for the development of adjustment problems later in life still needs to be elucidated. Further works are needed to have a better understanding of the detrimental effect of postnatal stress, including perinatal and maternal stress, on the later development of preterm born children. It would be beneficial for the development of targeted and individualized intervention.
  80 in total

Review 1.  How do glucocorticoids influence stress responses? Integrating permissive, suppressive, stimulatory, and preparative actions.

Authors:  R M Sapolsky; L M Romero; A U Munck
Journal:  Endocr Rev       Date:  2000-02       Impact factor: 19.871

Review 2.  The fetal and neonatal hypothalamic-pituitary-adrenal axis.

Authors:  P C Ng
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2000-05       Impact factor: 5.747

3.  Early Procedural Pain Is Associated with Regionally-Specific Alterations in Thalamic Development in Preterm Neonates.

Authors:  Emma G Duerden; Ruth E Grunau; Ting Guo; Justin Foong; Alexander Pearson; Stephanie Au-Young; Raphael Lavoie; M Mallar Chakravarty; Vann Chau; Anne Synnes; Steven P Miller
Journal:  J Neurosci       Date:  2017-12-18       Impact factor: 6.167

Review 4.  Effects of kangaroo mother care on maternal mood and interaction patterns between parents and their preterm, low birth weight infants: a systematic review.

Authors:  Eirini Athanasopoulou; John R E Fox
Journal:  Infant Ment Health J       Date:  2014 May-Jun

5.  Altered basal cortisol levels at 3, 6, 8 and 18 months in infants born at extremely low gestational age.

Authors:  Ruth E Grunau; David W Haley; Michael F Whitfield; Joanne Weinberg; Wayne Yu; Paul Thiessen
Journal:  J Pediatr       Date:  2007-02       Impact factor: 4.406

6.  Development of emotional and behavioral regulation in children born extremely preterm and very preterm: biological and social influences.

Authors:  Caron A C Clark; Lianne J Woodward; L John Horwood; Stephanie Moor
Journal:  Child Dev       Date:  2008 Sep-Oct

7.  Five-year follow-up of effects of neonatal intensive care and morphine infusion during mechanical ventilation on diurnal cortisol rhythm.

Authors:  Joke de Graaf; Erica L T van den Akker; Richard A van Lingen; Liesbeth J M Groot Jebbink; Frank H de Jong; Ruth E Grunau; Monique van Dijk; Dick Tibboel
Journal:  J Pediatr       Date:  2014-07-01       Impact factor: 4.406

8.  Synthesis of a cortisol-biotin conjugate and evaluation as a tracer in an immunoassay for salivary cortisol measurement.

Authors:  R A Dressendörfer; C Kirschbaum; W Rohde; F Stahl; C J Strasburger
Journal:  J Steroid Biochem Mol Biol       Date:  1992-12       Impact factor: 4.292

9.  National survey of problems and competencies among four- to sixteen-year-olds: parents' reports for normative and clinical samples.

Authors:  T M Achenbach; C T Howell; H C Quay; C K Conners
Journal:  Monogr Soc Res Child Dev       Date:  1991

10.  How do maternal PTSD and alexithymia interact to impact maternal behavior?

Authors:  Daniel S Schechter; Francesca Suardi; Aurelia Manini; Maria Isabel Cordero; Ana Sancho Rossignol; Gaëlle Merminod; Marianne Gex-Fabry; Dominik A Moser; Sandra Rusconi Serpa
Journal:  Child Psychiatry Hum Dev       Date:  2015-06
View more
  1 in total

1.  Optimizing Care for the Preterm Infant.

Authors:  Elizabeth Asztalos
Journal:  Children (Basel)       Date:  2022-05-25
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.