Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-22T14:23:16.673Z Has data issue: false hasContentIssue false

Association of maternal exposure to Superstorm Sandy and maternal cannabis use with development of psychopathology among offspring: the Stress in Pregnancy Study

Published online by Cambridge University Press:  26 May 2023

Yoko Nomura*
Affiliation:
Department of Psychology, CUNY Queens College and Graduate Center, Flushing, New York, USA; and Icahn School of Medicine at Mount Sinai, New York, USA
Jacob Ham
Affiliation:
Icahn School of Medicine at Mount Sinai, New York, USA
Patricia M. Pehme
Affiliation:
Department of Psychology, CUNY Queens College and Graduate Center, Flushing, New York, USA
Waiman Wong
Affiliation:
Department of Psychology, CUNY Queens College and Graduate Center, Flushing, New York, USA
Lexi Pritchett
Affiliation:
Department of Psychology, CUNY Queens College and Graduate Center, Flushing, New York, USA; and Icahn School of Medicine at Mount Sinai, New York, USA
Sima Rabinowitz
Affiliation:
Icahn School of Medicine at Mount Sinai, New York, USA
Nancy S. Foldi
Affiliation:
Department of Psychology, CUNY Queens College and Graduate Center, Flushing, New York, USA; and Department of Radiology, Weill Cornell Medicine, Brain Health Imaging Institute, New York, USA
Veronica J. Hinton
Affiliation:
Department of Psychology, CUNY Queens College and Graduate Center, Flushing, New York, USA
Priya J. Wickramaratne
Affiliation:
Columbia University Medical Center and New York State Psychiatric Institute, New York, USA
Yasmin L. Hurd
Affiliation:
Icahn School of Medicine at Mount Sinai, New York, USA; and Icahn School of Medicine at Mount Sinai, Addiction Institute of Mount Sinai, New York, USA
*
Correspondence: Yoko Nomura. Email: [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Background

Early-life adverse experiences can elevate the magnitude of the risk of developmental psychopathology, but the potential synergistic effects of multiple factors have not been well studied.

Aims

To determine whether prenatal exposures to maternal stress (Superstorm Sandy) and maternal cannabis use synergistically alter the risk of developmental psychopathology.

Method

The study included 163 children (53.4% girls), longitudinally tracked (ages 2–5 years) in relation to the effects of two early-life adverse exposures (Superstorm Sandy and maternal cannabis use). Offspring were grouped by exposure status (neither, only maternal cannabis use, only Superstorm Sandy or both). DSM-IV disorders for offspring were derived from structured clinical interviews; caregiver-reported ratings of family stress and social support were also assessed.

Results

A total of 40.5% had been exposed to Superstorm Sandy and 24.5% to maternal cannabis use. Offspring exposed to both (n = 13, 8.0%), relative to those exposed to neither, had a 31-fold increased risk of disruptive behavioural disorders (DBDs) and a seven-fold increased risk of anxiety disorders. The synergy index demonstrated that offspring with two exposures had synergistic elevation in risk of DBDs (synergy index, 2.06, P = 0.03) and anxiety disorders (synergy index, 2.60, P = 0.004), compared with the sum of single risks. Offspring with two exposures had the highest parenting stress and lowest social support.

Conclusions

Our findings are consistent with the double-hit model suggesting that offspring with multiple early-life adverse exposures (Superstorm Sandy and maternal cannabis use) have synergistically increased risks of mental health problems. Given the increasing frequency of major natural disasters and cannabis use, especially among women under stress, these findings have significant public health implications.

Type
Paper
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
Copyright © The Author(s), 2023. Published by Cambridge University Press on behalf of the Royal College of Psychiatrists

The developmental origin of health and disease hypothesis postulates that poor gestational quality as measured by exposure to suboptimal conditions, including stress, substance use and maternal infections, has a deleterious impact on development,Reference Barker1 particularly affecting the brain. Most neurodevelopmental processes (e.g. neuronal and/or glial genesis, differentiation, migration, synaptogenesis and myelination) are at least initiated, if not completed, during gestation.Reference Rice and Barone2 These processes are precisely governed by the brain's developmental clock, and any interference during gestation can result in its reprogramming, which can affect the risk for subsequent mental health problems.Reference O'Donnell and Meaney3

An important risk factor for altered neurodevelopmental programming is maternal stress during pregnancy. Preclinical research has demonstrated that maternal stress during gestation adversely affects behavioural and hormonal development.Reference Hamada and Matthews4 Although human studies have replicated these findings,Reference Howland, Sandman, Davis and Glynn5 a notable limitation is the ethical introduction of stress in human studies. Consequently, measures of human prenatal stress are generally broad, lack negative valence and typically consider everyday stressful events, which vary greatly among pregnant women. Quasi-experiments based on traumatic major disasters experienced by everyone have provided conditions in which highly acute stress is randomly assigned. Although such disasters have been increasing in occurrence, to date there have been only a few studies examining the impact of natural disasters (the Canadian Ice Storm,Reference Laplante, Brunet, Schmitz, Ciampi and King6 Hurricane KatrinaReference Xiong, Harville, Mattison, Elkind-Hirsch, Pridjian and Buekens7 and Superstorm SandyReference Nomura, Zhang and Hurd8,Reference Nomura, Rompala, Pritchett, Aushev, Chen and Hurd9 ) or human-made disasters (the Three Mile Island nuclear-plant explosion,Reference Hoffman and Hatch10 the Chernobyl nuclear plant explosion,Reference Huizink, Dick, Sihvola, Pulkkinen, Rose and Kaprio11 war and terrorismReference Meijer12,Reference Engel, Berkowitz, Wolff and Yehuda13 ) on child health outcomes.

To understand the long-term consequences of early life exposure to stress, a multifactorial conceptualisation of neurodevelopmental and psychiatric disease is emerging, in which multiple biologically significant events (or ‘hits’) are distributed across early life.Reference Koss and Gunnar14 One commonly used framework is the double-hit model,Reference van Camp, Cigalotti, Bouwalerh, Mairesse, Gatta and Palanza15 which posits that early life stressors, particularly those occurring during formative developmental periods, may render the organism more vulnerable to other stressors such that the joint effect of the two stressors is greater than the sum of their individual risks. In our current study, we assessed the ‘double-hit’ in children associated with prenatal exposure to stress associated with Superstorm Sandy and perinatal maternal cannabis use. We chose cannabis because the endocannabinoid system is a critical biological system in regulation of neurodevelopmental processes and modulation of stress effects.Reference Ruehle, Rey, Remmers and Lutz16 Moreover, the legalisation of cannabis and diminishing awareness of its risk is increasing cannabis use among women of reproductive age.Reference Ko, Farr, Tong, Creanga and Callaghan17 Given recent increases in both major disasters (including the recent COVID-19 pandemic) and cannabis use, examination of the double-hit model could provide considerable public health information regarding healthy child neurobehavioral development.

Method

This report follows the STROBE reporting guidelines for observational studies.

Participants

The study included mothers and their children from a longitudinal project (the Stress in Pregnancy (SIP) Study) that investigates the effects of prenatal psychosocial stress, such as that caused by Superstorm Sandy, on offspring development. Superstorm Sandy struck New York City in October 2012, leaving many dead and 8 million households without electricity; there were also gasoline shortages and public transport systems sustained damage.18

Pregnant women were initially recruited from two prenatal obstetrics clinics serving a racially and financially diverse population during their second trimester and followed throughout their pregnancy. Exclusion criteria included HIV infection, maternal psychosis, maternal age <15 years, life-threatening maternal medical complications, and congenital or chromosomal abnormalities of the fetus. For details, see Finik and Nomura (2017).Reference Finik and Nomura19 After the birth of the children, child–mother dyads (N = 358) were assessed annually. Among these, a subsample of 163 mothers with preschool-aged children (ages 2–5 years; mean (s.d.) = 3.19 (1.17)) were chosen for a diagnostic interview of psychiatric diagnostic outcomes. This subsample of preschool-aged participants did not differ significantly from the rest of the SIP cohort with respect to major demographic characteristics (Supplementary Table 1 available at https://doi.org/10.1192/bjo.2022.595).

All procedures contributing to this work complied with the ethical standards of the national and institutional committees on human experimentation and with the Helsinki Declaration of 1975, as revised in 2008. All procedures involving human subjects and/or patients were approved by the Institutional Review Board (IRB) at the City University of New York. All participants provided written consent according to the protocol approved by the same IRB.

Measures

Exposures

Prenatal superstorm sandy

Superstorm Sandy exposure status was defined as whether mothers were pregnant (N = 66, or 40.5%) or not (N = 97, or 59.5%) during the storm.

Perinatal cannabis use

Perinatal cannabis use was assessed during pregnancy and 24 months after the birth of the child. Prenatal cannabis use was ascertained using the Structured Clinical Interview for DSM-IV,Reference First, Gibbon, Hilsenroth and Segal20 conducted by trained clinical interviewers. Postnatal use was assessed using the Cannabis Use Disorders Identification Test-RevisedReference Adamson, Kay-Lambkin, Baker, Lewin and Thornton Kelly21 at 6, 12, 18 and 24 months and the Mini-International Neuropsychiatric interview at 24 months.Reference Sheehan, Lecrubier, Sheehan, Amorim, Janavs and Weiller22 Perinatal cannabis use was coded positive (1) for use prenatally or postnatally (6–24 months). Forty (24.5%) mothers reported perinatal cannabis use.

Outcomes

Primary measure

Child psychopathology

The Preschool Age Psychiatric Assessment (PAPA)Reference Egger, Angold, DelCarmen-Wiggins and Carter23 was used to ascertain diagnostic outcomes. PAPA is a diagnostic interview of caregivers assessing psychiatric disorders in children between the ages of 2–5 years. It is tailored to measure feelings and behaviours pertinent to young children and enables a definition of age-specific diagnostic criteria when considering developmental changes across the preschool period. The interviews were conducted by clinical interviewers with systematic training and monitoring from the designer of the instrument.Reference Egger, Erkanli, Keeler, Potts, Walter and Angold24 PAPA assesses various DSM-IV diagnostic criteria prevalent in young children, including phobia, anxiety disorders [separation anxiety disorder (SAD), selective mutism, generalised anxiety disorder (GAD), posttraumatic stress disorder (PTSD)], depressive disorders (major depression, dysthymia, and depressive disorders not otherwise specified), and disruptive behavioural disorders (DBDs) [conduct disorder, oppositional defiant disorder (ODD), and attention deficit/hyperactivity disorder (ADHD)]. When answers to gatekeeping questions for each diagnostic category were positive, the interviewers explored symptoms in depth and recorded frequency, duration, and age at first onset, based on a 3 month recall period, as well as lifetime occurrence and diagnoses. Diagnostic outcomes followed the DSM-IV diagnostic algorithms.

PAPA's reliability compares with those of measures widely used for older children and adults.Reference Egger, Erkanli, Keeler, Potts, Walter and Angold24 Interrater reliabilities were fair to good for dysthymia (k = 0.72), specific phobia (k = 0.46), social phobia (k = 0.54), SAD (k = 0.60), GAD (k = 0.59), selective mutism (k = 0.88), conduct disorder (k = 0.66), ODD (k = 0.62) and ADHD (k = 0.78).

Secondary measures

Postnatal parenting stress

Parenting Stress Index Short-formReference Abidin25 is a screening measure for identifying issues related to problems in the parent's or child's characteristics within the family unit. The three subscales capture problems within the family that influence the level of parenting stress. Those three subscales include parental distress (range 12–56), difficult child (range 12–57) and parent–child dysfunctional interaction (range 12–50). The total scale (range 36–138) captures the parenting stress within the family. The α for the total scale is 0.86.

Social support

MOS-Social Support SurveyReference Sherbourne, Stewart, Sherbourne and Stewart26 measures available social support in four distinct areas (emotional, tangible, affectionate and positive social interaction). The α for the subscales range from 0.91 to 0.96, with a value of 0.97 for the total score. Subscale and total scores range from 1 to 5.

Potential confounders

Child and maternal demographics

Child sex, child race, child ethnicity, maternal age, parents’ marital status, parity, and socioeconomic status (SES) were a priori determined as confounders. The child's race and ethnicity were reported by mothers. SES was extracted with four indicators (maternal education, pre-pregnancy occupation prestige,Reference Linver, Brooks-Gunn and Kohen27 work and welfare status) using latent class analysis.Reference Evans and Mills28 For details, see Nomura et al. (2021).Reference Nomura, Zhang and Hurd8

Normative prenatal stress

Normative prenatal stress was extracted using latent profile analysisReference Tein, Coxe and Cham29 with the Pregnancy-Related Anxiety Questionnaire-Revised (PRAQ-R),Reference Huizink, Delforterie, Scheinin, Tolvanen, Karlsson and Karlsson30 Perceived Stress Scale (PSS-14),Reference Cohen, Williamson, Spacapam and Oskamp31 life events,Reference Dohrenwend, Krasnoff, Askenasy and Dohrenwend32 maternal depression by the Edinburgh Postnatal Depression Scale (EPDS)Reference Murray and Carothers33 and anxiety by the State-Trait Anxiety Inventory (STAI),Reference Spielberger34 assessed during pregnancy. Internal consistency for the PRAQ-R, PSS-14, EPDS and STAI were α = 0.86, α = 0.91, α = 0.84 and α = 0.89, respectively.

Maternal substance use

Maternal substance use during pregnancy was ascertained via face-to-face clinical interview and self-report. Substances reported included tobacco, alcohol, cocaine, heroin, opioids, glue and prescription medications. Positive response was coded as 1, otherwise response was coded as 0.

Objective and subjective Superstorm Sandy-related traumas and challenges

Objective Superstorm Sandy-related challenge was assessed with Storm32,Reference Yong, Laplante, Elgbeili, Hillerer, Brunet and O'Hara35 which measures salient aspects of objective disaster exposure. Internal consistency was α = 0.90. Subjective (perceived) post-traumatic stress trauma symptoms were measured by the modified Impact of Events Scale-Revised.Reference Weiss, Marmar, Wilson and Keane36 The internal consistency was α = 0.91.

Statistical method

Children were grouped by maternal exposure status to Superstorm Sandy and cannabis. The exposure-group variable had four categories: children exposed to neither Superstorm Sandy nor cannabis (reference), Superstorm Sandy only, cannabis only, and both Superstorm Sandy and cannabis.

Cumulative lifetime risk of various psychiatric disorders was estimated using survival analysis techniques by means of a modified Kaplan–Meier method.Reference Williams37 Prior to the analysis, the proportional hazard assumption was tested with each diagnostic outcome, using the Schoenfeld residuals.Reference Schoenfeld38 Then, equality of survival distributions for the four groups was estimated using log-rank test. A Cox proportional hazards regression modelReference Cox39 was then used in three stages. The model in step 1 included sociodemographic and psychosocial confounders. The model in step 2 included postnatal psychosocial environment scales (family stress and social support) to evaluate the unique contribution of postnatal psychosocial environment over and above demographic and psychosocial confounders in step 1. In step 3, only the exposure group variable was included to evaluate the unique contribution of our exposures over and above contributions of the demographic confounders and postnatal psychosocial environment.

Lastly, to estimate the hazard risks of each diagnostic outcome, Cox proportional hazards regression models were then used in the three exposed groups relative to the reference group. Additive interaction – defined as the departure of disease rates from an additive model,Reference Rothman, Greenland and Walker40,Reference Li and Chambless41 based on Rothman's ‘index of synergism’ – was chosen to test the double-hit model. A synergy index was calculated to examine the magnitude of additive interaction. Synergy index values of 1 indicated that the sum of the two risks (Superstorm Sandy and cannabis use) equalled the risk of exposure to both, whereas synergy index values greater than 2 indicated appreciable synergistic acceleration of risk.Reference Rothman, Greenland and Walker40 To assess the significance of the synergy index, standard errors of each synergy index were calculated based on the approach of Cortina-Borja and colleagues.Reference Cortina-Borja, Smith, Combarros and Lehmann42 A 4 × 2 table of the numbers of cases and controls (of each disorder) in four groups by the two risks (Superstorm Sandy and cannabis use) was constructed. Then, with n 1, n 2 …. n 8 as the values of the eight cells, application of the delta methodReference Tanner43 yielded an asymptotic normal approximation to the standard error of ln(SI) as: $\sqrt {1/n_1 + 1/n_2 + \cdots + 1/n_8}$, where SI is the synergy index. The statistic Z = ln(SI)/s.e.(ln(SI)) had an asymptotically standard normal distribution under the null hypothesis of no interaction. We obtained P-values based on this method.

We then estimated the differences in levels of psychosocial family environment (family stress and social support) from 2–5 years of age. Generalised estimating equations (GEE)Reference Liang and Zeger44 facilitated analysis of longitudinal designsReference Ballinger45 by nesting multiple assessments at different ages and evaluating the overall differences among the four groups with all covariates. To explore group differences, pairwise comparisons were assessed a priori without adjustment of multiple testing.

The a priori level of significance, based on two-sided tests, was set at P = 0.05. All analyses were conducted using IBM SPSS Statistics, version 28.

Results

Demographic, psychosocial, and lifestyle characteristics

Table 1 shows the overall characteristics of the 163 participants as a whole and by exposure group; 53% were girls. Participants were racially diverse. In racial categories, 31 (19.0%) were Black, 15 (9.2%) were Asian and 50 (30.7%) were mixed or other non-White races. Ninety-four (57.7%) were Hispanic and 69 (42.3%) were non-Hispanic. There were no major differences among the four exposure groups with respect to major demographic variables. However, psychosocial and behavioural characteristics including cigarette smoking were more prevalent and normative prenatal stress (P = 0.01) was higher in the two cannabis exposure groups (cannabis-only and both Superstorm Sandy and cannabis).

Table 1 Demographic characteristics of the total sample population and subgroups

a. There were five cases with missing information. Reference group: no exposure to cannabis (CB) or Sandy Storm (SS); CB only: exposed to only cannabis; SS only: exposed to only SS; both: exposed to both cannabis and SS.

Proportional hazards assumption and differential risk of psychopathology by Superstorm Sandy and cannabis exposures

Inspection of the Schoenfeld residuals by our predictor on functions of time showed that there was no violation in the assumption with any of the diagnostic outcomes. Figure 1 shows the patterns of onset for any anxiety disorder (a) and any DBD (b) among children in the four groups. The test of equality of strata showed significant difference in the patterns of onset in any anxiety disorder (χ2(3) = 22.22, P < 0.0001) and any DBD (χ2(3) = 26.84, P < 0.0001). Among individual disorders, significant differences were found for SAD (P = 0.001), GAD (P < 0.0001), social phobia (P < 0.0001), dysthymia (P = 0.002), conduct disorder (P < 0.0001), ODD (P < 0.0001) and ADHD (P < 0.0001).

Fig. 1 Survival curves for any anxiety disorder and any disruptive behavioural disorder among children exposed to Superstorm Sandy (SS) and/or maternal cannabis (CB) use. Blue line, children not exposed to either SS or CB (N = 70); green line, children exposed to only CB (N = 27); red line, children exposed to only SS (N = 53); orange line, children exposed to both (N = 13). Significant difference among groups was found in the test of equality of strata (log-rank test), χ2(3) = 22.22, P < 0.0001 for any anxiety disorder and χ2(3) = 26.84, P < 0.0001 for any disruptive disorder. The cumulative risks of lifetime disorders were estimated after adjusting for confounders.

Table 2 shows the unique contribution of postnatal psychosocial factors (step 2) and exposure group (step 3) in diagnostic outcomes. With the exception of any depressive disorders, postnatal psychosocial environment on the composite disorder outcomes, including any anxiety (Δχ2(2) = 6.6, P = 0.04), any phobia (Δχ2(2) = 8.7, P = 0.01) and any DBD (Δχ2(2) = 7.1, P = 0.03), had significant contribution to the elevated cumulative risks over and above the confounders’ effects (column 3). Furthermore, our predictor (exposure group) was uniquely associated with elevated risks for any anxiety disorder (Δχ2(3) = 22.9, P < 0.001), any depressive disorder (Δχ2(2) = 12.1, P = 0.007) and any DBD (Δχ2(3) = 16.6, < 0.001) over and above what was already explained in steps 1 and 2 (column 4).

Table 2 The effect of exposures to maternal Superstorm Sandy (SS) and cannabis use (CB) in consideration of multiple potential confounders on child diagnostic outcomes

Log-rank test was used to estimate the equality of survival distributions among the four groups in survival analysis by means of a modified Kaplan–Meier method.

a. Step 1 includes all of the 11 covariates including child race and ethnicity, child sex, maternal age, marital status of the parents, parity, socioeconomic status, prenatal normative stress, prenatal substance use, post-traumatic stress symptoms related to SS and objective SS stress. χ2(11) represents the overall model fit of the covariates-only model

b. Step 2 includes an additional two indicators of postnatal environment (postnatal family stress and social support). Δχ2(2) shows the changes in the model fit from the covariates-only model (step 1).

c. Step 3 includes the exposure variable with four groups (neither, only CB, only SS, both CB and SS). Δχ2(3) shows the changes in the model fit from the previous (step 2).

Rates of individual disorders are shown in the first section of the column (cumulative rates over 5 years) in Table 3. For anxiety disorders, children exposed to both Superstorm Sandy and cannabis use had the highest rates of SAD (69.2%), GAD (46.2%) and selective mutism (7.7%), and over 75% had one form of anxiety disorder. Superstorm Sandy-only children had the next highest prevalence of anxiety disorders (37.7% SAD, 13.2% GAD and 47.2% any anxiety disorder), followed by cannabis-only children (18.5% SAD, 7.4% GAD and 25.9% any anxiety disorder). Within phobias, over 60% of children exposed to both and 18.5% in the cannabis-only group had social phobia. For DBDs, children exposed to both had the highest rates of any DBD (30.8%) – conduct disorder (15.4%), ODD (53.8%) and ADHD (46.2%) – followed by the two single exposure groups. The reference group, children exposed to neither, had the lowest rates of any DBD (2.9%) – conduct disorder (1.4%), ODD (2.9%) and ADHD (2.9%). Approximately one-quarter of children exposed to both Superstorm Sandy and cannabis use had dysthymia (23.1%).

Table 3 Risk of disorders among children with maternal cannabis (CB) and Superstorm Sandy (SS) exposure

a. Anxiety disorders do not include phobia and phobia does not include anxiety disorders.

RR = relative risk; SAD = separation anxiety disorder; GAD = generalised anxiety disorder; PTSD = post-traumatic stress disorder; MDD = major depressive disorder; DDNOS = depressive disorder – not otherwise specified; DBD = disruptive behavioural disorder; CD = conduct disorder; ODD = oppositional defiant disorder; ADHD = attention-deficit hyperactivity disorder.

Analysis was based on the proportional hazard model with covariates including child sex, child race, child ethnicity, maternal age, marital status of the parents, parity, family socioeconomic status, prenatal substance use, prenatal stress, post-traumatic stress symptoms due to Superstorm Sandy and severity of objective Superstorm Sandy exposures, as well as postnatal family stress and social support at age 3.

SI was calculated as follows. SAB = (hRAB−1)/(HRA + HRB−2); ln (SAB) = sqrt [Σnij ], where i is a subsample of each group for positive and j is for negative disorders.

Lifetime cumulative risks for each disorder were estimated for the three exposure groups relative to the reference group. These risks are shown in the second column of Table 3. A notable finding was the risk of DBDs for children exposed to both. These children had an over 31-fold increased risk for any DBD [hazard ratio (HR) = 31.2, P = 0.0002]. Among the specific DBDs, those exposed to both had a 26-fold increased risk for ADHD (HR = 26.3, P = 0.0003), a 16-fold increased risk for ODD (HR = 16.2, P = 0.004) and a 15-fold increased risk for conduct disorder (HR = 15.4, P = 0.005). Children exposed to both had a 54-fold increased risk for any depressive disorder (HR = 54.7, P = 0.03) and a more than seven-fold increased risk for any anxiety disorder (HR = 7.89, P = 0.0004). Among specific anxiety and depressive disorders, those exposed to both risks had a >54-fold increased risk for dysthymia (HR = 54.7, P = 0.03), a >48-fold increased risk for GAD (HR = 48.6, P = 0.0005) a >17-fold increased risk for social phobia (HR = 17.8, P = 0.0003) and a six-fold increased risk for SAD (HR = 6.6, P = 0.002). Children exposed to Superstorm Sandy only also had a substantial increased risk for any DBD (HR = 6.4, P = 0.03) and any anxiety disorder (HR = 3.3, P = 0.0002), whereas children exposed to cannabis only had an increased risk for any DBD (HR = 9.4, P = 0.01).

The synergy index for magnitude of additive interaction is shown in the third section of Table 3. Among overall categories, any DBD (synergy index, 2.06, P = 0.03) and any anxiety disorder (synergy index, 2.60, P = 0.004) showed significant synergistically increased risk. Among individual risks, risks for ADHD (synergy index, 13.30, P < 0.001), social phobia (synergy index, 6.57, P < 0.001), GAD (synergy index, 3.17, P = 0.006), SAD (synergy index, 2.90, P < 0.001), conduct disorder (synergy index, 2.32, P = 0.04) and ODD (synergy index, 1.98, P = 0.05) among children exposed to both were synergistically elevated.

Characteristics of postnatal family environment by exposure groups

Table 4 shows overall group differences in parenting stress and social support, and pairwise comparisons (last column) among the four groups. Generally, children exposed to both Superstorm Sandy and cannabis use had the highest levels of parenting stress and lowest levels of social support, followed by the cannabis-only group. Specifically, total parenting stress was highest in the group exposed to both. Available social support in all areas (emotional support, tangible support, affectionate support and positive social interaction) was lowest among the group exposed to both. However, families that experienced Superstorm Sandy only had comparable scores to the reference group that experienced neither Superstorm Sandy nor cannabis use.

Table 4 Characteristics of postnatal family environment in relation to maternal cannabis use and/or Superstorm Sandy exposure

a. The number refers to the group membership: group 1 (reference), exposed to neither cannabis (CB) nor Sandy Storm (SS); group 2 (CB only), exposed to only cannabis; group 3 (SS only), exposed to only SS; group 4 (both), exposed to both CB and SS. Only significant results from the pairwise comparisons are reported.

Analysis was based on the proportional hazard model with covariates including child sex, child race, child ethnicity, maternal age, marital status of the parents, parity, family socioeconomic status, prenatal substance use, prenatal stress, posttraumatic stress symptoms due to Superstorm Sandy and severity of objective Superstorm Sandy exposures.

Discussion

This investigation builds on our longitudinal study SIP study, which follows a cohort of mothers and children born around the time of Superstorm Sandy. To our knowledge, this is the first study to examine the joint effects of prenatal exposure to a major natural disaster and early life exposure to the mother's cannabis use on psychiatric outcomes among preschool-aged children. The results show that whereas both Superstorm Sandy and maternal cannabis use alone were associated with increased risks of DBDs and anxiety disorders, the synergistic risk of joint exposure was appreciably greater than the sum of the two individual risks, specifically for SAD, GAD, depressive disorders, social phobia, conduct disorder, ODD and ADHD. Our findings are consistent with the double-hit model of a synergistic impact of early life stress with cannabis exposure on future psychopathology risk.Reference van Camp, Cigalotti, Bouwalerh, Mairesse, Gatta and Palanza15

Our findings of heightened risks for developmental psychopathologies in children of mothers who experienced prenatal stress and perinatal cannabis use are in line with preclinical studies demonstrating that these prenatal environmental exposures can induce neurobehavioral disturbances relevant to psychopathology risk in offspring.Reference O'Donnell and Meaney3 Moreover, early life stress is known to affect the endocannabinoid system, which has been well documented to regulate biological stress processes. This strong interaction between stress and endocannabinoid systems, in turn, influences neural networks underlying the regulation of emotions.Reference Hill, Patel, Campolongo, Tasker, Wotjak and Brain46 The fact that the combination of stress and cannabis exposure resulted in a synergistically elevated risk for psychopathology has important public health and policy implications. However, as multiple factors need to be considered regarding the current population, caution must be used in interpreting the associations between cannabis, in addition to Superstorm Sandy, on child outcomes only in the framework of a double-hit model. Nevertheless, the results of this study provide an important foundation for future studies to replicate and expand aspects of causality.

Our study had several strengths. First, unlike most studies that define prenatal stress as everyday stress, maternal psychopathology or low SES, our study examined the effects of a large-scale natural disaster on developmental programming. Second, with the additional measurement of perinatal maternal cannabis use, we were able to obtain evidence of a synergistic, double-hit impact of both stressors on the risks of developmental psychopathology on offspring. Third, the use of a structured interview for child psychopathology instead of a caregiver-report scale, provided greater confidence in our estimates of increased risks for developmental psychopathology. Fourth, there are strengths in the use of longitudinal statistics: survival analysis enabled us to estimate the cumulative risk of each disorder over the first 5 years of life; and GEE enabled us to leverage the parallel measure of postnatal psychosocial family environment assessed annually from 2–5 years of age. GEE evaluate differences in postnatal stress and social support while incorporating missing data and intra-correlations within the individual participants. Fifth, the study provided a real-life model of the significant consequences of altered neurodevelopmental programming.

Our study also had limitations. It was based on a sample of 163 children, which was a subsample of a larger cohort (N = 358), as only children of preschool age were given the structural clinical interviews. However, as Supplementary Table 1 shows, there were no notable differences in demographic and stress variables between the subsample and the rest of the sample. Second, although clinical interviews are the gold standard for measuring preschool psychopathology, there is still the risk of shared variance due to having the same caregiver provide all reports. It is also known that maternal depression can influence mothers’ ratings of their children. We attempted to mitigate this risk by controlling for normative stress extracted by the latent profile analysis including maternal depression, anxiety and perceived stress. Third, although the data indicated increased synergistic risk for psychopathology in young children exposed to both Superstorm Sandy and cannabis use, the sample size of this highest risk group was small (n = 13), and it is possible that the small sample size may have inflated the risk estimates, leading to a lack of generalisability. However, it is important to note that we examined the cumulative risk over time (i.e., HR). HRs provide more accurate and robust estimates than odds ratios when estimates are based on a small sample size. Nevertheless, readers should interpret the magnitude of risks, especially for ADHD, conduct disorder and ODD, with caution. Fourth, there were no psychiatric diagnoses of mothers and fathers, which may have genetic contributions to offspring's diagnostic outcomes. Fifth, although exposure timing during pregnancy is an important developmental factor, our relatively small sample size (n = 163) prohibited further division by trimester of the exposed group. Finally, although our results show a robust and alarming increased risk associated with exposure to both Superstorm Sandy and cannabis use over and above various potential confounders and the postnatal psychosocial family environment in the staged analysis, it is still possible that other important confounders were overlooked. For example, perinatal cannabis exposure could be associated with the mother's prior abuse history.Reference Marroun H, Tiemeier, Jaddoe, Hofman, Mackenbach and Steegers47 Moreover, potential neurotoxicity associated with early-life exposure to cannabis was not examined in the offspring.

The current findings have significant public health implications, given the increasing frequency of major disasters (e.g., the COVID-19 pandemic, wildfires and extreme tropical storms) and the increase in legalisation and use of cannabis, especially among women under stress.Reference Hill, Patel, Campolongo, Tasker, Wotjak and Brain46 It is critical not only to acknowledge and tend to the needs of pregnant women given the enormous potential impact of stress from such disasters but also to educate and caution around the use of cannabis, be it recreational or to cope with life stressors.

Supplementary material

Supplementary material is available online at https://doi.org/10.1192/bjo.2022.595.

Data availability

The data that support the findings of this study are available from the corresponding author (Y.N.) upon reasonable request.

Acknowledgements

We thank the children and parents who consented to participate in this study. We thank Yvette Caro, Ph.D., and Katie Dana, Ph.D., for clinical interviews and former research staff and assistants at Queens College, CUNY, for their contributions to this study. Y.N. had full access to all data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

Author contributions

All authors meet four criteria in ICMJE for authorship. Y.N. formulated the research questions and designed the study. Y.N., J.H., P.M.P., L.P., S.R., V.J.H. and Y.L.H. carried out the study. Y.N., W.W. and P.J.W. analysed and interpreted the data. Y.N., J.H., P.M.P., L.P., S.R., N.S.F., V.J.H., P.J.W. and Y.L.H. wrote the article.

Funding

This research was supported by grant R01MH102729 from the National Institute of Mental Health and a PSC-CUNY, Queens College Research Enhancement, grant (to Y.N.) and by grant R01DA030359 from the National Institutes of Drug Abuse (to Y.L.H.).

Declaration of interest

None.

References

Barker, DJ. The Wellcome Foundation Lecture, 1994. The fetal origins of adult disease. Proc Biol Sci 1995; 262: 3743.Google ScholarPubMed
Rice, D, Barone, S Jr. Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models. Environ Health Perspect 2000; 108(Suppl 3): 511–33.Google ScholarPubMed
O'Donnell, KJ, Meaney, MJ. Fetal origins of mental health: the developmental origins of health and disease hypothesis. Am J Psychiatry 2017; 174: 319–28.CrossRefGoogle ScholarPubMed
Hamada, H, Matthews, SG. Prenatal programming of stress responsiveness and behaviours: progress and perspectives. J Neuroendocrinol 2019; 31: e12674.CrossRefGoogle Scholar
Howland, MA, Sandman, CA, Davis, EP, Glynn, LM. Prenatal maternal psychological distress and fetal developmental trajectories: associations with infant temperament. Dev Psychopathol 2020; 32: 1685–95.CrossRefGoogle ScholarPubMed
Laplante, DP, Brunet, A, Schmitz, N, Ciampi, A, King, S. Project Ice Storm: prenatal maternal stress affects cognitive and linguistic functioning in 5 1/2-year-old children. J Am Acad Child Adolesc Psychiatry 2008; 47: 1063–72.CrossRefGoogle ScholarPubMed
Xiong, X, Harville, EW, Mattison, DR, Elkind-Hirsch, K, Pridjian, G, Buekens, P. Exposure to Hurricane Katrina, post-traumatic stress disorder and birth outcomes. Am J Med Sci 2008; 336: 111–5.CrossRefGoogle ScholarPubMed
Nomura, Y, Zhang, W, Hurd, YL. Stress in pregnancy: clinical and adaptive behavior of offspring following Superstorm Sandy. Dev Psychopathol 2021: 111.Google ScholarPubMed
Nomura, Y, Rompala, G, Pritchett, L, Aushev, V, Chen, J, Hurd, YL. Natural disaster stress during pregnancy is linked to reprogramming of the placenta transcriptome in relation to anxiety and stress hormones in young offspring. Mol Psychiatry 2021; 26(11): 6520–30.CrossRefGoogle ScholarPubMed
Hoffman, S, Hatch, MC. Depressive symptomatology during pregnancy: evidence for an association with decreased fetal growth in pregnancies of lower social class women. Health Psychol 2000; 19(6): 535–43.CrossRefGoogle ScholarPubMed
Huizink, AC, Dick, DM, Sihvola, E, Pulkkinen, L, Rose, RJ, Kaprio, J. Chernobyl exposure as stressor during pregnancy and behaviour in adolescent offspring. Acta Psychiatr Scand 2007; 116: 438–46.CrossRefGoogle ScholarPubMed
Meijer, A. Child psychiatric sequelae of maternal war stress. Acta Psychiatr Scand 1985; 72: 505–11.CrossRefGoogle ScholarPubMed
Engel, SM, Berkowitz, GS, Wolff, MS, Yehuda, R. Psychological trauma associated with the World Trade Center attacks and its effect on pregnancy outcome. Paediatr Perinat Epidemiol 2005; 19: 334–41.CrossRefGoogle ScholarPubMed
Koss, KJ, Gunnar, MR. Annual research review: early adversity, the hypothalamic-pituitary-adrenocortical axis, and child psychopathology. J Child Psychol Psychiatry 2018; 59: 327–46.CrossRefGoogle ScholarPubMed
van Camp, G, Cigalotti, J, Bouwalerh, H, Mairesse, J, Gatta, E, Palanza, P, et al. Consequences of a double hit of stress during the perinatal period and midlife in female rats: mismatch or cumulative effect? Psychoneuroendocrinol 2018; 93: 4555.CrossRefGoogle ScholarPubMed
Ruehle, S, Rey, AA, Remmers, F, Lutz, B. The endocannabinoid system in anxiety, fear memory and habituation. J Psychopharmacol 2012; 26: 2339.CrossRefGoogle ScholarPubMed
Ko, JY, Farr, SL, Tong, VT, Creanga, AA, Callaghan, WM. Prevalence and patterns of marijuana use among pregnant and nonpregnant women of reproductive age. Am J Obstet Gynecol 2015; 213(2): 201.e1–10.CrossRefGoogle ScholarPubMed
Centers for Disease Control and Prevention (CDC). Deaths associated with hurricane Sandy-October-November 2012. MMWR Morb Mortal Wkly Rep 2013; 62(20): 393–7.Google Scholar
Finik, J, Nomura, Y. Cohort profile: stress in pregnancy (SIP) study. Int J Epidemiol 2017; 46: 1388–k. Available from: https://doi.org/10.1093/ije/dyw264.Google ScholarPubMed
First, MB, Gibbon, M. The structured clinical interview for DSM-IV Axis I Disorders (SCID-I) and the structured clinical interview for DSM-IV Axis II Disorders (SCID-II). In Comprehensive Handbook of Psychological Assessment, Vol. 2: Personality Assessment (eds Hilsenroth, MJ, Segal, DL): 134–43. John Wiley & Sons, Inc., 2004.Google Scholar
Adamson, SJ, Kay-Lambkin, FJ, Baker, AL, Lewin, TJ, Thornton Kelly, BJ, et al. An improved brief measure of cannabis misuse: the cannabis use disorders identification test-revised (CUDIT-R). Drug Alcohol Depend 2010; 110: 137–43.CrossRefGoogle ScholarPubMed
Sheehan, DV, Lecrubier, Y, Sheehan, KH, Amorim, P, Janavs, J, Weiller, E, et al. The mini-international neuropsychiatric interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. J Clin Psychiatry 1998; 59(Suppl 20): 2233.Google ScholarPubMed
Egger, HL, Angold, A. The Preschool Age Psychiatric Assessment (PAPA): a structured parent interview for diagnosing psychiatric disorders in preschool children. In Handbook of Infant, Toddler, and Preschool Mental Health Assessment (eds DelCarmen-Wiggins, R, Carter, A): 223–43. Oxford University Press, 2004.Google Scholar
Egger, HL, Erkanli, A, Keeler, G, Potts, E, Walter, BK, Angold, A. Test-retest reliability of the preschool age psychiatric assessment (PAPA). J Am Acad Child Adolesc Psychiatry 2006; 45: 538–49.CrossRefGoogle ScholarPubMed
Abidin, RR. Parenting Stress Index (4th edn). PAR, 2012.Google Scholar
Sherbourne, CD, Stewart, AL, Sherbourne, CD, Stewart, AL. MOS social support survey. Soc Sci Med 1991; 32: 705–14.CrossRefGoogle ScholarPubMed
Linver, MR, Brooks-Gunn, J, Kohen, DE. Family processes as pathways from income to young children's development. Dev Psychol 2002; 38: 719–34.CrossRefGoogle ScholarPubMed
Evans, GE, Mills, C. Identifying class structure: a latent class analysis of the criterion-related and construct validity of the Goldthorpe class schema. Euro Sociol Rev 1998; 14: 87106.CrossRefGoogle Scholar
Tein, JY, Coxe, S, Cham, H. Statistical power to detect the correct number of classes in latent profile analysis. Struct Equ Modeling 2013; 20(4): 640–57.CrossRefGoogle ScholarPubMed
Huizink, AC, Delforterie, MJ, Scheinin, NM, Tolvanen, M, Karlsson, L, Karlsson, H. Adaption of pregnancy anxiety questionnaire-revised for all pregnant women regardless of parity: PRAQ-R2. Arch Womens Ment Health 2016; 19: 125–32.CrossRefGoogle ScholarPubMed
Cohen, S, Williamson, G. Perceived stress in a probability sample of the United States. In The Social Psychology of Health: Claremont Symposium on Applied Social Psychology (eds Spacapam, S, Oskamp, S). Sage, 1988.Google Scholar
Dohrenwend, BS, Krasnoff, L, Askenasy, AR, Dohrenwend, BP. Exemplification of a method for scaling life events: the peri life events scale. J Health Soc Behav 1978; 19: 205–29.CrossRefGoogle ScholarPubMed
Murray, L, Carothers, AD. The validation of the Edinburgh post-natal depression scale on a community sample. Br J Psychiatry 1990; 157: 288–90.CrossRefGoogle ScholarPubMed
Spielberger, CD. State-Trait Anxiety Inventory (2nd edn). Consulting Psychologists Press, 1989.Google Scholar
Yong, PE, Laplante, DP, Elgbeili, G, Hillerer, KM, Brunet, A, O'Hara, M, et al. Prenatal maternal stress predicts stress reactivity at 2½ years of age: the Iowa flood study. Psychoneuroendocrinol 2015; 56: 6278.CrossRefGoogle Scholar
Weiss, DS, Marmar, CR. The Impact of Event Scale-Revised. In Assessing Psychological Trauma and PTSD (eds Wilson, JP, Keane, TM): 399411. Guilford Press, 1997.Google Scholar
Williams, RL. Product-limit survival functions with correlated survival times. Lifetime Data Anal 1995; 1: 171–86.CrossRefGoogle ScholarPubMed
Schoenfeld, D. Partial residuals for the proportional hazards regression model. Biometrika 1982; 69(1): 239–41.CrossRefGoogle Scholar
Cox, DR. Regression models and life-tables. J R Stat Soc Series B Stat Methodol 1972; 34(2): 187220.Google Scholar
Rothman, KJ, Greenland, S, Walker, AM. Concepts of interaction. Am J Epidemiol 1980; 112(4): 467–70.CrossRefGoogle ScholarPubMed
Li, R, Chambless, L. Test for additive interaction in proportional hazards models. Ann Epidemiol 2007; 17(3): 227–36.CrossRefGoogle ScholarPubMed
Cortina-Borja, M, Smith, AD, Combarros, O, Lehmann, DJ. The synergy factor: a statistic to measure interactions in complex diseases. BMC Res Notes 2009; 2: 105.CrossRefGoogle ScholarPubMed
Tanner, MA. Tools for Statistical Inference: Observed Data and Data Augmentation Methods. Springer-Verlag, 1991.CrossRefGoogle Scholar
Liang, KY, Zeger, SL. Longitudinal data analysis using generalized linear models. Biometrika 1986; 73(1): 1322.CrossRefGoogle Scholar
Ballinger, GA. Using generalized estimating equations for longitudinal data analysis. Organ Res Methods 2004; 7(2): 127–50.CrossRefGoogle Scholar
Hill, MN, Patel, S, Campolongo, P, Tasker, JG, Wotjak, CT, Brain, JS. Functional interactions between stress and the endocannabinoid system: from synaptic signaling to behavioral output. J Neuroscience 2010; 30(45): 14980–6.CrossRefGoogle ScholarPubMed
Marroun H, E, Tiemeier, H, Jaddoe, VW, Hofman, A, Mackenbach, JP, Steegers, EA, et al. Demographic, emotional and social determinants of cannabis use in early pregnancy: the generation R study. Drug Alcohol Depend 2008; 98(3): 218–26.CrossRefGoogle ScholarPubMed
Figure 0

Table 1 Demographic characteristics of the total sample population and subgroups

Figure 1

Fig. 1 Survival curves for any anxiety disorder and any disruptive behavioural disorder among children exposed to Superstorm Sandy (SS) and/or maternal cannabis (CB) use. Blue line, children not exposed to either SS or CB (N = 70); green line, children exposed to only CB (N = 27); red line, children exposed to only SS (N = 53); orange line, children exposed to both (N = 13). Significant difference among groups was found in the test of equality of strata (log-rank test), χ2(3) = 22.22, P < 0.0001 for any anxiety disorder and χ2(3) = 26.84, P < 0.0001 for any disruptive disorder. The cumulative risks of lifetime disorders were estimated after adjusting for confounders.

Figure 2

Table 2 The effect of exposures to maternal Superstorm Sandy (SS) and cannabis use (CB) in consideration of multiple potential confounders on child diagnostic outcomes

Figure 3

Table 3 Risk of disorders among children with maternal cannabis (CB) and Superstorm Sandy (SS) exposure

Figure 4

Table 4 Characteristics of postnatal family environment in relation to maternal cannabis use and/or Superstorm Sandy exposure

Supplementary material: File

Nomura et al. supplementary material

Table S1

Download Nomura et al. supplementary material(File)
File 22.1 KB
Submit a response

eLetters

No eLetters have been published for this article.