The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.
Superstorm Sandy exposure in utero is associated with neurobehavioral phenotypes and brain structure alterations in childhood: A machine learning approach
Abstract
Introduction: Prenatal maternal stress (PNMS), including exposure to natural disasters, has been shown to serve as a risk factor for future child psychopathology and suboptimal brain development, particularly among brain regions shown to be sensitive to stress and trauma exposure. However, statistical approaches deployed in most studies are usually constrained by a limited number of variables for the sake of statistical power. Explainable machine learning, on the other hand, enables the study of high data dimension and offers novel insights into the prominent subset of behavioral phenotypes and brain regions most susceptible to PNMS. In the present study, we aimed to identify the most important child neurobehavioral and brain features associated with in utero exposure to Superstorm Sandy (SS). Methods: By leveraging an explainable machine learning technique, the Shapley additive explanations method, we tested the marginal feature effect on SS exposures and examined the individual variable effects on disaster exposure. Results: Results show that certain brain regions are especially sensitive to in utero exposure to SS. Specifically, in utero SS exposure was associated with larger gray matter volume (GMV) in the right caudate, right hippocampus, and left amygdala and smaller GMV in the right parahippocampal gyrus. Additionally, higher aggression scores at age 5 distinctly correlated with SS exposure. Discussion: These findings suggest in utero SS exposure may be associated with greater aggression and suboptimal developmental alterations among various limbic and basal ganglia brain regions.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“in utero exposure to disaster-related stress may be associated with larger amygdala and hippocampal volumes and higher aggression at age 5. 30,31”
From Environmental roots of neonatal health: how social and structural exposures shape early-life outcomes (2026) · cites this paper as [30]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Antenatal maternal stress and long‐term effects on child neurodevelopment: how and why?
Talge, N. M., Neal, C., Glover, V., & the Early Stress, T. R. A. P. S. N. F. A. N. E. O. C. A. A. M. H. (2007) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2006.01714.x · Cited by 1,349
Neurobiology of Aggression and Violence
Siever, L. J. (2008) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2008.07111774 · Cited by 984
Prenatal developmental origins of future psychopathology: mechanisms and pathways
Monk, C., Lugo-Candelas, C., & Trumpff, C. (2019) · Annual Review of Clinical Psychology · doi:10.1146/annurev-clinpsy-050718-095539 · Cited by 388
Qin, S., Young, C. B., Duan, X., Chen, T., Supekar, K., & Menon, V. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.10.006 · Cited by 249
Lebel, C., Walton, M., Letourneau, N., Giesbrecht, G. F., Kaplan, B. J., & Dewey, D. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.12.004 · Cited by 237
Wen, D. J., Poh, J. S., Ni, S. N., Chong, Y.-S., Chen, H., Kwek, K., Shek, L. P., Gluckman, P. D., Fortier, M. V., Meaney, M. J., et al. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.74 · Cited by 186 · cited 7×
“MRI serves as an unparalleled technology to pinpoint the structural and functional brain changes in various brain regions of the limbic system, such as the amygdala and hippocampus, and frontal lobe, such as the prefrontal cortex, among offspring exposed to PNMS and how those changes underlie the consequent neurobehavi…”
BackgroundResultInfluentialWu, Y., Espinosa, K. M., Barnett, S. D., Kapse, A., Quistorff, J. L., Lopez, C., Andescavage, N., Pradhan, S., Lu, Y.-C., Kapse, K., et al. (2022) · JAMA Network Open · doi:10.1001/jamanetworkopen.2022.9244 · Cited by 113
El Marroun, H., Tiemeier, H., Muetzel, R. L., Thijssen, S., van der Knaap, N. J. F., Jaddoe, V. W. V., Fernández, G., Verhulst, F. C., & White, T. J. H. (2016) · Depression and Anxiety · doi:10.1002/da.22524 · Cited by 62
Research works printed but not linked: 39
- Acosta, 2019, Maternal pregnancy-related anxiety is associated with sexually dimorphic alterations in amygdala volume in 4-year-old children., Front. Behav. Neurosci., 13, 10.3389/fnbeh.2019.00175 · DOI · Paper page
- Bhatt, 2012, Distinct contributions of the amygdala and parahippocampal gyrus to suspicion in a repeated bargaining game., Proc. Natl. Acad. Sci. U.S.A., 109, 8728, 10.1073/pnas.1200738109 · DOI
- Bi, 2019, What is machine learning? A primer for the epidemiologist., Am. J. Epidemiol., 188, 2222, 10.1093/aje/kwz189 · DOI
- Buss, 2010, High pregnancy anxiety during mid-gestation is associated with decreased gray matter density in 6–9-year-old children., Psychoneuroendocrinology, 35, 141, 10.1016/j.psyneuen.2009.07.010 · DOI · Paper page
- Buss, 2012, Maternal cortisol over the course of pregnancy and subsequent child amygdala and hippocampus volumes and affective problems., Proc. Natl. Acad. Sci. U.S.A., 109, E1312, 10.1073/pnas.1201295109 · DOI · Paper page
- Cao-Lei, 2021, Prenatal maternal stress from a natural disaster and hippocampal volumes: Gene-by-environment interactions in young adolescents from project ice storm., Front. Behav. Neurosci., 15, 10.3389/fnbeh.2021.706660 · DOI
- Clemens, 2020, Report of the intergovernmental panel on climate change: Implications for the mental health policy of children and adolescents in Europe—a scoping review., Eur. Child Adolesc. Psychiatry, 31, 701, 10.1007/s00787-020-01615-3 · DOI · Paper page
- Chawla, 2002, SMOTE: Synthetic minority over-sampling technique., J. Artif. Intel. Res., 16, 321
- Crippa, 2015, Use of machine learning to identify children with autism and their motor abnormalities., J. Autism Dev. Disord., 45, 2146, 10.1007/s10803-015-2379-8 · DOI · Paper page
- Dale, 1999, Cortical surface-based analysis: I. Segmentation and surface reconstruction., Neuroimage, 9, 179, 10.1006/nimg.1998.0395 · DOI · Paper page
- Davis, 2017, Prenatal maternal cortisol concentrations predict neurodevelopment in middle childhood., Psychoneuroendocrinology, 75, 56, 10.1016/j.psyneuen.2016.10.005 · DOI · Paper page
- Dessie, 2021, A novel miRNA-based classification model of risks and stages for clear cell renal cell carcinoma patients., BMC Bioinformatics, 22, 10.1186/s12859-021-04189-2 · DOI
- Driscoll, 2022, Neuroanatomy, nucleus caudate, StatPearls.
- Elreedy, 2019, A comprehensive analysis of synthetic minority oversampling technique (SMOTE) for handling class imbalance., Inform. Sci., 505, 32, 10.1016/j.ins.2019.07.070 · DOI
- Finik, 2017, Cohort profile: Stress in pregnancy (SIP) study., Int. J. Epidemiol., 46, 1388, 10.1093/ije/dyw264 · DOI
- Glover, 2011, Annual research review: Prenatal stress and the origins of psychopathology: An evolutionary perspective., J. Child Psychol. Psychiatry, 52, 356, 10.1111/j.1469-7610.2011.02371.x · DOI · Paper page
- Güven, 2020, Combining functional near-infrared spectroscopy and EEG measurements for the diagnosis of attention-deficit hyperactivity disorder., Neural Comput. Appl., 32, 8367, 10.1007/s00521-019-04294-7 · DOI
- Jones, 2019, Larger amygdala volume mediates the association between prenatal maternal stress and higher levels of externalizing behaviors: Sex specific effects in project ice storm., Front. Hum. Neurosci., 13, 10.3389/fnhum.2019.00144 · DOI · Paper page
- King, 2012, Using natural disasters to study the effects of prenatal maternal stress on child health and development., Birth Defects Res. Part C Embryo Today Rev., 96, 273, 10.1002/bdrc.21026 · DOI · Paper page
- Lafortune, 2021, Effect of natural disaster-related prenatal maternal stress on child development and health: A meta-analytic review., Int. J. Environ. Res. Public Health, 18, 10.3390/ijerph18168332 · DOI
- Lautarescu, 2020, Prenatal stress: Effects on fetal and child brain development., Int. Rev. Neurobiol., 150, 17, 10.1016/bs.irn.2019.11.002 · DOI · Paper page
- Little, 2020, Multivariate models of brain volume for identification of children and adolescents with fetal alcohol spectrum disorder., Hum. Brain Mapp., 41, 1181, 10.1002/hbm.24867 · DOI
- Loomans, 2013, Psychosocial stress during pregnancy is related to adverse birth outcomes: Results from a large multi-ethnic community-based birth cohort., Eur. J. Public Health, 23, 485, 10.1093/eurpub/cks097 · DOI · Paper page
- Mareckova, 2022, Prenatal stress and its association with amygdala-related structural covariance patterns in youth., NeuroImage Clin., 34, 10.1016/j.nicl.2022.102976 · DOI
- Nomura, 2022, Stress in pregnancy: Clinical and adaptive behavior of offspring following Superstorm Sandy., Dev. Psychopathol., 34, 1249, 10.1017/S0954579421000304 · DOI
- Oskar, 2020, Machine learning within studies of early-life environmental exposures and child health: Review of the current literature and discussion of next steps., Curr. Environ. Health Rep., 7, 170, 10.1007/s40572-020-00282-5 · DOI
- Park, 2021, Deep learning feature extraction approach for hematopoietic cancer subtype classification., Int. J. Environ. Res. Public Health, 18, 10.3390/ijerph18042197 · DOI
- Reynolds, 2010, Behavior assessment system for children, Corsini. Encycl. Psychol., 1
- Reynolds, 2004, BASC-2: Behavior assessment system for children, 121
- Ring, 2002, Neuropsychiatry of the basal ganglia., J. Neurol. Neurosurg. Psychiatry, 72, 12, 10.1136/jnnp.72.1.12 · DOI
- Rodriguez, 2021, Detection of prenatal alcohol exposure using machine learning classification of resting-state functional network connectivity data., Alcohol, 93, 25, 10.1016/j.alcohol.2021.03.001 · DOI
- Sartori, 2018, Volumetric brain magnetic resonance imaging predicts functioning in bipolar disorder: A machine learning approach., J. Psychiatr. Res., 103, 237, 10.1016/j.jpsychires.2018.05.023 · DOI
- Saxe, 2017, Machine learning methods to predict child posttraumatic stress: A proof-of-concept study., BMC Psychiatry, 17, 10.1186/s12888-017-1384-1 · DOI
- Thijssen, 2015, Brain morphology of childhood aggressive behavior: A multi-informant study in school-age children., Cogn. Affect. Behav. Neurosci., 15, 564, 10.3758/s13415-015-0344-9 · DOI
- Tisdall, 2012, Volumetric navigators for prospective motion correction and selective reacquisition in neuroanatomical MRI., Magn. Reson. Med., 68, 389, 10.1002/mrm.23228 · DOI
- Van den Bergh, 2020, Prenatal developmental origins of behavior and mental health: The influence of maternal stress in pregnancy., Neurosci. Biobehav. Rev., 117, 26, 10.1016/j.neubiorev.2017.07.003 · DOI · Paper page
- Watts, 2021, Predicting offenses among individuals with psychiatric disorders-A machine learning approach., J. Psychiatr. Res., 138, 146, 10.1016/j.jpsychires.2021.03.026 · DOI
- Zakrison, 2020, The medical, public health, and emergency response to the impact of 2017 hurricane Irma in Cuba., Disaster Med. Public Health Prep., 14, 10, 10.1017/dmp.2019.71 · DOI
- Zhu, 2019, Emotion regulation of hippocampus using real-time fMRI neurofeedback in healthy human., Front. Hum. Neurosci., 13, 10.3389/fnhum.2019.00242 · DOI
Cited by
Nawaz, K., Babata, K., Scheid, L., Bitar, L., Ortiz, N. V., Kota, S., & Chalak, L. F. (2026) · Pediatric Research · doi:10.1038/s41390-026-05139-5 · Cited by 1
Metadata
- Authors
- Demirci, G. M., DeIngeniis, D., Wong, W. M., Shereen, A. D., Nomura, Y., & Tsai, C.-L.
- Venue
- Frontiers in Neuroscience
- Publisher
- Frontiers Media SA
- Published
- 2023-02-02
- Volume
- 17
- ISSN
- 1662-453X
- Cited by
- 8
- References
- 8
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.