Abstract
Stress following preterm birth can disrupt the emerging foundation of the neonatal brain. The current study examined how structural brain development is affected by a stressful early environment and whether changes in topological architecture at term-equivalent age could explain the increased vulnerability for behavioral symptoms during early childhood. Longitudinal changes in structural brain connectivity were quantified using diffusion-weighted imaging (DWI) and tractography in preterm born infants (gestational age,28 weeks), imaged at 30 and/or 40 weeks of gestation (N = 145, 43.5% female). A global index of postnatal stress was determined based on the number of invasive procedures during hospitalization (e.g., heel lance). Higher stress levels impaired structural connectivity growth in a subnetwork of 48 connections (p = 0.003), including the amygdala, insula, hippocampus, and posterior cingulate cortex. Findings were replicated in an independent validation sample (N = 123, 39.8% female, n = 91 with follow-up). Classifying infants into vulnerable and resilient based on having more or less internalizing symptoms at two to five years of age (n = 71) revealed lower connectivity in the hippocampus and amygdala for vulnerable relative to resilient infants (p< 0.001). Our findings suggest that higher stress exposure during hospital admission is associated with slower growth of structural connectivity. The preservation of global connectivity of the amygdala and hippocampus might reflect a stress-buffering or resilience-enhancing factor against a stressful early environment and early-childhood internalizing symptoms.
Original language | English |
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Pages (from-to) | 8948-8959 |
Number of pages | 12 |
Journal | Journal of Neuroscience |
Volume | 42 |
Issue number | 48 |
Early online date | 14 Nov 2022 |
DOIs | |
Publication status | Published - 30 Nov 2022 |
Bibliographical note
Funding Information:Received Jan. 21, 2022; revised June 29, 2022; accepted July 7, 2022. Author contributions: F.L., M.J.N.L.B., E.J.H., M.L.T., J.D., C.H.V., and M.P.v.d.H. designed research; F.L. performed research; F.L. and M.P.v.d.H. analyzed data; F.L. wrote the first draft of the paper; F.L., M.J.N.L.B., E.J.H., M.L.T., J.D., C.H.V., and M.P.v.d.H. edited the paper; F.L. wrote the paper. F.L. was supported by the Wilhelmina Children’s Hospital Grant D-17-010007. M.P.v.d.H. was supported by the Netherlands Organization for Scientific Research (NWO) VIDI Grant 452-16-015 and the European Research Council Grant ERC-2020-CoG 101001062. E.J.H. was supported by the European Research Council Grant ERC-2015-CoG 682591. The authors declare no competing financial interests. Correspondence should be addressed to Femke Lammertink at [email protected]. https://doi.org/10.1523/JNEUROSCI.0176-22.2022 Copyright © 2022 the authors
Publisher Copyright:
Copyright © 2022 the authors.
Funding
Received Jan. 21, 2022; revised June 29, 2022; accepted July 7, 2022. Author contributions: F.L., M.J.N.L.B., E.J.H., M.L.T., J.D., C.H.V., and M.P.v.d.H. designed research; F.L. performed research; F.L. and M.P.v.d.H. analyzed data; F.L. wrote the first draft of the paper; F.L., M.J.N.L.B., E.J.H., M.L.T., J.D., C.H.V., and M.P.v.d.H. edited the paper; F.L. wrote the paper. F.L. was supported by the Wilhelmina Children’s Hospital Grant D-17-010007. M.P.v.d.H. was supported by the Netherlands Organization for Scientific Research (NWO) VIDI Grant 452-16-015 and the European Research Council Grant ERC-2020-CoG 101001062. E.J.H. was supported by the European Research Council Grant ERC-2015-CoG 682591. The authors declare no competing financial interests. Correspondence should be addressed to Femke Lammertink at [email protected]. https://doi.org/10.1523/JNEUROSCI.0176-22.2022 Copyright © 2022 the authors
Funders | Funder number |
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European Research Council | ERC-2015-CoG 682591 |
Horizon 2020 Framework Programme | 101001062 |
NWO | 452-16-015 |
Wilhelmina Kinderziekenhuis | D-17-010007 |
Keywords
- brain development
- diffusion MRI
- internalizing symptoms
- postnatal stress
- prematurity
- resilience