Cited by 1,432Maternal Mental Health During Pregnancy and PostpartumStress Responses and CortisolEpigenetics and DNA Methylation

Prenatal exposure to maternal depression, neonatal methylation of human glucocorticoid receptor gene (NR3C1) and infant cortisol stress responses

Open access
Oberlander, Tim F., Weinberg, Joanne, Papsdorf, Michael, Grunau, Ruth, Misri, Shaila, Devlin, Angela M.·2008·Epigenetics

Abstract

BACKGROUND: In animal models, variations in early maternal care are associated with differences in hypothalamic-pituitary-adrenal(HPA) stress response in the offspring, mediated via changes in the epigenetic regulation of glucocorticoid receptor (GR) gene (Nr3c1) expression. OBJECTIVE: To study this in humans, relationships between prenatal exposure to maternal mood and the methylation status of a CpG-rich region in the promoter and exon 1F of the human GR gene (NR3C1) in newborns and HPA stress reactivity at age three months were examined. RESULTS: Prenatal exposure to increased third trimester maternal depressed/anxious mood was associated with increased methylation of NR3C1 at a predicted NGFI-A binding site. Increased NR3C1 methylation at this site was also associated with increased salivary cortisol stress responses at 3 months, controlling for prenatal SRI exposure, postnatal age and pre and postnatal maternal mood. METHODS: The methylation status of a CpG-rich region of the NR3C1 gene, including exon 1F, in genomic DNA from cord blood mononuclear cells was quantified by bisulfite pyrosequencing in infants of depressed mothers treated with a serotonin reuptake inhibitor antidepressant (SRI) (n = 33), infants of depressed nontreated mothers (n = 13) and infants of non depressed/non treated mothers (n = 36). To study the functional implications of the newborn methylation status of NR3C1 in newborns, HPA function was assessed at three months using salivary cortisol obtained before and following a non noxious stressor and at a late afternoon basal time. CONCLUSIONS: Methylation status of the human NR3C1 gene in newborns is sensitive to prenatal maternal mood and may offer a potential epigenetic process that links antenatal maternal mood and altered HPA stress reactivity during infancy.

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.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.4161/epi.3.2.6034

Cites

45 of 45 references verified0 citation errors · 0 not checkable

Statistics

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.

A few free checks a day · papers already verified open instantly · results are public

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 4

  1. [31]31. Oberlander TF, Weinberg J, Mayes L, Riggs W, Rurak D, Papsdorf M, Misri S, Grunau R. Hypothalamic-pituitary-adrenal (HPA) axis function in 3 month old infants with pre- natal serotonin reuptake inhibitor (SRI) antidepressant exposure. Abstract. XVIth Biennial International Conference on Infant Studies. Vancouver, BC 2008.
  2. [33]33. Prechtl HF, O'Brien MJ. Behavioural states of the full-term newborn: the emergence of a concept. In: Stratton P, editor. Psychobiology of the Human Newborn. New York, NY: John Wiley and Sons Ltd 1982; 53-73.
  3. [40]40. Abidin RR. Parenting Stress Index. Charlottesville, VA: Pediatric Psychology Press; 1990.
  4. [43]43. Kim J, Riggs KW, Misri S, Kent N, Oberlander TF, Grunau RE, Fitzgerald C, Rurak DW. Stereoselective disposition of fluoxetine and norfluoxetine during pregnancy and breast- feeding. Br J Clin Pharmacol 2006; 61:155-63.

Cited by

Sorted by citations

Authors
Oberlander, T. F., Weinberg, J., Papsdorf, M., Grunau, R., Misri, S., & Devlin, A. M.
Affiliations
  • University of British Columbia (CA)
  • Child and Family Research Institute (CA)
Venue
Epigenetics
Published
2008-03-24
Volume
3
Issue
2
Pages
97-106
ISSN
  • 1559-2294 (ISSN-L)
  • 1559-2308
OpenAlex
W2106670153
Cited by
1,432
References
45
Citations by year
2026: 30 · 2025: 42 · 2024: 50 · 2023: 53 · 2022: 56 · 2021: 82 · 2020: 104 · 2019: 65 · 2018: 91 · 2017: 95 · 2016: 117 · 2015: 123 · 2014: 124 · 2013: 100 · 2012: 122
FWCI
58.68
Type
journal article
Language
en
Open access
Locations
  • Epigenetics (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • March of Dimes Foundation (12-FY01-30)
  • Canadian Institutes of Health Research (54490, 57837, MOP54490)
  • National Institute on Alcohol Abuse and Alcoholism (R01AA007789)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Maternal Mental Health During Pregnancy and Postpartum
  • Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
Keywords
maternal depression, prenatal exposure, glucocorticoid receptor gene, NR3C1, DNA methylation, hypothalamic-pituitary-adrenal axis, cortisol stress response, serotonin reuptake inhibitors, umbilical cord blood, epigenetic regulation, maternal mood, infant development
MeSH terms
Adult, Base Sequence, Depression, Exons, Female, Fetal Blood, Humans, Hydrocortisone, Hypothalamo-Hypophyseal System, Infant, Leukocytes, Mononuclear, Molecular Sequence Data, Mothers, Pituitary-Adrenal System, Pregnancy, Pregnancy Complications, Promoter Regions, Genetic, Receptors, Glucocorticoid, Selective Serotonin Reuptake Inhibitors, Antidepressive Agents, Second-Generation, CpG Islands, DNA Methylation

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