Evidence map›Paper›PMID 30590340›Full record

ArticlePsychoneuroendocrinology2019

Maternal cortisol output in pregnancy and newborn telomere length: Evidence for sex-specific effects.

Michelle Bosquet Enlow, Georgios Sideridis, Valentina Bollati, Mirjam Hoxha, Michele R Hacker, Rosalind J Wright

Abstract read
In one paragraph

Article in Psychoneuroendocrinology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 2 pooled it
9.8field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 2 syntheses or guidelines pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Observational
  5. Article
  6. Article
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  9. Review
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  12. Article
  13. Pathomechanisms of Prenatally Programmed Adult Diseases.Antioxidants (Basel, Switzerland) · 2023
    Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Maternal Sociodemographic Factors and Antenatal Stress.International journal of environmental research and public health · 2021
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

Michelle Bosquet EnlowDepartment of Psychiatry, Boston Children's Hospital, 300 Longwood Ave, Mailstop BCH 3199, Boston, MA, 02115, USA; Department of Psychiatry, Harvard Medical School, Boston, MA, USA. Electronic address: michelle.bosquet@childrens.harvard.edu.
Georgios SideridisDepartment of Psychiatry, Harvard Medical School, Boston, MA, USA; Institutional Centers for Clinical and Translational Research, Boston Children's Hospital, 300 Longwood Ave, Mailstop BCH 3200, Boston, MA, 02115, USA.
Valentina BollatiEPIGET Lab, Department of Clinical Sciences and Community Health, Università degli Studi di Milano, via San Barnaba 8, 20122, Milan, Italy.
Mirjam HoxhaEPIGET Lab, Department of Clinical Sciences and Community Health, Università degli Studi di Milano, via San Barnaba 8, 20122, Milan, Italy.
Michele R HackerDepartment of Obstetrics and Gynecology, Beth Israel Deaconess Medical Center, 330 Brookline Avenue, KS3, Boston, MA, 02215, USA; Department of Obstetrics, Gynecology and Reproductive Biology, Harvard Medical School, Boston, MA, USA.
Rosalind J WrightDepartment of Pediatrics, Mount Sinai Kravis Children's Hospital, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, Box 1198, New York City, NY, 10029, USA; Institute for Exposomic Research, Icahn School of Medicine at Mount Sinai, New York City, NY, USA.
Boston Children's Hospital · USUniversity of Milan · ITBeth Israel Deaconess Medical Center · USMount Sinai Hospital · US

Funding

The Mount Sinai Transdisciplinary Center on Early Environmental ExposuresP30ES023515 · NIEHS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Robert O Wright · 2014 to 2026
$21.3M
Early life stress, telomere attrition, and child prefrontal cortex functioningR01HD082078 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI BOSQUET ENLOW, MICHELLE A · 2015 to 2020
$3.4M
Perinatal Programming of Infant Stress Reactivity and the Atopic PhenotypeR01HL095606 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BOSQUET ENLOW, MICHELLE A, WRIGHT, ROSALIND J · 2010 to 2013
$3.1M
Prenatal stress and epigenetic programming of the HPA axis and autonomic balanceR01HL114396 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI WRIGHT, ROSALIND J · 2012 to 2015
$2.8M
NHLBI NIH HHS R01 HL095606NHLBI NIH HHS R01 HL114396NICHD NIH HHS R01 HD082078NIEHS NIH HHS P30 ES023515
6 · The paper itself

Abstract

Newborn telomere length is a potential biomarker of the effects of maternal-fetal processes on offspring long-term health. A number of maternal psychosocial and environmental factors in pregnancy (e.g., stress, health, socioeconomic status) have been associated with shortened telomere length at birth. The physiological mechanisms responsible for potential effects of maternal factors on newborn telomere length have yet to be identified. Indirect evidence suggests that disruptions in maternal hypothalamic-pituitary-adrenal (HPA) axis functioning in pregnancy may be involved. Studies are needed that test whether maternal HPA axis functioning in pregnancy is associated with newborn telomere length. This study examined whether maternal HPA axis functioning across pregnancy, reflected in hair cortisol collected within one week after delivery, predicted newborn telomere length assessed from leukocyte cord blood collected at birth among 93 sociodemographically diverse mother-infant dyads. We further tested whether associations between maternal hair cortisol and newborn telomere length differed by infant sex, given documented sex differences in prenatal environmental exposure effects on offspring health, patterns of cortisol exposure during gestation, and telomere biology across the lifespan. In a multi-group structural equation modeling analysis that accounted for cortisol exposures across trimesters, maternal cortisol levels in pregnancy were not associated with newborn telomere length in the sample as a whole. However, significant sex differences emerged, with a significant positive association among females and a lack of a significant association among males. In addition, analyses revealed that cortisol levels were higher across trimesters among mothers of male infants than mothers of female infants. The results suggest that functioning of the maternal HPA axis in pregnancy may differ by fetal sex and have sex-specific effects on newborn telomere biology. These findings have implications for understanding the mechanisms by which maternal psychosocial and environmental exposures influence newborn telomere length and for elucidating mechanisms contributing to sex disparities in health.

Indexed as

FemaleHairHumansHydrocortisoneHypothalamo-Hypophyseal SystemInfant, NewbornMaleMaternal ExposureMothersPituitary-Adrenal SystemPregnancyPrenatal Exposure Delayed EffectsSex CharacteristicsSex FactorsSocial ClassStress, PsychologicalHydrocortisoneCord bloodHair cortisolHypothalamic-pituitary-adrenal (HPA) axisNewbornSex differencesTelomere length

Identifiers

PMID30590340
PMCPMC6420355
OpenAlexW2904292122

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.