4.0 Article

Association Between Maternal-Perceived Psychological Stress and Fetal Telomere Length

Journal

SOUTHERN MEDICAL JOURNAL
Volume 109, Issue 12, Pages 767-772

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.14423/SMJ.0000000000000567

Keywords

bootstrapping statistical methodology; fetal telomere length; maternal psychological stress; neonatal umbilical cord blood

Funding

  1. James and Esther King Biomedical Research Program
  2. Florida Department of Health [4 KB03, 1KG14-33987]
  3. University of South Florida Neuroscience Collaborative-Seed Grant Program
  4. University of South Florida College of Public Health Interdisciplinary Research Development Grant

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Objective: Our study aimed to investigate the association between maternal-perceived psychological stress and fetal telomere length. Methods: We recruited women in labor upon hospital delivery admission. Based on responses to the Perceived Stress Scale, we categorized participants as having high, normal, or low perceived stress. We collected umbilical cord blood samples (N = 71) and isolated genomic DNA from cord blood leukocytes using quantitative polymerase chain reaction. We used a ratio of relative telomere length derived by telomere- to-single-copy gene ratio (T/S ratio). We applied analysis of variance and bootstrapping statistical procedures. Results: Sixteen (22.5%) women were classified as having low perceived stress, 42 (59.2%) were classified as having normal perceived stress, and 13 (18.3%) were classified as having high perceived stress. Fetal telomere length differed significantly across the three stress groups in a dose-response pattern (T/S ratio of those with low perceived stress was greater than those with normal perceived stress, which was greater than those with high perceived stress [P < 0.05]). Conclusions: Our findings support our hypothesis that maternal-perceived psychological stress during pregnancy is associated with shorter fetal telomere length and suggest maternal stress as a possible marker for early intrauterine programming for accelerated chromosomal aging.

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