Evidence map›Paper›PMID 25349321›Full record

Trial reportPediatrics2014

Perinatal complications and aging indicators by midlife.

Idan Shalev, Avshalom Caspi, Antony Ambler, Daniel W Belsky, Simon Chapple, Harvey Jay Cohen, Salomon Israel, Richie Poulton, Sandhya Ramrakha, Christine D Rivera and 4 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Pediatrics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
–field-weighted citation impact
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

31 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
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  9. Article
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  11. Article
  12. Review
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  14. Article
  15. Article
  16. Article
  17. The fetal programming of telomere biology hypothesis: an update.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    Review
  18. Article
  19. Telomere Length in Newborns is Related to Maternal Stress During Pregnancy.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
    Article
  20. Intrauterine exposure to maternal stress alters Bdnf IV DNA methylation and telomere length in the brain of adult rat offspring.International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience · 2017
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Idan ShalevDepartment of Biobehavioral Health and The Network on Child Protection and Well-Being, Social Science Research Institute, The Pennsylvania State University, University Park, Pennsylvania; ius14@psu.edu.
Avshalom CaspiDepartments of Psychology & Neuroscience and Psychiatry and Behavioral Sciences, Institute for Genome Sciences and Policy, and Social, Genetic, and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, London, United Kingdom;
Antony AmblerSocial, Genetic, and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, London, United Kingdom; Dunedin Multidisciplinary Health and Development Research Unit, Department of Preventive and Social Medicine, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand;
Daniel W BelskyCenter for the Study of Aging and Human Development, Duke University Medical Center, Durham, North Carolina; Social Science Research Institute, Duke University, Durham, North Carolina;
Simon ChappleDunedin Multidisciplinary Health and Development Research Unit, Department of Preventive and Social Medicine, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand;
Harvey Jay CohenCenter for the Study of Aging and Human Development, Duke University Medical Center, Durham, North Carolina;
Salomon IsraelDepartments of Psychology & Neuroscience and.
Richie PoultonDunedin Multidisciplinary Health and Development Research Unit, Department of Preventive and Social Medicine, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand;
Sandhya RamrakhaDunedin Multidisciplinary Health and Development Research Unit, Department of Preventive and Social Medicine, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand;
Christine D RiveraCenter for Developmental Science, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; and.
Karen SugdenInstitute for Genome Sciences and Policy, and.
Benjamin WilliamsInstitute for Genome Sciences and Policy, and.
Dieter WolkeDepartment of Psychology, Lifespan Health and Wellbeing Group and Division of Mental Health and Wellbeing, Warwick Medical School, The University of Warwick, Coventry, United Kingdom.
Terrie E MoffittDepartments of Psychology & Neuroscience and Psychiatry and Behavioral Sciences, Institute for Genome Sciences and Policy, and Social, Genetic, and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, London, United Kingdom;

Funding

Resource Core 3 - Metabolomics CoreP30AG028716 · NIA · DUKE UNIVERSITY · PI Virginia B Kraus · 2006 to 2026
$24.6M
Is mental disorder a preventable cause of age-related disease? The Dunedin Study.R01AG032282 · NIA · DUKE UNIVERSITY · PI CASPI, AVSHALOM, MOFFITT, TERRIE E · 2009 to 2025
$9.5M
BEHAVIOR AND PHYSIOLOGY IN AGINGT32AG000029 · NIA · DUKE UNIVERSITY · PI Maria Marquine · 1985 to 2026
$9.3M
Generating new knowledge to support reversibility interventionsR01AG048895 · NIA · DUKE UNIVERSITY · PI MOFFITT, TERRIE E · 2014 to 2015
$311k
Medical Research Council G0100527Medical Research Council G0601483Medical Research Council G9806489Medical Research Council MR/K00381XMedical Research Council MR/K00381X/1NIA NIH HHS AG032282NIA NIH HHS P30 AG028716NIA NIH HHS P30-AG028716-08NIA NIH HHS R01 AG032282NIA NIH HHS R01 AG048895NIA NIH HHS T32 AG000029NIA NIH HHS T32-AG00029
6 · The paper itself

Abstract

backgroundPerinatal complications predict increased risk for morbidity and early mortality. Evidence of perinatal programming of adult mortality raises the question of what mechanisms embed this long-term effect. We tested a hypothesis related to the theory of developmental origins of health and disease: that perinatal complications assessed at birth predict indicators of accelerated aging by midlife.

methodsPerinatal complications, including both maternal and neonatal complications, were assessed in the Dunedin Multidisciplinary Health and Development Study cohort (N = 1037), a 38-year, prospective longitudinal study of a representative birth cohort. Two aging indicators were assessed at age 38 years, objectively by leukocyte telomere length (TL) and subjectively by perceived facial age.

resultsPerinatal complications predicted both leukocyte TL (β = -0.101; 95% confidence interval, -0.169 to -0.033; P = .004) and perceived age (β = 0.097; 95% confidence interval, 0.029 to 0.165; P = .005) by midlife. We repeated analyses with controls for measures of family history and social risk that could predispose to perinatal complications and accelerated aging, and for measures of poor health taken in between birth and the age-38 follow-up. These covariates attenuated, but did not fully explain the associations observed between perinatal complications and aging indicators.

conclusionsOur findings provide support for early-life developmental programming by linking newborns' perinatal complications to accelerated aging at midlife. We observed indications of accelerated aging "inside," as measured by leukocyte TL, an indicator of cellular aging, and "outside," as measured by perceived age, an indicator of declining tissue integrity. A better understanding of mechanisms underlying perinatal programming of adult aging is needed.

Indexed as

AdultAgingCohort StudiesFemaleHumansInfant, NewbornLongitudinal StudiesMalePerinatal CarePhotic StimulationPregnancyPregnancy ComplicationsProspective Studiesagingdevelopmental programmingperceived ageperinatal complicationstelomere length

Identifiers

PMID25349321
PMCPMC4210799

What OpenQuestion holds

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Registered trials

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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.