Evidence map›Paper›PMID 39455859›Full record

ReviewPediatric research2025

Neonatal multimorbidity and the phenotype of premature aging in preterm infants.

Jonathan S Litt, Mandy Brown Belfort, Todd M Everson, Sebastien Haneuse, Henning Tiemeier

Abstract readReview
In one paragraph

Review in Pediatric research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Observational
  2. Article
  3. Review
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

5 authors.

Jonathan S LittDepartment of Neonatology, Beth Israel Deaconess Medical Center, Boston, USA. jlitt@bidmc.harvard.edu.
Mandy Brown BelfortDepartment of Pediatrics, Harvard Medical School, Boston, USA.
Todd M EversonDepartment of Environmental Health, Emory University, Atlanta, USA.
Sebastien HaneuseDepartment of Biostatistics, Harvard TH Chan School of Public Health, Boston, USA.
Henning TiemeierDepartment of Social and Behavioral Sciences, Harvard TH Chan School of Public Health, Boston, USA.

Funding

Longitudinal trajectories of early childhood respiratory symptomatology and their impact on behavioral developmentK23HD088695 · NICHD · BETH ISRAEL DEACONESS MEDICAL CENTER · PI LITT, JONATHAN S · 2018 to 2022
$754k
NICHD NIH HHS K23 HD088695
6 · The paper itself

Abstract

Multimorbidity is the co-occurrence of multiple chronic health problems, associated with aging, frailty, and poor functioning. Children born preterm experience more multimorbid conditions in early life compared to term-born peers. Though neonatal multimorbidity is linked to poor health-related quality of life, functional outcomes, and peer group participation, gaps in our theoretical understanding and conceptualization remain. Drawing from life course epidemiology and the Developmental Origins of Heath and Disease models, we offer a framework that neonatal multimorbidity reflects maturational vulnerability posed by preterm birth. The impact of such vulnerability on health and development may be further amplified by adverse exposures and interventions within the environment of the neonatal intensive care unit. This can be exacerbated by disadvantaged home or community contexts after discharge. Uncovering the physiologic and social antecedents of multiple morbid conditions in the neonatal period and their biological underpinnings will allow for more accurate risk-prediction, counseling, and care planning for preterm infants and their families. According to this framework, the maturational vulnerability to multimorbidity imparted by preterm birth and its negative effects on health and development are not predetermined or static. Elucidating pathways of early biologic and physical aging will lead to improvements in care and outcomes. IMPACT: Multimorbidity is associated with significant frailty and dysfunction among older adults and is indicative of early physiologic aging. Preterm infants commonly experience multimorbidities in the newborn period, an underrecognized threat to long-term health and development. We offer a novel framework incorporating multimorbidity, early cellular aging, and life course health development to innovate risk-prediction, care-planning, and therapeutics.

Indexed as

Aging, PrematureInfant, PrematureMultimorbidityHumansInfant, NewbornPhenotypeQuality of Life

Identifiers

PMID39455859
PMCPMC12900265

What Socratic holds

Textmetadata
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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 Socratic graph.