Neonatal multimorbidity and the phenotype of premature aging in preterm infants

Jonathan S Litt1,2,3, Mandy Brown Belfort4,5, Todd M Everson6

  • 1Department of Neonatology, Beth Israel Deaconess Medical Center, Boston, USA. jlitt@bidmc.harvard.edu.

Pediatric Research
|October 25, 2024
PubMed

Insights

Preterm birth increases the risk of multimorbidity, the co-occurrence of multiple chronic conditions. This framework links neonatal multimorbidity to early aging, improving care for preterm infants.

Area of Science:

  • Neonatology
  • Developmental Pediatrics
  • Gerontology

Background:

  • Multimorbidity, the co-occurrence of multiple chronic conditions, is linked to aging, frailty, and poor functioning.
  • Children born preterm exhibit higher rates of multimorbidity in early life compared to term-born peers.
  • Neonatal multimorbidity is associated with diminished quality of life and functional outcomes, yet theoretical understanding is limited.

Purpose of the Study:

  • To propose a framework conceptualizing neonatal multimorbidity as a reflection of maturational vulnerability from preterm birth.
  • To integrate life course epidemiology and Developmental Origins of Health and Disease models.
  • To identify physiologic and social antecedents and biological underpinnings of neonatal multimorbidity for improved risk prediction and care.

Main Methods:

  • The study employs a conceptual framework integrating life course epidemiology and the Developmental Origins of Health and Disease models.
  • It examines the impact of neonatal intensive care unit exposures and post-discharge environments on health trajectories.
  • The framework considers early biologic and physical aging pathways.

Main Results:

  • Neonatal multimorbidity stems from maturational vulnerability associated with preterm birth.
  • Adverse exposures in the neonatal intensive care unit and disadvantaged post-discharge contexts can amplify negative health impacts.
  • Early biologic and physical aging pathways are crucial for understanding and improving long-term outcomes.

Conclusions:

  • Neonatal multimorbidity is an underrecognized threat to long-term health in preterm infants.
  • A novel framework incorporating multimorbidity, early cellular aging, and life course health development can enhance risk prediction, care planning, and therapeutics.
  • Understanding these pathways can lead to improved care and outcomes for preterm infants.

Related Concept Videos

Background and Environment Affect Phenotype02:27

Background and Environment Affect Phenotype

Although the genetic makeup of an organism plays a major role in determining the phenotype, there are also several environmental factors, such as temperature, oxygen availability, presence of mutagens, that can alter an organism’s phenotype.
An example of how genetic background affects phenotype can be seen in horses. The Extension gene in horses is responsible for their coat color. A wild-type gene (EE) produces black pigment in the coat, while a mutant gene (ee) produces red pigment. A...
6.5K
Nature and Nurture01:10

Nature and Nurture

Many human characteristics, like height, are shaped by both nature—in other words, by our genes—and by nurture, or our environment. For example, chronic stress during childhood inhibits the production of growth hormones and consequently reduces bone growth and height. Scientists estimate that 70-90% of variation in height is due to genetic differences among individuals, and 10-30% of variation in height is due to differences in the environments that individuals experience,...
20.4K
Mitochondria01:37

Mitochondria

Mitochondria are eukaryotic cellular organelles that are known to produce energy through a process called oxidative phosphorylation. Besides their primary function, mitochondria are involved in various cellular processes, including cell growth, differentiation, signaling, metabolism, and senescence. Age-related changes cause a decline in mitochondrial quality and integrity due to increased mitochondrial mutations and oxidative damage. Thus, aging can severely impact mitochondrial functions,...
11.3K