Related Experiment Video
Updated: Jul 11, 2025

A Rat Model of Mild Intrauterine Hypoperfusion with Microcoil Stenosis
Published on: January 7, 2018
From premature birth to premature kidney disease: does accelerated aging play a role?
Keia R Sanderson1, Christel Wekon-Kemeni2,3, Jennifer R Charlton4
1Department of Medicine-Nephrology, University of North Carolina, Chapel Hill, NC, USA. keia_sanderson@med.unc.edu.
Insights
Preterm birth may accelerate biological aging, increasing the risk of chronic kidney disease (CKD). Understanding this link could lead to new therapies for preventing advanced CKD in preterm infants.
Area of Science:
- Gerontology and Nephrology
- Developmental Biology and Chronic Disease
Background:
- Increased fetal viability has shifted focus from survival to long-term health outcomes after preterm birth.
- Growing evidence links preterm birth to accelerated biological aging and increased risk of chronic diseases.
- Chronic kidney disease (CKD) is characterized by an advanced biological age exceeding chronological age.
Purpose of the Study:
- To review the relationship between premature biological aging and chronic kidney disease (CKD) following preterm birth.
- To explore potential biological mechanisms linking preterm birth, accelerated aging, and CKD.
- To identify research gaps and potential therapeutic avenues for preventing advanced CKD.
Main Methods:
- Literature review summarizing key findings on aging, premature aging after preterm birth, and CKD.
- Analysis of existing evidence to identify plausible biological mechanisms connecting preterm birth and kidney disease.
- Synthesis of current research to highlight knowledge gaps in the premature aging paradigm.
Main Results:
- Preterm birth is associated with an accelerated biological aging phenotype.
- CKD shares a similar phenotype of advanced biological age.
- Significant knowledge gaps exist regarding the specific biological links between preterm birth and CKD.
Conclusions:
- Preterm birth may initiate a process of premature biological aging that increases susceptibility to CKD.
- Further research is crucial to elucidate the biological mechanisms underlying this premature aging paradigm.
- Understanding these mechanisms could pave the way for novel therapeutic strategies to prevent advanced CKD in individuals born preterm.
Abstract:
As the limits of fetal viability have increased over the past 30 years, there has been a growing body of evidence supporting the idea that chronic disease should be taken into greater consideration in addition to survival after preterm birth. Accumulating evidence also suggests there is early onset of biologic aging after preterm birth. Similarly, chronic kidney disease (CKD) is also associated with a phenotype of advanced biologic age which exceeds chronologic age. Yet, significant knowledge gaps remain regarding the link between premature biologic age after preterm birth and kidney disease. This review summarizes the four broad pillars of aging, the evidence of premature aging following preterm birth, and in the setting of CKD. The aim is to provide additional plausible biologic mechanisms to explore the link between preterm birth and CKD. There is a need for more research to further elucidate the biologic mechanisms of the premature aging paradigm and kidney disease after preterm birth. Given the emerging research on therapies for premature aging, this paradigm could create pathways for prevention of advanced CKD.
More Related Videos
Related Concept Videos
Chronic Kidney Disease I: Introduction
Acute Kidney Injury IV: Diagnostic Studies and Prevention
Chronic Kidney Disease II: Clinical Manifestations
Teratogenicity
Acute Kidney Injury II: Pathophysiology
Nephrons

