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Preterm Birth and Kidney Health: From the Womb to the Rest of Life
You-Lin Tain1,2, Chien-Ning Hsu3,4
1Division of Pediatric Nephrology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 833, Taiwan.
Insights
Preterm birth can harm kidney development, increasing lifelong chronic kidney disease (CKD) risk. Early screening and interventions for preterm infants are crucial for preventing future kidney problems.
Area of Science:
- Nephrology
- Developmental Biology
- Public Health
Background:
- Chronic kidney disease (CKD) is a growing global health concern.
- Maternal factors and preterm birth are significant risk factors for CKD.
- Impaired kidney development during nephrogenesis leads to fewer nephrons, predisposing individuals to CKD.
Purpose of the Study:
- To review the link between preterm birth, kidney development, and CKD risk.
- To explore mechanisms of kidney programming and secondary insults in preterm infants.
- To propose multidisciplinary solutions for mitigating CKD risk in this population.
Main Methods:
- Analysis of human studies on preterm birth and kidney outcomes.
- Summary of animal models illustrating kidney programming and nephron reduction.
- Consolidation of knowledge on common kidney programming mechanisms.
Main Results:
- Preterm birth is associated with adverse kidney outcomes.
- Animal models confirm kidney programming and reduced nephron counts.
- Postnatal factors like AKI, nephrotoxic drugs, and nutrition exacerbate CKD risk.
Conclusions:
- Advancements in preterm infant survival necessitate a focus on long-term kidney health.
- Early identification and management of risk factors are essential.
- Multidisciplinary approaches and early CKD screening can improve outcomes for preterm infants.
Abstract:
Chronic kidney disease (CKD) is a widespread condition often resulting from multiple factors, including maternal influences. These risk factors not only heighten the likelihood of developing CKD but increase the risk of a preterm birth. Adverse events during nephrogenesis can disrupt kidney development, leading to a reduced number of nephrons. As survival rates for preterm infants improve, more individuals are living into adulthood, thereby elevating their risk of CKD later in life. This review aims to explore the connections between preterm birth, kidney development, and the increased risk of CKD, while proposing practical solutions for the future through a multidisciplinary approach. We examine human studies linking preterm birth to negative kidney outcomes, summarize animal models demonstrating kidney programming and reduced nephron numbers, and consolidate knowledge on common mechanisms driving kidney programming. Additionally, we discuss factors in the postnatal care environment that may act as secondary insults contributing to CKD risk, such as acute kidney injury (AKI), the use of nephrotoxic drugs, preterm nutrition, and catch-up growth. Finally, we outline recommendations for action, emphasizing the importance of avoiding modifiable risk factors and implementing early CKD screening for children born preterm. Together, we can ensure that advancements in kidney health keep pace with improvements in preterm care.
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