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Updated: Jun 9, 2026

Analysis of Nephron Composition and Function in the Adult Zebrafish Kidney
Published on: August 9, 2014
Early origin of adult renal disease
Silvio Maringhini1, Ciro Corrado, Guido Maringhini
1Paediatric Nephrology Unit, G. Di Cristina Children's Hospital, A.R.N.A.S. Civico, Di Cristina, Fatebenefratelli, Palermo, Italy. s.maringhini@ospedalecivicopa.org
Insights
Kidney damage can begin in early life due to fetal programming and low birth weight, leading to adult renal insufficiency. Early prevention strategies are crucial for children at risk of kidney disease.
Area of Science:
- Nephrology
- Developmental Biology
- Public Health
Background:
- Renal failure can originate early in life, influenced by prenatal and postnatal factors.
- Fetal programming, involving maternal nutrition and epigenetic changes, impacts long-term kidney health.
- Low birth weight is a significant risk factor for developing hypertension and renal insufficiency later in life.
Purpose of the Study:
- To highlight the early origins of renal failure.
- To emphasize the role of fetal programming and early life events in kidney disease development.
- To advocate for early preventive measures in at-risk children.
Main Methods:
- Review of observational studies in humans.
- Analysis of experimental studies in animals.
- Synthesis of evidence on congenital abnormalities, postnatal events, and nutrition.
Main Results:
- Evidence indicates renal damage can initiate in utero and early childhood.
- Congenital abnormalities, poor nutrition, and adverse postnatal events contribute to adult renal damage.
- Low birth weight is linked to increased risk of hypertension and renal insufficiency.
Conclusions:
- Kidney disease has early developmental origins, starting in fetal life.
- Interventions during pregnancy and early childhood are critical for preventing adult renal insufficiency.
- Targeted prevention in high-risk children is essential for long-term kidney health.
Abstract:
Observational studies in humans and experimental studies in animals have clearly shown that renal failure may start early in life. 'Fetal programming' is regulated by adaptations occurring in uterus including maternal nutrition, placental blood supply, and epigenetic changes. Low birth weight predisposes to hypertension and renal insufficiency. Congenital abnormalities of the kidney and urinary tract, adverse postnatal events, wrong nutritional habits may produce renal damage that will become clinically relevant in adulthood. Prevention should start early in children at risk of renal disease.
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