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Published on: October 25, 2015
Fetal programming of renal function
Jörg Dötsch1, Christian Plank, Kerstin Amann
1Department of Pediatrics, University of Cologne, Kerpener Str. 62, 50937 Cologne, Germany. Joerg.doetsch@uk-koeln.de
Insights
Low birth weight can lead to adverse kidney outcomes in children due to fetal programming. Postnatal nutrition may influence these programmed renal outcomes.
Area of Science:
- Nephrology
- Developmental Biology
- Epidemiology
Background:
- Large epidemiological studies link low birth weight to adverse renal outcomes in childhood.
- Fetal programming, influenced by maternal factors like diabetes, smoking, and glucocorticoid use, can lead to conditions such as glomerular disease, hypertension, and renal failure.
- Clinical data on the impact of maternal glucocorticoid use during pregnancy on fetal renal programming are limited.
Purpose of the Study:
- To discuss the potential mechanisms underlying fetal programming of renal outcomes.
- To explore how factors during pregnancy and postnatal life may influence kidney development and long-term renal health.
Main Methods:
- Review of existing epidemiological data.
- Discussion of proposed biological mechanisms.
- Synthesis of current understanding on fetal programming and renal health.
Main Results:
- Low birth weight is associated with reduced nephron number due to diminished nephrogenesis.
- Alterations in the intrarenal renin-angiotensin-aldosterone system and endothelial dysfunction are implicated in adverse renal outcomes.
- Postnatal factors, such as nutritional intake, can modify the outcomes of fetal programming.
Conclusions:
- Fetal programming initiated by factors like low birth weight can have lasting adverse effects on renal health.
- Understanding these mechanisms is crucial for developing interventions to prevent childhood kidney disease.
- Further clinical research is needed to elucidate the precise impact of specific maternal exposures.
Abstract:
Results from large epidemiological studies suggest a clear relation between low birth weight and adverse renal outcome evident as early as during childhood. Such adverse outcomes may include glomerular disease, hypertension, and renal failure and contribute to a phenomenon called fetal programming. Other factors potentially leading to an adverse renal outcome following fetal programming are maternal diabetes mellitus, smoking, salt overload, and use of glucocorticoids during pregnancy. However, clinical data on the latter are scarce. Here, we discuss potential underlying mechanisms of fetal programming, including reduced nephron number via diminished nephrogenesis and other renal (e.g., via the intrarenal renin-angiotensin-aldosterone system) and non-renal (e.g., changes in endothelial function) alterations. It appears likely that the outcomes of fetal programming may be influenced or modified postnatally, for example, by the amount of nutrients given at critical times.
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