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Published on: October 26, 2020
Developmental programming of hypertension and kidney disease
1Section of Neonatology, Department of Pediatrics, Hypertension and Renal Center of Excellence, Tulane University Health Sciences Center, New Orleans, LA 70112, USA.
Insights
Early life factors like premature birth and low birth weight can program later health, increasing risks for hypertension and chronic kidney disease (CKD) due to reduced nephron endowment.
Area of Science:
- Developmental biology
- Nephrology
- Public health
Background:
- Developmental programming, or developmental origins of health and disease, links early life conditions to later health outcomes.
- Premature birth (<37 weeks gestation) and low birth weight (<2,500g) are associated with increased risk of late-onset diseases.
- Chronic kidney disease (CKD) and hypertension risk in these infants may stem from reduced nephron endowment.
Purpose of the Study:
- To discuss the impact of premature birth, low birth weight, intrauterine environment, and infant feeding on hypertension and renal disease development.
- To examine the kidney's role in the developmental programming of hypertension and CKD.
Main Methods:
- Literature review and synthesis of existing evidence.
- Analysis of factors influencing intrauterine development and nephron endowment.
- Discussion of the relationship between early life events and adult-onset disease.
Main Results:
- Reduced nephron endowment is a key factor in the susceptibility to CKD and hypertension in premature or LBW infants.
- Uteroplacental insufficiency, maternal diet, hyperglycemia, vitamin A deficiency, glucocorticoid disruption, and ethanol exposure can lead to low nephron number.
- The intrauterine environment and infant feeding significantly influence long-term renal and cardiovascular health.
Conclusions:
- Early life interventions targeting the intrauterine milieu and infant nutrition are crucial for preventing later-life hypertension and CKD.
- Understanding developmental programming is essential for improving long-term health outcomes in vulnerable infants.
- The kidney plays a central role in mediating the effects of early life exposures on adult health.
Abstract:
A growing body of evidence supports the concept that changes in the intrauterine milieu during "sensitive" periods of embryonic development or in infant diet after birth affect the developing individual, resulting in general health alterations later in life. This phenomenon is referred to as "developmental programming" or "developmental origins of health and disease." The risk of developing late-onset diseases such as hypertension, chronic kidney disease (CKD), obesity or type 2 diabetes is increased in infants born prematurely at <37 weeks of gestation or in low birth weight (LBW) infants weighing <2,500 g at birth. Both genetic and environmental events contribute to the programming of subsequent risks of CKD and hypertension in premature or LBW individuals. A number of observations suggest that susceptibility to subsequent CKD and hypertension in premature or LBW infants is mediated, at least in part, by reduced nephron endowment. The major factors influencing in utero environment that are associated with a low final nephron number include uteroplacental insufficiency, maternal low-protein diet, hyperglycemia, vitamin A deficiency, exposure to or interruption of endogenous glucocorticoids, and ethanol exposure. This paper discusses the effect of premature birth, LBW, intrauterine milieu, and infant feeding on the development of hypertension and renal disease in later life as well as examines the role of the kidney in developmental programming of hypertension and CKD.
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