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Obesity and preterm birth: additive risks in the progression of kidney disease in children
Carolyn L Abitbol1, Jayanthi Chandar, Maria M Rodríguez
1Division of Pediatric Nephrology (M714), University of Miami/Holtz Children's Hospital, 1611 NW 12th Avenue, Annex 5, Miami, FL 33126, USA. cabitbol@med.miami.edu
Insights
Preterm birth and obesity significantly increase the risk of kidney disease progression in children. Obese preterm children face the highest risk of renal demise during childhood.
Area of Science:
- Pediatric Nephrology
- Renal Disease Research
- Public Health
Background:
- Preterm birth is linked to reduced nephron mass, a risk factor for future kidney disease.
- Obesity is an emerging concern for pediatric kidney disease progression.
- Understanding the combined impact of preterm birth and obesity is crucial for early intervention.
Purpose of the Study:
- To investigate the independent and combined risks of obesity and preterm birth on kidney disease progression in children.
- To compare disease progression and renal histomorphometry in different pediatric groups.
Main Methods:
- Retrospective cohort study of 80 children with proteinuric kidney disease.
- Categorization into obese/non-obese and term/preterm birth groups.
- Analysis of disease progression, renal histomorphometry, and insulin resistance (HOMA-IR).
Main Results:
- Obese preterm children had a significantly higher risk of renal demise compared to obese term children (HR 2.4, P=0.04).
- Preterm birth was associated with reduced renal mass (OR 4.7, P=0.006), but obesity was not.
- Obesity led to glomerulomegaly in all obese children, irrespective of birth weight.
Conclusions:
- Obesity and preterm birth act as additive risk factors for kidney disease progression in children.
- Early identification and management of these risk factors are essential for improving long-term kidney health outcomes.
- The findings highlight the critical interplay between birth status and metabolic health in pediatric renal disease.
Abstract:
Preterm birth is associated with decreased nephron mass and obesity that may impact on kidney disease progression in later life. Our objectives were to examine the relative risks of obesity and preterm birth on the progression of kidney disease in children. In a retrospective cohort study, 80 (44 obese and 36 non-obese) patients with proteinuric kidney disease were studied for disease progression and glomerular histomorphometry. Of the obese, 22 had been born at term (Obese-T) and 22 had been preterm (Obese-PT). Seventeen non-obese children with focal glomerular sclerosis, born at term (NO-FSGS), and 19 non-obese preterm (NO-PT) children, served as controls. Insulin resistance as measured by the homeostatic model assessment (HOMA-IR) was elevated in all obese children. Obese-PT patients had increased risk of renal demise during childhood when compared with Obese-T children [hazard ratio 2.4; 95% Confidence interval (95% CI) 1.1 to 7.1; P = 0.04]. In obese children, although proteinuria often exceeded nephrotic range, average levels of serum albumin remained normal. Preterm patients were more likely to have reduced renal mass (odds ratio 4.7; P = 0.006), but obesity was not a factor. Renal histomorphometry showed glomerulomegaly in obese patients, regardless of birth weight. Obesity and preterm birth appear to impose additive risks for progression of kidney disease in childhood.
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