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Updated: Aug 20, 2025

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Published on: June 29, 2013
Fetal growth restriction followed by very preterm birth is associated with smaller kidneys but preserved kidney
Jonas Liefke1, Caroline Heijl2, Katarina Steding-Ehrenborg1
1Clinical Physiology, Department of Clinical Sciences Lund, Lund University, Skåne University Hospital, Lund, Sweden.
Insights
Adolescents born very preterm with fetal growth restriction (FGR) have smaller kidney volumes but normal kidney function. These structural changes may predict future kidney disease risk.
Area of Science:
- Nephrology
- Pediatric Nephrology
- Fetal Medicine
Background:
- Preterm birth and fetal growth restriction (FGR) are linked to long-term kidney disease and hypertension risks.
- Previous studies on preterm children show conflicting results regarding structural kidney changes and function.
- This study investigates kidney structure and function in adolescents born very preterm, with and without FGR.
Purpose of the Study:
- To assess kidney structure and function in adolescents born very preterm.
- To compare kidney parameters in adolescents with and without a history of FGR.
- To evaluate potential long-term consequences of FGR and preterm birth on renal health.
Main Methods:
- Magnetic resonance imaging (MRI) was used to measure cortical and medullary kidney volumes and T1/T2* mapping.
- Biochemical markers of kidney function and renin-angiotensin-aldosterone system (RAAS) activation were analyzed.
- Adolescents born very preterm with FGR were compared to those born preterm with appropriate for gestational age (AGA) and term-born AGA controls.
Main Results:
- Adolescents born very preterm with FGR exhibited significantly smaller total and medullary kidney volumes compared to term-born AGA controls.
- A decreased corticomedullary volume ratio was observed in preterm FGR and preterm AGA groups compared to term AGA.
- No significant differences were found in kidney function markers (biochemical) or RAAS activation between the groups.
Conclusions:
- Very preterm birth combined with FGR is associated with reduced total and medullary kidney volumes in adolescence.
- Despite structural changes, current markers of kidney function and RAAS activation were not different between groups.
- Diminished kidney volumes may serve as a prognostic marker for future kidney function decline.
Background:
Preterm birth and fetal growth restriction (FGR) are associated with structural and functional kidney changes, increasing long-term risk for chronic kidney disease and hypertension. However, recent studies in preterm children are conflicting, indicating structural changes but normal kidney function. This study therefore assessed kidney structure and function in a cohort of adolescents born very preterm with and without verified FGR.
Methods:
Adolescents born very preterm with FGR and two groups with appropriate birthweight (AGA) were included; one matched for gestational week at birth and one born at term. Cortical and medullary kidney volumes and T1 and T2* mapping values were assessed by magnetic resonance imaging. Biochemical markers of kidney function and renin-angiotensin-aldosterone system (RAAS) activation were analyzed.
Results:
Sixty-four adolescents were included (13-16 years; 48% girls). Very preterm birth with FGR showed smaller total (66 vs. 75 ml/m2; p = 0.01) and medullary volume (19 vs. 24 ml/m2; p < 0.0001) compared to term AGA. Corticomedullary volume ratio decreased from preterm FGR (2.4) to preterm AGA (2.2) to term AGA (1.9; p = 0.004). There were no differences in T1 or T2* values (all p ≥ 0.34) or in biochemical markers (all p ≥ 0.12) between groups.
Conclusions:
FGR with abnormal fetal blood flow followed by very preterm birth is associated with smaller total kidney and medullary kidney volumes, but not with markers of kidney dysfunction or RAAS activation in adolescence. Decreased total kidney and medullary volumes may still precede a long-term decrease in kidney function, and potentially be used as a prognostic marker. A higher resolution version of the Graphical abstract is available as Supplementary information.
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