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Use of Ultra-high Field MRI in Small Rodent Models of Polycystic Kidney Disease for In Vivo Phenotyping and Drug Monitoring
Published on: June 23, 2015
Chronic kidney disease associated with extremely premature birth and extremely low birth weight may progress through
Chinatsu Onodera1, Ken Ishikawa2, Hiroshi Sugawara2
1Department of Pediatrics, School of Medicine, Iwate Medical University, 2-1-1, Idaidori, Yahaba-Cho, Shiwa-Gun, Iwate Prefecture, 028-3694, Japan. chinaono@iwate-med.ac.jp.
Insights
Infants born with low birth weight or prematurely may develop chronic kidney disease (CKD) later in life. Early monitoring after neonatal intensive care unit (NICU) discharge is crucial for detecting kidney damage in these high-risk infants.
Area of Science:
- Pediatrics
- Nephrology
- Neonatology
Background:
- Infants born with low birth weight and/or premature birth (L/P-CKD) may have fewer nephrons, increasing susceptibility to kidney injury.
- Nephrotoxic exposures during early infancy can exacerbate kidney damage in these vulnerable infants.
- The long-term progression of L/P-CKD remains poorly understood.
Purpose of the Study:
- To present three cases of L/P-CKD diagnosed in adolescence after NICU discharge.
- To highlight the potential long-term renal consequences in extremely premature and low birth weight infants.
- To emphasize the need for extended follow-up protocols for these patients.
Main Methods:
- Case series of three extremely premature infants (24-26 weeks gestation, 606-906g birth weight) requiring prolonged NICU stays (117-311 days).
- Monitoring included serum creatinine, renal ultrasonography, and renal biopsy.
- Clinical data reviewed for potential causes of kidney damage, excluding common factors like infections or lifestyle issues.
Main Results:
- Patients developed proteinuria in adolescence (10-15 years) despite normal creatinine at NICU discharge.
- Renal ultrasonography showed smaller-than-normal kidneys.
- Renal biopsies revealed glomerulomegaly and perihilar glomerulosclerosis, suggesting glomerular hypertension.
Conclusions:
- L/P-CKD can manifest in adolescence, indicated by proteinuria and specific renal biopsy findings.
- The progression of CKD in these infants may be linked to growth spurts and delayed diagnosis.
- Establishing long-term follow-up from NICU discharge through adulthood is essential for managing L/P-CKD.
Abstract:
Chronic kidney disease associated with low birth weight and/or premature birth (L/P-CKD) in infants may result from a decreased number of nephrons at birth. These infants may develop acute kidney injury due to exposure to nephrotoxic substances or other events during nephrogenesis in early infancy. Nonetheless, L/P-CKD progression remains unclear. We present three cases of L/P-CKD diagnosed after neonatal intensive care unit (NICU) discharge. Three patients were born extremely prematurely (gestational age, 24-26 weeks) with extremely low birth weight (606-906 g). They were admitted to the NICU (117-311 days) anad received several nephrotoxic medications during the early postnatal period. They showed elevated serum creatinine levels at 4 weeks after birth, which decreased to normal levels at NICU discharge. Proteinuria was first detected during adolescence (10-15 years) on annual school urine screening, with a remarkable increase in their height (18 - 50.8 cm), without known episodes of urinary tract infection, dehydration, lifestyle-related issues, such as excessive salt/protein intake, and extreme lack of exercise that might have caused kidney damage. Their kidneys were smaller than normal on renal ultrasonography. Open renal biopsy findings indicated glomerulomegaly and perihilar glomerulosclerosis in two of the three patients, suggesting glomerular hypertension. The remarkable differences between the body height before CKD and the timing of diagnosis of CKD could contribute to the progress of CKD. Long-term follow-up of low birth weight and extremely premature infants, from NICU discharge until adulthood, should be established.
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