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Elevated serum creatinine levels in infants with congenital hypothyroidism: reflection of decreased renal function?
1Department of Pediatrics, School of Medicine, Niigata University, Japan. asamitds@medws1.med.niigata-u.ac.jp
Insights
Congenital hypothyroidism (CH) in infants can elevate serum creatinine levels, indicating impaired renal function. This condition is reversible with timely L-thyroxine (LT4) treatment, highlighting the importance of monitoring kidney function in affected infants.
Area of Science:
- Pediatric Endocrinology
- Nephrology
- Neonatal Screening
Background:
- Congenital hypothyroidism (CH) effects on pediatric renal function are understudied.
- Neonatal screening identifies infants with CH, enabling early intervention.
- Assessing renal function in hypothyroid infants is crucial for understanding disease impact.
Purpose of the Study:
- To evaluate renal function in infants diagnosed with CH via neonatal screening.
- To compare renal function markers between different severity groups of CH.
- To determine the reversibility of renal function changes after L-thyroxine (LT4) therapy.
Main Methods:
- Enrolled 80 hypothyroid infants and 20 controls.
- Categorized hypothyroid infants into mild-moderate (MHT) and severe (SHT) groups based on TSH and FT4 levels.
- Measured serum creatinine (SCr) before and 2 months after LT4 treatment.
Main Results:
- Severely hypothyroid (SHT) infants exhibited significantly higher SCr levels compared to MHT and control groups.
- LT4 therapy led to a 41.3% decrease in SCr in the SHT group, normalizing levels.
- No significant differences in blood urea nitrogen (BUN) were observed across groups.
Conclusions:
- Elevated serum creatinine is a key indicator of impaired renal function in infants with CH.
- Thyroid hormone replacement therapy effectively reverses these renal function abnormalities.
- Clinicians should consider potential renal function impairment in hypothyroid infants.
Unlabelled:
The effects of hypothyroid status on renal function have been poorly studied in children. We assessed the renal function of hypothyroid infants detected during neonatal mass screening for congenital hypothyroidism (CH). Eighty hypothyroid infants and 20 age-matched normal infants for controls were enrolled. The 80 patients, aged 1 mo, were divided into two groups based on the initial thyroid stimulating hormone (TSH) and free thyroxine (FT4) values: a mild-moderately hypothyroid (MHT) group (n = 64, 31M and 33F) and a severely hypothyroid (SHT) group (n = 16, 3M and 13F). Serum creatinine (SCr), TSH, FT4 and other chemicals were compared before and 2 mo after L-thyroxine (LT4) substitution therapy. The following results were obtained: SCr levels were significantly higher in the SHT group (33.2+/-10.0 micromol/L, p < 0.001) compared with the MHT group (20.6+/-6.4 micromol/L) and normal control group (21.0+/-4.4 micromol/L). Two months after the LT4 replacement therapy, the elevated SCr levels in the SHT group decreased by 41.3% to the level (19.5+/-6.0 micromol/L) very close to that in the MHT group (18.8+/-5.1 micromol/L). No significant differences were noted among BUN levels in the three groups. Although serum creatinine kinase levels were significantly higher in the SHT group (230.3+/-102.3 U/L, p < 0.001) than in the MHT group (121.1+/-60.8 U/L), rhabdomyolysis was not considered to be responsible for the impaired renal function.
Conclusion:
From these results we conclude that serum creatinine levels are elevated in congenitally hypothyroid infants. This is a reversible change with thyroid hormone replacement therapy. The possibility of impaired renal functions should be kept in mind when treating hypothyroid infants.
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