Reference ranges for analytes of thyroid function in children

F A Verburg1, C Kirchgässner, H Hebestreit

  • 1Department of Nuclear Medicine, University of Würzburg, Würzburg, Germany. fverburg@ukaachen.de

Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|April 13, 2011
PubMed

Insights

Establishing pediatric reference ranges for thyroid hormones is crucial for early detection of dysfunction. This study provides age-specific ranges for serum thyroid-stimulating hormone (TSH), free thyroxine (FT4), and free triiodothyronine (FT3) in children up to 18 years.

Area of Science:

  • Pediatric Endocrinology
  • Clinical Chemistry
  • Laboratory Medicine

Background:

  • Accurate diagnosis of pediatric thyroid dysfunction relies on age-specific reference ranges for key thyroid hormones.
  • Existing ranges may not adequately reflect physiological changes throughout childhood and adolescence.
  • The Immulite® 2000 assay is widely used, necessitating validated reference values for its application.

Purpose of the Study:

  • To establish age-specific reference ranges for serum thyroid-stimulating hormone (TSH), free thyroxine (FT4), and free triiodothyronine (FT3) in a pediatric population.
  • To characterize the age-related changes in these hormone reference ranges from birth through adolescence.
  • To provide data supporting the use of tailored reference intervals for improved clinical interpretation in children.

Main Methods:

  • Serum samples from 656 healthy children (newborn to 18 years) were analyzed using Immulite® 2000 assays for TSH, FT4, and FT3.
  • Non-normally distributed data required using the 2.5th and 97.5th percentiles to define reference ranges.
  • Age-related reference range curves were calculated using the linearity, median, and skewness method.

Main Results:

  • Thyroid hormone reference ranges exhibited wide variation at birth, decreasing significantly within the first two years of life.
  • Reference range width stabilized around age 4, with lower and upper limits progressively declining towards adult values by age 18.
  • Significant age-dependent shifts were observed for TSH, FT4, and FT3, particularly in early childhood.

Conclusions:

  • Age-specific reference ranges are essential for accurate interpretation of TSH, FT4, and FT3 levels in children.
  • The wide variability in early life necessitates careful consideration when assessing thyroid function in infants and newborns.
  • These established ranges facilitate prompt and reliable detection of pediatric thyroid dysfunction.

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