Pediatric Reference Intervals for Free Thyroxine and Free Triiodothyronine by Equilibrium Dialysis-Liquid

Sonia L La'ulu, Kyle J Rasmussen, Joely A Straseski1

  • 1ARUP Institute for Clinical and Experimental Pathology, Salt Lake City, Utah, USA, Phone: (800) 242-2787 ext. 3696

Insights

Pediatric thyroid hormone reference intervals (RIs) for free thyroxine (fT4) and free triiodothyronine (fT3) were established using advanced methods in over 2200 children. These new RIs differ significantly from adult ranges, highlighting the need for pediatric-specific guidelines.

Area of Science:

  • Pediatric Endocrinology
  • Clinical Chemistry
  • Mass Spectrometry

Background:

  • Thyroid hormone levels change during childhood development.
  • Accurate diagnosis of pediatric thyroid disease requires age-specific reference intervals (RIs).
  • Establishing pediatric RIs is challenging due to difficulties in recruiting sufficient healthy subjects.

Purpose of the Study:

  • To determine non-parametric RIs for free thyroxine (fT4) and free triiodothyronine (fT3) in healthy children aged 6 months to 17 years.
  • To utilize equilibrium dialysis-high performance liquid chromatography-tandem mass spectrometry for precise measurements.
  • To establish RIs based on a large cohort of over 2200 healthy pediatric subjects.

Main Methods:

  • Recruited 2213 healthy children (6 months-17 years), screened for thyroid autoantibodies and normal thyrotropin.
  • Employed equilibrium dialysis-high performance liquid chromatography-tandem mass spectrometry for accurate fT4 and fT3 quantification.
  • Ensured adequate age-group representation with at least 120 subjects per year of life, where possible.

Main Results:

  • Established non-parametric RIs for fT4: 18.0-34.7 pmol/L (6 months-6 years) and 14.2-25.7 pmol/L (7-17 years).
  • Established age- and sex-specific RIs for fT3 across different pediatric age bands.
  • Observed significant variations in fT3 RIs between sexes in the 13-17 year olds.

Conclusions:

  • Significant differences exist between pediatric and adult thyroid hormone reference intervals.
  • Well-characterized, pediatric-specific RIs are crucial for accurate thyroid disease diagnosis in children.
  • This study provides essential data for updating clinical guidelines for pediatric thyroid function testing.
Abstract

Related Concept Videos

Therapeutic Drug Monitoring: Drug Analysis Methods01:26

Therapeutic Drug Monitoring: Drug Analysis Methods

Therapeutic Drug Monitoring (TDM) is a clinical practice that measures specific drug levels in a patient's blood or body tissues to tailor drug therapy effectively. This monitoring is critical for managing drugs with narrow therapeutic indices like digoxin and phenytoin, ensuring they are both safe and effective. For instance, monitoring theophylline levels in asthma patients involves precision and sensitivity to adjust doses according to individual responses to therapy, ensuring efficacy and...
289
Pharmacokinetics in Pediatric Patients: Drug Distribution01:17

Pharmacokinetics in Pediatric Patients: Drug Distribution

Drug distribution in the pediatric population exhibits unique challenges and considerations due to the physiological differences between children, particularly neonates and infants, and adults. A crucial aspect of pediatric pharmacology is understanding how these differences impact the pharmacokinetics of various drugs, necessitating age-specific dosing strategies to ensure efficacy and safety.Neonates and infants have a higher total body water content, ~75%–90% of their body weight,...
461
Synthesis and Regulation of Thyroid Hormones01:20

Synthesis and Regulation of Thyroid Hormones

Low blood levels of the thyroid hormones — triiodothyronine (T3) and thyroxine (T4) — signal the hypothalamus to release the thyrotropin-releasing hormone (TRH). TRH then reaches the pituitary gland and stimulates the release of thyroid-stimulating hormone(TSH) into the bloodstream.
Upon reaching the thyroid gland, TSH stimulates the follicular cells' active uptake of iodide ions from the blood. The ions diffuse to the apical surface of the cells and are oxidized to iodine. The...
8.9K
Drug Dosing in Renal Diseases: Measurement of Serum Creatinine Concentration and Clearance01:25

Drug Dosing in Renal Diseases: Measurement of Serum Creatinine Concentration and Clearance

In healthy individuals, serum creatinine levels remain stable due to a balance between its constant production—primarily from muscle metabolism—and renal excretion. Creatinine is freely filtered by the glomeruli, making it a valuable marker for estimating renal function. When the glomerular filtration rate (GFR) decreases, the kidneys can only eliminate less creatinine, causing serum levels to rise.Serum creatinine concentration is widely used to estimate creatinine clearance...
340