Total fluoride intake and urinary excretion in German children aged 3-6 years

M Haftenberger1, G Viergutz, V Neumeister

  • 1Department of Paediatric Dentistry, University of Technology, Dresden, Germany.

Caries Research
|January 19, 2002
PubMed

Insights

Few studies examine total fluoride intake and urinary excretion in preschoolers. This study found preschoolers excrete about half of ingested fluoride, highlighting the need for larger studies on fluoride exposure and excretion rates.

Area of Science:

  • Pediatric Nutrition
  • Environmental Health
  • Toxicology

Background:

  • Limited research exists on total fluoride intake and urinary excretion in preschool-aged children.
  • Existing studies present conflicting results regarding fluoride metabolism in this age group.

Purpose of the Study:

  • To assess total daily fluoride intake from various sources in healthy preschool children.
  • To determine the proportion of ingested fluoride excreted in urine among these children.

Main Methods:

  • Utilized the duplicate-diet approach to measure fluoride intake from food and beverages.
  • Calculated fluoride intake from toothbrushing by quantifying swallowed toothpaste and rinsing water.
  • Recorded the use of fluoridated salt and fluoride supplements.

Main Results:

  • Average daily fluoride intake from food was 202.5 ± 116.2 µg F/day.
  • Average swallowed fluoride during toothbrushing was 273.9 ± 175.6 µg F/day.
  • Total daily fluoride ingestion averaged 930.7 ± 391.5 µg (53.0 ± 21.4 µg/kg body weight).
  • Approximately 51.5% of ingested fluoride was excreted in urine.

Conclusions:

  • Preschool children excrete a significant proportion of their total fluoride intake via urine.
  • Wide inter-individual variations in fluoride excretion necessitate further investigation in larger populations with diverse fluoride exposure levels.

Related Concept Videos

Pharmacokinetics in Pediatric Patients: Drug Excretion01:26

Pharmacokinetics in Pediatric Patients: Drug Excretion

In pediatric medicine, understanding the renal function and drug elimination nuances is crucial for administering safe and effective treatments. Newborns, in particular, display markedly slower renal functions than adults, profoundly affecting how drugs are cleared from their bodies. This slower drug clearance requires clinicians to extend the dosing intervals for many medications to prevent drug accumulation and toxicity while ensuring therapeutic efficacy.One key area where these adjustments...
One-Compartment Open Model: Urinary Excretion Data and Determination of k01:11

One-Compartment Open Model: Urinary Excretion Data and Determination of k

The one-compartment open model leverages urinary excretion data to estimate renal clearance, which gauges the kidney's capacity to expel a drug. This method offers several benefits, including directly measuring drug elimination and assessing the kidney's contribution to overall drug clearance. However, this approach has limitations. It assumes sole renal excretion of the drug, which is not true for all drugs. Accurate urinary excretion and plasma drug concentration measurement can also be...
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 (Clcr), a...
Drug Dosing: Infants and Children01:29

Drug Dosing: Infants and Children

Pediatric patient dosages diverge from adults due to disparities in body surface area, total body water, and extracellular fluid per kilogram of body weight. The dosing regimen considers the variations in pharmacokinetics and pharmacology across distinct age groups, encompassing preterm newborns, infants, young children, older children, and adolescents. Calculation of pediatric patient doses is predicated on determining body surface area, which exhibits a superior correlation with the child's...
Drug Dosing in Renal Diseases: Measurement of Glomerular Filtration Rate01:25

Drug Dosing in Renal Diseases: Measurement of Glomerular Filtration Rate

The glomerular filtration rate (GFR) is a critical indicator of kidney health, reflecting how well the kidneys filter blood. Changes in GFR can signal potential kidney impairment, necessitating accurate measurement methods to monitor kidney function effectively.Various molecules can serve as markers for GFR measurement, with the ideal marker meeting several specific criteria. It must freely filter at the glomerulus, avoid reabsorption or secretion by the renal tubules, remain unmetabolized, not...
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption01:23

Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption

Understanding the physiological differences in the pediatric population is crucial for effective pharmacotherapy. Neonates, infants, and children exhibit significant variations in gastric pH, gastric emptying time, intestinal transit time, and biliary function. These variations profoundly affect oral drug absorption, necessitating a nuanced approach to pediatric dosing.Neonates present with a unique physiological profile, having a gastric pH greater than 4 and faster and more irregular gastric...