Related Experiment Video
Updated: Jun 4, 2026

Semi-Targeted Ultra-High-Performance Chromatography Coupled to Mass Spectrometry Analysis of Phenolic Metabolites in Plasma of Elderly Adults
Published on: April 22, 2022
Aromatase inhibitors to augment height: continued caution and study required.
1Saban Research Institute, Childrens Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, CA 90027, USA. mgeffner@chla.usc.edu
Aromatase inhibitors (AIs) may increase height potential in children by slowing bone maturation. However, extensive research is needed to confirm efficacy and safety in pediatric populations.
Area of Science:
- Pediatric Endocrinology
- Pharmacology
Background:
- Aromatase inhibitors (AIs) block androgen-to-estrogen conversion.
- Estrogen is crucial for growth plate fusion in children.
- AIs are approved for breast cancer but explored off-label for short stature.
Purpose of the Study:
- To evaluate the potential of AIs to enhance height in children.
- To highlight the need for rigorous studies on AI efficacy and safety in pediatric populations.
Main Methods:
- Review of existing research trials on AI use in children.
- Analysis of limited data from Finland and Florida studies.
- Observation of off-label AI use in the United States.
Main Results:
- Limited data suggests potential efficacy in slowing epiphysial maturation.
- Fewer than 110 children globally treated in research protocols by 2008.
- Many children treated off-label in the US, with unknown outcomes.
Conclusions:
- Aromatase inhibitors show promise for increasing height potential in children.
- Significant gaps exist in understanding the long-term efficacy and safety of AIs in pediatric use.
- Well-designed, long-term studies are imperative for pediatric AI application.
Related Concept Videos
Nature and Nurture
Oral Hypoglycemic Agents: Biguanides and Glitazones
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors
Acarbose and miglitol are typically...
Drug Dosing: Obese Patients
Dosage Regimen: Individualization
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase