Ann Pediatr Endocrinol Metab.  2013 Mar;18(1):13-18. 10.6065/apem.2013.18.1.13.

Response to three years of growth hormone therapy in girls with Turner syndrome

Affiliations
  • 1Department of Pediatrics, Hallym University College of Medicine, Seoul, Korea.
  • 2Department of Pediatrics, Ajou University School of Medicine, Suwon, Korea. pedhwang@ajou.ac.kr

Abstract

PURPOSE
Short stature is the most common finding in patients with Turner syndrome. Improving the final adult height in these patients is a challenge both for the patients and physicians. We investigated the clinical response of patients to growth hormone treatment for height improvement over the period of three years.
METHODS
Review of medical records from 27 patients with Turner syndrome treated with recombinant human growth hormone for more than 3 years was done. Differences in the changes of height standard deviation scores according to karyotype were measured and factors influencing the height changes were analyzed.
RESULTS
The response to recombinant human growth hormone was an increase in the height of the subjects to a mean value of 1.1 standard deviation for subjects with Turner syndrome at the end of the 3-year treatment. The height increment in the first year was highest. The height standard deviation score in the third year was negatively correlated with the age at the beginning of the recombinant human growth hormone treatment. Different karyotypes in subjects did not seem to affect the height changes.
CONCLUSION
Early growth hormone administration in subjects with Turner syndrome is helpful to improve height response to the treatment.

Keyword

Turner syndrome; Growth hormone; Treatment outcome

MeSH Terms

Adult
Growth Hormone
Human Growth Hormone
Humans
Karyotype
Medical Records
Treatment Outcome
Turner Syndrome
Growth Hormone
Human Growth Hormone

Figure

  • Fig. 1 Changes in height standard deviation scores for Korean Turner syndrome (TSSDS, continuous line) and normal population (standard deviation score [SDS], dashes) patients during growth hormone (GH) treatment. P-values indicate the differences between each point in time and the previous observation.

  • Fig. 2 Changes in standard deviation score for the height of Korean Turner syndrome patients according to the karyotypes of the subjects. GH, growth hormone.

  • Fig. 3 Relationship between the age at the commencementof growth hormone (GH) administration and the standard deviation scores of height at the third year.


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