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Oxandrolone increases final height in Turner syndrome
Author(s) -
CROCK P.,
WERTHER G. A.,
WETTENHALL H. N. B.
Publication year - 1990
Publication title -
journal of paediatrics and child health
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.631
H-Index - 76
eISSN - 1440-1754
pISSN - 1034-4810
DOI - 10.1111/j.1440-1754.1990.tb02434.x
Subject(s) - oxandrolone , medicine , turner syndrome , anabolic steroid , bone age , anabolism , pediatrics , growth hormone , hormone
In order to examine whether the anabolic steroid oxandrolone has any long‐term effect on height in Turner syndrome, the short‐ and long‐term effects were studied in a group of 35 individuals with the syndrome. At commencement of treatment, age range was 8.2–16 years (mean 12.9); oxandrolone dosage was 0.07‐0.26 mg/kg per day (mean 0.14 mg/kg per day) and continued for 12 months‐6 years (mean 33 months), ending at 12–18.5 years (mean 15.6 years). Height velocity increased significantly on therapy from 3.3 ± 0.1 to 5.8 ± 0.3 cm/year at 6 and 12 months, and maintained at 4.8 ± 0.3 cm/year by two years (all P <0.001). Girls who were younger and whose bone age was delayed grew faster ( P <0.001). Oxandrolone dose correlated with height velocity at 12 ( r = 0.39, P <0.05) and 18 months ( r = 0.31, P <0.05). Both height standard deviation score (SDS) and estimated mature height (EMH) increased significantly by the end of treatment (‐0.31 ± 0.2, and to 0.45 ± 0.2, and 140.4 ± 1.1 cm to 144.4 ± 1.1 cm respectively (both P <0.0001). in 23 patients who had completed growth at a mean age of 20.6 ± 0.83 years, final height was 145.5 ± 1.3 cm. This was not significantly different from EMH of 144.9 ± 1.3 cm at the end of therapy, and based on a pre‐treatment EMH of 140.5 ± 1.3 cm, represented a mean height gain of 5 cm. Furthermore, based on height SDS for Turner syndrome at age 18 of 0.2 ± 0.2, compared with pre‐treatment height SDS of ‐0.32 ± 0.2, there was an increased SDS by the end of therapy of 0.5, equivalent to 4–5 cm. Side effects of oxandrolone were minor and infrequent, limited to increased muscularity and some degree of voice deepening. It is concluded that in Turner syndrome use of the anabolic steroid oxandrolone: (i) increases height velocity for up to 2 years of treatment; (ii) increases final height by 4–5 cm, based on both bone age EMH prediction and use of height standard deviation scores; (iii) is associated with reliable prediction of final height at end of therapy using Greulich‐Pyle/ayley‐Pinneau methods. Oxandrolone is an effective, economic, safe and well‐tolerated promoter of growth in Turner syndrome.