ANALYSIS OF BONE-AGE MATURATION AND GROWTH VELOCITY IN ISOLATED GROWTH-HORMONE (GH) DEFICIENT BOYS WITH AND WITHOUT GONADAL SUPPRESSION TREATMENT AND IN GH DEFICIENT BOYS WITH ASSOCIATED GONADOTROPIN-DEFICIENCY
M. Satoh et al., ANALYSIS OF BONE-AGE MATURATION AND GROWTH VELOCITY IN ISOLATED GROWTH-HORMONE (GH) DEFICIENT BOYS WITH AND WITHOUT GONADAL SUPPRESSION TREATMENT AND IN GH DEFICIENT BOYS WITH ASSOCIATED GONADOTROPIN-DEFICIENCY, Journal of pediatric endocrinology & metabolism, 10(6), 1997, pp. 615-622
Bone age maturation and growth velocity were analyzed longitudinally b
y the TW2 RUS method standardized for Japanese children in 45 GH-treat
ed boys with idiopathic GH deficiency (GHD). The patients were divided
into three groups: Group I consisted of four isolated GHD patients wh
o underwent spontaneous puberty without gonadotropin suppression treat
ment (GST) and had a mean final height of 151.9 cm; Group II consisted
of 24 GHD patients with associated gonadotropin deficiency who receiv
ed sex hormone replacement treatment (GRT) and had a mean final height
of 165.3 cm; Group III consisted of 17 isolated GHD patients who unde
rwent spontaneous puberty and had a mean final height of 158.3 cm afte
r being treated with combined GH and GST. Bone age matured along with
chronological age in Group I, whereas bone age in Group II decelerated
significantly after a bone age of 12 years and did not reach a bone a
ge of 14 years, Bone age maturation in Group III showed an intermediat
e pattern between Groups I and II; bone age decelerated significantly
after a bone age of 12 years but mean bone age advanced beyond a bone
age of 14 years. Height velocity in Group I during GH treatment decele
rated rapidly after the pubertal growth spurt, as usually seen in norm
al puberty, A definite pubertal growth spurt was not observed in the h
eight velocity of Group II during GH treatment before receiving GRT; t
he mean height velocity gradually declined, remaining at 3.5-4.5 cm/ye
ar even after 18 years, Mean height velocity in Group III during GH tr
eatment and GST showed a similar tendency as Group II, but it declined
more rapidly. Since a growth velocity of around 3 cm/year was preserv
ed with GH treatment despite the decline in growth velocity, the slowe
r the advance of bone age, the longer the treatment period and, theref
ore, the taller the final height achieved by GST compared to Group I.
It is recommended to start GST at a bone age between 11.5 years and 13
years. The timing, namely when to start GRT in GHD with gonadotropin
deficiency or when to stop GST in isolated GHD, can be estimated accor
ding to the patient's desired final height and bone age-growth potenti
al.