Final height in girls with Turner syndrome after long-term growth hormone treatment in three dosages and low dose estrogens

被引:169
|
作者
van Pareren, YK
Keizer-Schrama, SMPFD
Stijnen, T
Sas, TCJ
Jansen, M
Otten, BJ
Hoorweg-Nijman, JJG
Vulsma, T
Stokvis-Brantsma, WH
Rouwé, CW
Reeser, HM
Gerver, WJ
Gosen, JJ
Rongen-Westerlaken, C
Drop, SLS
机构
[1] Erasmus MC Sophia Childrens Hosp, Dept Pediat, Div Endocrinol, NL-3015 GJ Rotterdam, Netherlands
[2] Erasmus Univ, Dept Epidemiol & Biostat, NL-3015 GJ Rotterdam, Netherlands
[3] Wilhelmina Childrens Hosp, NL-3584 EA Utrecht, Netherlands
[4] Univ Nijmegen St Radboud Hosp, NL-6523 GA Nijmegen, Netherlands
[5] Free Univ Amsterdam Hosp, NL-1081 HV Amsterdam, Netherlands
[6] Univ Amsterdam, Acad Med Ctr, Emma Childrens Hosp, NL-1105 AZ Amsterdam, Netherlands
[7] Leiden Univ, Ctr Med, NL-2333 ZA Leiden, Netherlands
[8] Univ Groningen, Univ Med Ctr Groningen, Beatrix Childrens Hosp, NL-9713 GZ Groningen, Netherlands
[9] Juliana Childrens Hosp, NL-2566 MJ The Hague, Netherlands
[10] Acad Hosp Maastricht, NL-6229 HX Maastricht, Netherlands
[11] Rijnland Hosp, NL-2353 GA Leiderdorp, Netherlands
[12] Canisius Wilhelmina Hosp, NL-6532 SZ Nijmegen, Netherlands
来源
关键词
D O I
10.1210/jc.2002-021171
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although GH treatment for short stature in Turner syndrome is an accepted treatment in many countries, which GH dosage to use and which age to start puberty induction are issues of debate. This study shows final height (FH) in 60 girls with Turner syndrome treated in a randomized dose-response trial, combining GH treatment with low dose estrogens at a relatively young age. Girls were randomly assigned to group A (4 IU/m(2) . d; similar to0.045 mg/kg/d), group B (first year, 4 IU/m(2).d; thereafter 6 IU/m(2).d), or group C (first year, 4 IU/m(2).d; second year, 6 IU/m(2).d; thereafter, 8 IU/m(2).d). After a minimum of 4 yr of GH treatment, at a mean age of 12.7 +/- 0.7 yr, low dose micronized 17beta-estradiol was given orally. After a mean duration of GH treatment of 8.6 +/- 1.9 yr, FH was reached at a mean age of 15.8 +/- 0.9 yr. FH, expressed in centimeters or SD score, was 157.6 +/- 6.5 or - 1.6 +/- 1.0 in group A, 162.9 +/- 6.1 or -0.7 +/- 1.0 in group B, and 163.6 6.0 or -0.6 +/- 1.0 in group C. The difference in FH in centimeters, corrected for height SD score and age at start of treatment, was significant between groups A and B [regression coefficient, 4.1; 95% confidence interval (CI), 1.4,6.9; P < 0.01], and groups A and C (coefficient, 5.0; 95% CI, 2.3,7.7; P < 0.001)9 but not between groups B and C (coefficient, 0.9; 95% CI, - 1.8, 3.6). Fifty of the 60 girls (83%) had reached a normal FH (FH SD score, more than -2). After starting estrogen treatment, the decrease in height velocity (HV) changed significantly to a stable HV, without affecting bone maturation (change in bone age/change in chronological age). The following variables contributed significantly to predicting FH SD score: GH dose, height SD score (ref. normal girls), chronological age at start of treatment, and HV in the first year of GH treatment. GH treatment was well tolerated. In conclusion, GH treatment leads to a normalization of FH in most girls, even when puberty is induced at a normal pubertal age. The optimal GH dosage depends on height and age at the start of treatment and first year HV.
引用
收藏
页码:1119 / 1125
页数:7
相关论文
共 50 条
  • [31] Favorable final height outcome in girls with Ullrich-Turner syndrome treated with low-dose growth hormone together with oxandrolone despite starting treatment after 10 years of age
    Stahnke, N
    Keller, E
    Landy, H
    JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2002, 15 (02): : 129 - 138
  • [32] Final height in Turner syndrome patients treated with growth hormone
    Pasquino, AM
    Passeri, F
    Municchi, G
    Segni, M
    Pucarelli, I
    Larizza, D
    Bossi, G
    Severi, F
    Galasso, C
    HORMONE RESEARCH, 1996, 46 (06) : 269 - 272
  • [33] Carbohydrate metabolism during long-term growth hormone (GH) treatment and after discontinuation of GH treatment in girls with turner syndrome participating in a randomized dose-response study
    Sas, TCJ
    Keizer-Schrama, SMPFD
    Stijnen, T
    Aanstoot, HJ
    Drop, SLS
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (02): : 769 - 775
  • [34] Final height in girls with Turner's syndrome treated with once or twice daily growth hormone injections
    Sas, TCJ
    Keizer-Schrama, SMPFD
    Stijnen, T
    van Teunenbroek, A
    Hokken-Koelega, ACS
    Waelkens, JJJ
    Massa, GG
    Vulsma, T
    Gerver, WJ
    Reeser, HM
    Delemarre-van de Waal, HE
    Jansen, M
    Drop, SLS
    ARCHIVES OF DISEASE IN CHILDHOOD, 1999, 80 (01) : 36 - 41
  • [35] LONG-TERM GROWTH HORMONE TREATMENT AUGMENTS FINAL ADULT HEIGHT IN PATIENTS WITH ACHONDROPLASIA
    Harada, Daisuke
    Namba, Noriyuki
    Hanioka, Yuki
    Ueyama, Kaoru
    Sakamoto, Natsuko
    Izui, Masafumi
    Nagamatsu, Yuiko
    Kashiwagi, Hiroko
    Yamamuro, Miho
    Ishiura, Yoshihito
    Ogitani, Ayako
    Seino, Yoshiki
    HORMONE RESEARCH IN PAEDIATRICS, 2017, 88 : 95 - 95
  • [36] Final height after long-term treatment with recombinant human growth hormone (RHGH) in children with uremic growth failure
    Nissel, Richard
    Ucur, Esat
    Mehls, Otto
    Haffner, Dieter
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2006, 21 : 367 - 368
  • [37] Long-term results of growth hormone therapy in Turner syndrome
    Bramswig, JH
    ENDOCRINE, 2001, 15 (01) : 5 - 13
  • [38] Long-term results of growth hormone therapy in turner syndrome
    J. H. Bramswig
    Endocrine, 2001, 15 : 5 - 13
  • [39] Growth hormone treatment regimens in girls with Turner syndrome
    Keizer-Schrama, SMPFD
    Sas, TCJ
    ACTA PAEDIATRICA, 1999, 88 : 126 - 129
  • [40] Accurate Long-Term Prediction of Height during the First Four Years of Growth Hormone Treatment in Prepubertal Children with Growth Hormone Deficiency or Turner Syndrome
    Ranke, Michael B.
    Lindberg, Anders
    Brosz, Mathias
    Kaspers, Stefan
    Loftus, Jane
    Wollmann, Hartmut
    Koltowska-Haggstrom, Maria
    Roelants, Mathieu
    HORMONE RESEARCH IN PAEDIATRICS, 2012, 78 (01): : 8 - 17