Long-term effects of previous oxandrolone treatment in adult women with Turner syndrome

被引:16
作者
Freriks, Kim [1 ]
Sas, Theo C. J. [2 ,3 ]
Traas, Maaike A. F. [4 ]
Netea-Maier, Romana T. [1 ]
den Heijer, Martin [1 ]
Hermus, Ad R. M. M. [1 ]
Wit, Jan M. [5 ]
van Alfen-van der Velden, Janielle A. E. M. [6 ]
Otten, Barto J. [6 ]
Keizer-Schrama, Sabine M. P. F. de Muinck [3 ]
Gotthardt, Martin [7 ]
Dejonckere, Philippe H. [8 ]
Zandwijken, Gladys R. J. [9 ]
Menke, Leonie A. [5 ,10 ]
Timmers, Henri J. L. M. [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Endocrinol 471, NL-6500 HB Nijmegen, Netherlands
[2] Albert Schweitzer Hosp, Dept Paediat, Dordrecht, Netherlands
[3] Erasmus MC, Dept Paediat, Rotterdam, Netherlands
[4] Gelre Hosp Apeldoorn, Dept Obstet & Gynaecol, Apeldoorn, Netherlands
[5] Leiden Univ, Dept Paediat, Med Ctr, Leiden, Netherlands
[6] Radboud Univ Nijmegen, Med Ctr, Dept Paediat, NL-6500 HB Nijmegen, Netherlands
[7] Radboud Univ Nijmegen, Med Ctr, Dept Nucl Med, NL-6500 HB Nijmegen, Netherlands
[8] Univ Med Ctr Utrecht, Dept Phoniatr, Utrecht, Netherlands
[9] Dutch Growth Res Fdn, Rotterdam, Netherlands
[10] Haga Hosp, Dept Paediat, The Hague, Netherlands
关键词
GROWTH-HORMONE TREATMENT; TREATED GIRLS; FINAL HEIGHT; BODY PROPORTIONS; INSULIN; COMBINATION; FREQUENCY; THERAPY; DENSITY; GLUCOSE;
D O I
10.1530/EJE-12-0404
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Short stature is a prominent feature of Turner syndrome (TS), which is partially overcome by GH treatment. We have previously reported the results of a trial on the effect of oxandrolone (Ox) in girls with TS. Ox in a dose of 0.03 mg/kg per day (Ox 0.03) significantly increased adult height gain, whereas Ox mg/kg per day (0.06) did not, at the cost of deceleration of breast development and mild virilization. The aim of this follow-up study in adult participants of the pediatric trial was to investigate the long-term effects of previous Ox treatment. Design and methods: During the previous randomized controlled trial, 133 girls were treated with GH combined with placebo (Pl), Ox 0.03, or Ox 0.06 from 8 years of age and estrogen from 12 years. Sixty-eight women (Pl, n=23; Ox 0.03, n=27; and Ox 0.06, n=18) participated in the double-blind follow-up study (mean age, 24.0 years; mean time since stopping GH, 8.7 years; and mean time of Ox/Pl use, 4.9 years). We assessed height, body proportions, breast size, virilization, and body composition. Results: Height gain (final minus predicted adult height) was maintained at follow-up (Ox 0.03 10.2 +/- 4.9 cm, Ox 0.06 9.7 +/- 4.4 cm vs Pl 8.0 +/- 4.6 cm). Breast size, Tanner breast stage, and body composition were not different between groups. Ox-treated women reported more subjective virilization and had a lower voice frequency. Conclusion: Ox 0.03 mg/kg per day has a beneficial effect on adult height gain in TS patients. Despite previously reported deceleration of breast development during Ox 0.03 treatment, adult breast size is not affected. Mild virilization persists in only a small minority of patients. The long-term evaluation indicates that Ox 0.03 treatment is effective and safe. European Journal of Endocrinology 168 91-99
引用
收藏
页码:91 / 99
页数:9
相关论文
共 35 条
[21]   Efficacy and Safety of Oxandrolone in Growth Hormone-Treated Girls with Turner Syndrome [J].
Menke, Leonie A. ;
Sas, Theo C. J. ;
Keizer-Schrama, Sabine M. P. F. de Muinck ;
Zandwijken, Gladys R. J. ;
de Ridder, Maria A. J. ;
Odink, Roelof J. ;
Jansen, Maarten ;
Delemarre-van de Waal, Henriette A. ;
Stokvis-Brantsma, Wilhelmina H. ;
Waelkens, Johan J. ;
Westerlaken, Ciska ;
Reeser, H. Maarten ;
van Trotsenburg, A. S. Paul ;
Gevers, Evelien F. ;
van Buuren, Stef ;
DeJonckere, Philippe H. ;
Hokken-Koelega, Anita C. S. ;
Otten, Barto J. ;
Wit, Jan M. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2010, 95 (03) :1151-1160
[22]  
Nielsen J, 1990, Birth Defects Orig Artic Ser, V26, P209
[23]  
Nilsson KO, 1996, J CLIN ENDOCR METAB, V81, P635, DOI 10.1210/jcem.81.2.8636281
[24]   Excess visceral and hepatic adipose tissue in Turner syndrome determined by magnetic resonance imaging: Estrogen deficiency associated with hepatic adipose content [J].
Ostberg, JE ;
Thomas, EL ;
Hamilton, G ;
Attar, MJH ;
Bell, JD ;
Conway, GS .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (05) :2631-2635
[25]   Reference values for height, height velocity and weight in Turner's Syndrome [J].
RongenWesterlaken, C ;
Corel, L ;
vandenBroeck, J ;
Massa, G ;
Karlberg, J ;
AlbertssonWikland, K ;
Naeraa, RW ;
Wit, JM ;
Otten, BJ ;
KeizerSchrama, SMPFD ;
DelemarrevandeWaal, HA ;
Oostdijk, W ;
Gons, MH ;
Drayer, NM ;
Reeser, HM ;
Gerver, WJ ;
Waelkens, JJJ ;
vanTeunenbroek, A ;
Rikken, B ;
Alm, J ;
Aronson, S ;
Gustafsson, J ;
Hagenas, L ;
Hager, A ;
Ivarsson, SA ;
Kristrom, B ;
Marcus, C ;
Moell, C ;
Nilsson, KO ;
Ritzen, M ;
Tuvemo, T ;
Westgren, U ;
Westphal, O ;
Aman, Y .
ACTA PAEDIATRICA, 1997, 86 (09) :937-942
[26]   Growth hormone therapy of Turner's syndrome: Beneficial effect on adult height [J].
Rosenfeld, RG ;
Attie, KM ;
Frane, J ;
Brasel, JA ;
Burstein, S ;
Cara, JF ;
Chernausek, S ;
Gotlin, RW ;
Kuntze, J ;
Lippe, BM ;
Mahoney, CP ;
Moore, WV ;
Saenger, P ;
Johanson, AJ .
JOURNAL OF PEDIATRICS, 1998, 132 (02) :319-324
[27]   Normalization of height in girls with Turner syndrome after long-term growth hormone treatment:: Results of a randomized dose-response trial [J].
Sas, TCJ ;
Keizer-Schrama, SMPFD ;
Stijnen, T ;
Jansen, M ;
Otten, BJ ;
Hoorweg-Nijman, JJG ;
Vulsma, T ;
Massa, GG ;
Rouwé, CW ;
Reeser, HM ;
Gerver, WJ ;
Gosen, JJ ;
Rongen-Westerlaken, C ;
Drop, SLS .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (12) :4607-4612
[28]   Body proportions during long-term growth hormone treatment in girls with Turner syndrome participating in a randomized dose-response trial [J].
Sas, TCJ ;
Gerver, WJM ;
de Bruin, R ;
Stijnen, T ;
Keizer-Schrama, SMPFD ;
Cole, TJ ;
van Teunenbroek, A ;
Drop, SL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (12) :4622-4628
[29]  
Stahnke N, 2002, J PEDIATR ENDOCR MET, V15, P129
[30]   Impact of growth hormone supplementation on adult height in Turner syndrome: Results of the Canadian randomized controlled trial [J].
Stephure, DK ;
Anglin, G ;
Chipman, J ;
Daneman, D ;
Dean, HJ ;
Guyda, HJ ;
Holland, FJ ;
Quigley, C ;
Van Vliet, G ;
Stephure, DK ;
Anglin, G ;
Van Vliet, G ;
Hall, JG ;
Preece, MA ;
Taylor, W ;
Daneman, A ;
Riley, B ;
Salisbury, SR ;
Curtis, JA ;
Szots, F ;
Barnes, RD ;
Legault, L ;
Polychronakos, C ;
Rodd, C ;
MacMillan, AB ;
Vander Meulen, JA ;
Alexander, DS ;
Couch, RM ;
McCoy, EE ;
Metzger, D ;
Kitson, HF ;
Stewart, LL ;
Tze, WJ ;
Taback, SP ;
Collu, R ;
Deal, CL ;
Huot, C ;
Faught, KA ;
Lawson, ML ;
Muirhead, SE ;
Best, TB ;
Bruce, GA ;
Khoury, K ;
Bailey, JD ;
Ehrlich, RM ;
Perlman, K ;
Rovet, J ;
Boulton, BC ;
Clarson, CL ;
Jenner, MRF .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (06) :3360-3366