GROWTH-HORMONE THERAPY IN TURNERS SYNDROME - AN UPDATE ON FINAL HEIGHT

被引:0
作者
ROSENFELD, RG
ATTIE, KM
FRANE, J
JOHANSON, AJ
KUNTZE, J
BRASEL, JA
BURSTEIN, S
CARA, JF
CHERNAUSEK, S
GOTLIN, RW
LIPPE, BM
MAHONEY, PC
MOORE, WV
SAENGER, P
机构
[1] UNIV KANSAS,MED CTR,LAWRENCE,KS 66045
[2] MONTEFIORE HOSP & MED CTR,NEW YORK,NY
[3] CHILDRENS HOSP,MED CTR,CINCINNATI,OH
[4] MASON CLIN,SEATTLE,WA 98111
[5] UNIV CALIF LOS ANGELES,SCH MED,LOS ANGELES,CA 90024
[6] UNIV CHICAGO,CHICAGO,IL 60637
[7] UNIV CALIF LOS ANGELES,MED CTR,LOS ANGELES,CA 90024
[8] GENENTECH INC,SAN FRANCISCO,CA 94080
[9] UNIV TENNESSEE,KNOXVILLE,TN 37996
[10] UNIV COLORADO,MED CTR,BOULDER,CO 80309
关键词
GROWTH HORMONE; OXANDROLONE; TURNERS SYNDROME; HEIGHT VELOCITY; FINAL HEIGHT;
D O I
暂无
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The Genentech National Cooperative Study of growth hormone (GH) therapy in Turner's syndrome was initiated in 1983; 70 girls with Turner's syndrome were randomly assigned to observation or to treatment with GH alone, oxandrolone alone, or a combination of GH plus oxandrolone for a period of 12-24 months. After completion of this phase, patients receiving GH alone were continued on GH, while all other patients received the combination of GH plus oxandrolone. Data are currently available on the 62 girls who were treated for a minimum of 3-6 years. When compared with the height velocities anticipated for girls of comparable ages with untreated Turner's syndrome, both GH alone and a combination of GH plus oxandrolone resulted in an increase in height velocity, which was most prominent during the first 2 years of treatment and was sustained for at least 6 years. Although GH therapy is continuing at present in half of the patients, 14 of 17 girls (82%) receiving GH alone and 42 of 45 girls (93%) receiving combination therapy have exceeded their projected adult heights. For the 30 girls who have stopped therapy. the current mean height is 151.9 cm, compared with their original mean projected adult height of 143.8 cm. These results demonstrate that GH therapy can result in short-term (3-6 years) acceleration of growth, as well as in improved adult height.
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页码:3 / 6
页数:4
相关论文
共 12 条
  • [1] GROWTH CURVE FOR GIRLS WITH TURNER SYNDROME
    LYON, AJ
    PREECE, MA
    GRANT, DB
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1985, 60 (10) : 932 - 935
  • [2] GROWTH-HORMONE TREATMENT OF TURNER SYNDROME PATIENTS WITH INSUFFICIENT GROWTH-HORMONE RESPONSE TO PHARMACOLOGICAL STIMULATION TESTS
    MASSA, G
    VANDERSCHEURENLODEWEYCKX, M
    CRAEN, M
    VANDEWEGHE, M
    VANVLIET, G
    [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1991, 150 (07) : 460 - 463
  • [3] NILSSON KO, 1989, ACTA PAEDIATR SC S, V356, P160
  • [4] CHROMOSOMAL AND CLINICAL FINDINGS IN 110 FEMALES WITH TURNER SYNDROME
    PALMER, CG
    REICHMANN, A
    [J]. HUMAN GENETICS, 1976, 35 (01) : 35 - 49
  • [5] PARK E, 1983, PEDIATR RES, V17, P1
  • [6] RANKE MB, 1991, TURNERS SYNDROME GRO
  • [7] METHIONYL HUMAN GROWTH-HORMONE IN TURNERS SYNDROME
    RONGENWESTERLAKEN, C
    WIT, JM
    DROP, SLS
    OTTEN, BJ
    OOSTDIJK, W
    DELEMARREVANDENWAAL, HA
    GONS, MH
    BOT, A
    VANDENBRANDE, JL
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1988, 63 (10) : 1211 - 1217
  • [8] 3-YEAR RESULTS OF A RANDOMIZED PROSPECTIVE TRIAL OF METHIONYL HUMAN GROWTH-HORMONE AND OXANDROLONE IN TURNER SYNDROME
    ROSENFELD, RG
    HINTZ, RL
    JOHANSON, AJ
    SHERMAN, B
    BRASEL, JA
    BURSTEIN, S
    CHERNAUSEK, S
    COMPTON, P
    FRANE, J
    GOTLIN, RW
    KUNTZE, J
    LIPPE, BM
    MAHONEY, PC
    MOORE, WV
    NEW, MI
    SAENGER, P
    SYBERT, V
    [J]. JOURNAL OF PEDIATRICS, 1988, 113 (02) : 393 - 400
  • [9] METHIONYL HUMAN GROWTH-HORMONE AND OXANDROLONE IN TURNER SYNDROME - PRELIMINARY-RESULTS OF A PROSPECTIVE RANDOMIZED TRIAL
    ROSENFELD, RG
    HINTZ, RL
    JOHANSON, AJ
    BRASEL, JA
    BURSTEIN, S
    CHERNAUSEK, SD
    CLABOTS, T
    FRANE, J
    GOTLIN, RW
    KUNTZE, J
    LIPPE, BM
    MAHONEY, PC
    MOORE, WV
    NEW, MI
    SAENGER, P
    STONER, E
    SYBERT, V
    [J]. JOURNAL OF PEDIATRICS, 1986, 109 (06) : 936 - 943
  • [10] ROSENFELD RG, 1992, IN PRESS J PEDIATR