Growth, development, puberty and adult height before and during treatment in children with congenital isolated growth hormone deficiency

被引:21
作者
Smuel, Keren [1 ]
Kauli, Rivka [1 ]
Lilos, Pearl [1 ]
Laron, Zvi [1 ]
机构
[1] Tel Aviv Univ, Sackler Fac Med, Schneider Childrens Med Ctr, Endocrinol & Diabet Res Unit, IL-69978 Tel Aviv, Israel
关键词
Congenital IGHD; GHRH-R mutations; hGH treatment; Growth; Puberty; hGH-1A gene deletion; Skinfold thickness; Adiposity; BMI; Age at first ejaculation; Menarche; ISOLATED GH DEFICIENCY; FINAL HEIGHT; ANTIBODY-FORMATION; GENE DELETION; TESTICULAR SIZE; MUTATION; BOYS; HGH; AGE; ADOLESCENCE;
D O I
10.1016/j.ghir.2015.05.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective: To describe the growth, development and puberty in children with congenital IGHD before and during hGH treatment. Subjects: Patients with cIGHD treated by hGH between the years 1958-1992. Setting: All patients were diagnosed, treated and followed in our clinic. Participants: Data were found in 37/41 patients (21 m, 16 f). 34 had hGH-1A deletions, 7 GHRH-R mutations. Patients, referred after age 25, were excluded. Results: The birth length of 10/37 neonates was 48.29 +/- 2.26 (44-50) cm. Birth weight of 28/37 neonates was 3380 +/- 370 g (m), 3230 +/- 409 g (f). Neuromotor milestones were variable. Age at referral was 5.7 +/- 4.2 y (m) and 5.6 +/- 3.8 y (f). Initiation of hGH treatment (35 mu g/kg/d) was 7.5 +/- 4.8, (0.8-15.08) y (m) and 6.8 +/- 4.36 (0.8-16.5)y (f). Height SDS increased from -43 to -1.8 (m) and from -4.5 to -2.6 (f). Head circumference increased from -2.6 to -1.3 (m) and from -2.7 to -2.3 (f). BMI increased from 15.8 to 20.6 (m) and from 15.5 to 20.4 (f). There was a negative correlation between age of hGH initiation and change in height SDS (r = -0.66; rho < 0.01), same for bone age (r = -0.69; rho < 0.01). Upper/lower body ratio decreased from 2.5 +/- 2.1 (m +/- SD) to 1.08 +/- 0.1 (rho < 0.0005). Puberty was delayed in boys, less so in girls. Mean age of 1st ejaculation (14 m) was 17.6 +/- 2.2y and of menarche (14 f. was 13.7 +/- 1.2 y. In both genders there was a positive correlation between age at start of hGH and age at onset of puberty (r = 0.57; rho < 0.01). All reached full sexual development but the penile and testicular sizes were below normal. There was a positive correlation between length of hGH treatment and final testicular volume (r = 0.597, rho = 0.05) and a negative correlation between the age at initiation of hGH treatment and final testicular volume(r = -0.523, rho = 0.018). All were obese and hGH treatment increased the adiposity progressively (r = 0.418, rho = 0.013). Conclusion: Early diagnosis and treatment of cIGHD enables normal or near normal growth, development and puberty. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:182 / 188
页数:7
相关论文
共 63 条
[1]   Isolated Growth Hormone Deficiency (GHD) in Childhood and Adolescence: Recent Advances [J].
Alatzoglou, Kyriaki S. ;
Webb, Emma Alice ;
Le Tissier, Paul ;
Dattani, Mehul T. .
ENDOCRINE REVIEWS, 2014, 35 (03) :376-432
[2]   Phenotype-Genotype Correlations in Congenital Isolated Growth Hormone Deficiency (IGHD) [J].
Alatzoglou, Kyriaki S. ;
Dattani, Mehul T. .
INDIAN JOURNAL OF PEDIATRICS, 2012, 79 (01) :99-106
[3]   Expanding the Spectrum of Mutations in GH1 and GHRHR: Genetic Screening in a Large Cohort of Patients with Congenital Isolated Growth Hormone Deficiency [J].
Alatzoglou, Kyriaki S. ;
Turton, James P. ;
Kelberman, Daniel ;
Clayton, Peter E. ;
Mehta, Ameeta ;
Buchanan, Charles ;
Aylwin, Simon ;
Crowne, Elisabeth C. ;
Christesen, Henrik T. ;
Hertel, Niels T. ;
Trainer, Peter J. ;
Savage, Martin O. ;
Raza, Jamal ;
Banerjee, Kausik ;
Sinha, Sunil K. ;
Ten, Svetlana ;
Mushtaq, Talat ;
Brauner, Raja ;
Cheetham, Timothy D. ;
Hindmarsh, Peter C. ;
Mullis, Primus E. ;
Dattani, Mehul T. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2009, 94 (09) :3191-3199
[4]  
Argente J, 2001, J PEDIATR ENDOCR MET, V14, P1003
[5]  
Arnhold I.J., 2014, J PEDIAT ENDOCRINOL, V12, P499
[6]   Clinical and molecular characterization of Brazilian patients with growth hormone gene deletions [J].
Arnhold, IJP ;
Osorio, MGF ;
Oliveira, SB ;
Estefan, V ;
Kamijo, T ;
Krishnamani, MRS ;
Cogan, JD ;
Phillips, JA ;
Mendonca, BB .
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 1998, 31 (04) :491-497
[7]  
Arrigo T., 2014, J PEDIAT ENDOCRINOL, V11, P45
[8]   Onset of Breast Development in a Longitudinal Cohort [J].
Biro, Frank M. ;
Greenspan, Louise C. ;
Galvez, Maida P. ;
Pinney, Susan M. ;
Teitelbaum, Susan ;
Windham, Gayle C. ;
Deardorff, Julianna ;
Herrick, Robert L. ;
Succop, Paul A. ;
Hiatt, Robert A. ;
Kushi, Lawrence H. ;
Wolff, Mary S. .
PEDIATRICS, 2013, 132 (06) :1019-1027
[9]   Biphasic response of subscapular skinfold thickness to hGH or IGF-1 administration to patients with congenital IGHD, congenital MPHD and Laron syndrome [J].
Bisker-Kassif, Orly ;
Kauli, Rivka ;
Lilos, Pearl ;
Laron, Zvi .
OBESITY RESEARCH & CLINICAL PRACTICE, 2014, 8 (01) :E55-E62
[10]   CATCH-UP GROWTH IN EARLY TREATED PATIENTS WITH GROWTH-HORMONE DEFICIENCY [J].
BOERSMA, B ;
RIKKEN, B ;
WIT, JM ;
JANSEN, M ;
DEMUINCKKEIZERSCHRAMA, SMPF ;
OOSTDIJK, W ;
OTTEN, BJ ;
VULSMA, T .
ARCHIVES OF DISEASE IN CHILDHOOD, 1995, 72 (05) :427-431