Anabolic effects of growth hormone treatment in young children with cystic fibrosis

被引:33
|
作者
Alemzadeh, R [1 ]
Upchurch, L [1 ]
McCarthy, V [1 ]
机构
[1] Univ Tennessee, Grad Sch Med, Dept Pediat, Knoxville, TN 37920 USA
关键词
cystic fibrosis; growth hormone; malnutrition; growth failure;
D O I
10.1080/07315724.1998.10718788
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Malnutrition is commonly found in children with Cystic Fibrosis (CF) and is characterized by poor weight gain and linear growth. Almost one-third of children with CF are below 5th percentile for weight and height. Intensive nutritional supplementation may not result in sustained improvement in weight gain and linear growth. Objective: To evaluate the anabolic effects of GH, Humatrope (Eli Lilly, 0.05 mg/kg/day) was administered to five children with CF (3 males/2 females) for an average period of 2 years. Methods: All patients were maintained on caloric intake of 1.3-2.0 times the recommended daily allowance. Patients underwent standard growth hormone (GH) stimulation studies and measurement of IGF-1 and IGFBP-3. Results: The mean +/- SE for age and skeletal age were 3.2 +/- 0.85 years and 2.0 +/- 0.45 years, respectively. Growth was assessed by determining both weight and height, which were normalized for age and sex by calculating Z scores using MANES I reference data. Differences in Z scores between clinic visits (Delta Z) were calculated for both weight and height to determine changes in growth velocity. The mean Z scores for weight and height were markedly attenuated in CF children as compared with healthy children (-1.95 +/- 0.23 and -2.8 +/- 0.27, respectively). The mean +/- SE for maximum stimulated GH value, IGF-1 and IGFBP-3 were 9.2 +/- 1.2 ng/dl, 67 +/- 6 ng/ml, and 1.7 +/- 0.22 mg/L, respectively. GH treatment improved weight and height Z scores (-0.11 +/- 0.05 and -0.94 +/- 0.18, p<0.01) significantly. The Delta Z scores for weight and height were significantly increased during first and second year of GM treatment (p<0.02). Also, the average values of IGF-1 and IGFBP-3 were significantly increased as compared to pretreatment values (186 +/- 37 ng/ml and 3.0 +/- 0.22 mg/L, p<0.01). Conclusions: GM treatment significantly improves weight and linear growth in young patients with CF. These data suggest that anabolic effects of GM may be beneficial for treatment of malnutrition in children with CF.
引用
收藏
页码:419 / 424
页数:6
相关论文
共 50 条
  • [41] Growth failure in cystic fibrosis
    McNaughton, S
    Stormont, DA
    Shepherd, RW
    Francis, PWJ
    Dean, B
    JOURNAL OF PAEDIATRICS AND CHILD HEALTH, 1999, 35 (01) : 86 - 92
  • [42] Effects of the Sex Steroid Hormone Estradiol on Biofilm Growth of Cystic Fibrosis Pseudomonas aeruginosa Isolates
    Al-Zawity, Jiwar
    Afzal, Faria
    Awan, Aysha
    Nordhoff, Daniela
    Kleimann, Alexander
    Wesner, Daniel
    Montier, Tristan
    Le Gall, Tony
    Muller, Mareike
    FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2022, 12
  • [43] Effects of early recombinant human growth hormone treatment in young Chinese children with Prader–Willi syndrome
    Ying Gao
    Li-Li Yang
    Yang-Li Dai
    Zheng Shen
    Qiong Zhou
    Chao-Chun Zou
    Orphanet Journal of Rare Diseases, 18
  • [44] EFFECT OF HYPERSOMATOSTATINEMIA ON GROWTH-HORMONE SECRETION IN CYSTIC-FIBROSIS PATIENTS WITH DIABETES
    CULLER, FL
    MEACHAM, LR
    NEUROENDOCRINOLOGY, 1993, 58 (04) : 473 - 477
  • [45] THE CLINICAL SIGNIFICANCE OF OROPHARYNGEAL CULTURES IN YOUNG CHILDREN WITH CYSTIC FIBROSIS
    Breuer, O.
    Caudri, D.
    Akesson, L.
    Stick, S.
    Schultz, A.
    RESPIROLOGY, 2018, 23 : 142 - 142
  • [46] Low bone mineral density in young children with cystic fibrosis
    Sermet-Gaudelus, Isabelle
    Souberbielle, Lean Claude
    Ruiz, Jean Charles
    Vrielynck, Stephanie
    Heuillon, Blandine
    Azhar, Imrana
    Cazenave, Aline
    Lawson-Body, Ethel
    Chedevergne, Frederique
    Lenoir, Gerard
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2007, 175 (09) : 951 - 957
  • [47] Effects of Growth Hormone Treatment on Growth in Children with Juvenile Idiopathic Arthritis
    Simon, D.
    Bechtold, S.
    HORMONE RESEARCH, 2009, 72 : 55 - 59
  • [48] Auxological and Endocrinological Features in Children and Adolescents with Cystic Fibrosis
    Ferrari, Vittorio
    Terlizzi, Vito
    Stagi, Stefano
    JOURNAL OF CLINICAL MEDICINE, 2022, 11 (14)
  • [49] Quantitative Ultrasound in Spanish Children and Young Adults With Cystic Fibrosis
    Lopez-Rodriguez, Maria J.
    Lavado-Garcia, Jesus M.
    Canal-Macias, Maria L.
    Calderon-Garcia, Julian F.
    Moran, Jose M.
    Pedrera-Zamorano, Juan D.
    BIOLOGICAL RESEARCH FOR NURSING, 2013, 15 (03) : 280 - 284
  • [50] Interpretation of lung function in infants and young children with cystic fibrosis
    Ramsey, Kathryn A.
    Ranganathan, Sarath
    RESPIROLOGY, 2014, 19 (06) : 792 - 799