Literature DB >> 31462537

GH-IGF-1 Axis in Children with Cystic Fibrosis.

Sara Pagani1, Elena Bozzola2, Gloria Acquafredda3, Vito Terlizzi4, Valeria Raia5, Fabio Majo6, Alberto Villani2, Mauro Bozzola7.   

Abstract

OBJECTIVE: To verify whether growth hormone receptor (GHR) gene expression plays a role in growth of children with cystic fibrosis (CF), as a consequence of the chronic inflammatory condition and malnutrition.
DESIGN: We enrolled 49 prepubertal patients (24 males and 25 females) affected by CF in a stable clinical condition, 19 of whom had been diagnosed through newborn screening and 30 following presentation of symptoms. Patients had no significant comorbidity affecting growth or cystic fibrosis transmembrane conductance regulator (CFTR)-related diabetes requiring insulin therapy. Blood was collected during two follow-up visits to measure insulin-like growth factor (IGF-I), growth hormone-binding protein (GHBP), and GHR gene expression. Recruited as a control group were 52 healthy children, sex- and age-matched, were recruited as a control group.
METHODS: We compared body mass index (BMI), height, weight, IGF-I, GHBP, and GHR gene expression values (evaluated by Chemiluminescent Immunometric assay; ELISA and real-time PCR, respectively) in CF patients diagnosed through newborn screening (NBS) or by symptoms (late diagnosis [LD]) and in healthy controls.
RESULTS: BMI increased significantly in patients between the time of diagnosis and check-up (P<0.001), particularly in the LD group; median value was lower at diagnosis and significantly higher (P<0.001) at follow-up visits compared to controls. At initial evaluation, higher levels of IGF-I (not statistically significant) were found in both the NBS group and the LD group compared to the control group. At the second evaluation, significantly higher levels of IGF-I (P=0.003) were found in both the NBS and LD groups compared to controls; GHR mRNA expression had significantly increased (P=0.013) in LD patients compared with the first evaluation and was significantly higher in the NBS and LD groups than in controls. GHBP values had significantly increased (P=0.047) in the NBS group after one year of therapy compared to first visit levels and were significantly higher (P<0,0001) in the NBS and LD groups compared to controls.
CONCLUSION: In our LD patients during childhood, we observed good auxological values and a GH/IGF-I axis function within normal range for the factor evaluated. However, earlier diagnosis through NBS might further minimize and prevent growth retardation, by reducing the duration of symptoms before treatment.
© 2019 Marshfield Clinic.

Entities:  

Keywords:  Cystic fibrosis: growth; Growth hormone receptor; IGF-I; Newborn screening

Mesh:

Substances:

Year:  2019        PMID: 31462537      PMCID: PMC6886888          DOI: 10.3121/cmr.2019.1476

Source DB:  PubMed          Journal:  Clin Med Res        ISSN: 1539-4182


  23 in total

Review 1.  Cystic fibrosis adult care: consensus conference report.

Authors:  James R Yankaskas; Bruce C Marshall; Beth Sufian; Richard H Simon; David Rodman
Journal:  Chest       Date:  2004-01       Impact factor: 9.410

2.  Growth in Prepubertal Children With Cystic Fibrosis Treated With Ivacaftor.

Authors:  Michael S Stalvey; Jesse Pace; Minoo Niknian; Mark N Higgins; Valerie Tarn; Joy Davis; Sonya L Heltshe; Steven M Rowe
Journal:  Pediatrics       Date:  2017-02       Impact factor: 7.124

3.  Cystic fibrosis - Comparison between patients in paediatric and adult age.

Authors:  V Santos; A V Cardoso; C Lopes; P Azevedo; F Gamboa; A Amorim
Journal:  Rev Port Pneumol (2006)       Date:  2016-10-13

Review 4.  Manifestations of cystic fibrosis diagnosed in adulthood.

Authors:  Jerry A Nick; David M Rodman
Journal:  Curr Opin Pulm Med       Date:  2005-11       Impact factor: 3.155

5.  Growth Deficiency in Cystic Fibrosis Is Observable at Birth and Predictive of Early Pulmonary Function.

Authors:  Rebecca Darrah; Rebecca Nelson; Elizabeth G Damato; Michael Decker; Anne Matthews; Craig A Hodges
Journal:  Biol Res Nurs       Date:  2016-04-13       Impact factor: 2.522

6.  Deregulation of the growth hormone/insulin-like growth factor-1 axis in adults with cystic fibrosis.

Authors:  C Pascucci; R V De Biase; D Savi; S Quattrucci; A M Isidori; C Lubrano; L Gnessi; A Lenzi
Journal:  J Endocrinol Invest       Date:  2017-11-02       Impact factor: 4.256

7.  Growth Hormone Receptor Gene Expression Increase Reflects Nutritional Status Improvement in Patients Affected by Crohn's Disease.

Authors:  Sara Pagani; Elena Bozzola; Caterina Strisciuglio; Cristina Meazza; Erasmo Miele; M Malamisura; Paola De Angelis; Mauro Bozzola
Journal:  Front Pediatr       Date:  2018-11-12       Impact factor: 3.418

Review 8.  Endocrine Disorders in Cystic Fibrosis.

Authors:  Scott M Blackman; Vin Tangpricha
Journal:  Pediatr Clin North Am       Date:  2016-08       Impact factor: 3.278

9.  Serum insulin-like growth factor-1 (IGF-1) during CF pulmonary exacerbation: trends and biomarker correlations.

Authors:  A H Gifford; A B Nymon; A Ashare
Journal:  Pediatr Pulmonol       Date:  2013-06-18

Review 10.  Inflammatory Diseases and Growth: Effects on the GH-IGF Axis and on Growth Plate.

Authors:  Francesca Cirillo; Pietro Lazzeroni; Chiara Sartori; Maria Elisabeth Street
Journal:  Int J Mol Sci       Date:  2017-08-31       Impact factor: 5.923

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  2 in total

1.  Zinc status and growth in infants and young children with cystic fibrosis.

Authors:  Sarah E Bauer; HuiChuan J Lai; Catherine M McDonald; Fadi Asfour; James E Slaven; Clement L Ren
Journal:  Pediatr Pulmonol       Date:  2021-09-17

Review 2.  Auxological and Endocrinological Features in Children and Adolescents with Cystic Fibrosis.

Authors:  Vittorio Ferrari; Vito Terlizzi; Stefano Stagi
Journal:  J Clin Med       Date:  2022-07-13       Impact factor: 4.964

  2 in total

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