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Efficacy of Growth Hormone Treatment in Children with Type 1 Diabetes Mellitus and Growth Hormone Deficiency-An Analysis of KIGS Data.
Bonfig, Walter; Lindberg, Anders; Carlsson, Martin; Cutfield, Wayne; Dunger, David; Camacho-Hübner, Cecilia; Holl, Reinhard W.
Afiliación
  • Bonfig W; Department of Pediatrics, Klinikum Wels-Grieskirchen, Wels, Austria; Department of Pediatrics, Technical University München, Munich, Germany. Electronic address: walter.bonfig@mri.tum.de.
  • Lindberg A; Pfizer Health AB, Sollentuna, Sweden.
  • Carlsson M; Pfizer Health AB, Sollentuna, Sweden.
  • Cutfield W; Liggins Institute, University of Auckland, Auckland, New Zealand.
  • Dunger D; Department of Pediatrics and the Wellcome Trust-MRC Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom.
  • Camacho-Hübner C; Pfizer Inc, Endocrine Care, New York, NY.
  • Holl RW; Institute of Epidemiology and Medical Biometry, University of Ulm, Ulm, Germany; German Center for Diabetes Research (DZD), Munich-Neuherberg, Germany.
J Pediatr ; 198: 260-264, 2018 07.
Article en En | MEDLINE | ID: mdl-29656861
ABSTRACT

OBJECTIVE:

To analyze first-year treatment growth response and growth hormone (GH) dosage in prepubertal patients with the combination of type 1 diabetes mellitus (T1DM) and growth hormone deficiency (GHD). STUDY

DESIGN:

A total of 69 patients with T1DM and GHD treated with GH have been enrolled in KIGS (Pfizer International Growth Database). Of these, 24 prepubertal patients had developed T1DM before GHD and were included in this analysis. Of 30 570 patients with GHD without T1DM, 15 024 were prepubertal and served as controls. Values are expressed as mean ± SD.

RESULTS:

Patients with T1DM and GHD had similar characteristics compared with the GHD-alone group. Neither age (10.2 ± 3.13 vs 8.42 ± 3.46 years, P = .14), height SDS corrected for midparental height SDS at start of treatment (-1.62 ± 1.38 vs -1.61 ± 1.51, P = .80), nor GH dosage (0.24 ± 0.08 mg/kg/wk vs 0.20 ± 0.04 mg/kg/wk, P = .09) were different between those with and without T1DM. First-year catch-up growth was comparable between the 2 patient groups (first treatment year height velocity 7.54 ± 3.11 cm/year compared with 8.35 ± 2.54 cm/year in control patients, P = .38). Height SDS of children with T1DM and GHD improved from -2.62 ± 1.04 to -1.88 ± 1.11 over 1 year of GH treatment.

CONCLUSION:

Short-term response to GH therapy appeared similar in subjects with T1DM who then developed GHD and in those with GHD alone. Thus, T1DM does not appear to compromise GH response in children with GHD and should not exclude GH treatment in these children. GH treatment was safe in both subgroups of patients.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estatura / Hormona de Crecimiento Humana / Diabetes Mellitus Tipo 1 Tipo de estudio: Observational_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: J Pediatr Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estatura / Hormona de Crecimiento Humana / Diabetes Mellitus Tipo 1 Tipo de estudio: Observational_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: J Pediatr Año: 2018 Tipo del documento: Article
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