Seven years of follow up of trabecular bone score, bone mineral density, body composition and quality of life in adults with growth hormone deficiency treated with rhGH replacement in a single center

Author:

Allo Miguel Gonzalo1,Serraclara Plá Alicia2,Partida Muñoz Myriam Lorena2,Martínez Díaz-Guerra Guillermo2,Hawkins Federico2

Affiliation:

1. Endocrinology Service, 12 de Octubre University Hospital, Avenida Cordoba S/N, 28026 Madrid, Spain

2. Endocrinology Service, 12 de Octubre University Hospital, University Complutense, Madrid, Spain

Abstract

Background: Adult growth hormone deficiency (AGHD) is characterized by impaired physical activity, diminished quality of life (QoL), weight and fat mass gain, decreased muscle mass and decreased bone mineral density (BMD). The aim of this study was to evaluate the effects of long-term treatment (7 years) with recombinant human growth hormone (rhGH) on metabolic parameters, body composition (BC), BMD, bone microarchitecture and QoL. Patients and Methods: In this prospective study, BMD and BC were assessed by dual-energy X-ray absorptiometry (DXA). Bone microarchitecture was assessed with the trabecular bone score (TBS). The QoL-AGHDA test was used to assess QoL. Results: A total of 18 AGHD patients (mean age, 37.39 ± 12.42) were included. Body weight and body mass index (BMI) showed a significant increase after 7 years ( p = 0.03 and p = 0.001, respectively). There was a significant tendency of body fat mass (BFM) ( p = 0.028) and lean body mass (LBM) ( p = 0.005) to increase during the 7 years of rhGH treatment. There was a significant increase in lumbar spine (LS) BMD ( p = 0.01). TBS showed a nonsignificant decrease after 7 years of treatment, with a change of -0.86% ± 1.95. QoL showed a large and significant improvement ( p = 0.02). Conclusion: Long-term rhGH treatment in AGHD patients induces a large and sustained improvement in QoL. Metabolic effects are variable with an increase in LBM as well as in BMI and BFM. There is a positive effect on BMD based on the increase in LS BMD, which stabilizes during long-term therapy and is not associated with a similar increase in bone microarchitecture.

Publisher

SAGE Publications

Subject

Endocrinology, Diabetes and Metabolism

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