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Vasculometabolic effects in patients with congenital growth hormone deficiency with and without GH replacement
Isabela Peixoto Biscotto1, Valéria Aparecida Costa Hong2, Rafael Loch Batista3
1Unidade de Endocrinologia do Desenvolvimento, Laboratório de Hormônios e Genética Molecular LIM42, Disciplina de Endocrinologia, Departamento de Clínica Médica do Hospital das Clínicas da Faculdade de Medicina da Universidade São Paulo, Av. Dr. Eneas de Carvalho Aguiar, 255, Sao Paulo, SP, 05403-000, Brazil. isapbiscotto@gmail.com.
Insights
Adults with congenital growth hormone deficiency (GHD) not on GH replacement therapy (GHRT) had unfavorable body composition but similar vascular properties compared to those on GHRT. GHRT decisions for adults with GHD remain individualized.
Area of Science:
- Endocrinology
- Metabolic Disorders
- Vascular Biology
Background:
- Congenital growth hormone deficiency (GHD) in adults can lead to adverse metabolic and body composition changes.
- The impact of GH replacement therapy (GHRT) on vascular properties in adults with GHD requires further investigation.
Purpose of the Study:
- To evaluate and compare metabolic profiles and vascular properties in adult patients with congenital GHD, with and without GH replacement therapy (GHRT).
Main Methods:
- A cross-sectional study involving 81 adult subjects: 29 GHD patients on GHRT, 20 GHD patients without GHRT, and 32 controls.
- Assessment included anthropometric parameters, body composition (DXA), metabolic profiles, and vascular properties (carotid intima-media thickness, pulse wave velocity, flow-mediated dilation).
Main Results:
- Patients without GHRT exhibited significantly higher waist-to-height ratio, body fat percentage, and fat mass index compared to those on GHRT.
- Patients without GHRT showed unfavorable lipid profiles with higher triglycerides and lower HDL cholesterol than controls.
- No significant differences in vascular properties were observed among the three groups.
Conclusions:
- Adults with congenital GHD without GHRT present with poorer body composition but do not show differences in vascular properties compared to those receiving GHRT.
- These findings support an individualized approach to GHRT in adults with GHD, considering metabolic and body composition outcomes.
Purpose:
To evaluated the metabolic profiles and vascular properties in congenital growth hormone (GH) deficiency (GHD) and its replacement in adults.
Patients And Methods:
Cross-sectional study conducted in a single tertiary center for pituitary diseases. Eighty-one adult subjects were divided into three groups: (1) 29 GHD patients with daily subcutaneous GH replacement therapy (GHRT) during adulthood; (2) 20 GHD patients without GHRT during adulthood and (3) 32 controls. Only patients with adequate adherence to others pituitary hormone deficiencies were included. Anthropometric parameters, body composition by dual-energy X-ray absorptiometry, metabolic profiles and vascular properties (carotid intima media thickness, pulse wave velocity and flow-mediated dilation) were compared among the groups.
Results:
Waist-to-height ratio (WHR), body fat percentages and fat mass index (FMI) were lower in patients with GHRT than patients without GHRT during adulthood (0.49 ± 0.06 vs. 0.53 ± 0.06 p = 0.026, 30 ± 10 vs. 40 ± 11 p = 0.003 and 7.3 ± 4 vs. 10 ± 3.5 p = 0.041, respectively). In addition, association between longer GHRT and lower body fat percentage was observed (r = - 0.326, p = 0.04). We found higher triglyceride (113.5 ± 62 vs. 78 ± 36, p = 0.025) and lower HDL cholesterol (51 ± 17 vs. 66 ± 23, p = 0.029) levels in patients without GHRT during adulthood in comparison to controls. No statistical differences were observed for vascular properties among the groups.
Conclusions:
No differences in vascular properties were observed in congenital GHD adult patients with or without GHRT despite patients without GHRT had an unfavorable body composition. GHRT currently remains an individualized decision in adults with GHD and these findings bring new insight into the treatment and follow-up of these patients.
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