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DOI 10.1016/j.medcli.2016.06.002

Медицинская библиотека · Medicina clinica · 2016

[Body composition and metabolic risk in small for gestational age children treated with growth hormone].

Aurensanz Clemente Esther, Samper Villagrasa Pilar, Ayerza Casas Ariadna, Ruiz Frontera Pablo, Moreno Aznar Luis Alberto, Bueno Lozano Gloria

Клиническое исследованиеСтатьяПеревод в очереди

Аннотация

BACKGROUND AND

OBJECTIVES

Small for gestational age (SGA) children are at increased risk of metabolic syndrome. Our objective is to evaluate changes in body composition produced by growth hormone (GH) treatment.

PATIENTS AND METHOD: A group of 28 SGA children without catch-up growth and undergoing treatment with GH was selected for evaluation. Over the course of 3 years from the beginning of the treatment with GH, the children's body composition variables (bone mineral density [BMD], fat and lean body mass proportion) were evaluated annually with dual-energy X-ray absorptiometry. A study of correlation between metabolic and body composition variables was also made.

RESULTS

Treatment with GH produces a reduction in fat mass proportion in relation to lean body mass, decreasing from 25.94±6.09 to 22.88±5.38% (P=.034). In the abdominal regions we observe an increase in lean mass, from 1,356,91±426,71 to 2,570,96±814,36g (P=.000) and a tendency for visceral fat deposits to decrease. BMD in lumbar vertebrae improved from -1.55±0.68 to -0.90±0.79Z (P=.019).

CONCLUSIONS

Treatment with GH produces changes in body composition, improving BMD and increasing the proportion of lean body mass with a reduction in fat mass. If these changes persisted into adulthood, they may cause a reduction in the metabolic and cardiovascular risk in this group of patients.

Для цитирования: Aurensanz Clemente Esther, Samper Villagrasa Pilar, Ayerza Casas Ariadna, Ruiz Frontera Pablo, Moreno Aznar Luis Alberto, Bueno Lozano Gloria. [Body composition and metabolic risk in small for gestational age children treated with growth hormone].. Medicina clinica. 2016. DOI: 10.1016/j.medcli.2016.06.002.

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