Effects of growth hormone-releasing hormone on visceral fat, metabolic, and cardiovascular indices in human studies

被引:32
作者
Stanley, Takara L.
Grinspoon, Steven K.
机构
[1] Massachusetts Gen Hosp, Neuroendocrine Unit, Program Nutr Metab, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
基金
美国国家卫生研究院;
关键词
Growth hormone; Visceral obesity; Obesity; Growth hormone-releasing hormone; Cardiovascular risk; HIV-INFECTED PATIENTS; RANDOMIZED CONTROLLED-TRIAL; CARDIOMETABOLIC RISK-FACTORS; HEPATIC-STEROID METABOLISM; CORONARY-HEART-DISEASE; EXCESS ABDOMINAL FAT; GH-DEFICIENT ADULTS; OBESE SUBJECTS; BODY-COMPOSITION; ADIPOSE-TISSUE;
D O I
10.1016/j.ghir.2014.12.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Increased visceral adipose tissue (VAT) is associated with reductions in endogenous GH secretion, possibly as a result of hyperinsulinemia, increased circulating free fatty acid, increased somatostatin tone, and reduced ghrelin. Reduced GH may, in turn, further exacerbate visceral fat accumulation because of decreased hormone-sensitive lipolysis in this depot. Data from multiple populations demonstrate that both reduced GH and increased VAT appear to contribute independently to dyslipidemia, increased systemic inflammation, and increased cardiovascular risk. The reductions in GH in states of visceral adiposity are characterized by reduced basal and pulsatile GH secretion with intact pulse frequency. Treatment with GH-releasing hormone (GHRH) provides a means to reverse these abnormalities, increasing endogenous basal and pulsatile GH secretion without altering pulse frequency. This review describes data from HIV-infected individuals and individuals with general obesity showing that treatment with GHRH significantly reduces visceral fat, ameliorates dyslipidemia, and reduces markers of cardiovascular risk Further research is needed regarding the long-term efficacy and safety of this treatment modality. (C) 2014 Elsevier Ltd. All rights reserved.
引用
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页码:59 / 65
页数:7
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