Skip to main content Accessibility help
×
Hostname: page-component-76fb5796d-45l2p Total loading time: 0 Render date: 2024-04-25T15:01:03.551Z Has data issue: false hasContentIssue false

18 - Impact of gender and age on growth hormone responsiveness

from Part III - Growth hormone replacement therapy in adults with growth hormone deficiency

Published online by Cambridge University Press:  08 January 2010

Anders Juul
Affiliation:
National University Hospital, Copenhagen
Jens O. L. Jorgensen
Affiliation:
Aarhus Kommunehospital, Aarhus, Denmark
Get access

Summary

Introduction

Growth hormone (GH) is a potent metabolic hormone of importance for body composition, bone mass, serum lipids, physical fitness and mental capacity. Accumulated experience has shown that although the majority of GH-deficient patients benefit from replacement therapy with GH, the response to GH differs between individuals. The basis of this variation in sensitivity is not fully understood. This review will focus on the impact of gender and age on several outcome measures.

GH secretion in healthy individuals – effects of age and gender

The secretion of GH peaks during puberty and declines thereafter with advancing age. Studies of the 24-hour GH serum concentration have shown a reduction, ranging from 32 to 45%, in elderly subjects (aged 55–85) compared with younger to middle-aged individuals (aged 18–45) (Ho et al., 1987; Vermeulen, 1987; Corpas et al., 1992). In healthy men aged 21–71 a 14% decrease in GH secretion, and a 6% decrease in GH half-life has been calculated for every advancing decade (Iranmanesh et al., 1991). In addition, the somatotroph responsiveness to GH releasing hormone (GHRH) (Pavlov et al., 1986; Iovino, Monteleone & Steardo, 1989), and to insulin-induced hypoglycaemia is impaired in the elderly (Kalk et al., 1973), but stimulation with combinations of arginine and GHRH seems less dependent on age (Ghigo et al., 1990). At present the mechanisms underlying the reduced GH secretion in ageing are not fully understood. The restoration of the somatotroph responsiveness after repeat stimulation (Corpas et al., 1992) indicates a functional and reversable state.

Obese subjects are characterized by reduced serum GH concentrations (Weltman et al., 1994) and blunted response to stimuli of GH secretion (Williams et al., 1984).

Type
Chapter
Information
Growth Hormone in Adults
Physiological and Clinical Aspects
, pp. 373 - 396
Publisher: Cambridge University Press
Print publication year: 2000

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×