The physiology of endocrine systems with ageing

被引:185
|
作者
van den Beld, Annewieke W. [1 ,2 ]
Kaufman, Jean-Marc [3 ]
Zillikens, M. Carola [1 ]
Lamberts, Steven W. J. [1 ]
Egan, Josephine M. [4 ]
van der Lely, Aart J. [1 ]
机构
[1] Erasmus MC, Div Endocrinol, Dept Internal Med, Rotterdam, Netherlands
[2] Groene Hart Hosp, Dept Internal Med, Gouda, Netherlands
[3] Ghent Univ Hosp, Dept Endocrinol, Unit Osteoporosis & Metab Bone Dis, Ghent, Belgium
[4] NIA, Lab Clin Invest, Baltimore, MD 21224 USA
来源
LANCET DIABETES & ENDOCRINOLOGY | 2018年 / 6卷 / 08期
关键词
SUBCLINICAL THYROID-DYSFUNCTION; INSULIN-SECRETION; GLUCOSE-TOLERANCE; DEHYDROEPIANDROSTERONE DHEA; POSTMENOPAUSAL WOMEN; HORMONE-THERAPY; ANDROGEN LEVELS; FREE-THYROXINE; RENAL-FUNCTION; FRACTURE RISK;
D O I
10.1016/S2213-8587(18)30026-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
During ageing, the secretory patterns of the hormones produced by the hypothalamic-pituitary axis change, as does the sensitivity of the axis to negative feedback by end hormones. Additionally, glucose homoeostasis tends towards disequilibrium with increasing age. Along with these endocrine alterations, a loss of bone and muscle mass and strength occurs, coupled with an increase in fat mass. In addition, ageing-induced effects are difficult to disentangle from the influence of other factors that are common in older people, such as chronic diseases, inflammation, and low nutritional status, all of which can also affect endocrine systems. Traditionally, the decrease in hormone activity during the ageing process has been considered to be detrimental because of the related decline in bodily functions. The concept of hormone replacement therapy was suggested as a therapeutic intervention to stop or reverse this decline. However, clearly some of these changes are a beneficial adaptation to ageing, whereas hormonal intervention often causes important adverse effects. In this paper, we discuss the effects of age on the different hypothalamic-pituitary-hormonal organ axes, as well as age-related changes in calcium and bone metabolism and glucose homoeostasis.
引用
收藏
页码:647 / 658
页数:12
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