Skip to main content Accessibility help
×
Hostname: page-component-68945f75b7-z8dg2 Total loading time: 0 Render date: 2024-08-06T02:52:40.097Z Has data issue: false hasContentIssue false

12 - Erythropoietin and aging

from Part III - Anemia of aging

Published online by Cambridge University Press:  21 October 2009

Lodovico Balducci
Affiliation:
H. Lee Moffitt Cancer Center & Research Institute, Florida
William Ershler
Affiliation:
Institute for Advanced Studies in Aging and Geriatric Medicine, Washington DC
Giovanni de Gaetano
Affiliation:
Catholic University, Campobasso
Get access

Summary

Introduction

Anemia represents a common problem among the elderly, with a prevalence of 5–10% for the community-dwelling elderly between 65 and 74 years, and over 20% for seniors 85 years and over. In hospitalized elderly patients and in skilled nursing facilities, anemia prevalence ranges from 40 to 50%. The recent appreciation of the numerous adverse consequences of anemia has generated interest in a more complete understanding of anemia in the elderly. Erythropoietin (EPO) is a hormone central to the regulation of red-blood-cell production that increases in response to falling hemoglobin concentration. Paradoxically, although EPO levels rise slightly with age in non-anemic elderly people, the expected EPO response to anemia appears significantly blunted in the elderly, supporting a relative endogenous EPO deficiency. This relative EPO deficiency, possibly attributable to occult renal insufficiency, may play a central role in the rising prevalence of anemia with advancing age and unexplained anemia in the elderly.

Erythropoiesis

Hematopoiesis, the production of blood elements, occurs in an orderly hierarchical fashion. Maintenance of mature peripheral blood cells (i.e., platelets, red blood cells or erythrocytes, neutrophils, eosinophils, basophils, monocytes, lymphocytes, natural killer cells, and dendritic cells) demands ongoing production to meet losses and respond to stresses. A pluripotent hematopoietic stem cell produces committed progenitors of myeloid, erythroid, and megakaryocytic lineages.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2007

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
×