Skip Navigation


Age and Ageing Advance Access originally published online on February 28, 2009
Age and Ageing 2009 38(3):283-289; doi:10.1093/ageing/afp011
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
38/3/283    most recent
afp011v1
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Semba, R. D.
Right arrow Articles by Fried, L. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Semba, R. D.
Right arrow Articles by Fried, L. P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2009. Published by Oxford University Press on behalf of the British Geriatrics Society. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Elevated serum advanced glycation end products and their circulating receptors are associated with anaemia in older community-dwelling women

Richard D. Semba1, Luigi Ferrucci2, Kai Sun1, Kushang V. Patel3, Jack M. Guralnik3 and Linda P. Fried1,4

1 Johns Hopkins University School of Medicine, Baltimore, MD, USA
2 Clinical Research Branch, National Institute on Aging, Baltimore, MD, USA
3 Laboratory of Epidemiology, Demography, and Biometry, National Institute on Aging, Bethesda, MD, USA
4 Mailman School of Public Health, Columbia University, New York, NY, USA

Address correspondence to: R. Semba. Tel: (+1) 410 955 3572, Fax: (+1) 410 955 0629. Email: rdsemba{at}jhmi.edu

Objective: to determine whether serum carboxymethyl-lysine, a dominant advanced glycation end product (AGE), and circulating total receptor for AGEs (sRAGE) and endogenous secretory receptor for AGEs (esRAGE) are associated with anaemia.

Design: cross-sectional analysis.

Setting: moderately severely disabled women, ≥65 years, living in the community in Baltimore, MD (the Women's Health and Aging Study I).

Participants: 519 women with and without anaemia.

Main outcome measure: haemoglobin and anaemia (haemoglobin <12 g/dL).

Results: of 519 women, 128 (24.7%) had anaemia. All odds ratios (OR) were expressed per one standard deviation. Serum CML was associated with anaemia [OR 1.47, 95% confidence interval (CI) 1.11–1.95, P = 0.008] in a multivariate logistic regression model adjusting for age, race, smoking, education and chronic diseases. Serum sRAGE (ng/mL) and esRAGE (ng/mL) were associated with anaemia (OR 1.52, 95% CI 1.21–1.92, P = 0.0004; OR 1.49, 95% CI 1.18–1.87, P = 0.0006, respectively) in separate multivariate logistic regression models, adjusting for the same covariates mentioned above. Serum CML (P = 0.004), sRAGE (P < 0.0001) and esRAGE (P < 0.0001) were inversely and independently associated with haemoglobin concentrations.

Conclusion: AGEs and circulating RAGE are independently associated with haemoglobin and anaemia in older women. AGEs are amenable to interventions, as serum AGEs can be lowered by a change in dietary pattern and pharmacological treatment.

Keywords: advanced glycation end products, anaemia, haemoglobin, women, elderly

Received 5 June 2008; accepted in revised form 4 December 2008.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.