Journal of Renal Nutrition
Volume 20, Issue 2 , Pages 74-81, March 2010

Serum Carboxymethyl-Lysine, a Dominant Advanced Glycation End Product, Is Associated With Chronic Kidney Disease: The Baltimore Longitudinal Study of Aging

  • Richard D. Semba, MD, MPH

      Affiliations

    • Department of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore, Maryland
    • Corresponding Author InformationAddress reprint requests to Richard Semba, MD, MPH, Department of Ophthalmology, Johns Hopkins University School of Medicine, 550 N. Broadway, Suite 700, Baltimore, MD 21205.
  • ,
  • Jeffrey C. Fink, MD, MS

      Affiliations

    • Division of Nephrology, Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland
  • ,
  • Kai Sun, MS

      Affiliations

    • Department of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore, Maryland
  • ,
  • B. Gwen Windham, MD, MHS

      Affiliations

    • Longitudinal Studies Section, Clinical Research Branch, National Institute on Aging, Baltimore, Maryland
  • ,
  • Luigi Ferrucci, MD, PhD

      Affiliations

    • Longitudinal Studies Section, Clinical Research Branch, National Institute on Aging, Baltimore, Maryland

published online 23 October 2009.

Objective

Advanced glycation end products (AGEs) are modifiable risk factors for renal disease that were primarily studied in persons with diabetes or endstage renal disease. Our objective was to characterize the relationship between AGEs and renal function in community-dwelling adults.

Design

The presence of serum L-carboxymethyl-lysine (CML), a dominant AGE, was compared with renal function in a cross-sectional analysis.

Setting

This study was part of the Baltimore Longitudinal Study of Aging in Baltimore, Maryland.

Patients or Other Participants

Participants included community-dwelling men and women, aged 26 to 93 years, seen during a regular follow-up visit to the Baltimore Longitudinal Study of Aging between 2002 and 2007.

Main Outcome Measures

The main outcome measures included chronic kidney disease (CKD) at stage ≥3 of the National Kidney Foundation classification (estimated glomerular filtration rate [eGFR] of<60 mL/minute/1.73 m2) and eGFR.

Results

Of 750 adults, 121 (16.1%) had CKD. Serum CML was associated with CKD (odds ratio expressed per one standard deviation, 1.37; 95% confidence interval, 1.11 to 1.67; P=.003) in a multivariate logistic regression model adjusting for age, race, smoking, and chronic diseases. Serum CML was associated with eGFR (mL/minute/1.73 m2) (β=−2.21, standard error=0.57, P=.0001) in a multivariate linear regression model, adjusting for age, race, smoking, and chronic diseases. After excluding patients with diabetes, serum CML was associated with CKD (odds ratio per one standard deviation, 1.38; 95% confidence interval, 1.12 to 1.70; P=.003) and eGFR (β=−2.09, standard error=0.59, P=.0005), adjusting for the same covariates.

Conclusion

Serum CML, a dominant AGE, is independently associated with CKD and eGFR.

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PII: S1051-2276(09)00219-2

doi:10.1053/j.jrn.2009.08.001

Journal of Renal Nutrition
Volume 20, Issue 2 , Pages 74-81, March 2010