Serum Carboxymethyl-Lysine, Disability, and Frailty in Older Persons: The Cardiovascular Health Study

被引:29
作者
Whitson, Heather E. [1 ,2 ]
Arnold, Alice M. [3 ]
Yee, Laura M. [3 ]
Mukamal, Kenneth J. [4 ]
Kizer, Jorge R. [5 ,6 ]
Djousse, Luc [4 ]
Ix, Joachim H. [7 ,8 ,9 ]
Siscovick, David [10 ]
Tracy, Russell P. [11 ]
Thielke, Stephen M. [12 ,13 ]
Hirsch, Calvin [14 ]
Newman, Anne B. [15 ]
Zieman, Susan [16 ]
机构
[1] Duke Univ, Dept Med, Durham, NC USA
[2] GRECC, Durham VA Med Ctr, Durham, NC USA
[3] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[4] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[5] Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
[6] Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10467 USA
[7] Univ Calif San Diego, Dept Med, San Diego, CA 92103 USA
[8] Univ Calif San Diego, Dept Prevent & Family Med, San Diego, CA 92103 USA
[9] Vet Affairs San Diego Healthcare Syst, Nephrol Sect, San Diego, CA USA
[10] Univ Washington, Dept Med, Seattle, WA USA
[11] Univ Vermont, Dept Pathol, Colchester, VT USA
[12] Puget Sound VA Med Ctr, Seattle, WA USA
[13] Univ Washington, Dept Psychiat, Seattle, WA 98195 USA
[14] Univ Calif Davis, Dept Med, Davis, CA USA
[15] Univ Pittsburgh, Dept Epidemiol, Pittsburgh, PA 15260 USA
[16] NIA, NIH, Bethesda, MD 20892 USA
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2014年 / 69卷 / 06期
关键词
Biomarkers; Disablement process; Epidemiology; Frailty; Metabolism; GLYCATION END-PRODUCTS; DISEASE MORTALITY; OXIDATIVE STRESS; CROSS-LINKING; ADULTS; ENDPRODUCTS; WOMEN; COMPLICATIONS; PHENOTYPE; FOODS;
D O I
10.1093/gerona/glt155
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background. Advanced glycation endproducts are biologically active compounds that accumulate in disordered metabolism and normal aging. Carboxymethyl-lysine (CML), a ubiquitous human advanced glycation endproduct, has been associated with age-related conditions and mortality. Our objective was to ascertain the relationship between CML and geriatric outcomes (disability and frailty) in a large cohort of older men and women. Methods. In 1996-1997, serum CML was measured in 3,373 Cardiovascular Health Study participants (mean age 78.1 +/- 4.8 years). Disability, defined as difficulty in any of six activities of daily living, was assessed every 6-12 months for 14 years. Frailty was defined according to five standard criteria at the 1996-1997 visit. Cox proportional hazard models estimated the relationship between CML and incident disability (N = 2,643). Logistic regression models estimated the relationship between CML and prevalent frailty. Results. Adjusting for multiple potential confounders, higher CML was associated with incident disability (hazard ratio per standard deviation [225 ng/mL] increase: 1.05, 95% CI 1.01-1.11). In men, odds of frailty increased with higher CML values (odds ratio = 1.30 per standard deviation, 95% CI 1.14-1.48), but the relationship was attenuated by adjustment for cognitive status, kidney function, and arthritis. CML was not associated with frailty in women. Conclusions. Higher serum CML levels in late life are associated with incident disability and prevalent frailty. Further work is needed to understand CML's value as a risk stratifier, biomarker, or target for interventions that promote healthy aging.
引用
收藏
页码:710 / 716
页数:7
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