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  Vol. 162 No. 20, November 11, 2002 TABLE OF CONTENTS
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Frailty and Activation of the Inflammation and Coagulation Systems With and Without Clinical Comorbidities

Results From the Cardiovascular Health Study

Jeremy Walston, MD; Mary Ann McBurnie, PhD; Anne Newman, MD, MPH; Russell P. Tracy, PhD; Willem J. Kop, PhD; Calvin H. Hirsch, MD; John Gottdiener, MD; Linda P. Fried, MD, MPH; for the Cardiovascular Health Study Investigators

Arch Intern Med. 2002;162:2333-2341.

Background  The biological basis of frailty has been difficult to establish owing to the lack of a standard definition, its complexity, and its frequent coexistence with illness.

Objective  To establish the biological correlates of frailty in the presence and absence of concurrent cardiovascular disease and diabetes mellitus.

Methods  Participants were 4735 community-dwelling adults 65 years and older. Frail, intermediate, and nonfrail subjects were identified by a validated screening tool and exclusion criteria. Bivariate relationships between frailty level and physiological measures were evaluated by Pearson {chi}2 tests for categorical variables and analysis of variance F tests for continuous variables. Multinomial logistic regression was performed to evaluate multivariable relationships between frailty status and physiological measures.

Results  Of 4735 Cardiovascular Health Study participants, 299 (6.3%) were identified as frail, 2147 (45.3%) as intermediate, and 2289 (48.3%) as not frail. Frail vs nonfrail participants had increased mean ± SD levels of C-reactive protein (5.5 ± 9.8 vs 2.7 ± 4.0 mg/L), factor VIII (13 790 ± 4480 vs 11 860 ± 3460 mg/dL), and, in a smaller subset, D dimer (647 ± 1033 vs 224 ± 258 ng/mL) (P<=.001 for all, {chi}2 test for trend). These differences persisted when individuals with cardiovascular disease and diabetes were excluded and after adjustment for age, sex, and race.

Conclusions  These findings support the hypothesis that there is a specific physiological basis to the geriatric syndrome of frailty that is characterized in part by increased inflammation and elevated markers of blood clotting and that these physiological differences persist when those with diabetes and cardiovascular disease are excluded.


From Johns Hopkins Medical Institutions, Baltimore, Md (Drs Walston and Fried); University of Washington, Seattle (Dr McBurnie); University of Pittsburgh, Pittsburgh, Pa (Dr Newman); University of Vermont, Burlington (Dr Tracy); Uniformed Services University of the Health Sciences, Bethesda, Md (Dr Kop); University of California, Davis, Sacramento (Dr Hirsch); and St Francis Hospital, Roslyn, NY (Dr Gottdiener).



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