Patterns of Comorbid Inflammatory Diseases in Frail Older Women: The Women's Health and Aging Studies I and II

被引:76
作者
Chang, Sandy S. [1 ]
Weiss, Carlos O. [2 ,3 ]
Xue, Qian-Li [2 ,3 ]
Fried, Linda P. [4 ]
机构
[1] Yale Univ, Sch Med, Sect Geriatr, Dept Internal Med, New Haven, CT 06520 USA
[2] Johns Hopkins Univ, Sch Med, Dept Med, Div Geriatr Med & Gerontol, Baltimore, MD 21205 USA
[3] Johns Hopkins Med Inst, Ctr Aging & Hlth, Baltimore, MD 21205 USA
[4] Columbia Univ, Dept Epidemiol, Mailman Sch Publ Hlth, New York, NY USA
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2010年 / 65卷 / 04期
关键词
Frailty; Comorbidity; Inflammation; CARDIOVASCULAR-DISEASE; MARKERS; PROGRESSION; BIOMARKERS; DISABILITY;
D O I
10.1093/gerona/glp181
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. Developing interventions to prevent frailty in older adults is a priority as it increases the risk for disability, institutionalization, and death. Single chronic inflammatory diseases are known to increase the risk of frailty. Identification of comorbid inflammatory diseases that synergistically might heighten this risk would provide further insight into therapeutic approaches to prevent frailty. The study aims were to characterize whether there are specific inflammatory disease pairs that are associated with frailty and to determine whether the risk of frailty is affected by synergistic interactions between these inflammatory diseases. Methods. Data were from the Women's Health and Aging Studies I and II and complementary cohorts 01 community-dwelling women aged 70-79 years front Baltimore, Maryland (n = 620). Multivariable logistic regression analyses were performed to evaluate the relationships between these diseases and frailty. Results. Among the frail (11.3%), 15.2% had both depressive symptoms and anemia and 14.5% had pulmonary disease and anemia. The risk of frailty was synergistically increased in those with depressive symptoms and anemia (adjusted risk ratios = 11.93. 95% confidence interval [CI] 4.10-34.76) and those with pulmonary disease and anemia (risk ratios = 5.57. 95% CI 2.14-14.48), compared with those without either disease in each pair. The attributable proportions of frail cases due to interaction between the diseases of each pair were 0.56 (95% CI 0.07-1.05) and 0.61 (95% CI 0.18-1.05), respectively. Conclusions. Synergistic interactions between specific inflammatory diseases may heighten the risk of frailty. These findings suggest that a common etiologic pathway may exist among co-occurring inflammatory diseases and that their improved comanagemcm may be an approach to reducing frailty.
引用
收藏
页码:407 / 413
页数:7
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