Frailty, Inflammatory Markers, and Waitlist Mortality Among Patients With End-stage Renal Disease in a Prospective Cohort Study
Autor: | Jacqueline Garonzik-Wang, Silas P. Norman, Christine E. Haugen, Ravi Varadhan, Mara A. McAdams-DeMarco, Ashton A. Shaffer, Hao Ying, Jeremy D. Walston, Fatima Warsame, Niraj M. Desai, Dorry L. Segev, Alvin G. Thomas |
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Rok vydání: | 2018 |
Předmět: |
Male
medicine.medical_specialty Waiting Lists Population 030232 urology & nephrology Inflammation Disease 030230 surgery urologic and male genital diseases Risk Assessment Article End stage renal disease 03 medical and health sciences 0302 clinical medicine Predictive Value of Tests Internal medicine Humans Medicine Prospective Studies Registries education Prospective cohort study Kidney transplantation Aged Transplantation education.field_of_study Frailty business.industry Middle Aged medicine.disease Kidney Transplantation C-Reactive Protein Receptors Tumor Necrosis Factor Type I Predictive value of tests Kidney Failure Chronic Female Independent Living Waitlist mortality medicine.symptom business Biomarkers |
Zdroj: | Transplantation. 102:1740-1746 |
ISSN: | 1534-6080 0041-1337 |
DOI: | 10.1097/tp.0000000000002213 |
Popis: | Among community-dwelling older adults, frailty is associated with heightened markers of inflammation and subsequent mortality. Although frailty is common among end-stage renal disease (ESRD) patients, the role of frailty and markers of inflammation in this population remains unclear. We quantified these associations in patients on the kidney transplant waitlist and tested whether frailty and/or markers of inflammation improve waitlist mortality risk prediction.We studied 1975 ESRD patients on the kidney transplant waitlist (November 1, 2009, to February 28, 2017) in a multi-center cohort study of frailty. Serum inflammatory markers (interleukin-6 [IL-6], soluble tumor necrosis factor-α receptor-1 [sTNFR1], and C-reactive protein [CRP]) were analyzed in 605 of these participants; we calculated the inflammatory index score using IL-6 and sTNFR1. We compared the C-statistic of an established registry-based prediction model for waitlist mortality adding frailty and/or inflammatory markers (1 SD change in log IL-6, sTNFR1, CRP, or inflammatory index).The registry-based model had moderate predictive ability (c-statistic = 0.655). Frailty was associated with increased mortality (2.19; 95% confidence interval [CI], 1.26-3.79) but did not improve risk prediction (c-statistic = 0.646; P = 0.65). Like frailty, IL-6 (2.13; 95% CI, 1.41-3.22), sTNFR1 (1.70; 95% CI, 1.12-2.59), CRP (1.68; 95% CI, 1.06-2.67), and the inflammatory index (2.09; 95% CI, 1.38-3.16) were associated with increased mortality risk; unlike frailty, adding IL-6 (c-statistic = 0.777; P = 0.02), CRP (c-statistic = 0.728; P = 0.02), or inflammatory index (c-statistic = 0.777; P = 0.02) substantially improved mortality risk prediction.Frailty and markers of inflammation were associated with increased waitlist mortality risk, but only markers of inflammation significantly improved ESRD risk prediction. These findings help clarify the accelerated aging physiology of ESRD and highlight easy-to-measure markers of increased waitlist mortality risk. |
Databáze: | OpenAIRE |
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