Racial differences in inflammation and outcomes of aging among kidney transplant candidates

被引:8
|
作者
Shrestha, Prakriti [1 ]
Haugen, Christine E. [1 ]
Chu, Nadia M. [1 ,2 ]
Shaffer, Ashton [1 ]
Garonzik-Wang, Jacqueline [1 ]
Norman, Silas P. [3 ]
Walston, Jeremy D. [4 ]
Segev, Dorry L. [1 ,2 ]
McAdams-DeMarco, Mara A. [1 ,2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Surg, Baltimore, MD 21205 USA
[2] Johns Hopkins Sch Publ Hlth, Dept Epidemiol, 615 N Wolfe St,W6033, Baltimore, MD 21205 USA
[3] Univ Michigan, Dept Med, Div Nephrol, Ann Arbor, MI 48109 USA
[4] Johns Hopkins Univ, Sch Med, Dept Med, Div Geriatr, Baltimore, MD 21205 USA
关键词
End-stage renal disease; Inflammation; Race; Frailty; HRQOL; OLDER-ADULTS; WOMENS HEALTH; ALL-CAUSE; FRAILTY; MORTALITY; PHENOTYPE; CYTOKINES; DISEASE; GENDER; RISK;
D O I
10.1186/s12882-019-1360-8
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
BackgroundInflammation is more common among African Americans (AAs), and it is associated with frailty, poor physical performance, and mortality in community-dwelling older adults. Given the elevated inflammation levels among end-stage renal disease (ESRD) patients, inflammation may be associated with adverse health outcomes such as frailty, physical impairment, and poor health-related quality of life (HRQOL), and these associations may differ between AA and non-AA ESRD patients.MethodsOne thousand three ESRD participants were recruited at kidney transplant evaluation (4/2014-5/2017), and inflammatory markers (interleukin-6 [IL-6], tumor necrosis factor-a receptor-1 [TNFR1], C-reactive protein [CRP]) were measured. We quantified the association with frailty (Fried phenotype), physical impairment (Short Physical Performance Battery [SPPB]), and fair/poor HRQOL at evaluation using adjusted modified Poisson regression and tested whether these associations differed by race (AA vs. non-AA).ResultsNon-AAs had lower levels of TNFR1 (9.7ng/ml vs 14.0ng/ml, p<0.001) and inflammatory index (6.7 vs 6.8, p<0.001) compared to AAs, but similar levels of IL-6 (4.5pg/ml vs 4.3pg/ml, p>0.9) and CRP (4.7 g/ml vs 4.9 g/ml, p=0.4). Non-AAs had an increased risk of frailty with elevated IL-6 (RR=1.58, 95% CI:1.27-1.96, p<0.001), TNFR1 (RR=1.60, 95% CI:1.25-2.05, p<0.001), CRP (RR=1.41, 95% CI:1.10-1.82, p<0.01), and inflammatory index (RR=1.82, 95% CI:1.44-2.31, p<0.001). The associations between elevated inflammatory markers and frailty were not present among AAs. Similar results were seen with SPPB impairment and poor/fair HRQOL.ConclusionsNon-AAs with elevated inflammatory markers may need closer follow-up and may benefit from prehabilitation to improve physical function, reduce frailty burden, and improve quality of life prior to transplant.
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页数:8
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