Association of kidney function with inflammatory and procoagulant markers in a diverse cohort: a cross-sectional analysis from the Multi-Ethnic Study of Atherosclerosis (MESA).
Association of kidney function with inflammatory and procoagulant markers in a diverse cohort: a cross-sectional analysis from the Multi-Ethnic Study of Atherosclerosis (MESA).
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DOI:
10.1186/1471-2369-9-9
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发表时间:
2008-08-05
期刊:
影响因子:
2.3
通讯作者:
Shlipak, Michael
中科院分区:
文献类型:
--
作者:
Keller, Christopher;Katz, Ronit;Cushman, Mary;Fried, Linda F.;Shlipak, Michael
Prior studies using creatinine-based estimated glomerular filtration rate (eGFR) have found limited associations between kidney function and markers of inflammation. Using eGFR and cystatin C, a novel marker of kidney function, the authors investigated the association of kidney function with multiple biomarkers in a diverse cohort. The Multi-Ethnic Study of Atherosclerosis consists of 6,814 participants of white, African-American, Hispanic, and Chinese descent, enrolled from 2000–2002 from six U.S. communities. Measurements at the enrollment visit included serum creatinine, cystatin C, and six inflammatory and procoagulant biomarkers. Creatinine-based eGFR was estimated using the four-variable Modification of Diet in Renal Disease equation, and chronic kidney disease was defined by an eGFR < 60 mL/min/1.73 m2. Adjusted partial correlations between cystatin C and all biomarkers were statistically significant: C-reactive protein (r = 0.08), interleukin-6 (r = 0.16), tumor necrosis factor-α soluble receptor 1 (TNF-αR1; r = 0.75), intercellular adhesion molecule-1 (r = 0.21), fibrinogen (r = 0.14), and factor VIII (r = 0.11; two-sided p < 0.01 for all). In participants without chronic kidney disease, higher creatinine-based eGFR was associated only with higher TNF-αR1 levels. In a cohort characterized by ethnic diversity, cystatin C was directly associated with multiple procoagulant and inflammatory markers. Creatinine-based eGFR had similar associations with these biomarkers among subjects with chronic kidney disease.
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影响因子:
2.8
作者:
Albert, MA;Glynn, RJ;Ridker, PM
通讯作者:
Ridker, PM
影响因子:
13.2
作者:
Coll, E;Botey, A;Darnell, A
通讯作者:
Darnell, A
影响因子:
19.6
作者:
Levey, AS;Eckardt, KU;Eknoyan, G
通讯作者:
Eknoyan, G
DOI:
10.1111/j.1432-1033.1988.tb14384.x
发表时间:
1988-11-01
期刊:
EUROPEAN JOURNAL OF BIOCHEMISTRY
影响因子:
--
作者:
CASTELL, JV;GEIGER, T;HEINRICH, PC
通讯作者:
HEINRICH, PC
影响因子:
3.8
作者:
BEMELMANS, MHA;GOUMA, DJ;BUURMAN, WA
通讯作者:
BUURMAN, WA