Background
Studies in chronic kidney disease populations suggest that the non-GFR determinants of serum levels of the low molecular weight (LMW) protein filtration markers cystatin C, beta-2 microglobulin (B2M) and beta trace protein (BTP) are less affected by age, sex and ethnicity than those of creatinine.
Study Design
Cross-sectional study.
Setting & Participants
Predominantly elderly participants selected from the Age, Gene/Environment Susceptibility Kidney Study [AGES-Kidney, N=683, mean (SD) age 79 (4), GFR 62 (17) ml/min/1.73 m2] and from the Multi-Ethnic Study of Atherosclerosis Kidney Study [MESA-Kidney, N=273, mean (SD) age 70.5 (9), GFR 73 (19) ml/min/1.73 m2].
Predictors
Demographic and clinical factors hypothesized to be associated with conditions affecting non-GFR determinants of the filtration markers.
Outcomes
mGFR and eGFRs based on creatinine, cystatin C, B2M and BTP (eGFRcr, eGFRcys, eGFRB2M and eGFRBTP, respectively). Residual associations of factors with eGFR after accounting for mGFR as the parameter of interest.
Results
eGFRcys, eGFRB2M and eGFRBTP had significantly less strong residual associations with age and sex than eGFRcr in both AGES-Kidney and MESA-Kidney, and were not associated with ethnicity (black vs. white) in MESA-Kidney. After adjusting for age, sex and ethnicity, residual associations with most clinical factors were smaller than observed with age and sex. eGFRcys, eGFRB2M, but not eGFRBTP had significant residual associations with CRP in both studies.
Limitations
Small sample size may limit power to detect associations. Participants may be healthier than the general population.
Conclusions
Similar to previous studies in chronic kidney disease, in community-dwelling elders, cystatin C, B2M and BTP are less affected than creatinine by age and sex and are not affected by ethnicity. Both cystatin C and B2M may be affected by inflammation. These findings are important for the development and use of GFR estimating equations based on LMW serum proteins throughout the range in GFR.