作者
Kendra E. Wulczyn,Tariq Shafi,Amanda H. Anderson,Hernan Rincon-Choles,Clary B. Clish,Michelle Denburg,Harold I. Feldman,Jiang He,Chi‐yuan Hsu,Tanika N. Kelly,Paul L. Kimmel,Rupal Mehta,Robert G. Nelson,Ramachandran S. Vasan,Ana C. Ricardo,Vallabh O. Shah,Anand Srivastava,Dawei Xie,Eugene P. Rhee,Sahir Kalim,Laura M. Dember,J. Richard Landis,Raymond R. Townsend,Lawrence J. Appel,Jeffrey C. Fink,Mahboob Rahman,Edward Horwitz,Jonathan J. Taliercio,Panduranga S. Rao,James Sondheimer,James P. Lash,Hao Chen,Alan S. Go,Afshin Parsa,Tracy L. Rankin
摘要
Abstract
Rationale & Objective
The toxins contributing to uremic symptoms in patients with CKD are unknown. We sought to apply complementary statistical modeling approaches to data from untargeted plasma metabolomic profiling to identify solutes associated with uremic symptoms in patients with CKD. Study Design
Cross-sectional. Setting & Participants
1,761 Chronic Renal Insufficiency Cohort (CRIC) participants with CKD not on dialysis. Predictors
Measurement of 448 known plasma metabolites. Outcomes
The uremic symptoms fatigue, anorexia, pruritus, nausea, paresthesia, and pain were assessed by single items on the Kidney Disease Quality of Life-36 (KDQOL) instrument. Analytical Approach
Multivariable adjusted linear regression, Lasso linear regression, and random forest models were used to identify metabolites associated with symptom severity. After adjustment for multiple comparisons, metabolites selected in at least two of the three modeling approaches were deemed "overall" significant. Results
Participant mean eGFR was 43 mL/min/1.73 m2, with 44% self-identifying as female and 41% Non-Hispanic Black. The prevalence of uremic symptoms ranged from 22 – 55%. We identified 17 metabolites for which a higher level was associated with greater severity of at least one uremic symptom, and 9 metabolites inversely associated with uremic symptom severity. Many of these metabolites demonstrated at least a moderate correlation with eGFR (Pearson's r ≥ 0.5), and some were also associated with risk of developing kidney failure or death in multivariable adjusted Cox regression models. Limitations
Lack of a second independent cohort for external validation of our findings. Conclusions
Metabolomic profiling was used to identify multiple solutes associated with uremic symptoms in adults with CKD, but future validation and mechanistic studies are needed.