4.6 Article

Biphasic Dynamics of Inflammatory Markers Following Hemodialysis Initiation: Results From the International MONitoring Dialysis Outcome Initiative

Journal

KIDNEY INTERNATIONAL REPORTS
Volume 8, Issue 1, Pages 75-80

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ekir.2022.10.020

Keywords

albumin; dynamics; end-stage kidney disease; inflammation; mortality; neutrophil-lymphocyte ratio

Funding

  1. National Institute of Diabetes and Digestive and Kidney Diseases K23 award [DK132680-01]

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This study investigated the longitudinal changes in inflammatory markers in hemodialysis patients and their relationship with survival time. The results showed a distinct biphasic pattern of change in inflammatory markers in patients who died, while a sustained decline in inflammation was observed in survivors.
Introduction: Inflammation is highly prevalent among patients with end-stage kidney disease and is associated with adverse outcomes. We aimed to investigate longitudinal changes in inflammatory markers in a diverse international incident hemodialysis patient population.Methods: The MONitoring Dialysis Outcomes (MONDO) Consortium encompasses hemodialysis data-bases from 31 countries in Europe, North America, South America, and Asia. The MONDO database was queried for inflammatory markers (total white blood cell count [WBC], neutrophil count, lymphocyte count, serum albumin, and C-reactive protein [CRP]) and hemoglobin levels in incident hemodialysis patients. Laboratory parameters were measured every month. Patients were stratified by survival time (#6 months, >6 to 12 months, >12 to 18 months, >18 to 24 months, >24 to 30 months, >30 to 36 months, and >36 months) following dialysis initiation. We used cubic B-spline basis function to evaluate temporal changes in inflammatory parameters in relationship with patient survival. Results: We studied 18,726 incident hemodialysis patients. Their age at dialysis initiation was 71.3 +/- 11.9 years; 10,802 (58%) were males. Within the first 6 months, 2068 (11%) patients died, and 12,295 patients (67%) survived >36 months (survivor cohort). Hemodialysis patients who died showed a distinct biphasic pattern of change in inflammatory markers where an initial decline of inflammation was followed by a rapid rise that was consistently evident approximately 6 months before death. This pattern was similar in all patients who died and was consistent across the survival time intervals. In contrast, in the survivor cohort, we observed initial decline of inflammation followed by sustained low levels of inflammatory biomarkers.Conclusion: Our international study of incident hemodialysis patients highlights a temporal relationship between serial measurements of inflammatory markers and patient survival. This finding may inform the development of prognostic models, such as the integration of dynamic changes in inflammatory markers for individual risk profiling and guiding preventive and therapeutic interventions.

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