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

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

Journal

Kidney international reports
ISSN: 2468-0249
Titre abrégé: Kidney Int Rep
Pays: United States
ID NLM: 101684752

Informations de publication

Date de publication:
Jan 2023
Historique:
received: 01 05 2022
revised: 28 09 2022
accepted: 17 10 2022
entrez: 16 1 2023
pubmed: 17 1 2023
medline: 17 1 2023
Statut: epublish

Résumé

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. The MONitoring Dialysis Outcomes (MONDO) Consortium encompasses hemodialysis databases 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. 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. 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.

Identifiants

pubmed: 36644346
doi: 10.1016/j.ekir.2022.10.020
pii: S2468-0249(22)01833-2
pmc: PMC9831940
doi:

Types de publication

Journal Article

Langues

eng

Pagination

75-80

Informations de copyright

© 2022 Published by Elsevier Inc. on behalf of the International Society of Nephrology.

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Auteurs

Dalia E Yousif (DE)

Division of Nephrology, Department of Medicine, Soba University Hospital, Khartoum, Sudan.
Research Division, Renal Research Institute, New York, New York, USA.

Xiaoling Ye (X)

Research Division, Renal Research Institute, New York, New York, USA.

Stefano Stuard (S)

Fresenius Medical Care EMEA, Bad Homburg, Germany.

Juan Berbessi (J)

Fresenius Medical Care Global Medical Office, Buenos Aires, Argentina.

Adrian M Guinsburg (AM)

Fresenius Medical Care Global Medical Office, Buenos Aires, Argentina.

Len A Usvyat (LA)

Fresenius Medical Care, Waltham, Massachusetts, USA.

Jochen G Raimann (JG)

Research Division, Renal Research Institute, New York, New York, USA.

Jeroen P Kooman (JP)

Division of Nephrology, Department of Internal Medicine, Maastricht University Medical Center, Maastricht, the Netherlands.

Frank M van der Sande (FM)

Division of Nephrology, Department of Internal Medicine, Maastricht University Medical Center, Maastricht, the Netherlands.

Neill Duncan (N)

Faculty of Medicine, Imperial College London, London, UK.

Kevin J Woollard (KJ)

Faculty of Medicine, Imperial College London, London, UK.

Rupert Bright (R)

Faculty of Medicine, Imperial College London, London, UK.

Charles Pusey (C)

Faculty of Medicine, Imperial College London, London, UK.

Vineet Gupta (V)

Division of Hospital Medicine, Department of Medicine, University of California San Diego, San Diego, California, USA.

Joachim H Ix (JH)

Herbert Wertheim School of Public Health, University of California San Diego, San Diego, California, USA.
Nephrology Section, Veteran Affairs San Diego Healthcare System, La Jolla, California, USA.
Division of Nephrology and Hypertension, University of California San Diego, San Diego, California, USA.

Peter Kotanko (P)

Research Division, Renal Research Institute, New York, New York, USA.
Division of Nephrology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Rakesh Malhotra (R)

Division of Nephrology and Hypertension, University of California San Diego, San Diego, California, USA.

Classifications MeSH