Anemia in Patients After Stem Cell Transplantation and in Kidney Transplant Recipients.


Journal

Transplantation proceedings
ISSN: 1873-2623
Titre abrégé: Transplant Proc
Pays: United States
ID NLM: 0243532

Informations de publication

Date de publication:
04 May 2024
Historique:
received: 31 01 2024
accepted: 29 03 2024
medline: 6 5 2024
pubmed: 6 5 2024
entrez: 5 5 2024
Statut: aheadofprint

Résumé

Hematopoietic stem cell transplant (HSCT) is the treatment of choice in various hematologic diseases, and kidney transplantation (KTx) is the best therapy for end-stage kidney disease. Chronic kidney disease (CKD) occurs relatively often after both types of transplantations. Anemia after both HSCT and KTx may be due to CKD and other reasons. This study aimed to assess the prevalence of anemia to CKD in 156 prevalent patients after HSCT and 80 after KTx. According to the World Health Organization's definition (hemoglobin <13 g/dL for men and <12 g/dL for women), the prevalence of anemia in the studied cohort after HSCT was 13% in women and 35% in men and for those after KTx, it was29% in men and 11%. Anemia in KTx was found in 46% of patients, whereas CKD was present in 53%. After HSCT, anemia was associated with CKD in 56% of women and 17% of men. In KTx, anemia and CKD was diagnosed in 21% of patients. Patients with anemia after KTx had significantly lower glomerular filtration rate (GFR), hemoglobin, and significantly higher creatinine levels. Age was related to the estimated GFR (eGFR; r = -0.39, P < .001) in patients who underwent HSCT and had anemia. In patients without anemia, age was negatively related to eGFR (r = -0.56, P < .001) and the hemoglobin-to-platelet count (r = 0.62, P < .001). In KTx, hemoglobin was related to eGFR (r = 0.35, P < .001), and age was related to eGFR (r = -0.20, P < .05). The type of induction therapy immunosuppressive regimen (anti-thymocyte globulin vs basiliximab vs no induction) did not affect the prevalence of anemia in the KTx population studied. Anemia is relatively common in CKD after HSCT. In both CKD and coexistent anemia, nephrology referral is to be considered to optimize therapy, including nephroprotection.

Identifiants

pubmed: 38705734
pii: S0041-1345(24)00200-8
doi: 10.1016/j.transproceed.2024.03.028
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest All the authors declare no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Aleksandra Kaszyńska (A)

Department of Nephrology, Dialysis and Internal Medicine, Warsaw Medical University, Warsaw Poland.

Małgorzata Kępska-Dzilińska (M)

Department of Nephrology, Dialysis and Internal Medicine, Warsaw Medical University, Warsaw Poland.

Ewa Karakulska-Prystupiuk (E)

Department of Hematology, Transplantation and Internal Medicine, Warsaw Medical University, Warsaw Poland.

Ewa Wojtaszek (E)

Department of Nephrology, Dialysis and Internal Medicine, Warsaw Medical University, Warsaw Poland.

Grzegorz Basak (G)

Department of Hematology, Transplantation and Internal Medicine, Warsaw Medical University, Warsaw Poland.

Slawomir Nazarewski (S)

Department of General, Vascular, Endocrine and Transplant Surgery, Warsaw Medical University, Warsaw, Poland.

Zbigniew Galązka (Z)

Department of General, Vascular, Endocrine and Transplant Surgery, Warsaw Medical University, Warsaw, Poland.

Jolanta Malyszko (J)

Department of Nephrology, Dialysis and Internal Medicine, Warsaw Medical University, Warsaw Poland. Electronic address: jolmal@poczta.onet.pl.

Classifications MeSH