scholarly journals Red blood cell alloimmunization in multi-transfused patients with chronic kidney disease in Port Harcourt, South-South Nigeria

2018 ◽  
Vol 18 (4) ◽  
pp. 979 ◽  
Author(s):  
Esther Ifeoma Obi ◽  
Crosdale Ogho Pughikumo ◽  
Richard Ishmael Oko-jaja
2013 ◽  
Vol 28 (6) ◽  
pp. 1504-1515 ◽  
Author(s):  
Karminder S. Gill ◽  
Paul Muntner ◽  
Richard A. Lafayette ◽  
Jeffrey Petersen ◽  
Jeffrey C. Fink ◽  
...  

2016 ◽  
Vol 41 (4) ◽  
pp. 317-323 ◽  
Author(s):  
Natalia Borges Bonan ◽  
Thiago M. Steiner ◽  
Viktoriya Kuntsevich ◽  
Grazia Maria Virzì ◽  
Marina Azevedo ◽  
...  

Background: We tested the effect of uremia on red blood cell (RBC) eryptosis, CD14++/CD16+ monocytes and erythrophagocytosis. Design: RBC and monocytes from chronic kidney disease (CKD) stages 3/4 (P-CKD3/4) or hemodialysis (HD) patients and healthy controls (HCs) cells incubated with sera pools from patients with CKD stages 2/3 (S-CKD2/3) or 4/5 (S-CKD4/5) were evaluated to assess eryptosis, monocyte phenotypes and reactive oxygen species (ROS) by cytometer. Erythrophagocytosis was evaluated by subsequent co-incubation of preincubated HC-monocytes and autologous-RBC. Results: HC-eryptosis (1.3 ± 0.9%) was lower than in HD (4.3 ± 0.5%) and HC-RBC incubated with S-CKD4/5 (5.6 ± 1%). CD14++/CD16+ were augmented in P-CKD3/4 (34.6 ± 8%) and HC-monocytes incubated with S-CKD4/5 (26.4 ± 7%) than in HC (5.4 ± 1%). In these cells, ROS was increased (44.5 ± 9%; control 9.6 ± 2%) and inhibited by N-acetylcysteine (25 ± 13%). Erythrophagocytosis was increased in CD14++/CD16+ (60.8 ± 10%) than in CD14++/CD16- (15.5 ± 2%). Conclusions: Sera pools from CKD patients increase eryptosis and promote a proinflammatory monocyte phenotype. Both processes increased erythrophagocytosis, thereby suggesting a novel pathway for renal anemia.


2015 ◽  
Vol 24 (6) ◽  
pp. 654-662 ◽  
Author(s):  
Karminder Gill ◽  
Jeffrey C. Fink ◽  
David T. Gilbertson ◽  
Keri L. Monda ◽  
Paul Muntner ◽  
...  

2020 ◽  
Vol 35 (5) ◽  
pp. e177-e177
Author(s):  
Shafini Mohamed Yusoff ◽  
Rosnah Bahar ◽  
Mohd Nazri Hassan ◽  
Noor Haslina Mohd Noor ◽  
Marini Ramli ◽  
...  

2019 ◽  
Vol 44 (5) ◽  
pp. 1158-1165 ◽  
Author(s):  
Jiu-Hong Li ◽  
Jun-Feng Luo ◽  
Ying Jiang ◽  
Yong-Jian Ma ◽  
Yong-Qiang Ji ◽  
...  

Background: Although reduced red blood cell (RBC) lifespan has been reported to be a contributory factor to anemia in patients with end-stage chronic kidney disease (CKD), there are limited data regarding RBC lifespan in early-stage CKD. Serum erythropoietin (EPO) is considered a primary causative factor of renal anemia. The aims of this study were to compare the RBC lifespan, serum EPO levels, and other renal anemia indicators across CKD-stage groups of patients and to analyze the impacts of etiological factors on renal anemia. Methods: A cohort of 74 non-smoking patients with CKD were enrolled, including 15 in stage 1, 18 in stage 2, 15 in stage 3, 15 in stage 4, and 11 in stage 5. RBC lifespan was determined by CO breath tests. Potential correlations of hemoglobin (Hb) concentration with RBC lifespan, reticulocyte count (Ret), and levels of EPO, ferritin, folic acid, and vitamin B12 were analyzed. Results: CKD progression was associated with decreases in (Hb) and RBC lifespan. RBC lifespan durations in CKD stages 1–5 were 122 ± 50, 112 ± 26, 90 ± 32, 88 ± 28, and 60 ± 24 days, respectively. RBC lifespan means for the stage 3, 4 and 5 groups were significantly shorter than those for the stage 1 and 2 groups. Serum EPO did not differ significantly between the CKD stage groups. (Hb) correlated directly with RBC lifespan (r = 0.372, p = 0.002) and Ret (r = 0.308, p = 0.011), but did not correlate with serum EPO, ferritin, folic acid, or vitamin B12 levels. Conclusions: Reduced RBC lifespan in early-stage CKD, demonstrated in this study, suggests that increased RBC destruction may play a more important etiological role in renal anemia than other indicators in patients with CKD.


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