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Williams, A.* ; Bissinger, R.* ; Shamaa, H.* ; Patel, S.* ; Bourne, L.* ; Artunc, F. ; Qadri, S.M.*

Pathophysiology of red blood cell dysfunction in diabetes and its complications.

Pathophysiology 30, 327-345 (2023)
Verlagsversion DOI PMC
Creative Commons Lizenzvertrag
Diabetes Mellitus (DM) is a complex metabolic disorder associated with multiple microvascular complications leading to nephropathy, retinopathy, and neuropathy. Mounting evidence suggests that red blood cell (RBC) alterations are both a cause and consequence of disturbances related to DM-associated complications. Importantly, a significant proportion of DM patients develop varying degrees of anemia of confounding etiology, leading to increased morbidity. In chronic hyperglycemia, RBCs display morphological, enzymatic, and biophysical changes, which in turn prime them for swift phagocytic clearance from circulation. A multitude of endogenous factors, such as oxidative and dicarbonyl stress, uremic toxins, extracellular hypertonicity, sorbitol accumulation, and deranged nitric oxide metabolism, have been implicated in pathological RBC changes in DM. This review collates clinical laboratory findings of changes in hematology indices in DM patients and discusses recent reports on the putative mechanisms underpinning shortened RBC survival and disturbed cell membrane architecture within the diabetic milieu. Specifically, RBC cell death signaling, RBC metabolism, procoagulant RBC phenotype, RBC-triggered endothelial cell dysfunction, and changes in RBC deformability and aggregation in the context of DM are discussed. Understanding the mechanisms of RBC alterations in DM provides valuable insights into the clinical significance of the crosstalk between RBCs and microangiopathy in DM.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Schlagwörter Anemia ; Cell Death ; Complications ; Deformability ; Diabetes ; Metabolism ; Microcirculation ; Red Blood Cells ; Thrombosis; Chronic Kidney-disease; Increased Erythrocyte Adhesion; Iron-deficiency Anemia; Distribution Width; Phosphatidylserine Exposure; Endothelial-cells; Hemoglobin A1c; Erythropoietin Deficiency; Eryptotic Erythrocytes; Glyoxalase System
Sprache englisch
Veröffentlichungsjahr 2023
HGF-Berichtsjahr 2023
ISSN (print) / ISBN 0928-4680
e-ISSN 1873-149X
Zeitschrift Pathophysiology
Quellenangaben Band: 30, Heft: 3, Seiten: 327-345 Artikelnummer: , Supplement: ,
Verlag MDPI
Verlagsort St Alban-anlage 66, Ch-4052 Basel, Switzerland
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Diabetes Research and Metabolic Diseases (IDM)
POF Topic(s) 90000 - German Center for Diabetes Research
Forschungsfeld(er) Helmholtz Diabetes Center
PSP-Element(e) G-502400-001
Förderungen Ontario Tech University STAR award
natural sciences and engineering research council of canada
DOI 10.3390/pathophysiology30030026
WOS ID 001074402600001
Scopus ID 85173530790
PubMed ID 37606388
Erfassungsdatum 2023-10-06
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