
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Hemolytic anemia other diagnostic studies
Introduction
Overview
Overview
Other possible diagnostic studies in the workup for hemolytic anemia include ferritin, urine hemosiderin, and flow cytometry.
Other diagnostic studies
Other diagnostic studies
- Ferritin[1]: Ferritin is often increased in chronic hemolytic conditions. Ferritin is a marker of total body iron. It is unknown exactly how a high ferritin level relates to hemolytic anemia, but it is known that ferritin is an acute phase reactant that is elevated in chronic conditions. In hereditary spherocytosis, for example, a small fraction of patients have ferritin levels above 500 ng/ml. In the case of anemia of chronic disease.
- Urine hemosiderin[2]: This is a marker of intravascular hemolysis. In some cases it is useful to distinguish whether hemolysis occurs intravascularly (within blood vessels) or extravascularly (such as in the spleen). Both urine hemosiderin and LDH are more specific markers of intravascular hemolysis. Assessment of urine hemosiderin can help with the diagnostic workup of hemolytic anemia can sometimes help guide the management plan. Warm autoimmune hemolytic anemia, for example, is due to IgG antibodies binding red blood cells and causing extravascular hemolysis. The urine hemosiderin would be low in this case. This is treated with steroids. Cold agglutinin disease, on the other hand, is less likely to be associated with extravascular hemolysis so is not treated with steroids.
- Flow cytometry[3]: Flow cytometry can be done on red blood cells to assess for paroxysmal nocturnal hemoglobinuria, or PNH, which is one cause of hemolysis. Flow cytometry assesses for cell surface markers on red blood cells. PNH is characterized by the absence of CD55 (decay accelerating factor) and CD59 (membrane inhibitor of reactive lysis), which are complement inhibitory proteins that prevent destruction of red blood cells by complement.
References
References
- ↑ Fervenza FC, Croatt AJ, Bittar CM, Rosenthal DW, Lager DJ, Leung N; et al. (2008). “Induction of heme oxygenase-1 and ferritin in the kidney in warm antibody hemolytic anemia”. Am J Kidney Dis. 52 (5): 972–7. doi:10.1053/j.ajkd.2008.07.012. PMC 2709285. PMID 18805612.
- ↑ Hikosaka K, Ikutani M, Shito M, Kazuma K, Gulshan M, Nagai Y; et al. (2014). “Deficiency of nicotinamide mononucleotide adenylyltransferase 3 (nmnat3) causes hemolytic anemia by altering the glycolytic flow in mature erythrocytes”. J Biol Chem. 289 (21): 14796–811. doi:10.1074/jbc.M114.554378. PMC 4031534. PMID 24739386.
- ↑ Kelly R, Richards S, Hillmen P, Hill A (2009). “The pathophysiology of paroxysmal nocturnal hemoglobinuria and treatment with eculizumab”. Ther Clin Risk Manag. 5: 911–21. PMC 2789686. PMID 20011245.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Shyam Patel [2]
