Course of iron parameters in HFE‐hemochromatosis patients during initial treatment with erythrocytapheresis compared to phlebotomy. Issue 6 (16th February 2016)
- Record Type:
- Journal Article
- Title:
- Course of iron parameters in HFE‐hemochromatosis patients during initial treatment with erythrocytapheresis compared to phlebotomy. Issue 6 (16th February 2016)
- Main Title:
- Course of iron parameters in HFE‐hemochromatosis patients during initial treatment with erythrocytapheresis compared to phlebotomy
- Authors:
- Rombout‐Sestrienkova, Eva
Koek, Ger H.
Neslo, Rabin
van Kraaij, Marian
Menheere, Paul P.
Masclee, Ad
Swinkels, Dorine W. - Abstract:
- Abstract : Current treatment for newly diagnosed patients with hereditary hemochromatosis (HH) and iron overload consist of weekly phlebotomy or less frequent and more personalized erythrocytapheresis. Previous observations during phlebotomy suggest an increase in intestinal iron uptake caused by lowering of hepcidin as a result of intensive bloodletting. It is not known whether such an effect is present or even more pronounced using erythrocytapheresis since a larger amount of iron is extracted per procedure. In this study we aimed to assess the effect of erythrocytapheresis on the course of iron parameters, with special focus on serum hepcidin. We performed a retrospective proof‐of‐principle observational study, comparing serum iron parameters in 12 males during the depletion phase using either phlebotomy ( n = 6) or erythrocytapheresis ( n = 6). Decreases in serum ferritin over time were similar for both treatments but more pronounced using erythrocytapheresis when expressed per treatment procedure. Hemoglobin did not change during erythrocytapheresis, whereas during phlebotomy decreased with 10%. Increase of erythropoietin and soluble transferrin receptor and decrease in transferrin saturation were similar for both treatments. Reduction in serum hepcidin was higher (50% versus 25% of initial value) and occurred more early using phlebotomy (10 versus 20 weeks after start). In aggregate, compared to phlebotomy, the less frequent and more personalized erythrocytapheresisAbstract : Current treatment for newly diagnosed patients with hereditary hemochromatosis (HH) and iron overload consist of weekly phlebotomy or less frequent and more personalized erythrocytapheresis. Previous observations during phlebotomy suggest an increase in intestinal iron uptake caused by lowering of hepcidin as a result of intensive bloodletting. It is not known whether such an effect is present or even more pronounced using erythrocytapheresis since a larger amount of iron is extracted per procedure. In this study we aimed to assess the effect of erythrocytapheresis on the course of iron parameters, with special focus on serum hepcidin. We performed a retrospective proof‐of‐principle observational study, comparing serum iron parameters in 12 males during the depletion phase using either phlebotomy ( n = 6) or erythrocytapheresis ( n = 6). Decreases in serum ferritin over time were similar for both treatments but more pronounced using erythrocytapheresis when expressed per treatment procedure. Hemoglobin did not change during erythrocytapheresis, whereas during phlebotomy decreased with 10%. Increase of erythropoietin and soluble transferrin receptor and decrease in transferrin saturation were similar for both treatments. Reduction in serum hepcidin was higher (50% versus 25% of initial value) and occurred more early using phlebotomy (10 versus 20 weeks after start). In aggregate, compared to phlebotomy, the less frequent and more personalized erythrocytapheresis leads to a more pronounced decrease in serum ferritin per treatment procedure, without a larger decrease in serum hepcidin. This may be clinically relevant and may prevent an increase in intestinal iron uptake and an ensuing vicious circle of more frequent treatment procedures. J. Clin. Apheresis 31:564–570, 2016. © 2015 Wiley Periodicals, Inc. … (more)
- Is Part Of:
- Journal of clinical apheresis. Volume 31:Issue 6(2016)
- Journal:
- Journal of clinical apheresis
- Issue:
- Volume 31:Issue 6(2016)
- Issue Display:
- Volume 31, Issue 6 (2016)
- Year:
- 2016
- Volume:
- 31
- Issue:
- 6
- Issue Sort Value:
- 2016-0031-0006-0000
- Page Start:
- 564
- Page End:
- 570
- Publication Date:
- 2016-02-16
- Subjects:
- hereditary hemochromatosis -- erythrocytapheresis -- phlebotomy -- iron parameters -- hepcidin
Hemapheresis -- Periodicals
Blood -- Transfusion -- Periodicals
Blood -- Transfusion, Autologous -- Periodicals
Cell separation -- Periodicals
Leukapheresis -- Periodicals
Plasmapheresis -- Periodicals
615.39 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-1101 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jca.21451 ↗
- Languages:
- English
- ISSNs:
- 0733-2459
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4958.381500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 234.xml