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dc.contributor.authorHosseini, Poorya
dc.contributor.authorAbidi, Sabia Z.
dc.contributor.authorDu, E
dc.contributor.authorPapageorgiou, Dimitrios P.
dc.contributor.authorChoi, Youngwoon
dc.contributor.authorHiggins, John M.
dc.contributor.authorKato, Gregory J.
dc.contributor.authorSuresh, Subra
dc.contributor.authorDao, Ming
dc.contributor.authorYaqoob, Zahid
dc.contributor.authorSo, Peter T. C.
dc.contributor.authorPark, YongKeun, Ph.D. Massachusetts Institute of Technology
dc.date.accessioned2018-04-26T20:21:07Z
dc.date.available2018-04-26T20:21:07Z
dc.date.issued2016-08
dc.date.submitted2016-05
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/114975
dc.description.abstractHydroxyurea (HU) has been used clinically to reduce the frequency of painful crisis and the need for blood transfusion in sickle cell disease (SCD) patients. However, the mechanisms underlying such beneficial effects of HU treatment are still not fully understood. Studies have indicated a weak correlation between clinical outcome and molecular markers, and the scientific quest to develop companion biophysical markers have mostly targeted studies of blood properties under hypoxia. Using a common-path interferometric technique, we measure biomechanical and morphological properties of individual red blood cells in SCD patients as a function of cell density, and investigate the correlation of these biophysical properties with drug intake as well as other clinically measured parameters. Our results show that patient-specific HU effects on the cellular biophysical properties are detectable at normoxia, and that these properties are strongly correlated with the clinically measured mean cellular volume rather than fetal hemoglobin level.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant 1R01HL121386-01A1)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant 9P41EB015871-26A1)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant 5R01NS051320)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant 5U01HL114476)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant 4R44EB012415)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Grant CBET-0939511)en_US
dc.publisherNational Academy of Sciences (U.S.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/PNAS.1610435113en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceNational Academy of Sciencesen_US
dc.titleCellular normoxic biophysical markers of hydroxyurea treatment in sickle cell diseaseen_US
dc.typeArticleen_US
dc.identifier.citationHosseini, Poorya et al. “Cellular Normoxic Biophysical Markers of Hydroxyurea Treatment in Sickle Cell Disease.” Proceedings of the National Academy of Sciences 113, 34 (August 2016): 9527–9532 © 2016 National Academy of Sciencesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Laser Biomedical Research Centeren_US
dc.contributor.mitauthorHosseini, Poorya
dc.contributor.mitauthorPapageorgiou, Dimitrios P.
dc.contributor.mitauthorDao, Ming
dc.contributor.mitauthorYaqoob, Zahid
dc.contributor.mitauthorSo, Peter T. C.
dc.relation.journalProceedings of the National Academy of Sciencesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-04-13T18:42:16Z
dspace.orderedauthorsHosseini, Poorya; Abidi, Sabia Z.; Du, E; Papageorgiou, Dimitrios P.; Choi, Youngwoon; Park, YongKeun; Higgins, John M.; Kato, Gregory J.; Suresh, Subra; Dao, Ming; Yaqoob, Zahid; So, Peter T. C.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-7347-7887
dc.identifier.orcidhttps://orcid.org/0000-0003-2678-4491
dc.identifier.orcidhttps://orcid.org/0000-0001-5372-385X
dc.identifier.orcidhttps://orcid.org/0000-0003-4698-6488
mit.licensePUBLISHER_POLICYen_US


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