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Stability over time of hematological variables in 197 children with sickle cell anemia

dc.contributor.authorOdenheimer, Daniel J.en_US
dc.contributor.authorWhitten, Charles F.en_US
dc.contributor.authorRucknagel, Donald L.en_US
dc.contributor.authorSarnaik, Sharada A.en_US
dc.contributor.authorSing, Charles F.en_US
dc.date.accessioned2006-04-28T16:47:31Z
dc.date.available2006-04-28T16:47:31Z
dc.date.issued1984-07en_US
dc.identifier.citationOdenheimer, Daniel J.; Whitten, Charles F.; Rucknagel, Donald A.; Sarnaik, Sharada A.; Sing, Charles F. (1984)."Stability over time of hematological variables in 197 children with sickle cell anemia." American Journal of Medical Genetics 18(3): 461-470. <http://hdl.handle.net/2027.42/38236>en_US
dc.identifier.issn0148-7299en_US
dc.identifier.issn1096-8628en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38236
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6206724&dopt=citationen_US
dc.description.abstractOne hundred ninety-seven children with sickle cell anemia were followed for 4 years at the Wayne State Comprehensive Sickle Cell Center to evaluate the stability of the hematological variables (Hb, Hct, RBC count, MCV, %HbF and %HBA 2 ) over time. The mean values of the hematological measurements taken during three separate 16-month intervals were used to represent an individual's values. The correlations of the hematological variables between intervals ranged from a low of 0.46 for %HBA 2 to a high of 0.91 for %HbF. Correlations that spanned two intervals (an average of 32 months) were of the same magnitude as those that spanned only one interval (an average of 16 months), suggesting that there was no decrease in the degree of stability of these variables as the time between measurements increased. The stability of the correlations between variables within intervals, and the stability of the coefficients of the first two principal components of the six hematological variables over time suggested that the relationships among variables were also stable. In a recent report [Odenheimer et al, 1983], we used the values of the six hematological variables collected at an individual's first visit to the sickle cell center to identify four hematologically distinct subgroups of children. In the current report, we found that as many as 83% of the individuals remained in the same subgroup in at least two of the three follow-up intervals, suggesting that the factors that contributed to this classification were the result of stable, rather than transient phenomena.en_US
dc.format.extent614573 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherGeneticsen_US
dc.titleStability over time of hematological variables in 197 children with sickle cell anemiaen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Ann Arbor, Detroiten_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Ann Arbor, Detroiten_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Ann Arbor, Detroit ; Department of Human Genetics, Box 015, University of Michigan Medical School, 1137 E. Catherine Street, Ann Arbor, MI 48109en_US
dc.contributor.affiliationotherComprehensive Sickle Cell Center and Department of Pediatrics, Wayne State University, Detroiten_US
dc.contributor.affiliationotherComprehensive Sickle Cell Center and Department of Pediatrics, Wayne State University, Detroiten_US
dc.identifier.pmid6206724en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38236/1/1320180316_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/ajmg.1320180316en_US
dc.identifier.sourceAmerican Journal of Medical Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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