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Potential Effect of an Apoprotein B-based Algorithm on Management of New Patients with Hypertriglyceridemia Referred to a Specialty Lipid Clinic

dc.contributor.authorBrook, Robert D.en_US
dc.contributor.authorDoshi, Hardiken_US
dc.contributor.authorBard, Robert L.en_US
dc.contributor.authorRubenfire, Melvynen_US
dc.date.accessioned2009-06-01T19:17:13Z
dc.date.available2010-06-02T14:34:29Zen_US
dc.date.issued2009-05en_US
dc.identifier.citationBrook, Robert D.; Doshi, Hardik; Bard, Robert L.; Rubenfire, Melvyn (2009). "Potential Effect of an Apoprotein B-based Algorithm on Management of New Patients with Hypertriglyceridemia Referred to a Specialty Lipid Clinic." Clinical Cardiology 32(5): 251-255. <http://hdl.handle.net/2027.42/62999>en_US
dc.identifier.issn0160-9289en_US
dc.identifier.issn1932-8737en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/62999
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=19452482&dopt=citationen_US
dc.description.abstractBackground In patients with hypertriglyceridemia, non-high density lipoprotein cholesterol (nonHDL-C) is a targeted goal. However, apoprotein B100 (apoB) may be superior in predicting cardiovascular risk so we assessed the utility of an apoB-based. Methods New patients (n = 125) who had both apoB and standard lipids measured on the same day were included and we determined the concordances of having achieved goal lipid levels based upon proposed apoB versus nonHDL-C (ATP III) targets in patients with elevated TG (≥150 mg·dl −1 ) levels. Results Although apoB was correlated with nonHDL-C (r = 0.47, p ≤ 0.001), the tests had only a fair level of agreement when categorizing the percentage of patients achieving lipid goals for their degree of cardiovascular risk (Κ = 0.22). Among patients with an elevation in nonHDL-C above ATP III goals, between 12–42% had achieved target apoB. On the contrary, between 44–50% of patients were found to be at nonHDL-C but not apoB target. The results were not substantively altered if the analyses were confined to patients with TG values between 200–499 mg·dl −1 , rather than all patients with TG levels ≥ 150 mg·dl −1 , as specifically outlined in ATP III guidelines. In total, > 50% of all subjects would have been treated either more or less aggressively following an apoB-based therapeutic algorithm. Conclusions Our findings confirm that the majority of patients referred with hypertriglyceridemia would be managed differently by following an apoB-based treatment algorithm compared to ATP III guidelines. Although many patients would be candidates for more intense therapy, many would be treated less aggressively. Copyright © 2009 Wiley Periodicals, Inc.en_US
dc.format.extent102769 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Periodicals, Inc.en_US
dc.subject.otherMedicine and Healthcareen_US
dc.subject.otherCardiovascular Diseaseen_US
dc.titlePotential Effect of an Apoprotein B-based Algorithm on Management of New Patients with Hypertriglyceridemia Referred to a Specialty Lipid Clinicen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialitiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Cardiovascular Medicine, University of Michigan, Ann Arbor, Michigan ; Division of Cardiovascular Medicine University of Michigan Ann Arbor, MI, 48106en_US
dc.contributor.affiliationumDivision of Cardiovascular Medicine, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDivision of Cardiovascular Medicine, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDivision of Cardiovascular Medicine, University of Michigan, Ann Arbor, Michiganen_US
dc.identifier.pmid19452482en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/62999/1/20399_ftp.pdf
dc.identifier.doi10.1002/clc.20399en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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