Literature DB >> 7706525

Limited discriminant value of lipoprotein AI, lipoprotein Lp(a) and other lipoprotein particles in patients with and without early onset ischaemic heart disease.

D T Vallance1, H A Staunton, A F Winder.   

Abstract

AIMS: To assess whether the ability of lipoprotein related variables to discriminate between individuals with or without premature clinical ischaemic heart disease (IHD) was improved using data on high density lipoprotein-lipoprotein AI (HDL-LpAI) fractions, alone or in combination with data on Lp(a).
METHODS: Lipid and apolipoprotein concentrations were measured in 26 middle-aged men (mean age 50.3 years) with early onset IHD and coronary artery bypass grafting prior to sampling, and in 26 matched lipaemic and 26 normolipaemic asymptomatic controls.
RESULTS: Triglyceride and Lp(a) concentrations were higher, while HDL cholesterol and apolipoprotein A-I (apoA-I) concentrations were lower in patients than in controls. LpAI concentrations were also lower in IHD patients and were correlated with HDL and apoA-I in both IHD and control groups. Lp(a) was not correlated with any other lipid or apolipoprotein measured in either patients or controls. Univariate discriminant function analysis showed that the proportion correctly classified as patients or controls was marginally greater using LpAI concentrations as the discriminator, which was not increased in combination with Lp(a). Serum triglycerides, HDL cholesterol, apoA-I and Lp(a) alone all had similar, but weaker, discriminant power, which increased in various combinations with LpAI.
CONCLUSIONS: LpAI particle measurement may be useful in research to define mechanisms of cardiovascular protection by HDL but the discriminating power for IHD was only marginally superior to measuring total apoA-I or Lp(a) concentrations. Little further advantage arose through combining LpAI data with other variables.

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Year:  1995        PMID: 7706525      PMCID: PMC502267          DOI: 10.1136/jcp.48.1.70

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  34 in total

1.  Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge.

Authors:  W T Friedewald; R I Levy; D S Fredrickson
Journal:  Clin Chem       Date:  1972-06       Impact factor: 8.327

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Authors:  R F Atmeh; J Shepherd; C J Packard
Journal:  Biochim Biophys Acta       Date:  1983-04-13

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Journal:  J Biol Chem       Date:  1984-10-10       Impact factor: 5.157

4.  Unrecognized dyslipoproteinemia in United Kingdom families recruited to a genetic register because of unexplained coronary heart disease.

Authors:  A Staunton; D T Vallance; A Child; A J Camm; A F Winder
Journal:  J Lab Clin Med       Date:  1994-06

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Journal:  N Engl J Med       Date:  1983-08-18       Impact factor: 91.245

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Journal:  Biochim Biophys Acta       Date:  1983-08-29

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Journal:  Proc Natl Acad Sci U S A       Date:  1980-01       Impact factor: 11.205

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Authors:  M C Cheung; J J Albers
Journal:  J Lipid Res       Date:  1982-07       Impact factor: 5.922

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Authors:  P Avogaro; G B Bon; G Cazzolato; G B Quinci
Journal:  Lancet       Date:  1979-04-28       Impact factor: 79.321

10.  Prevalence of coronary heart disease in the Framingham Offspring Study: role of lipoprotein cholesterols.

Authors:  P W Wilson; R J Garrison; W P Castelli; M Feinleib; P M McNamara; W B Kannel
Journal:  Am J Cardiol       Date:  1980-10       Impact factor: 2.778

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  1 in total

Review 1.  ACP Broad Sheet no 151: September 1997. Investigation of dyslipidaemias.

Authors:  A F Winder; W Richmond; D T Vallance
Journal:  J Clin Pathol       Date:  1997-09       Impact factor: 3.411

  1 in total

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