Journal of Clinical Lipidology
Volume 4, Issue 4 , Pages 259-264, July 2010

Is directly measured low-density lipoprotein clinically equivalent to calculated low-density lipoprotein?

  • Lawrence Baruch, MD

      Affiliations

    • James J. Peters VA Medical Center (Medical Service), 130 West Kingsbridge Road, Bronx, NY 10468
    • Mt. Sinai School of Medicine, New York, NY
    • Corresponding Author InformationCorresponding author:
  • ,
  • Sanjay Agarwal, MD

      Affiliations

    • Valley Hospital, Ridgewood, NJ
  • ,
  • Bhanu Gupta, MD

      Affiliations

    • Mayo Clinic, Rochester, MN
  • ,
  • Ann Haynos, BA

      Affiliations

    • University of Nevada, Reno, NV
  • ,
  • Swapna Johnson, MD

      Affiliations

    • James J. Peters VA Medical Center (Medical Service), 130 West Kingsbridge Road, Bronx, NY 10468
  • ,
  • Katelyn Kelly-Johnson, BS

      Affiliations

    • James J. Peters VA Medical Center (Medical Service), 130 West Kingsbridge Road, Bronx, NY 10468
  • ,
  • Calvin Eng, MD

      Affiliations

    • James J. Peters VA Medical Center (Medical Service), 130 West Kingsbridge Road, Bronx, NY 10468
    • Mt. Sinai School of Medicine, New York, NY

Received 10 March 2010; accepted 31 May 2010. published online 28 June 2010.

Background

Low-density lipoprotein cholesterol (LDL-C) can either be calculated or measured directly. Clinical guidelines recommend the use of calculated LDL-C (C-LDL-C) to guide therapy because the evidence base for cholesterol management is derived almost exclusively from trials that use C-LDL-C, with direct measurement of LDL-C (D-LDL-C) being reserved for those patients who are nonfasting or with significant hypertriglyceridemia.

Objective

Our aim was to determine the clinical equivalence of directly measured-LDL-C, using a Siemens Advia Chemistry System, and fasting C-LDL-C.

Methods

Eighty-one subjects recruited for two cholesterol treatment studies had at least one C-LDL-C and D-LDL-C performed simultaneously; 64 had a repeat lipid assessment after 4 to 6 weeks of therapy, resulting in 145 pairs of C-LDL-C and D-LDL-C.

Results

There was significant correlation between D-LDL-C and C-LDL-C (r2 = 0.86). Correlation was significantly better in those with lower total cholesterol, triglycerides, and high-density lipoprotein. In 60% of subjects, the difference between D-LDL-C and C-LDL-C was more than 5 mg/dL and greater than 6%. Clinical concordance between D-LDL-C and C-LDL-C was present in 40% of patients, whereas clinical discordance was noted in 25%. One-third had greater than a 15 mg/dL difference between D-LDL-C and C-LDL-C, whereas 25% had a greater than 20 mg/dL difference. In 47% of subjects, the difference between D-LDL-C and C-LDL-C at baseline and follow-up changed by a minimum of 10% or 10 mg/dL.

Conclusions

Our findings suggest that D-LDL-C is not clinically equivalent to C-LDL-C. This puts into question the current recommendation of using D-LDL-C in situations in which C-LDL-C would be inaccurate.

Keywords: Health policy, Hypercholesterolemia, LDL-C cholesterol, Lipids

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PII: S1933-2874(10)00225-4

doi:10.1016/j.jacl.2010.05.003

Journal of Clinical Lipidology
Volume 4, Issue 4 , Pages 259-264, July 2010