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

被引:14
|
作者
Baruch, Lawrence [1 ,2 ]
Agarwal, Sanjay [3 ]
Gupta, Bhanu [4 ]
Haynos, Ann [5 ]
Johnson, Swapna [1 ]
Kelly-Johnson, Katelyn [1 ]
Eng, Calvin [1 ,2 ]
机构
[1] James J Peters VA Med Ctr, Med Serv, Bronx, NY 10468 USA
[2] Mt Sinai Sch Med, New York, NY USA
[3] Valley Hosp, Ridgewood, NJ USA
[4] Mayo Clin, Rochester, MN USA
[5] Univ Nevada, Reno, NV 89557 USA
关键词
Health policy; Hypercholesterolemia; LDL-C cholesterol; Lipids; CORONARY-HEART-DISEASE; CARDIOVASCULAR-DISEASE; POSITION STATEMENT; APOLIPOPROTEIN-B; CHOLESTEROL; RISK; RATIOS;
D O I
10.1016/j.jacl.2010.05.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 (r(2) = 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 ing/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. Published by Elsevier Inc on behalf of the National Lipid Association.
引用
收藏
页码:259 / 264
页数:6
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