Fj. Vandis et al., DIRECT MEASUREMENT OF SERUM LOW-DENSITY-LIPOPROTEIN CHOLESTEROL IN PATIENTS WITH ACUTE MYOCARDIAL-INFARCTION ON ADMISSION TO THE EMERGENCY ROOM, The American journal of cardiology, 77(14), 1996, pp. 1232
In most clinical laboratories low-density lipoprotein (LDL) levels are
estimated by use of a mathematic formula, the Friedewald equation, ra
ther than measured directly.(1) Although the Friedewald estimate is re
liable when the triglyceride level is <400, it is influenced by the fe
d or fasting state. Postprandial elevation of triglycerides is respons
ible for lowering LDL levels by the Friedewald estimate: 7% reduction
of LDL 2 hours after a meal and 2.5% reduction of LDL 5 hours after a
meal.(2) Lipid measurement during an acute myocardial infarction prese
nts a number of problems to clinicians wanting to address secondary pr
evention of disease: Lipid measurements are accurate only in the first
24 hours after the event, and patients are usually admitted to hospit
als in the nonfasting state.(3) In addition, the triglyceride level ma
y be elevated 25% over the baseline or preinfarction level early after
myocardial infarction and may also yield falsely lower estimates of L
DL cholesterol levels.(3) LDL cholesterol may be directly measured in
nonfasting patients with the ultracentrifuge. Ultracentrifugation is a
technically demanding procedure requiring 48 hours of preparation inv
olving the analytic ultracentrifuge, a piece of equipment not usually
found in most clinical laboratories.(4) In addition to ultracentrifuga
tion, the newly developed immunoseparation method of LDL measurement 5
does not require a fasting specimen, may be performed in 3 hours, and
is easier to use technically, The following study compares immunosepa
ration, ultracentrifugation, and the Friedewald estimate of LDL in pat
ients admitted to the hospital for treatment of an acute myocardial in
farction.