Persisting chylomicron remnant concentrations have been linked to premature
atherosclerosis. The analysis of persisting chylomicron remnant concentrat
ions by an oral triglyceride tolerance test, however, is time-consuming for
the study subjects and requires large resources in the laboratory. Therefo
re, only small numbers of subjects have been studied in the past.
We describe major improvements of the testing procedure in regard of compos
ition of the fatty meal, of patient testing, and measurement of postprandia
l remnants. Shifting the time of the (ready-to-use) fatty drink from the mo
rning hours to bedtime was well accepted by the study subjects and allowed
the analysis of blood samples drawn at the morning with minimal impact on t
he participants' time and with minimal interferences by confounding factors
(e.g. smoking, additional food intake, physical activity). Chylomicron rem
nants were measured by fluorometry of the supernatant after ultracentrifuga
tion. This procedure was sensitive, was specific for chylomicron remnants,
and was easy to perform. The biological validity of the improved procedure
was evaluated by studying type III hyperlipoproteinemia patients and normol
ipemic apolipoprotein (Apo) E2 homozygotes.
In conclusion, this improved test permits the rapid testing for persisting
chylomicron remnants in the clinical routine and in large epidemiological s
tudies. (C) 2001 The Canadian Society of Clinical Chemists. All rights rese
rved.