E. Spector et al., HOLOGIC QDR-2000 WHOLE-BODY SCANS - A COMPARISON OF 3 COMBINATIONS OFSCAN MODES AND ANALYSIS SOFTWARE, Osteoporosis international, 5(6), 1995, pp. 440-445
This study reports on the short-term in vivo precision and absolute me
asurements of three combinations of whole-body scan modes and analysis
software using a Hologic QDR 2000 dual-energy X-ray densitometer. A g
roup of 21 normal, healthy volunteers (11 male and 10 female) were sca
nned six times, receiving one pencil-beam and one array whole-body sca
n on three occasions approximately 1 week apart. The following combina
tions of scan modes and analysis software were used: pencil-beam scans
analyzed with Hologic's standard whole-body software (PB scans); the
same pencil-beam analyzed with Hologic's newer ''enhanced'' software (
EPB scans); and array scans analyzed with the enhanced software (EA sc
ans). Precision values (% coefficient of variation, %CV) were calculat
ed for whole-body and regional bone mineral content (BMC), bone minera
l density (BMD), fat mass, lean mass, %fat and total mass. In general,
there was no significant difference among the three scan types with r
espect to short-term precision of BMD and only slight differences in t
he precision of BMC. Precision of BMC and BMD for all three scan types
was excellent: <1% CV for whole-body values, with most regional value
s in the 1%-2% range. Pencil-beam scans demonstrated significantly bet
ter soft tissue precision than did array scans. Precision errors for w
hole-body lean mass were: 0.9% (PB), 1.1% (EPB) and 1.9% (EA). Precisi
on errors for whole-body fat mass were: 1.7% (PB), 2.4% (EPB) and 5.6%
(EA). EPB precision errors were slightly higher than PB precision err
ors for lean, fat and %fat measurements of all regions except the head
, although these differences were significant only for the fat and % f
at of the arms and legs. In addition EPB precision values exhibited gr
eater individual variability than PB precision values. Finally, absolu
te values of bone and soft tissue were compared among the three combin
ations of scan and analysis modes. BMC, BMD, fat mass, %fat and lean m
ass were significantly different between PB scans and either of the EP
B or EA scans. Differences were as large as 20%-25% for certain region
al fat and BMD measurements. Additional work may be needed to examine
the relative accuracy of the scan mode/software combinations and to id
entify reasons for the differences in soft tissue precision with the a
rray whole-body scan mode.