We assessed the reprducibility ofX-ray fluorescence-based lead measurements from multiple me emeits made on a low-concen on per of pris phainitom and in five sects measured five times oni two occasions. Over a 6-month period, 220 measurements of the same phantom were obine and showed astandrdeviation of 1.29 pg Pb (g plaster of paY) ' (1,2) and industrial (3,4) lead levels. Second, when used as an index of cumulative exposure, in vivo bone lead measurements have proven valuable in discriminating between occupationally and nonoccupationally exposed persons (5). Third, and most importantly, it has been established that a strong relationship exists between elevated blood lead and bone lead in retired lead workers, highlighting the importance of an endogenous lead exposure (6,7).With the knowledge that the body's lead stores can be mobilized back into the circulatory system, research questions are now addressing the subclinical toxicity of lead (8) released from bone. The release of this endogenous lead store may be a direct result of changes in bone mineral status such as that experienced by women with the onset of menopause (9). The outcomes of such studies will depend strongly on determining changes in bone lead over a reasonable length of time. It is therefore important that in vivo bone lead measurements be reproducible.Because published data on the reproducibility of bone lead measurements are limited (10-12), we set out to define the short-and long-term reproducibility of bone lead concentrations determined by our measurement system both in phantoms and in human subjects. We also present preliminary data that examine the differences in tibia lead between the right and left legs within individuals.
Materials and MethodsWe determined the lead concentration in phantoms and in subjects with an improved 09Cd K X-ray fluorescence system. Details of the instrumentation of this upgraded system have been described previously (1).A bare cylindrical plaster of paris phantom with a nominal concentration of 23 pg Pb (g plaster of paris)Y was selected to define in vitro reproducibility. The phantom was measured over a 6-month period, during which 220 measurements were recorded. Each measurement lasted 1800 sec (clock time), and care was taken to reproduce the position of the phantom to eliminate the effects of any concentration inhomogeneity along or around the phantom.Five subjects (three male, two female) participated in the reproducibility trials. They were selected on the basis that their leg sizes represented a wide range of measurement geometries. We assessed leg size by the circumference at the midpoint between the medial malleolus and the tuberosity of the tibia. Two sets of five measurements were performed at the midpoint of the anteromedial aspect of the left tibia of each subject. For each individual a set of measurements was acquired mostly within a 5-day period. We made the first set of measurements in September 1992 and the second series in July 1993. Before the second set of measurements were repeated, howe...