2006
DOI: 10.1002/ajim.20253
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Plasma‐lead concentration: Investigations into its usefulness for biological monitoring of occupational lead exposure

Abstract: Plasma lead is not significantly altered by variation in a single day's exposure and, therefore, the choice of time of the day is not critical for sampling. However, plasma lead is negatively correlated to blood hemoglobin and mild hemolysis (not visible by the eye) in a sample may increase plasma lead with up to 30%. Finally, plasma provides lead exposure information that differs from whole blood, but it is not clear which one of these is the biomarker with the closest relation to exposure and/or effects.

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Cited by 23 publications
(12 citation statements)
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References 17 publications
(39 reference statements)
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“…The present data clearly show the well-known anaemic effect of Pb exposure (Bergdahl et al 2006). Previous authors have described the relationship between exposure and B-Hb by use of B–Pb as a biomarker (Gennart et al 1992).…”
Section: Discussionsupporting
confidence: 87%
“…The present data clearly show the well-known anaemic effect of Pb exposure (Bergdahl et al 2006). Previous authors have described the relationship between exposure and B-Hb by use of B–Pb as a biomarker (Gennart et al 1992).…”
Section: Discussionsupporting
confidence: 87%
“…It is possible that serum (Pb‐S) or plasma (Pb‐P) Pb concentrations may be better indexes of Pb exposure, distribution and the associated health risks [12]. This is because the toxic effects of Pb are primarily associated with the most rapidly exchangeable Pb fraction in the bloodstream, which is the Pb fraction in serum or plasma [13,14]. Importantly, maternal Pb‐P concentrations were shown to vary independently from maternal Pb‐B levels [15,16].…”
mentioning
confidence: 99%
“…The technique has been applied to assessing lead exposures in adults (Cake et al 1996;Hernandez-Avila et al 1998;Manton et al 2001;Smith et al 2002;Tellez-Rojo et al 2004). A direct comparison of lead concentrations in plasma and serum yielded similar results (Bergdahl et al 2006); however, the interchangeability of plasma and serum lead measurements for biomonitoring of lead exposure or body burden had not been thoroughly evaluated in large numbers of subjects (Bergdahl et al 2006;Manton et al 2001;Smith et al 2002).…”
Section: Health Effectsmentioning
confidence: 86%
“…The concentration of lead in plasma is extremely difficult to measure accurately because levels in plasma are near the quantitation limits of most analytical techniques (e.g., approximately 0.4 μg/L at blood lead concentration of 100 μg/L (Bergdahl and Skerfving 1997;Bergdahl et al 1997a) and because hemolysis that occurs with typical analytical practices can contribute substantial measurement error (Bergdahl et al 1998(Bergdahl et al , 2006Cavalleri et al 1978;Smith et al 1998a). Recent advances in inductively-coupled plasma mass spectrometry (ICP-MS) offer sensitivity sufficient for measurements of lead in plasma (Schütz et al 1996).…”
Section: Health Effectsmentioning
confidence: 99%