Hair Analysis Panel Discussion: Section 4.1
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				4.1 Distinguishing Between Endogenous and Exogenous Sources of Metals
				
All of the panelists agreed that using hair analysis as an exposure or diagnostic tool for metal contamination is severely limited by difficulties in distinguishing between internal and external sources of metals. It is further complicated by the natural occurrence of many of the trace elements (several of which are essential nutrients) within the body. The group recognized, however, that this distinction is not a limitation when a metabolite or a substance with no external source is being measured (e.g., organic compounds such as methyl mercury or many drugs of abuse).
Dr. Kosnett led discussions on the difficulties that exist in 
				distinguishing endogenous and exogenous substances in hair. Other 
				panelists expanded upon these issues. Individual points are summarized 
				below.
				
- Hair analysis data do not necessarily enable you to determine 
					where the measured contaminant came from and how it got there. 
					High hair levels may provide "markers of potential exposure," 
					but that does not tell us how much is internally incorporated. 
					If hair analysis is used in ATSDR's evaluations of exposures 
					to contaminants in air (e.g., in the form of particulates), 
					water, or soil/dust, it must be realized that this distinction 
					cannot necessarily be made (MK).
 - An Alaskan study of arsenic levels in tap water, urine, 
					and nails (Harrington et al. 1978), reveals some interesting 
					trends. Individuals drinking bottled water, but bathing in tap 
					water with arsenic averaging 345 micrograms per liter (µg/L), 
					had higher average levels of arsenic in hair (5.7 parts per 
					million, or ppm) compared to those drinking and bathing in tap 
					water with arsenic containing 30 µg/L (0.46 ppm arsenic in hair). 
					Urine levels were similar, however. This example helps illustrate 
					the difficulties in using hair concentrations alone to draw 
					inferences regarding the magnitude of the internally absorbed 
					dose of a metal (MK).
 - Though they are not applicable to the example above (based 
					on arsenic toxicokinetics), another reviewer noted that the 
					following caveats could further confound the interpretation 
					of such a scenario: (1) other exposures could be occurring (e.g., 
					cooking, brushing teeth), (2) dermal absorption could be occurring, 
					and/or (3) a pool of the contaminant could be sequestered in 
					and later released from the bone (e.g., this can be true with 
					tetracycline) (RB).
 - Effect of washing hair. Dr. Kosnett described various 
					studies that have looked at the role and/or effectiveness of 
					washing hair in order to distinguish between endogenous and 
					exogenous sources of arsenic. These studies suggest that no 
					truly good washing method exists to remove arsenic: If hair 
					is not washed aggressively, exogenous arsenic will remain. If 
					hair is washed too aggressively, endogenous arsenic may be removed.
 
— Smith (1964) showed that detected concentrations of arsenic in 
				hair will vary depending on washing method, with no method shown 
				to be capable of removing all arsenic. The results of applying different 
				washing methods (to hair purposely externally contaminated with 
				12.08 ppm arsenic) are highlighted in Table 4-1. The arsenic concentration 
				in hair before contamination was measured at 0.14 ppm. 
				
				
Table 4-1. Effect of washing method and time on arsenic levels in hair
| Washing Method | Washing Time (mins) | Arsenic (ppm) | 
| Water | 5 | 9.16 | 
| 15 | 5.78 | |
| 30 | 5.05 | |
| 60 | 5.03—6.21 | |
| Detergent (5%) | 60 | 4.20—9.93 | 
| HCl (N) | 60 | 4.92—6.26 | 
| NaOH (N) | 60 | 0.40—0.70 | 
Source: Smith 1964 
— Van den Berg et al. (1968) showed similar findings. Depending 
				on the washing regime, this study revealed that even after 1,600 
				minutes of washing, externally deposited arsenic was still detected 
				(MK).
				
				
Measuring total concentrations in hair. Depending on the purpose of your testing, it may not be critical to distinguish between internal and external contamination. For example, in an industrial hygiene exposure investigation, identifying elevated levels of an element may be enough to suggest that the potential for exposure exists and protective measures are needed. While urine data may reveal that existing protective measures have prevented internal exposures, knowledge that employees have exposure potential may be important (e.g., contamination could be carried home) (MK, TC, MG). Several panelists reiterated, however, the limitations of using such data for clinical evaluation or interpretation.


