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Interpreting Population Level Biomonitoring
Data in a Risk-Based Context:
A Canadian Perspective

Annie St-Amand1, Kate Werry1, Andy Nong1,
Sean M. Hays2, Lesa L. Aylward2
1Healthy Environments and Consumer Safety Branch, Health Canada;
2Summit Toxicology LLP

September 10, 2013
Population Biomonitoring Data: 
Canadian Health Measures Survey
Survey Parameters
• Cross‐sectional survey design
• Ongoing: 2007‐2009 (Cycle 1), 2009‐
2011 (Cycle 2), 2012‐2013 (Cycle 3 –
data collection in progress)
• National estimates for general 
population:
N= 5600‐6400

• Ages 3‐79 years (3‐5, 6‐11, 12‐19, 20‐
39, 40‐59, 60‐79)
• Health questionnaire – home interview
• Direct measures (blood/urine)– mobile 
clinic
Interpretation Tools
Biomonitoring Equivalents (BE)
“Safe” human dose

RfD, TDI: mg/kg-d

Uncertainty
Factors

Human (equivalent)
Point of Departure

Human
urine/blood level

BE: µg/L

Uncertainty
Factors

Human
Pharmacokinetics

BE - Concentration of biomarker that is
consistent with existing exposure guidance
or reference values such as RfDs, TDIs,
etc (Hays et al., 2007).

POD: mg/kg-d

Human
urine/blood level

BEPOD: µg/L
Screening of Biomonitoring Data
One Chemical

BEPOD

Medium
priority

BE
Low
priority

Hazard Quotient (HQ)
Increasing priority for
follow-up

High
priority

Many Chemicals

Source: LaKind et al., 2008

HQ = [ Biomarker ]
BE
HQ > 1
indicates biomonitoring data
exceeds exposure guidance
value
HQ Screening: Persistent Chemicals
CHMS 2007‐11
Cadmium
CHMS 2009‐11 (urine)
High
BEPOD
4.6 µg/L
Medium
BE
1.5 µg/L

Low
HQ Screening: Short‐lived Chemicals 
CHMS 2009‐11 (urine)
Inorganic Arsenic: DMA + MMA
(µg As/L urine)
High
BEPOD
16 µg/L
Medium
BE
5.8 µg/L

Low

10
Estimated Cancer Risk Levels 
CHMS 2009‐11
1.E-02

Cancer Risk

1.E-03

1.E-04

1.E-05

1.E-06

1.E-07
Arsenic (6-79 years) DDT (20-79 years) HCB (20-79 years)
Discussion
• HQs < 1 for majority of biomarkers
– suggest exposure levels are below existing
guidance values

• HQs > 1 at upper bound of the CHMS
population distributions for inorganic arsenic
and cadmium.
• BEs do not represent diagnostic criteria
• BEs are interim values (screening)
Conclusion
• Cadmium and inorganic arsenic: more detailed
examinations required
• Useful for prioritization efforts
www.health.gc.ca/biomonitoring
Thank you!

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