Biomarkers in Public Health: Development and Applications

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Biomarkers in Public Health: Development and Applications Irina Stepanov, Ph.D. Assistant Professor Division of Environmental Health Sciences and Masonic Cancer Center University of Minnesota

Transcript of Biomarkers in Public Health: Development and Applications

Page 1: Biomarkers in Public Health: Development and Applications

Biomarkers in Public Health: Development and Applications

Irina Stepanov, Ph.D. Assistant Professor

Division of Environmental Health Sciences and Masonic Cancer Center University of Minnesota

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Biomarker paradigm

Exposure Clinical disease

1987, U.S. National Research Council

Internal dose Biologically effective dose

Early biological effect

Altered structure/ function

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Biomarker paradigm

Exposure Internal dose Biologically effective dose

Early biological effect

Altered structure/ function

Clinical disease

Susceptibility

1987, U.S. National Research Council

Exposure and Effect

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What is a biomarker?

An indicator of exposure, effect, susceptibility, or clinical disease that can be measured in a biological system

Category Examples Unchanged exogenous agents (exposure) Asbestos fibers, metals

Metabolized exogenous agents (exposure, susceptibility)

Phenol for benzene, cotinine for nicotine, metabolite ratios

Endogenous molecules exposure effect susceptibility

Porphyrin ratios (metals, dioxins) DNA and protein adducts Gene polymorphisms

Cellular/tissue changes (effect, susceptibility)

Neutrophil to lymphocyte ratios, sperm counts

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Research publications on biomarkers

Results of PubMed search

Number of publications

time periods

(17) 0

100,000

200,000

300,000

400,000

500,000

600,000

1900 - 1950 1950 - 2000 2000 - present

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Genetic risk Environmental risk (exposures)

10% 90%

Cancer and degenerative diseases

Most diseases are believed to result from a complex interaction between an individual’s genetic make-up and environmental agents

Adapted from M.T. Smith and S.M. Rappaport, Environ Health Perspect, 117(8): A334-A335 (2009).

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Exposure assessment approaches

Questionnaires Interviews Diaries Biomarker measurements

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Different biological sample types for the biomarker-based exposure assessment

Kuhnle G. Nutritional biomarkers for objective dietary assessment. J Sci Food Agric 2012; 92: 1145–1149

Exposure frequency questionnaire

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Advantages and disadvantages of different biological sample types Type Advantages Disadvantages Blood Easy to collect, regularly replenished,

a way for chemicals to travel within the body

Invasive, cultural rejection, short lifespan

Urine Non-invasive, large amounts Metabolites are measured, more than a single time point or 24-h collections are often needed

Adipose tissue Good matrix for analysis of non-polar chemicals

Invasive

Breast milk Ease of collection, may reflect historical exposures to lipid-soluble chemicals

Limited application

Hair Non-invasive, temporal distribution Not many methods are validated, trace levels, potential of external incorporation

Nails Non-invasive, reflect long-term cumulative exposure

Not many methods are validated, trace levels

Saliva Non-invasive Not widely used

Exhaled air Non-invasive Limited application (volatile compounds)

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Characteristics of a good biomarker?

Specificity (to exposure, disease)

Sensitivity (in response to changes in exposure, disease)

Technical feasibility (collection, measurement)

Reproducibility (frame of reference)

Biological relevance (timeframe, mechanism of effect and disease)

Predictive value

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Biomarker development

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Hypothesis driven

Biomarker development strategies

Food

Dietary intervention with extremes (nil/high) of food

Confirmation of suitability of candidate biomarker

Biomarker validation

Food composition data; Bioavailability; Metabolism

Identification of likely candidate markers

Development of specific analytical method

Analysis of candidate biomarkers in collected specimens

Kuhnle G. J Sci Food Agric 2012;92:1145–1149; Gross et al. CEBP 2011;20(6):1107-1111

Technical feasibility

Specificity

Sensitivity

Application in epidemiological or clinical settings

1-methylhistidine

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Hypothesis driven

Biomarker development strategies

Food

Dietary intervention with extremes (nil/high) of food

Confirmation of suitability of candidate biomarker

Biomarker validation

Food composition data; Bioavailability; Metabolism

Identification of likely candidate markers

Development of specific analytical method

Analysis of candidate biomarkers in collected specimens

Kuhnle G. J Sci Food Agric 2012;92:1145–1149;

Technical feasibility

Specificity

Sensitivity

Application in epidemiological or clinical settings

Discovery driven

Food

Dietary intervention with extremes (nil/high) of food

Analysis of candidate biomarkers in collected specimens

Multivariate analysis to identify differences and candidate markers

Biomarker validation

Application in epidemiological or clinical settings

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Examples of biomarker applications in Environmental Health

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Lead (Pb)

banned banned, copper is used instead

outlawed since 1978

however…

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Temporal changes in blood Pb levels

CDC, MMWR, May 27, 2005 / 54(20);513-516

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Aflatoxin exposure an hepatocellular carcinoma (HCC)

G S Qian, R K Ross, M C Yu, et al. Cancer Epidemiol Biomarkers Prev 1994;3:3-10.

0

10

20

30

40

50

60

none Aflatoxin positive HBsAg positive HBsAg andaflatoxin positive

1 3.4

7.3

59.4

Rel

ativ

e ris

k of

hep

atoc

ellu

lar c

arci

nom

a

“… On the other hand, cohort analysis using all cases of HCC revealed no strong or statistically significant association between HCC risk and dietary aflatoxin consumption as determined from the in-person food frequency interview combined with the survey of market foods in the study region…”

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Use of biomarkers in environmental health

Identifying priority exposures Identifying at-risk populations Recognizing time-trends in population exposures Evaluation of exposure reduction and prevention activities Checking the validity of traditional exposure models Establishing reference ranges for comparison

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Application of biomarkers in tobacco carcinogenesis studies

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Stepanov Lab research focus: Applying biomarker-based approach to characterize and quantify the links between exposures and health outcomes

Chemical toxicants and carcinogens in

environmental sources

Biomarkers: Exposure

Metabolism Effect

Cancer Inflammation-driven

diseases Neurobehavioral

abnormalities

Quantitative links

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Biomarker expertise

Tobacco exposures

Tobacco-specific N-nitrosamines

Cotinine (nicotine)

Polycyclic aromatic hydrocarbons (1-HOP)

HPB-releasing DNA adducts

Oxidative DNA damage

8-oxo-dG

8-oxo-dA

M1dG

Trace elements (sample collection and processing)

Manganese

Iron

Cadmium

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100,000,000 people died from tobacco use in the 20th century

1,000,000,000 people will die from tobacco use in the 21st century

Why do we study tobacco?

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• 19 types of cancer

• Respiratory • Cardiovascular

Main health consequences of smoking

Over 7,000 constituents • Nicotine

• Numerous toxicants

• More than 70 carcinogens

Addiction

Toxicity

Carcinogenicity

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Why do we study tobacco?

Understand the diversity of tobacco products and related risks

Understand mechanisms of diseases caused by tobacco use

Identify susceptible individuals

Develop preventive measures

Build science base for tobacco product regulation by the FDA

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Focus on NNN and NNK

The most important carcinogens in smokeless tobacco

NNN: oral and esophageal cancer NNK: lung and pancreatic cancer

N

NN O

NNNN

NCH3

O N O

NNK

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Cancer deaths due to smoking (US)

ACS, Cancer Facts and Figures 2010

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Research approach

?

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Exposure measurement

Product analysis

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Biomarkers of NNK and NNN intake

N

NN O

NNN

N

NN OO

OHHO

HOOOC

NNN-N-Gluc

N

NN

CH3

OO

NNK

N

NN

CH3

OO

OHOOC

OHHO

HO

NO

OHHO

HOOOC

NN

CH3

OOH

NNAL-N-Gluc

NNAL-O-Gluc

N

NN

CH3

OOH

NNAL

Total NNN

Total NNAL

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Measuring the relationship between product content and constituent intake Habitual users of various brands

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Urinary total NNAL in US smokers of different cigarette brands

NNK in cigarette smoke Total NNAL in smokers’ urine

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Brand A Brand B

NN

K, n

g/m

g ni

cotin

e

0

0.1

0.2

0.3

0.4

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0.6

Brand A (48) Brand B (20)

Tota

l NN

AL, p

mol

/nm

ol c

otin

ine

P = 0.04

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Relationship between constituent levels and biomarkers of intake in smokeless users

Smokeless tobacco users (343) Products with wide range of nicotine and TSNA levels Multiple regression analysis for biomarkers (P-values)

Covariates

Urinary biomarkers

Total nicotine equivalents

Total NNN (NNN intake)

Total NNAL (NNK intake)

Constituent level in product 0.155 <0.001 <0.001

Dip weight 0.086 0.068 <0.001

Total daily dip duration <0.001 <0.001 <0.001

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Measuring the relationship between product content and constituent intake Switching studies

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Total NNAL in urine of smokeless tobacco users assigned to low-TSNA products

Hatsukami et al. J Natl Cancer Inst. 2004;96:844-852

Snus (low-TSNA product)

Nicotine patch

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Research approach

?

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Understanding individual susceptibility

N

NCH3

O N O

NNK

metabolic activation

DNA damage

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18,244 men (45-64 years old) enrolled between 1986 and 1989 use of tobacco and alcohol, usual diet, and medical history 10-ml blood sample and a single spot urine sample

Yuan et al, Carcinogenesis (2011);32:1366-1371

Linking exposure to cancer risk

Shanghai Prospective Cohort

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Relationship between TSNA exposure and cancer risk in humans

J.-M. Yuan et al, Carcinogenesis 32(9): 1366-1371 (2011); I. Stepanov et al. Int J Cancer 134:2278-2283 (2014)

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Ongoing non-tobacco studies

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Oxidative DNA damage in Taconite Workers Health Study

Oxidative DNA damage in Taconite Workers Health Study

Oxidative stress and inflammation, induced by the dust from taconite operations and mediated by iron exposure, are important contributors to the development of cancer and cardiovascular disease in taconite workers.

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The leading cause of blindness among older adults in the developed world

Approximately 30% of individuals over 75 years are affected

Indications of increased oxidative mitochondrial DNA damage in the retinal pigment epithelium

Oxidative DNA damage in age-related macular degeneration (AMD)

11-55 ng mtDNA