Epigenetic correlates of human socioeconomic status

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Epigenetic correlates of human socioeconomic status Clyde Hertzman

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Epigenetic correlates of human socioeconomic status. Clyde Hertzman. Gradient in all Cause Mortality: UK Whitehall Study (1980s). CHD Mortality - UK Whitehall Study. The Challenge of the Gradient. ubiquitous in wealthy and majority world countries by income, education, or occupation - PowerPoint PPT Presentation

Transcript of Epigenetic correlates of human socioeconomic status

Page 1: Epigenetic correlates of human socioeconomic status

Epigenetic correlates of human socioeconomic status

Clyde Hertzman

Page 2: Epigenetic correlates of human socioeconomic status

Gradient in all Cause Mortality: UK Whitehall Study (1980s)

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CHD Mortality - UK Whitehall Study

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The Challenge of the Gradient

• ubiquitous in wealthy and majority world countries by income, education, or occupation

• cuts across a wide range of disease processes

• not explained by traditional risk factors

• replicates itself on new conditions as they emerge

• occurs among males and females

• ‘flattens up’

• begins life as gradient in ‘developmental health’

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Sensitive Periods in Early Brain Development

VisionVision

0 1 2 3 7654

High

Low

Years

Habitual ways of Habitual ways of respondingrespondingEmotional Emotional

controlcontrol

SymboSymboll

Peer social skillsPeer social skillsNumbersNumbers

HearingHearing

Graph developed by Council for Early Child Development (ref: Nash, 1997; Early Years Study, 1999; Shonkoff, 2000.)

Pre-school years School years

LanguaLanguagege

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Canada: % vulnerable by SES

Source: NLSCY/UEY 1999-2000; EDI 1999-2000

% V

ulne

rabl

e

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Jamaica: % vulnerable by SES%

Vul

nera

ble

SES

% V

ulne

rabl

e

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Kosovo: % vulnerable by SES%

Vul

nera

ble

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Life Course Impacts of EarlyExperiences

2nd Decade

3rd/4th Decade

5th/6th

DecadeOld Age

• School Failure

• Teen Pregnancy

• Criminality

• Obesity

• Elevated BloodPressure

• Depression

• Coronary Heart Disease

• Diabetes

• Premature Aging

• Memory Loss

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Biological embedding occurs when

• experience gets under the skin and alters human biodevelopment;

• systematic differences in experience in different social environments lead to different biodevelopmental states;

• the differences are stable and long-term;they influence health, well-being, learning, and/or behaviour over the life course.

Hypothesis: Biological embedding

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Archeology of Biological EmbeddingArcheology of Biological EmbeddingArcheology of Biological EmbeddingArcheology of Biological Embedding

Experience/BehaviorExperience/BehaviorExperience/BehaviorExperience/Behavior

Gene ExpressionGene ExpressionGene ExpressionGene Expression

Cell/SynapseCell/SynapseCell/SynapseCell/Synapse

Neural CircuitryNeural CircuitryNeural CircuitryNeural Circuitry

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Shallow Archeology

Candidate Systems• HPA axis --- cortisol

• ANS system --- epinephrine/ne

• Prefrontal cortex

• Social affiliation --- amygdala/locus cereleus

• Immune function -- the ‘peripheral brain’

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Candidate System: Prefrontal Cortex SES Differences by School Age

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Deep Archeology

‘Social Epigenesis’ and other processes that can influence

gene expression.

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Biological Embedding: The ‘Meaney-

Szyf Paradigm’

• rat pups from high and low licking/suckling mothers cross-fostered to remove genetic effect

• differential qualities of nurturance occurs during sensitive period of brain development

• differential nurturance leads to epigenetic modification of key DNA regulatory loci through methylation

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The ‘Meaney-Szyf Paradigm’ (cont’d)

• epigenetic modification leads to lifelong change in HPA axis response to stress

• this change affects learning and behaviour across the rat life course

• inter-generational transmission (high licked female pups become high licking mothers, and vice versa)

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The Opportunity

If early experience really does ‘get under the skin’ to influence brain and biological development through epigenetic processes, then:

• similar environments & experiences should leave a consistent set of epigenetic ‘marks’ on different populations, and/or create great opportunities for understanding gene-environment-epigenetic interplay.

• the variation in epigenetic marks in children from diverse environments (& experiences) globally should teach us a great deal about biological embedding.

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SES, Life Course and Epigenesis: An Hypothesis Generating Study

• The opportunity: 1958 British Birth Cohort (>17,000 members at birth), with >4000 phenotypic variables collected at birth and 7 follow-ups, with fresh lymphocytes collected at age 45.

• The goal: to identify a full range of gene loci where experience may have become ‘biologically embedded’ through methylation.

• Done to date: examined >20,000 regulatory regions of 40 cohort members, sampled according to a factorial design, based upon extremes of SES in childhood and adulthood (also, abuse and maternal smoking)

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The Team

• Population health/life course epidemiology: Clyde Hertzman, Chris Power

• Epigenetics: Moshe Szyf, Marcus Pembry

• Bio-informatics: Michael Hallett, Matt Suderman

• Laboratory: Nada Borghol

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So far:

• 1252 loci differentially methylated according to childhood SES (smaller signatures for adult SES and social mobility)

• 794 loci differentially methylated by maternal smoking

• Approx. 4000 loci differentially methylated by retrospective reports of abuse in childhood

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1958 Cohort

• Replication• Expression?? • Gene analysis• Exploit 4000 phenotypes with larger

sample sizes

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Consistency in different populations?

The Wisconsin Study of Families and Work

The BC GECKO Study: ‘On and Off-diagonal children’ in ‘On and Off-diagonal

neighbourhoods’

Developing country studies

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Mid- Brain affiliation/attachment

PFC executive function/

impulsivity

HPA stress response

Abuse

Chronic diseases

Health behaviors Mental health

Epigenome

Exposure

Endophenotype

Phenotype

Is this the way forward?

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Exposure

Epigenome

Biochemical/Biophysical Pathway

Phenotype

(Prenatal)Maternal Smoking

Childhood Abuse

Childhood SES

Exposure Specific Pathways

Common Pathways

Exposure Specific Pathways

Exposure Specific Pathways

Outcome(s)Outcome(s)

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