Lec 8 Flashcards

Risk Factors for Chronic Pain (50 cards)

1
Q

Chronic Pain

A

-pain persisting beyond 3 months, this is beyond the expected time of tissue healing
-the nervous system has changed, pain persists even when the original injury is gone, nonfucntional pain

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2
Q

Acute Pain

A

a signal, protective, useful, expected to resolve as tissue heals

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3
Q

Pain as Perception

A

-shaped by the brain, not just by tissue, this is why psychological and social factors matter so much
-without the brain you have no painful experience, based on physiological but also personality, mood, SES, gender and many other factors interacting in the brain

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4
Q

Chronic Pain Prevelance

A

-1 in 5 adults worldwide live with chronic pain
-its the leading cause of disability
-more years lived with disability than any other condition globally

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5
Q

Economic Burden

A

-estimated $635 billion annually in the US alone, more than cancer, heart disease, and diabetes combined

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6
Q

Opioid Use & Chronic Pain

A

-chronic pain is the driver of opioid prescribing and a key factor in the opioid crisis

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7
Q

Yakoi Study Problem

A

-most psych studies test whether associations exist
-they dont test whether models can forecast new cases
-the replication crisis is largely a prediction failure

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8
Q

Yakoi Study Core Idea

A

-prediction and explanation are different goals requiring different methods
-a model that explains may be useless at predicting
-out-of-sample accuracy is the true test of a model
-more data beats better theory when the goal is prediction

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9
Q

Yakoi Study Solution

A

-use cross-validation, test your model on data it has never seen
-use large datasets
-change the question: can I predict pain for this person

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10
Q

Prediction Goals

A

-prediction refers to the capacity of a model to predict disease states from high dimensional data
-the problem is that many studies have claims to establish prediction while only providing correlation
-the goal is to generalize these predictions is new individuals that were never encountered before

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11
Q

Steps toward Prediction Goals

A

-predict the risk of developing pain or worsening of their pain
-improve personalized treatment
-improve allocation of health care resources
-refine diagnoses and phenotypes
-provide mechanistic insights
-pain clinics have wait times of 1-2 yrs
-these methods can expand diagnoses and can improve mechanistic insights to find targets for interventions
-there is a mosaic of factors that shapes pain in each individual

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12
Q

Risk Factor

A

something measurable before chronic pain develops that increases its likelihood

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13
Q

Differences in Pain

A

-same injury->persistent, disabling pain
-leads to depression, lost work, opioid use for high-impact pain
-same injury->recovery within weeks
-returns to work, normal life
-different types of pain, even if at the same pain level, have different meanings (3/10 stomach pain is not experienced the same as 3/10 cancer pain)

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14
Q

Predicts Worse Outcomes

A

-fear avoidance behaviours
-psychiatric comorbidities
-high baseline pain
-low general health status

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15
Q

Predicts Recovery

A

-low fear avoidance
-good baseline function
-strong social support
-positive recovery expectations

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16
Q

Biopsychosocial Model

A

biology, psychology, social context

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17
Q

Biology

A

genetics, sex, neurological sensitivity, inflammatory markers

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18
Q

Sex Differences

A

women report chronic pain more often and show greater pain sensitivity on lab tests, not fully explained by hormones alone

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19
Q

Genetic Variance

A

-genes influence pain sensitivity, polygenic factors, opioid response and susceptibility to chronic pain
-each variant has a tiny effect, thousands of ppl are needed to detect them reliably

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20
Q

Brain Imaging

A

-brain based biomarkers predicting subjective experience of pain has become an obsession for the field, with limited results
-not the most ethical to research, but would be helpful to locate pain objectively
-current resting scanning does not have enough insight

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21
Q

Psychology

A

fear avoidance, catasrophisizing, depression, anxiety

22
Q

Fear Avoidance

A

avoiding movement that could cause harm or worsen the pain
-lose physical fitness and functional decline over time
-high fear avoidance roughly double the odds of a poor outcome at one year

23
Q

Social Context

A

work environment, SES, healthcare access

24
Q

Reductionisim Problem

A

-building simple models that appear theoretically elegant but have limited capacity to predict actual human behaviour
-developing complex models that can accurately predict bahviour but fail to respect known psychological or neurobiological constraints
-using machine learning to find intersection between findings in blood, genes, bone, and brain to go beyond the constraints to optimize predictions

25
Problems w/Tradition Research
a) Explains but doesnt predict b) Results dont always replicate
26
Explanation Problem
-studies identify which factors are associated with pain, but rarely test whether they can predict which specific patient will develop chronic pain
27
Replication Problem
-effects found in small samples frequently disappear in larger studies, small samples find patterns that dont exist in the real world
28
Explantion
-what factors are associated with chronic pain -identifies correlates -builds theory -small samples ok
29
Prediction
-will this person develop chronic pain in 5 years -forecasts individual outcomes -needs to generalize -requires large samples -what big data enables
30
UK Biobank Stats
-500 000 participants recruited 2006-2010 -40-69 age range at enrolment -22 assessment centres across the UK -15+ years of ongoing follow-up -many more participants and much more data than most studies
31
Biobank Collection
a) Biological Samples -blood, urine, saliva for genetics studies and biomarkers b) Questionnaires -pain, mental health, lifestyle, medical history c) Brain & body imaging -MRI for 100 000 participants d) Health Records Linkage -hospital visits, perceriptions, diagnoses
32
Why is the Biobank Useful
a) Detect Small Genetic Effects b) Build Models That Actually Generalize c) Ask Longitudinal Questions d) Combine Data Types
33
Genetic Effect Detection
-each genetic variant contributes a small amount -w/500 000 people and genomic data you can reliably find them
34
Generalized Models
-large samples let you test your model on held out data, if it predicts well there, it will predict well in the real world
35
Longitudinal Questions
-who develops chronic pain over time -not just who has it now -participants are followed for years with health record linkage
36
Combined Data Types
-genetics + brain imaging + questionnaires+ prescriptions -the combo is what no single clinical study can afford
37
Findings from Biobank
a) prognostic risk score for development and spread of chronic pain b) Biological markers and psychosocial factors predict chronic pain conditions
38
Prognostic Risk Score
-taking 99 risk factors and use machine learning to make prediction about pain -trying to predict phenotypes -train the model integrating each of the factors together, each attributing a different weight for how they predict pain when considering the 99 predicators together
39
Predictors (strongest to weakest)
1. Mood 2.Sleep 3.Personality 4.Life Stressors 5. Demographics/ Occupational
40
Weakness of Demographics
demographics and occupational by themselves seem like strong predictors, but when observed in a multimodal context, they become redundant, better explained by other, stronger predictors, so what is remaining from those categories become weaker predictors
41
Biomarker x Psychosocial Interaction
-when measure all biology in acute or chronic were under 0.6, which is not clear at all, but psychosocial were all above 0.7 -a factor for this is bc its self reported, but also bc these factors are more prominent than biological -psychosocial risk factors outperfirm biomarkers, in the realm of self report -biomarkers work best for pain spreading -if we switch the target of the model, if we train the machine on the diagnosis, then they are some elements that can predict many things, but not self report
42
Synergy
-trying to create synergy between biomarkers and psychosocial -likelihood of diagnosis increases when high biomarkers are accompanied by high psychosocial factors -considering the patient as a whole and not just their biomarkers
43
Unknowns
1. Whats the direction of Causality 2. Why do treatments work for some people and not others 3. Who is missing from big data
44
Direction of Causality
-does depression cause chronic pain, or does chronic pain cause depression
45
Selective Treatment Success
-pain management program which have good evidence dont help everyone -risk factors may explain who benefits
46
Missing Data
-the UK biobank over-represents healthy, educated white participants, do our risk factors findings geenralize to other populations
47
Ethical Considerations
1. Risk Scores & Stigma 2. Consent & Data Use 3. Who benefits from research
48
Risk Scores & Stigma
-if we can predict who will develop chronic pain, what do we do with that info -could risk scores lead to discrimination in insurance or employment
49
Consent & Data Use
-biobank participants consented broadly -does that consent apply to AI usage
50
Benefit of Research
-if the biobank underrepresents marganlized, does it work equally well for everyone?