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The Pathophysiology and Clinical Course of Nicotine Addiction

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The Pathophysiology and Clinical Course of Nicotine Addiction. Joseph R DiFranza MD University of Massachusetts Medical School. Nicotine Addiction- Case histories. We asked smokers what does it feel like to need a cigarette?. Wanting. “Wanting” is the first symptom of nicotine withdrawal. - PowerPoint PPT Presentation
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The Pathophysiology and Clinical Course of Nicotine Addiction Joseph R DiFranza MD University of Massachusetts Medical School
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Page 1: The Pathophysiology and Clinical Course of Nicotine Addiction

The Pathophysiology and Clinical Course of Nicotine Addiction

Joseph R DiFranza MD

University of Massachusetts Medical School

Page 2: The Pathophysiology and Clinical Course of Nicotine Addiction

Nicotine Addiction- Case histories

We asked smokers what does it feel like to need a cigarette?

Page 3: The Pathophysiology and Clinical Course of Nicotine Addiction

Wanting

“Wanting” is the first symptom of nicotine withdrawal.

Wanting is a mild transient desire to smoke that is easily ignored.

Page 4: The Pathophysiology and Clinical Course of Nicotine Addiction

Craving

Craving is more intense than wanting and intrudes upon the person’s thoughts.

It is more persistent and difficult to ignore. “I feel like someone inside of me is really

telling me to smoke.”

Page 5: The Pathophysiology and Clinical Course of Nicotine Addiction

Craving

Craving a cigarette “just, like, pops in your head, like someone is sending you a message.”

Craving is like “being hungry, but instead of your stomach saying it, it’s your brain…it’s just hungry, except for a cigarette.”

Page 6: The Pathophysiology and Clinical Course of Nicotine Addiction

Needing Needing is an intense and urgent desire to

smoke that is impossible to ignore. The individual must smoke to restore a normal mental or physical state.

“You really want one. You know you need it. You know you’ll feel normal after smoking, and you have to smoke to feel normal again.”

“Pretty urgent… you need it and you can’t get your mind off it.”

Page 7: The Pathophysiology and Clinical Course of Nicotine Addiction

Withdrawal recurs after each cigarette Wanting then Craving then Needing

Page 8: The Pathophysiology and Clinical Course of Nicotine Addiction

Addiction develops in the same sequence in all smokers No withdrawal symptoms Wanting Wanting and Craving Wanting, Craving and Needing

Page 9: The Pathophysiology and Clinical Course of Nicotine Addiction

Clinical Staging of Nicotine Addiction Stage 1. Can remain abstinent indefinitely without

withdrawal symptoms Stage 2. Wanting “If I go too long without smoking, the

first thing I will notice is a mild desire to smoke that I can ignore.”

Stage 3. Craving “If I go too long without smoking, the desire for a cigarette becomes so strong that it is hard to ignore and it interrupts my thinking.”

Stage 4. Needing “If I go too long without smoking, I just can’t function right, and I know I will have to smoke just to feel normal again.”

Page 10: The Pathophysiology and Clinical Course of Nicotine Addiction

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Mean Adult FTND Scores by Stage

Page 11: The Pathophysiology and Clinical Course of Nicotine Addiction

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Mean Adolescent HONC Scores by Stage

Page 12: The Pathophysiology and Clinical Course of Nicotine Addiction

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Mean Adult HONC Scores by Stage

Page 13: The Pathophysiology and Clinical Course of Nicotine Addiction

The Latency to Withdrawal

“A little light bulb goes off and it’s like, alright, time [to smoke].”

The latency is the interval between smoking one cigarette and wanting, craving, or needing another.

Latency-to-wanting Latency-to-craving Latency-to-needing

Page 14: The Pathophysiology and Clinical Course of Nicotine Addiction

The Latency to Withdrawal

At the onset of addiction the latency-to-wanting may be longer than a month.

Repeated tobacco use causes the latencies to shrink.

The shortening of the latency drives the escalation in smoking.

Page 15: The Pathophysiology and Clinical Course of Nicotine Addiction

The Latency to Withdrawal

After smoking for 6 weeks, a 16-year-old girl noticed a latency-to-craving of 2 days

which shortened to 4 hours by age 161/2, …to 2 hours by age 17, …to 1.5 hours by age 18, …to 1 hour by age 19, …and to 30-45 minutes by age 21.

Page 16: The Pathophysiology and Clinical Course of Nicotine Addiction

The Latency to Withdrawal-Factors of 2

1) 1 week (1 cig/wk)

2) 3.5 days (2 cig/wk)

3) 42 hours

4) 21 hours

5) 11.5 hours

6) 5.6 hours

7) 2.8 hours

8) 1.4 hours

9) 42 minutes (1 ppd)

10) 21 minutes (2 ppd)

In adolescents, smoking 2 cigs/wk increases the risk for heavy adult smoking 174 fold.

Page 17: The Pathophysiology and Clinical Course of Nicotine Addiction

Smokers have Latencies of days or weeks With a half life of 2 hours, how can nicotine

have such a prolonged impact?

Page 18: The Pathophysiology and Clinical Course of Nicotine Addiction

The neuroscience shows…

One dose of nicotine increases noradrenaline synthesis in the hippocampus for at least a month.

One dose lowers neural activation thresholds for a month.

One dose affects tyrosine hydroxylase activity for a month.

One dose in adolescent rats affects behavior during adulthood.

Page 19: The Pathophysiology and Clinical Course of Nicotine Addiction

The neuroscience shows…

Nicotine changes the transcription of hundreds of genes in the brain.

Nicotine triggers a series of events that cannot be stopped by removing it.

Page 20: The Pathophysiology and Clinical Course of Nicotine Addiction

What could change in the brain that would cause addiction after one dose?

Page 21: The Pathophysiology and Clinical Course of Nicotine Addiction

HomeostasisThe brain seeks balance.

Page 22: The Pathophysiology and Clinical Course of Nicotine Addiction

HomeostasisNicotine disturbs the balance.

Page 23: The Pathophysiology and Clinical Course of Nicotine Addiction

HomeostasisThe brain compensates to regain balance.

Page 24: The Pathophysiology and Clinical Course of Nicotine Addiction

HomeostasisWithout nicotine the brain is disturbed.

Page 25: The Pathophysiology and Clinical Course of Nicotine Addiction

Insular cortex activity during withdrawal – “A little light bulb goes off, time to smoke.”

Nonsmokers Smokers

Page 26: The Pathophysiology and Clinical Course of Nicotine Addiction

HomeostasisNicotine is needed to restore balance.

Page 27: The Pathophysiology and Clinical Course of Nicotine Addiction

HomeostasisCraving occurs whenever the effect of nicotine wears off.

Page 28: The Pathophysiology and Clinical Course of Nicotine Addiction

HomeostasisNow you have to smoke just to feel normal.

Page 29: The Pathophysiology and Clinical Course of Nicotine Addiction

Homeostasis

The Latency to Withdrawal determines how long it is before the effect of each dose of nicotine wears off.

Page 30: The Pathophysiology and Clinical Course of Nicotine Addiction

The Latency to Withdrawal

Page 31: The Pathophysiology and Clinical Course of Nicotine Addiction

The Latency to Withdrawal

Page 32: The Pathophysiology and Clinical Course of Nicotine Addiction

The Latency to Withdrawal

Page 33: The Pathophysiology and Clinical Course of Nicotine Addiction

Do the Stages of Nicotine Addiction coincide with actual physical changes in the brain?

Page 34: The Pathophysiology and Clinical Course of Nicotine Addiction

Fractional Anisotropy is an MRI measure of structural complexity.Low FA High FA

Page 35: The Pathophysiology and Clinical Course of Nicotine Addiction

Our data show smokers have higher FA than nonsmokers in the dorsal anterior cingulate bundle (p=0.05).

Page 36: The Pathophysiology and Clinical Course of Nicotine Addiction

Smoking during adolescence increases FA.

Smokers generally have higher FA than nonsmokers.

Yet FA decreases as addiction increases.

FA correlates inversely with the FTND score: r = -.52, r = -.58, and r = -.64.

Page 37: The Pathophysiology and Clinical Course of Nicotine Addiction
Page 38: The Pathophysiology and Clinical Course of Nicotine Addiction
Page 39: The Pathophysiology and Clinical Course of Nicotine Addiction

FA decreases with advancing Stage of Addiction: r= -.85

FA decreases with advancing addiction as measured by the Hooked on Nicotine Checklist :

r = -.96

Page 40: The Pathophysiology and Clinical Course of Nicotine Addiction

The dorsal anterior cingulate gyrus- the location of maximal correlation between FA and Stage of Addiction (top), and FA and FTND (bottom)

Page 41: The Pathophysiology and Clinical Course of Nicotine Addiction

The dorsal anterior cingulate gyrus- The location of maximum correlation between FA and HONC

Page 42: The Pathophysiology and Clinical Course of Nicotine Addiction

Interpretation

Increasing FA in new smokers represents the adaptations that cause wanting, craving and needing.

Decreasing FA in adult smokers represents the adaptations that cause the Latency to Withdrawal to grow shorter.

Page 43: The Pathophysiology and Clinical Course of Nicotine Addiction

Smokers have more structural connection between the dorsal anterior cingulate and the prefrontal cortex than nonsmokers.

Page 44: The Pathophysiology and Clinical Course of Nicotine Addiction

Structural connectivity increases between the dorsal anterior cingulate and prefrontal cortex with advancing Stage of Addiction.

Page 45: The Pathophysiology and Clinical Course of Nicotine Addiction

During withdrawal the anterior cingulate shows greater functional connectivity with… Superior medial

frontal cortex Inferior parietal Precuneus Middle Cingulate Middle temporal

Page 46: The Pathophysiology and Clinical Course of Nicotine Addiction

Correlations between Functional Connectivity and Withdrawal

Craving

Correlated CircuitryPeak

Correlation Coefficient

ACC - Superior Frontal

0.74

ACC - R Precuneus 0.76

ACC - L Precuneus 0.75

ACC - L Putamen 0.77

ACC - Inf. Parietal 0.77

Page 47: The Pathophysiology and Clinical Course of Nicotine Addiction

Summary

Advancing stages of addiction are associated with decreased organizational complexity in the anterior cingulate white matter and increased structural connectivity between it and the frontal cortex.

These structural changes appear to be involved with craving as withdrawal craving correlates well with activity in this circuit.

Page 48: The Pathophysiology and Clinical Course of Nicotine Addiction

How quickly does addiction develop?

Page 49: The Pathophysiology and Clinical Course of Nicotine Addiction

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Endorsement of HONC symptoms of addiction by 10th Year NZ Youth

Page 50: The Pathophysiology and Clinical Course of Nicotine Addiction

The clinical data indicate that… One cigarette must rapidly change the brain.

Page 51: The Pathophysiology and Clinical Course of Nicotine Addiction

The neuroscience shows…

The nicotine from one cigarette occupies 88% of the brain’s nicotinic receptors.

One dose stimulates an increase in the number of brain nicotine receptors over night.

One dose initiates drug sensitization.

Page 52: The Pathophysiology and Clinical Course of Nicotine Addiction

Nicotine-Induced Behavioral Sensitization

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1 2 3 4 5 6Day

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Average of Nicotine animals (n=4)

Average of Control animals (n=4)

Page 53: The Pathophysiology and Clinical Course of Nicotine Addiction

5%

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Page 54: The Pathophysiology and Clinical Course of Nicotine Addiction

Conclusion

Nicotine hard-wires addiction into the brain. This process begins with the first cigarette. Addiction develops through 4 stages. The shortening of the latency to withdrawal

drives the progression to daily smoking.

Page 55: The Pathophysiology and Clinical Course of Nicotine Addiction

Is addiction reversible?

If the brain erases all trace of the addiction, after a long abstinence, people should again have the very long latencies of novice smokers.

Page 56: The Pathophysiology and Clinical Course of Nicotine Addiction

How much do people need to smoke after a relapse? The latency doubles in

length over three months. After that it barely

changes.

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Page 57: The Pathophysiology and Clinical Course of Nicotine Addiction

The neuroscience shows…

New adaptations develop in the brains of rats weeks after nicotine is stopped.

In humans, smoking cessation triggers an increase in nerve growth factor.

Page 58: The Pathophysiology and Clinical Course of Nicotine Addiction

Recommended reading

A sensitization-homeostasis model of nicotine craving, withdrawal, and tolerance: Integrating the clinical and basic science literature. DiFranza and Wellman. Nicotine & Tobacco Research. 2005; vol 7: 9-26.

The natural history and diagnosis of nicotine addiction. DiFranza et al. Current Pediatric Reviews, 2011; vol 7: 88-96.


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