| Purpose: |
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In the current study, the investigators propose to test: (1) whether brain activation and
connectivity in a resting state, assessed by ASL perfusion MRI, BOLD fMRI, and diffusion
tensor imaging (DTI) predicts smoking relapse, and (2) whether brain activation, assessed by
BOLD fMRI during performance of neurobehavioral probes for executive cognitive function,
stress and cue reactivity, predicts smoking relapse.
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| Study Summary: |
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Our previous work demonstrated that, among non-treatment seeking smokers, regional cerebral
blood flow (rCBF) is increased following 14 hours of overnight abstinence, as compared to
smoking as usual. Specifically, increased rCBF was observed in the anterior cingulate,
medial and left orbitofrontal cortex. Two smoking urges items ("cravings for a cigarette"
and "urges to smoke at this time") that predict relapse were strongly correlated with CBF
increases in several regions that comprise the brain's reward and visual circuitry (Wang et
al., 2007). In addition, two other studies by our group using BOLD fMRI showed that smokers
with genotypes associated with smoking relapse exhibit a reduction in BOLD signal in the
bilateral dorsolateral PFC and MF/CG during nicotine withdrawal as well as impairments in
working memory at high levels of task difficulty (Loughead et al., 2009). In a follow-up
experiment, it was found that the smoking cessation medication varenicline reverses this
deficit (Loughead et al., in press). In the current study, we propose to extend these
findings in a smoking cessation treatment population by testing: (1) whether brain
activation and connectivity in a resting state, assessed by ASL perfusion MRI, BOLD fMRI,
and diffusion tensor imaging (DTI) predicts smoking relapse, and (2) whether brain
activation, assessed by BOLD fMRI during performance of neurobehavioral probes for executive
cognitive function, stress and cue reactivity, predicts smoking relapse. Following
eligibility screening (week 0), 100 treatment-seeking smokers will complete two 1.5 hour
pre-quit neuroimaging assessments (one following 24 hours of overnight abstinence and the
other after smoking-as-usual (weeks 1 and weeks 2-3; order counterbalanced). All will
receive standardized behavioral smoking cessation counseling (week 4) to prepare for a
scheduled quit attempt (week 5). They will make brief visits to the Center (weeks 5, 6, 7, 8
& 9) to receive booster counseling and assess smoking status. The primary endpoints for
assessing quitting success are: 8 weeks post-target quit date (week 13) and 24-weeks post
target quit date (week 29). At the 8-week post-target quit date all participants will be
contacted for a telephone survey and those who self-report not smoking for the past 7 days
will be asked to come to the Center for biochemical confirmation. Lastly, a subset of
participants (15 smokers who report having been abstinent for at least the past 7 days and
15 smokers who relapsed within the first few weeks of the TQD) will be asked to complete a
third MRI scan to examine changes in brain activity related to cessation. Only those
participants reporting being quit at this time point will be contacted again at 24 weeks.
Identification of the neural substrates of relapse following a quit attempt could inform the
development of novel medications. Further, the identification of a "brain signature" that
predicts relapse may allow for the use of fMRI to screen novel medications and identify
those that reverse the liability profile.
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| Criteria: |
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Inclusion Criteria:
1. Treatment-seeking smokers between the ages of 18 and 65, reporting consumption of at
least 10 cigarettes per day for at least the past 6 months.
2. Capable of giving written informed consent, which includes compliance with the
requirements and restrictions listed in the combined consent and HIPAA form, and are
fluent, English-speaking.
3. Provide a baseline CO reading greater than 10 parts per million (ppm) at eligibility
screening.
4. Women of childbearing potential must consent to use a medically accepted method of
birth control (e.g., condoms and spermicide, oral contraceptive, Depo-Provera
injection, contraceptive patch, tubal ligation or abstinence from sex) for the
duration of the study.
Exclusion Criteria:
Smoking Behavior
1. Use of chewing tobacco, snuff, or snus.
2. Current enrollment or plans to enroll in another research or smoking cessation
program in at least the next 7 months.
3. Anticipated use (within next 7 months) of other nicotine substitutes or smoking
cessation treatments/ medications.
4. Provide a baseline CO reading less than or equal to 10ppm.
Alcohol/Drug Exclusion Criteria:
1. Lifetime history of substance abuse and/or currently receiving treatment for
substance abuse (e.g., alcohol, opioids, cocaine, marijuana or stimulants).
2. Current alcohol consumption that exceeds greater than 25 standard drinks/week for men
and greater than 20 standard drinks/week for women over the last 6 months.
3. Breath alcohol reading (BrAC) greater than or equal to 0.01 at the Eligibility
Screening or any fMRI scanning session.
4. A positive urine drug screen (cocaine, opiates, benzodiazepines, tri-cyclic
antidepressants, amphetamines, methamphetamines, barbiturates, methadone, and
phencyclidine) at the Eligibility Screening or any fMRI scanning session.
Medication Exclusion Criteria:
Current use or recent discontinuation (within last 2-weeks) of the following psychotropic
medications:
1. Antipsychotics (typical and atypical),
2. Mood-stabilizers,
3. Anti-depressants (tricyclics, SSRI's, selective and nonselective MAOIs,
Wellbutrin/Zyban),
4. Anti-panic agents,
5. Anti-obsessive agents,
6. Anti-anxiety agents,
7. Prescription (e.g., Provigil, Ritalin) or over-the-counter stimulants,
8. Diet Pills/Anorectics,
9. Systemic Steroids,
10. Varenicline,
11. Daily use of prescription medications for chronic pain.
Medical Exclusion Criteria:
1. Women who are pregnant, breast-feeding or planning a pregnancy for the duration of
the study.
2. History or current diagnosis of psychosis, bipolar disorder, schizophrenia, or any
Axis 1 disorder as identified by the MINI (Mini International Neuropsychiatric
Interview) or self reported; for major depression, only a current diagnosis will be
considered ineligible.
3. History or current diagnosis of Attention-Deficit Hyperactivity Disorder (ADHD).
4. History of epilepsy or a seizure disorder.
5. Low or borderline intellectual functioning - determined by receiving a score of less
than 90 on the Shipley Institute of Living Scale (SILS) which correlates with the
Wechsler Adult Intelligence Scale-Revised (WAIS-R) Estimated IQ Test (administered at
the eligibility screening visit).
fMRI-Related Exclusion Criteria:
1. Participation in study #810493 or #809858 within the last 6 months.
2. History of claustrophobia.
3. Being left-handed.
4. Color blindness.
5. Lifetime history of stroke.
6. Any impairment preventing participants from using the response pad necessary for the
cognitive testing.
7. Having a cochlear implant or wearing bilateral hearing aids.
8. Self-reported history of head trauma, brain or spinal tumor.
9. Self-reported use of pacemakers, certain metallic implants, or presence of metal in
the eye.
10. Circumstances or conditions that may interfere with magnetic resonance imaging (MRI).
11. Self-reported history of gunshot wounds.
12. Weight greater than 250lbs at any session.
General Exclusion:
1. Participation (within the last 6 months) in other studies at our center involving
cognitive testing (N-back, CPT or Go-No-Go Task).
2. Any medical condition or medication that could compromise participant safety or
interfere with imaging, as determined by the Principal Investigator and/or Study
Physician.
3. Inability to provide informed consent or complete any of the study tasks as
determined by the Principal Investigator and/or Study Physician.
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