Understanding how nicotine affects depression and brain function

* INCLUSION CRITERIA:

To be eligible for this study, an individual must meet all the following criteria assessed under the currently approved NIDA IRP screening protocol for the evaluation of potential research subjects (here referred to as the NIDA screening protocol). This is a protocol led by the Office of the Clinical Director (OCD) at the National Institute on Drug Abuse Intramural Research Program (NIDA IRP) to assess potential research participants eligibility for entering clinical protocols at the NIDA/IRP. Additional details can be found in the NIDA screening protocol documents. As routinely done at the NIDA IRP, the screening procedures and data collected under the NIDA

screening protocol will capture information above and beyond what is necessary to determine eligibility for this protocol but allows the Investigators to assess the eligibility criteria for this protocol.

In order to be eligible to participate in this study, an individual must meet all of the following criteria:

All Participants:

1. Able and willing to provide written informed consent.
2. Both sexes and all ethnic origins, age between 18 and 60 at the time of consent.
3. Absence of pregnancy and breastfeeding.
4. Have a Breath Alcohol Value of 0 on all study visit days involving scanning. Participant may be rescheduled if this value is greater than 0.

MDD Subjects:

1. Meet DSM-5 diagnostic criteria for current MDD at screening Clinical judgement will be used to interpret criteria.
2. Have a baseline (Hamilton Depression) HAM-D score indicative of current depression as evaluated by clinical staff.
3. Current stable serotonin modulating drug (e.g. SSRI/SNRI/serotonin modulator) treatment is allowed (no changes in the last 2 months). Specific medications will be evaluated by the MAI

Remitted MDD Subjects:

1. Meet DSM-5 diagnostic criteria for remitted MDD (full remission or partial remission or past depression) Clinical judgement will be used to interpret criteria.
2. HAM-D score indicating no clinically relevant depression as evaluated by clinical staff.
3. Current stable serotonin modulating drug (e.g. SSRI/SNRI/serotonin modulator) treatment is allowed (no changes in the last 2 months). Specific medications will be evaluated by the MAI.

Control Subjects (without MDD):

1. Control participants must not have current/lifetime MDD. Clinical judgement will be used to interpret criteria.
2. HAM-D score indicating no clinically-relevant depression as evaluated by clinical staff.

Daily Nicotine Users (Study Arm 2):

1. Uses nicotine daily for at least six months
2. Positive urine screen for cotinine

EXCLUSION CRITERIA (STUDY ARM 1):

An individual who meets any of the following criteria will be excluded from participation in this study:

1. Subjects with suicidal ideation where outpatient treatment is determined unsafe.
2. Lifetime history or current diagnosis of any of the following psychiatric illnesses: organic mental disorder, schizophrenia, schizoaffective disorder, delusional disorder, psychotic disorders not otherwise specified, bipolar disorder, patients with mood congruent or mood incongruent psychotic features. The MAI and/or PI/LI will reserve the right to exclude based psychiatric history not explicitly described in this criterion

   a. Within the control group, current use of antidepressants for psychiatric reasons will be exclusionary. The MAI reserves the right to evaluate use of antidepressants for non-psychiatric uses as appropriate for participation in the study.
3. Are cognitively impaired or have a learning disability severe enough to have required intervention throughout most or all of K-12 education. The MAI will reserve the right to evaluate if a participant s history of educational placement is likely to represent a learning disability that could significantly impact the data gathered in this study based on the severity and type of learning disability. Justification: Cognitive impairment and learning disabilities may be associated with altered brain functioning in regions recruited during laboratory task performance.
4. Heavy caffeine users (consume greater than 500 mg on a regular or daily basis. This is approximately five 8 fl oz cups of coffee). Participants will be asked to not deviate from their typical caffeine use on all scanning days.
5. May not have used any nicotine product weekly or more frequently than weekly in the past year; must never have been daily nicotine users for more than 1 month.
6. Must have an expired carbon monoxide level of less than or equal to 5 ppm and cotinine levels consistent with a non-smoker. Depending on the commercially available test used, a level equivalent to a non-smoker status will be used, ideally indicative of a urine cotinine level of around 10 ng/ml. However, given the known limitations of rapid tests to return specific quantifications of cotinine levels, if the present test is unable to quantify cotinine at this level, the lowest level of detection will be used as a cut off and MAI/PI discretion may be used to determine whether this cut off coupled with participant history and environmental factors indicates personal nicotine use versus secondhand smoke environment. If expired carbon monoxide level is greater than 5 ppm and cotinine levels consistent with a non-smoker, the MAI/PI will reserve the right to assess the participant's full clinical picture to determine the source of CO readings over 5 ppm. If the source is unlikely to be from personal nicotine use (e.g., negative cotinine test and participant states exposure to secondhand smoke environment, etc.), the CO test may be re-run until a lower reading is obtained, or the participant can be rescheduled.
7. History of moderate or severe substance use disorder in the past 6 months (other than caffeine)
8. Current pharmacological treatment for opioid use disorder (i.e., use of methadone)
9. Current use of illegal drugs other than marijuana as measured by urine drug screen Marijuana will not be allowed in the 24 hours prior to scanning based on self-report. Study day can be rescheduled to accommodate.
10. Participants may not use anticholinergic drugs (i.e., scopolamine), dopamine enhancing drugs (i.e. methylphenidate), or other medications that may impact MRI measures (i.e. benzodiazepines) prior to any scanning visit within a timeframe that is likely to directly

    impact the study questions. MAI discretion regarding timeframe of allowed use will be based on half-life, pharmacology of the drug in question, and pattern of use by the participant. Scanning visit timing can be adjusted to accommodate.
11. May not use drugs that directly enhance dopamine (i.e., methylphenidate) in the week prior to any scanning visit. Scanning visit timing can be adjusted to accommodate.
12. Any past or present significant cardiovascular, cerebrovascular, or respiratory conditions, including arrhythmias, acute coronary syndrome, ischemic heart disease, or, uncontrolled hypertension. The MAI may use their clinical judgement to interpret this criterion.
13. Body mass index (BMI) lower than 18.5 kg/m\^2
14. Contraindications to MRI as determined by MRI Safety Screening form and mock scanner trial (when available).
15. Abnormal structural MRI or significant head trauma. The MAI may use their clinical judgement to interpret this criterion.
16. Current neurological illness including but not limited to frequent migraines, multiple sclerosis, movement disorder. The MAI may use their clinical judgement to interpret this criterion.
17. Lifetime history of significant seizure disorder
18. Any other serious or unstable medical illness as defined by self-report, the evaluation of vital signs or other observation that in the view of the investigators would compromise the safety of an individual during participation

    All data collected will be evaluated by members of the study team to decide if there is an existing medical illness that would compromise participation in this research
19. Subjects that cannot speak English. Justification: To include non-English speakers, we would have to translate the consent and other study documents and hire and train bilingual staff, which would require resources that we do not have and could not justify, given the

small sample size for each experiment. Additionally, the data integrity of some of the cognitive tasks and standardized questionnaires used in this study would be compromised as they have only been validated in English. Most importantly, ongoing communication regarding safety procedures is necessary when participants are undergoing MRI procedures. The inability to effectively communicate MRI safety procedures in a language other than English could compromise the safety of non-English speaking participants

Exclusion Criteria (Study Arm 2)

1. Subjects with active suicidal ideation where outpatient treatment is determined unsafe.
2. Current psychiatric symptoms in which the ability to adhere to study protocol is determined to be impaired by clinical staff/MAI (e.g., difficulty understanding or answering questions, difficulty remaining still in the fMRI scanner)
3. Are cognitively impaired or have a learning disability severe enough to have required intervention throughout most or all of K-12 education. The MAI will reserve the right to evaluate if a participant s history of educational placement is likely to represent a learning disability that could significantly impact the data gathered in this study based on the severity and type of learning disability.

   Justification: Cognitive impairment and learning disabilities may be associated with altered brain functioning in regions recruited

   during laboratory task performance.
4. Heavy caffeine users (consume greater than 500 mg on a regular or daily basis. This is approximately five 8 fl oz cups of coffee). Participants will be asked to not deviate from their typical caffeine use on all scanning days.
5. Active severe substance use disorder in the past 6 months (other than caffeine and nicotine)
6. Contraindications to MRI as determined by MRI Safety Screening form and mock scanner trial (when available).
7. Abnormal structural MRI, significant head trauma, current neurological illness likely to impact fMRI signal or ability to comply with study requirements (e.g., staying still in scanner). The MAI may use their clinical judgement to evaluate this criterion.
8. Any serious or unstable medical illness as defined by self-report, the evaluation of vital signs or other observation that in the view of the investigators, would compromise the safety of an individual during participation. All data collected will be evaluated by members of the study team to decide if there is an existing medical illness that would compromise participation in this research
9. Subjects that cannot speak English. Justification: To include non-English speakers, we would have to translate the consent and other study documents and hire and train bilingual staff, which would require resources that we do not have and could not justify, given the small sample size for each experiment. Additionally, the data integrity of some of the cognitive tasks and standardized questionnaires used in this study would be compromised as they have only been validated in English. Most importantly, ongoing communication regarding safety procedures is necessary when participants are undergoing MRI procedures. The inability to effectively communicate MRI safety procedures in a language other than English could compromise the safety of non-English speaking participants