Matching Genotypes and Serotonergic Medications for Alcoholism

Completed · Phase 1 · Has a placebo group

Conditions studied: Alcoholism

In brief

Sertraline, a serotonin-specific reuptake inhibitor (SSRI) that increases basal serotonin levels, was shown to reduce alcohol consumption in lower risk/severity and later onset (LOA) but not higher risk/severity earlier onset alcoholic individuals (EOA). By contrast, ondansetron, a 5-HT3 receptor reduced alcohol consumption in EOAs but not LOAs. To explain this contrast in clinical efficacy, one approach suggests that differential serotonergic response is based on a functional polymorphism of the 5-HTTLPR promoter region of the serotonin re-uptake transporter (SERT). These alleles have typically been classified as biallelic genotypes: LL, SS and SL. The LL variant is postulated to be associated with EOA and the SS/SL variants associated with LOA. To test this hypothesis the investigators therefore propose to match and mismatch serotonergic treatments to genetic polymorphic variants \[in 132 non-treatment seeking alcohol dependent volunteers\] in a double-blind placebo controlled 2 x 2 design human laboratory study. The investigators propose to randomize non-treatment-seeking alcohol dependent persons based on their 5'-HTTLPR variant genotype (LL or SS/SL) into one of two counterbalanced arms: participants in the first arm (LL) will first receive one drug (either 200mg/day of sertraline or ondansetron 0.5mg/day) for three weeks followed by an alcohol self-administration experiment (ASAE), \[with a 1 week down-titration period if sertraline received first, during the first week of the "placebo period"\] then receive placebo for two more weeks (this will be a single-blind portion to use as a comparison group and to wash out the pharmacodynamic effects of the first drug) followed by a second ASAE. Participants will then receive the second drug for three weeks followed by a third ASAE \[all will receive medication for an additional 1 week period and those receiving sertraline last will be down-titrated\]. Participants in the second arm (SS/SL) will receive the same medications in the same balanced design. Individuals in both arms will receive weekly medication management to enhance medication adherence. The long-term objective of this research is to prospectively examine serotonergic treatment matching for alcohol dependence based on genotyping. Of equal importance, the investigators also recognize the strong contribution of additional genetic and environmental influences on alcohol consumption.

Key facts

Study ID: NCT01113164
Run by: Brown University
People needed: 79
Starts: 2008-09-01
Expected to finish: 2012-02-01
Last updated by the study team: 2012-02-22

Who can join

Age: 21 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

Must be between 21 and 65 years old (inclusive).
Participants may be male or female and must be in good health as confirmed by medical history, baseline physical examination, ECG, laboratory tests, urinalysis and vital signs.
Female participants must be:
Postmenopausal for at least one year, surgically sterile, or Practicing an effective method of birth control before entry and throughout the study; have a negative urine pregnancy test at baseline screening and prior to the alcohol challenge sessions.
Participants must understand that this is not a treatment study.
A diagnosis of Alcohol dependence using Module E of the structured clinical interview for the DSM-IV (SCID). Alcohol dependent as defined by an AUDIT score ≥ 12 and men must consume ≥ 35 and women ≥ 28 standardized alcoholic beverages a week.
Participants must be willing to take oral medication, adhere to the medication regimen and be willing to return for weekly visits and the alcohol challenge sessions.
Participants must be able to read and comprehend written instructions and comprehend and complete all scale and inventories required by the protocol.
Participants must have signed an informed consent indicating they understand the purpose of and procedures required for the study and willingness to participate.

You may not qualify if…

Pregnancy or breast feeding women.
Positive urine drug screen at baseline for any illegal substance other than marijuana.
Participants will be excluded if they have: (a) clinically significant medical abnormalities (i.e. ECG, hematological assessment, bilirubin > 150% of the upper limit of normal or ALT or AST elevations >300% the upper limit of normal, biochemistry including urinalysis, electrolytes,). (Persons with medical conditions that are adequately controlled by their primary care physician will not be excluded.)
Current use of psychotropic medications that cannot be discontinued
Medical contraindications for use of sertraline or ondansetron
Taking drugs that interfere with the metabolism of either drug that cannot be stopped per study physician.
Allergic to sertraline or ondansetron
Must have a breath alcohol concentration (BrAC) = 0.000 at the beginning of the alcohol challenge sessions.
Creatinine clearance ≤ 60 dl/min.
Individuals with a reasonable expectation of being institutionalized during the course of the trial or pending legal charges.
Participants who have significant alcohol withdrawal symptoms (clinical institute withdrawal assessment for alcohol revised (CIWA-Ar) >10.
lifetime depression or a history of suicide
history of seizures (e.g. epilepsy) or migraine headaches -

Where it is running

Center for Alcohol and Addiction Studies — Providence, Rhode Island, United States

Full record on ClinicalTrials.gov

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