PPARγ activation by pioglitazone does not suppress cravings for alcohol, and is associated with a risk of myopathy in treatment seeking alcohol dependent patients: a randomized controlled proof of principle study

• Published in: Psychopharmacology Vol. 237; no. 8; pp. 2367 - 2380
• Main Authors: Schwandt, Melanie L., Diazgranados, Nancy, Umhau, John C., Kwako, Laura E., George, David T., Heilig, Markus
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.08.2020; Springer Nature B.V
• Subjects: Addictions; Adult; Alcohol; Alcoholism - drug therapy; Alcoholism - metabolism; Animals; Biomedical and Life Sciences; Biomedicine; Cerebrospinal fluid; Clinical trials; Craving - drug effects; Craving - physiology; Double-Blind Method; Drug addiction; Drug dependence; Female; Humans; Hypoglycemic Agents - adverse effects; Hypoglycemic Agents - therapeutic use; Imagination - drug effects; Imagination - physiology; Inflammation; Interleukin 6; Lipopolysaccharides; Lipopolysaccharides - adverse effects; Male; Middle Aged; Monocyte chemoattractant protein 1; Muscular Diseases - chemically induced; Muscular Diseases - diagnosis; Muscular Diseases - metabolism; Myopathy; Neurosciences; Original Investigation; Pharmacology/Toxicology; Pioglitazone; Pioglitazone - adverse effects; Pioglitazone - therapeutic use; PPAR gamma - metabolism; Proof of Concept Study; Psychiatry; Recurrence; Tumor necrosis factor-α; Withdrawal; Young Adult; Alcohol craving; Alcohol dependence; Proinflammatory cytokines; Pioglitazone
• ISSN: 0033-3158; 1432-2072; 1432-2072
• DOI: 10.1007/s00213-020-05540-w

Rationale Proinflammatory processes have been implicated in alcohol addiction, craving, and relapse, while studies in experimental animals have suggested that activation of peroxisome proliferator-activated receptor gamma (PPAR γ ) inhibits proinflammatory signaling. Accordingly, it is hypothesized that medications with PPAR γ activity may have therapeutic potential in alcohol dependence. Objectives We conducted a double-blind, placebo-controlled mechanistic proof of principle study in alcohol-dependent inpatients to investigate the effect of pioglitazone on alcohol craving. Methods Participants were treated for withdrawal, if needed, and then randomized to pioglitazone (target dose 45 mg/day) or placebo. Once at target dose, they completed two experimental manipulations: guided imagery, which used personalized auditory scripts to induce alcohol cravings, and a low-dose challenge with i.v. lipopolysaccharide (LPS; 0.8 ng/kg) or placebo, on two separate sessions, in counterbalanced order. Behavioral and endocrine responses as well as CSF levels of proinflammatory cytokines were evaluated. Results The study was prematurely terminated after randomization of 16 subjects, following an independent review that established a high risk of myopathy in the active treatment group. Analysis of those who completed the study indicated that pioglitazone was associated with elevated, rather than suppressed alcohol cravings in response to alcohol-associated stimuli. LPS did not induce cravings for alcohol and thus did not lend itself to evaluating pioglitazone effects; however, pioglitazone increased the neuroendocrine stress response to LPS. CSF levels of IL-6, TNF-α, or MCP-1 were unaffected by pioglitazone treatment. Conclusions Both safety and efficacy biomarker data suggest that pioglitazone lacks potential as a medication for the treatment of alcohol dependence. Clinical trial registration NCT01631630