4.1 Article

Plasma pro- and anti-inflammatory cytokines may relate to cocaine use, cognitive functioning, and depressive symptoms in cocaine use disorder

Journal

AMERICAN JOURNAL OF DRUG AND ALCOHOL ABUSE
Volume 47, Issue 1, Pages 52-64

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/00952990.2020.1828439

Keywords

Cocaine use disorder; cognition; cytokine; depression; elastic net; inflammation

Funding

  1. National Institute on Drug Abuse [P50DA009262, R01DA030878, K08DA040006]
  2. University of Texas Health Sciences Center at Houston under McGovern Research Scholars Endowment
  3. la Caixa Foundation [100010434, LCF/BQ/DI19/11730047]
  4. University of Texas Health Sciences Center at Houston under Louis A. Faillace, M.D. Endowment

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The study found that certain cytokines are associated with cocaine use, cognition, and depression, but contrary to the hypothesis, higher pro-inflammatory cytokines were related to better functioning. Cytokines were selected at low frequencies and had weak relationships with outcomes.
Background Inflammation is implicated in cocaine use and associated problems, including depression and cognitive impairment. Objective We assessed 18 cytokines, cocaine use, cognition, and depression in individuals with Cocaine Use Disorder. Our general hypothesis was that higher pro-inflammatory cytokines would relate to more cocaine use, poorer cognition, and more depression, while higher anti-inflammatory cytokines would relate to less cocaine use, better cognition, and less depression. Methods Data were collected from 85 individuals (76.5% male, 80% African American) aged 18-65. The ASI, Shipley-2, and BDI-II assessed frequency and duration of cocaine use, cognition, and depression. Cytokines were tested using Bio-Plex Pro (TM) assays. Elastic net regression identified which cytokines related to each measure, controlling for confounds. Results Lower IL-29 (B = -0.08, bootstrapped 95%CI = [-0.24,0.07]), scD163 (B = -0.11, bootstrapped 95%CI = [-0.27,0.04]), Eotaxin-1 CCL11 (B = -0.11, bootstrapped 95%CI = [-0.30,0.08]), and higher APRIL/TNFSF13 (B = 0.11, bootstrapped 95%CI = [-0.08,0.30]) related to more frequent cocaine use. Lower IL-29 (B = -0.24, bootstrapped 95% CI = [-2.26,1.79]) and IL-20 (B = -1.62, bootstrapped 95%CI = [-3.53,0.29]) related to longer duration of cocaine use. Higher Eotaxin-2 CCL24 (B = 2.79, bootstrapped 95%CI = [-0.59,6.17]) and TWEAK (B = 2.83, bootstrapped 95%CI = [-0.80,6.45]) related to better cognition. Finally, higher IL-20 (B = -1.83, bootstrapped 95%CI = [-3.70,0.04]) and Osteocalcin (B = -1.56, bootstrapped 95%CI = [-3.81,0.70]) related to lower depressive symptoms. However, none of these relationships survived bootstrapped analyses. Conclusion Pro- and anti-inflammatory cytokines may relate to cocaine use, cognition, and depression, but inconsistent with our hypotheses, higher pro-inflammatory cytokines related to better functioning in several domains. Additionally, cytokines were selected at low frequencies and demonstrated weak relationships with outcomes. These preliminary findings suggest complex relationships between inflammation and cocaine use.

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