Table 2 Summary of all results from subgroup analyses and meta-regression models analyzing the effects of psychoplastogens on peripheral BDNF.

From: Effects of psychoplastogens on blood levels of brain-derived neurotrophic factor (BDNF) in humans: a systematic review and meta-analysis

Subgroup analyses

 

Overall

Healthy

Depression

Plasma

Serum

All psychoplastogens

0.02 [–0.08 to 0.13]

–0.01 [–0.17 to 0.14]

0.10 [–0.06 to 0.26]

0.05 [–0.09 to 0.19]

–0.04 [–0.21 to 0.13]

Ketamine

0.03 [–0.11 to 0.17]

–0.08 [–0.25 to 0.08]

0.10 [–0.07 to 0.27]

0.09 [–0.17 to 0.34]

–0.05 [–0.26 to 0.17]

Classic psychedelics

0.05 [–0.16 to 0.26]

0.04 [–0.20 to 0.28]

0.09 [–4.15 to 4.33]

Meta-regressions

 

Dose

Timing (h)

Age

Missing values

mBDNF

Multiple infusions

All psychoplastogens

0.0005* [0–0.001]

–0.0008 [–0.01 to 0.01]

0.77* [0.13–1.42]

0.007 [–0.26 to 0.27]

Ketamine

0.0007* [0.0002–0.001]

–0.003 [–0.02 to 0.01]

0.76 [–0.18 to 1.70]

0.10 [–0.14 to 0.34]

0.26 [–0.05 to 0.56]

Classic psychedelics

0.01 [–0.01 to 0.03]

0.005 [–0.08 to 0.09]

0.68 [–2.01 to 3.37]

–0.32 [–1.43 to 0.79]

LSD

0.002 [–0.01 to 0.01]

0.02 [–0.04 to 0.09]

–0.03 [–0.09 to 0.03]

0.59 [–1.26 to 2.44]

Psilocybin

0.006 [–0.37 to 0.38]

–0.06 [–0.33 to 0.22]

0.09 [–0.32 to 0.51]

7.06 [–3.43 to 17.56]

 

Design

Control group

Risk of bias

Crossover RCT

Parallel RCT

Placebo

Baseline + placebo

Some concerns

High

All psychoplastogens

–0.18 [–0.44 to 0.08]

–0.13 [–0.38 to 0.11]

–0.006 [–0.27 to 0.25]

-0.31* [–0.55 to –0.06]

–0.005 [–0.23 to 0.22]

0.26* [0.05–0.46]

Ketamine

–0.46 [–1.12 to 0.20]

–0.26* [–0.48 to –0.04]

–0.19 [–1.53 to 1.15]

0.04 [–0.22 to 0.31]

0.32* [0.02–0.62]

Classic psychedelics

–0.32 [–1.43 to 0.79]

0.005 [–1.07 to 1.08]

–0.40 [–1.19 to 0.39]

0.35 [–0.04 to 0.74]

LSD

0.13 [–0.45 to 0.71]

–0.32 [–0.91 to 0.28]

0.34 [–0.02–0.71]

  1. Missing fields indicate insufficient data available for analysis. Data are shown as standardized mean difference with 95% confidence intervals. In the moderator analyses, contrasts were as follows: mBDNF vs. total BDNF, multiple vs. single infusions, crossover or parallel RCT vs. non-randomized open-label trials, placebo control groups vs. baseline only control, and some concerns or high risk of bias vs. low risk of bias. *p < 0.05.