Evidence of increased risk of five psychiatric disorders due to antidepressants

Lu Hou1, Zhiqiang Du2, Rongrong Lu2

  • 1Department of Psychiatry, Huai'an Third People's Hospital, Huai'an, 223021, Jiangsu, China.

Abstract

Insights

Antidepressants (ATDs) may causally increase the risk of psychiatric disorders, including convulsion, schizophrenia, OCD, substance abuse, and suicide or self-harm. Further research is needed to balance ATD benefits against these potential risks.

Area of Science:

  • Psychiatric genetics
  • Pharmacogenomics
  • Epidemiology

Background:

  • Antidepressant (ATD) use is associated with psychiatric disorders.
  • Causal links between ATDs and psychiatric conditions remain unclear.
  • Genetic studies offer insights into potential causality.

Purpose of the Study:

  • To investigate the causal relationship between ATDs and five psychiatric disorders.
  • Utilizing the Two-sample Mendelian Randomization (TSMR) method.
  • Assessing causality for convulsion (CONV), schizophrenia (SCZ), obsessive-compulsive disorder (OCD), substance abuse (SA), and suicide or self-harm (SOSH).

Main Methods:

  • Two-sample Mendelian Randomization (TSMR) analysis.
  • Inverse Variance Weighted (IVW) method for primary causality assessment.
  • Weighted median, Weighted mode, and MR Egger methods for validation.
  • Sensitivity analyses including MR-Egger intercept, Cochran's Q, and leave-one-out tests to detect heterogeneity and pleiotropy.

Main Results:

  • Significant positive causal relationships were found between genetically predicted ATDs and CONV, SCZ, OCD, SA, and SOSH.
  • Specific odds ratios (OR) and confidence intervals (CI) highlight the strength of these associations.
  • Sensitivity analyses confirmed the robustness and reliability of the findings.

Conclusions:

  • Antidepressants (ATDs) are identified as potential risk factors for CONV, SCZ, OCD, SA, and SOSH.
  • Clinical practice requires a comprehensive evaluation of ATD therapeutic effects versus potential risks.
  • Individualized treatment plans and increased clinical vigilance are recommended for patients using ATDs.

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