4.7 Article

Risk of depression, suicide and psychosis with hydroxychloroquine treatment for rheumatoid arthritis: a multinational network cohort study

Journal

RHEUMATOLOGY
Volume 60, Issue 7, Pages 3222-3234

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/rheumatology/keaa771

Keywords

HCQ; safety; epidemiology; RA; psychosis; depression

Categories

Funding

  1. National Institute for Health Research (NIHR) Oxford Biomedical Research Centre (BRC)
  2. US National Institutes of Health
  3. US Department of Veterans Affairs
  4. Janssen Research Development
  5. Korea Health Industry Development Institute (KHIDI) - Ministry of Health & Welfare, Republic of Korea [HI16C0992]
  6. Versus Arthritis [21605]
  7. MRC-DTP [MR/K501256/1]
  8. Innovation Fund Denmark [5153-00002B]
  9. Novo Nordisk Foundation [NNF14CC0001]
  10. VINCI [VA HSR RES 13-457]
  11. NIHR Senior Research Fellowship
  12. Innovative Medicines Initiative 2 Joint Undertaking (JU) [806968]
  13. European Union
  14. European Federation of Pharmaceutical Industries Associations
  15. MRC [1959917, 2122671] Funding Source: UKRI

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This study found that the use of hydroxychloroquine to treat rheumatoid arthritis does not appear to increase the risk of depression, suicide/suicidal ideation, or psychosis compared to sulfasalazine. No consistent short-term or long-term effects were observed. Further investigation is needed for higher doses or different indications of use.
Objectives. Concern has been raised in the rheumatology community regarding recent regulatory warnings that HCQ used in the coronavirus disease 2019 pandemic could cause acute psychiatric events. We aimed to study whether there is risk of incident depression, suicidal ideation or psychosis associated with HCQ as used for RA. Methods. We performed a new-user cohort study using claims and electronic medical records from 10 sources and 3 countries (Germany, UK and USA). RA patients >= 18 years of age and initiating HCQ were compared with those initiating SSZ (active comparator) and followed up in the short (30 days) and long term (on treatment). Study outcomes included depression, suicide/suicidal ideation and hospitalization for psychosis. Propensity score stratification and calibration using negative control outcomes were used to address confounding. Cox models were fitted to estimate database-specific calibrated hazard ratios (HRs), with estimates pooled where I-2 <40%. Results. A total of 918 144 and 290 383 users of HCQ and SSZ, respectively, were included. No consistent risk of psychiatric events was observed with short-term HCQ (compared with SSZ) use, with meta-analytic HRs of 0.96 (95% CI 0.79, 1.16) for depression, 0.94 (95% CI 0.49, 1.77) for suicide/suicidal ideation and 1.03 (95% CI 0.66, 1.60) for psychosis. No consistent long-term risk was seen, with meta-analytic HRs of 0.94 (95% CI 0.71, 1.26) for depression, 0.77 (95% CI 0.56, 1.07) for suicide/suicidal ideation and 0.99 (95% CI 0.72, 1.35) for psychosis. Conclusion. HCQ as used to treat RA does not appear to increase the risk of depression, suicide/suicidal ideation or psychosis compared with SSZ. No effects were seen in the short or long term. Use at a higher dose or for different indications needs further investigation.

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