Cognitive Impairments in Patients with Rheumatoid Arthritis and Comorbid Anxiety and Depressive Disorders: Outcomes

A A Abramkin1, T A Lisitsyna2, D Yu Veltishchev3,4

  • 1Nasonova Research Institute of Rheumatology, Moscow, Russia. angrydoctor2015@yandex.ru.

Insights

Mild cognitive impairments (MCIs) are common in rheumatoid arthritis (RA) patients with anxiety and depressive disorders (ADDs). Psychopharmacotherapy (PPT) can reduce MCI rates over five years, suggesting personalized treatment benefits RA patients with ADDs.

Area of Science:

  • Rheumatology
  • Neuropsychiatry
  • Clinical Psychology

Background:

  • Rheumatoid arthritis (RA) frequently co-occurs with anxiety and depressive disorders (ADDs).
  • Cognitive impairments (CIs) are highly prevalent in RA patients, impacting quality of life.
  • Understanding the long-term trajectory of CIs in RA with comorbid ADDs is crucial for effective management.

Purpose of the Study:

  • To assess baseline rates and five-year outcomes of mild cognitive impairments (MCIs) in RA patients with ADDs.
  • To evaluate the impact of traditional synthetic disease-modifying antirheumatic drugs (csDMARDs), biologic DMARDs (bDMARDs), and psychopharmacotherapy (PPT) on MCI progression.
  • To identify factors associated with MCI development and persistence over five years.

Main Methods:

  • A cohort of 128 RA patients with diagnosed ADDs were assessed for cognitive function.
  • Patients received csDMARDs alone or with bDMARDs and/or PPT; 42.3% accepted PPT.
  • Multivariable logistic regression analyzed factors associated with MCI at the five-year follow-up.

Main Results:

  • MCIs were diagnosed in 73.2% of RA patients at baseline, primarily affecting logical thinking and memory.
  • Cognitive impairment rates increased in patients not receiving PPT over five years (69% to 85.7%).
  • Patients receiving PPT showed significantly lower CI rates (62.5%) compared to no-PPT groups (85.7%) at five years.
  • Favorable CI outcomes were linked to lower baseline depression scores, improved depression symptoms, and ADD remission.
  • Higher baseline DAS28 scores (OR 1.29) and lower ADD remission rates (OR 0.25) were associated with MCI.

Conclusions:

  • ADDs and MCIs are highly prevalent in RA patients, with CIs often persisting or worsening.
  • Psychopharmacotherapy (PPT) is associated with reduced long-term MCI rates in RA patients with ADDs.
  • Personalized PPT, including antidepressants and neuroleptics, may mitigate MCI progression in this patient population.

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