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Occurrence and relative risk of stroke in incident and prevalent contemporary rheumatoid arthritis
  1. Marie Holmqvist1,
  2. Emma Gränsmark1,
  3. Ängla Mantel1,
  4. Lars Alfredsson2,
  5. Lennart T H Jacobsson3,
  6. Solveig Wallberg-Jonsson4,
  7. Johan Askling1
  1. 1Clinical Epidemiology Unit, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden
  2. 2Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden
  3. 3Rheumatology, Department of Medicine, Malmö University Hospital, Malm, Sweden
  4. 4Institution of Public Health and Clinical Medicine/Rheumatology, Umeå University Hospital, Umea, Sweden
  1. Correspondence to Dr Marie Holmqvist, Karolinska Institutet, Clinical Epidemiology Unit, Department of Medicine Solna, T2, Karolinska Universitetssjukhuset, Stockholm 17176, Sweden; marie.holmqvist{at}ki.se

Abstract

Objective In contrast with the wealth of data on ischaemic heart disease in rheumatoid arthritis (RA), data on stroke are scarce and contradictory. Despite the high clinical and aetiological relevance, there is no data regarding when (if ever) after RA diagnosis there is an increased risk. Our objective was to assess the risk of stroke (by subtype) in contemporary patients with RA, particularly in relation to time since RA diagnosis.

Methods One incident RA cohort diagnosed between 1997 and 2009 (n=8077) and one nationwide prevalent RA cohort followed at Swedish rheumatology clinics between 2005 and 2009 ((n=39 065) were assembled). Each cohort member was matched to a general population comparator. Information on first-time hospitalisations for stroke up to 2009 was retrieved from the Swedish Patient Register. HR and 95% CI were estimated using Cox models.

Results In prevalent unselected RA, the HR of ischaemic stroke was 1.29 (95% CI 1.18 to 1.41). In the incident RA cohort, the overall risk increase was small and non-significant (overall HR 1.11, 95% CI 0.95 to 1.30). When stratified by RA disease duration, an increased risk of ischaemic stroke was indeed detectable but only after 10 or more years since RA diagnosis (HR>10 years: 2.33, 95% CI 1.25 to 4.34). Risk of haemorrhagic stroke was increased in prevalent but not in incident RA.

Conclusion The magnitude of stroke risk is lower than for ischaemic heart disease in RA, and the evolvement of this risk from RA diagnosis may be slower. This suggests different driving forces behind these two RA co-morbidities and has implications for the clinical follow-up of patients with RA.

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Footnotes

  • Competing interests None.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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