Table 2:

Association between atrial fibrillation (baseline and follow–up) and cognitive and functional outcomes among participants of the ONTARGET and TRANSCEND trials

OutcomeAll participants (no atrial fibrillation at baseline), no. %
n = 29 916
No atrial fibrillation, no. %
n = 27 864
Atrial fibrillation at baseline, no. %
n =1 016
New atrial fibrillation at follow-up, no. %
n = 2 052
All atrial fibrillation (baseline and follow-up), no. %
n = 3 068
Composite outcome*n = 29 916
7 972 (26.7)
n = 27 864
7 269 (26.1)
n = 1 016
347 (34.1)
n = 2 052
703 (34.3)
n = 3 068
1 050 (34.2)
Decrease in MMSE score ≥ 3n = 27 003
4 524 (16.8)
n = 25 114
4 169 (16.6)
n = 843
171 (20.3)
n = 1 889
355 (18.8)
n = 2 732
526 (19.3)
Dementia during follow-upn = 27 386
2 157 (7.9)
n = 25 521
1 972 (7.7)
n = 890
114 (12.8)
n = 1 865
185 (9.9)
n = 2 755
299 (10.9)
Loss of independence in ADLn = 27 160
2 006 (7.4)
n = 25 272
1 775 (7.0)
n = 857
122 (14.2)
n = 1 888
231 (12.2)
n = 2 745
353 (12.9)
Admission to long-term caren = 29 070
1 345 (4.6)
n = 27 052
1 183 (4.4)
n = 953
74 (7.8)
n = 2 018
162 (8.0)
n = 2 971
236 (7.9)
  • Note: ADL = activities of daily living, MMSE = Mini–Mental State Examination.

  • * Decrease in MMSE score of 3 points or more, new diagnosis of dementia at follow-up, loss of independence with performing ADL and admission to a long-term care facilty.