Table 1. Baseline characteristics of the participants completing the MRI protocol.
Characteristics | Placebo group (n = 83) | Active treatment groupa (n = 85) | ||
Mean or n | SD or % | Mean or n | SD or % | |
Age, years | 76.2 | 4.5 | 77.0 | 5.2 |
Women, n (%) | 52 | 62.7 | 50 | 58.8 |
Years of education | 14.8 | 3.5 | 14.3 | 3.6 |
Body Mass Index, kg/m2 b | 26.6 | 4.2 | 25.3 | 3.4 |
Systolic blood pressure, mmHg | 147 | 19 | 148 | 25 |
Diastolic blood pressure, mmHg | 80 | 11 | 80 | 11 |
TICS-M score | 24.8 | 2.7 | 24.9 | 2.8 |
MMSE score | 28.3 | 1.5 | 28.3 | 1.8 |
Initial brain volume, mL | 1376 | 71 | 1387 | 86 |
Depression score (GDS) c | 7.5 | 5.2 | 5.6 | 4.0 |
Ever-smoker, n (%) | 43 | 51.8 | 38 | 44.7 |
No ankle vibration sense, n (%) | 50 | 60.2 | 55 | 64.7 |
Hemoglobin, g/L | 138 | 12 | 138 | 13 |
MCV, fL | 93.0 | 4.3 | 92.3 | 4.4 |
Creatinine, µmol/L | 97 | 17 | 96 | 18 |
APOE ε4 positive, n (%) | 29 | 34.9 | 22 | 25.9 |
MTHFR 677C>T allele frequency (%) | 34.9 | 34.7 | ||
TCN2 776C>G allele frequency (%) | 30.1 | 37.1 | ||
Use of B vitamins at baseline, n (%) | 17 | 20.5 | 14 | 16.5 |
Use of fish-oils, omega-3, n (%) | 31 | 37.3 | 36 | 42.4 |
Diabetes any time, n (%) | 10 | 12.05 | 4 | 4.7 |
Use of CVD drugs baseline, n (%) | 36 | 43.4 | 42 | 49.4 |
Use of centrally acting drugs, n (%) | 20 | 24.1 | 23 | 27.1 |
Use of aspirin baseline (%) | 28 | 33.7 | 26 | 30.6 |
Other NSAIDs baseline | 12 | 14.5 | 18 | 21.2 |
Stroke, TIA, MRI infarct at baseline | 15 | 18.1 | 13 | 15.3 |
History of MI baseline | 6 | 7.3 | 6 | 7.1 |
Alcohol consumption (units/week) | 7.2 d | 8.6 | 8.2 | 9.3 |
Abbreviations: APOE, gene for apolipoprotein E; CVD, cardiovascular disease; GDS, Geriatric Depression Scale; MCV, mean red cell volume; MI, myocardial infarct; MMSE, mini-mental state examination; MTHFR, gene for methylenetetrahydrofolate reductase; NSAID, non-steroidal anti-inflammatory drug; TIA, transient ischemic attack; TICS-M, telephone interview of cognitive status, modified. Except where indicated by superscript letters, none of the factors differed between the placebo and active treatment groups.
Active treatment group received daily supplements of folic acid (0.8 mg), vitamin B12 (0.5 mg) and vitamin B6 (20 mg) for 24 months.
P = 0.022;
P = 0.009;
Excluding one high outlier.