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. 2012 Oct 29;4(5):43. doi: 10.1186/alzrt146

Table 1.

Baseline characteristics of subjects who completed the 24-week, double blind, placebo controlled portion of the study.

Placebo (n = 11) Curcumin 2 gm/day (n = 9) Curcumin 4 gm/day (n = 10)
Age in years 70.2 (12.4) 76.7 (5.6) 75.3 (6.9) P = 0.71
Gender, number of women (%) 6 (55%) 6 (67%) 7 (70%) P = 0.74
Years of education (S.D.) 14.3 (2.5) 16.7 (1.3) 15.0 (2.7) P = 0.08
Number on AchE-I's (%) 11 (100%) 7 (78%) 10 (100%) P = 0.08
Number on memantine (%) 8 (73%) 7 (78%) 8 (80%) P = 0.92
MMSE (S.D., range) 23.2 (2.3, 20-27) 21.4 (3.2, 17-28) 22.8 (3.4, 18-27) P = 0.41
ADAS-Cog score (S.D.) 18.2 (4.9) 20.9 (7.4) 19.3 (3.4) P = 0.64
NPI total score (S.D.) 8.5 (12.4) 8.9 (9.6) 11.7 (16.9) P = 0.84
ADCS-ADL score (S.D.) 66.7 (3.6) (n = 10) 60.3 (10.9) 61.0 (8.4) P = 0.18

Note that ADCS-ADL score was not available on one subject in the placebo arm. AchE-I, acetylcholinesterase inhibitor; ADAS-Cog, Alzheimer's Disease Assessment Scale - Cognitive Subscale; ADCS-ADL, Alzheimer's Disease Cooperative Study - Activities of Daily Living; MMSE, Mini-Mental State Examination; NPI, Neuropsychiatric Inventory; S.D., standard deviation.

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