Cg. Trolin et al., DECREASED METHIONINE ADENOSYLTRANSFERASE ACTIVITY IN ERYTHROCYTES OF PATIENTS WITH DEMENTIA DISORDERS, European neuropsychopharmacology, 5(2), 1995, pp. 107-114
ATP:l-methionine S-adenosyltransferase (EC 2.5.1.6, MAT) activity was
analyzed in erythrocytes from nine patients with a clinical diagnosis
of probable Alzheimer's disease (Pro.AD), four with possible Alzheimer
's disease (Pos.AD), three with mild cognitive dysfunction (MCD) and t
wo with dementia of vascular origin (VD), and 10 age-matched control s
ubjects. Significantly lower kinetic parameters (V-max and K-m towards
methionine) for MAT were observed in all the dementia cases. In the s
ubgroup of Pro.AD patients who also had low plasma levels of vitamin B
-12 (B-12), the reduction in MAT K-m was significantly correlated with
an increase in the serum levels of homocysteine, while no such correl
ation was observed in all the other dementia groups. Treatment for 6 m
onths of this subgroup of Pro.AD patients with B-12 (1 mg x 7 days + 1
mg/week, i.m.), S-adenosylmethionine (SAM, 200 mg twice daily, p.o.)
and folate (2.5 mg every 2 days, p.o.) caused a significant decrease i
n homocysteine in parallel with a significant increase in K-m for MAT.
These findings support the hypothesis that aberrations in the B-12 de
pendent transmethylation reactions might be involved in the pathogenes
is of dementia, and suggest that the evaluation of erythrocyte MAT act
ivity may be a useful marker for the detection of such an aberration.