Disturbances of folate metabolism may be related directly to schizophrenia. Susser et al.
+(2) found that a folate-sensitive defect in homocysteine metabolism contributes to the development of schizophrenia. Hyperhomocysteinemia in pregnant women increases the risk of neural tube defects; folate treatment may normalize homocysteine metabolism, thus reducing the risk
+(3). Studies of nutritional status in pregnancy have found that mothers of fetuses affected with neural tube defects have normal or mildly low levels of folate
+(4). Not all of the known risks for neural tube defects, such as maternal age, birth order, or febrile illness, operate through folate-dependent mechanisms.