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Department of Neurology
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Homocysteine metabolism and the vitamins involved are relevant for the metabolic and structural integrity of the central nervous system. Disturbances of homocysteine metabolism, e.g. due to genetic, nutritional or iatrogenic reasons, can lead to neurodegeneration and vascular disease. Manipulation of homocysteine metabolism may improve the clinical course of such disease.
Keywords: Homocysteine, folate, vitamin B6, vitamin B12, S-adenosylmethionine, glutathione, metabolism, genetics, neurodegeneration, Alzheimer’s disease, cognitive decline, aging, neurooncology, epilepsy, stroke.
1 group leader, 2 postdocs, 1 PhD student, 2 technicians
The genetic conditions of homocysteine metabolism are associated with DNA methylation, with the concentration of homocysteine metabolites in the plasma and the cerebrospinal fluid, with the clinical course of neurodegenerative diseases, with neurotoxicity of methotrexate chemotherapy, and with the incidence of primary brain tumours. Metabolites of homocysteine metabolism in the plasma or the cerebrospinal fluid are associated with neurodegeneration, cerebrovascular disease, seizures and sepsis.
We investigate to what extend the manipulation of homocysteine metabolism can influence Alzheimer’s disease, cerebrovascular disease, effects and side effects of antiepileptic drugs as well as of methotrexate, and the progression of primary brain tumours.
Techniques and equipment of molecular biology, biochemistry, cell culture, histology and transgenic animal models.
Deutsche Krebshilfe, European Research Advisory Board, Betty and David
Koetser Foundation for Brain Research, European Association of
Leukodystrophies, Hilde-Rüdiger-Stiftung der Commerzbank, industrial
funding.
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