NfL levels may mediate link between dementia, LRRK2 variants

Scientists have discovered that long-term changes in a biomarker of nerve damage, called neurofilament light chain (NfL), could be used to predict cognitive decline in people with Parkinson’s disease due to certain mutations. They found that a slower progression of dementia in people with LRRK2-associated Parkinson’s compared with those…

Deep Brain Stimulation Found to Ease Symptoms in Parkinson’s

Subthalamic deep brain stimulation (DBS) significantly eases motor and non-motor symptoms in people with early-onset Parkinson’s disease, a new study suggests. In fact, data showed that individuals with this early-onset form of the neurodegenerative disorder saw more than a 50% improvement, or lessening of motor symptoms, on one…

Swedish Biobank Promises to Help Unveil Genetics of Parkinson’s

A new biobank in Sweden, containing blood samples from patients with Parkinson’s disease and age- and sex-matched healthy people — along with data regarding the individuals’ lifestyles and medical histories — may help researchers investigate the underlying mechanisms of the neurodegenerative disorder and find new treatments. The biobank is…

Genetic Parkinson’s More Common Than Thought, Global Survey Reveals

Cases of inherited Parkinson’s disease may be more frequent than previously reported, results from an online global survey suggest. The survey, which was conducted by members of The Michael J. Fox Foundation Global Genetic Parkinson’s Study Group (MJFF-GGPSG), also revealed the willingness of investigators to share clinical information on…

Mutations in Gene Associated With Hereditary Parkinson’s Disease Lead to Toxic Accumulation of Manganese

Researchers have found that mutations in a gene linked to hereditary forms of Parkinson’s disease — SLC30A10 — cause accumulation of toxic levels of manganese inside cells, which disturbs protein transport and alters nerve cell function, leading to parkinsonian symptoms. The study “SLC30A10 Mutation Involved in Parkinsonism Results in Manganese Accumulation within…

Tiny Changes in Alpha-synuclein Protein Could Be an Important Driver in Parkinson’s, Study Suggests

Researchers have found that selective mutations in the protein alpha-synuclein affect its binding to cell membranes with potential implications in Parkinson’s disease (PD) and therapeutic strategies. The study, “Alpha-Synuclein Disease Mutations Are Structurally Defective and Locally Affect Membrane Binding,” was published in the Journal of the American Chemical Society.