Pharmacotherapy for Frontotemporal Dementia.
Rita KhouryYu LiuQuratulanne SheheryarGeorge T GrossbergPublished in: CNS drugs (2021)
Frontotemporal dementia is a heterogeneous spectrum of neurodegenerative disorders. The neuropathological inclusions are tau proteins, TAR DNA binding protein 43 kDa-TDP-43, or fused in sarcoma-ubiquitinated inclusions. Genetically, several autosomal mutations account for the heritability of the disorder. Phenotypically, frontotemporal dementia can present with a behavioral variant or a language variant called primary progressive aphasia. To date, there are no approved symptomatic or disease-modifying treatments for frontotemporal dementia. Currently used therapies are supported by low-level of evidence (mostly uncontrolled) studies. The off-label use of drugs is also limited by their side-effect profile including an increased risk of confusion, parkinsonian symptoms, and risk of mortality. Emerging disease-modifying treatments currently target the progranulin and the expansion on chromosome 9 open reading frame 72 genes as well as tau deposits. Advancing our understanding of the pathophysiology of the disease and improving the design of future clinical trials are much needed to optimize the chances to obtain positive outcomes.
Keyphrases
- binding protein
- clinical trial
- cerebrospinal fluid
- multiple sclerosis
- circulating tumor
- minimally invasive
- cardiovascular events
- genome wide
- current status
- single molecule
- working memory
- heat shock protein
- copy number
- amyotrophic lateral sclerosis
- risk factors
- smoking cessation
- case control
- randomized controlled trial
- cardiovascular disease
- adipose tissue
- genome wide identification
- dna methylation
- metabolic syndrome
- insulin resistance
- drug induced