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Case Study: A Precision Medicine Approach to Multifactorial Dementia and Alzheimer's Disease.
Ross, Mary Kay; Raji, Cyrus; Lokken, Kristine L; Bredesen, Dale E; Roach, Jared C; Funk, Cory C; Price, Nathan; Rappaport, Noa; Hood, Leroy; Heath, James R.
Afiliación
  • Ross MK; Brain Health and Research Institute, Seattle, WA, USA.
  • Raji C; Washington University School of Medicine, St. Louis, MO, USA.
  • Lokken KL; Department of Psychiatry and Behavioral Neurobiology, University of Alabama-Birmingham, Birmingham, AL, USA.
  • Bredesen DE; Department of Molecular and Medical Pharmacology, UCLA, Los Angeles, CA, USA.
  • Roach JC; Institute for Systems Biology, 401 Terry Ave N, Seattle, WA, USA, 98109.
  • Funk CC; Institute for Systems Biology, 401 Terry Ave N, Seattle, WA, USA, 98109.
  • Price N; Institute for Systems Biology, 401 Terry Ave N, Seattle, WA, USA, 98109.
  • Rappaport N; Institute for Systems Biology, 401 Terry Ave N, Seattle, WA, USA, 98109.
  • Hood L; Institute for Systems Biology, 401 Terry Ave N, Seattle, WA, USA, 98109.
  • Heath JR; Institute for Systems Biology, 401 Terry Ave N, Seattle, WA, USA, 98109.
Article en En | MEDLINE | ID: mdl-35237464
We report a case of a patient with mixed dementia successfully treated with a personalized multimodal therapy. Monotherapeutics are inadequate for the treatment of Alzheimer's disease (AD) and mixed dementia; therefore, we approach treatment through an adaptive personalized multimodal program. Many multimodal programs are pre-determined, and thus may not address the underlying contributors to cognitive decline in each particular individual. The combination of a targeted, personalized, precision medicine approach using a multimodal program promises advantages over monotherapies and untargeted multimodal therapies for multifactorial dementia. In this case study, we describe successful treatment for a patient diagnosed with AD, using a multimodal, programmatic, precision medicine intervention encompassing therapies targeting multiple dementia diastheses. We describe specific interventions used in this case that are derived from a comprehensive protocol for AD precision medicine. After treatment, our patient demonstrated improvements in quantitative neuropsychological testing, volumetric neuroimaging, PET scans, and serum chemistries, accompanied by symptomatic improvement over a 3.5-year period. This case outcome supports the need for rigorous trials of comprehensive, targeted combination therapies to stabilize, restore, and prevent cognitive decline in individuals with potentially many underlying causes of such decline and dementia. Our multimodal therapy included personalized treatments to address each potential perturbation to neuroplasticity. In particular, neuroinflammation and metabolic subsystems influence cognitive function and hippocampal volume. In this patient with a primary biliary cholangitis (PBC) multimorbidity component, we introduced a personalized diet that helped reduce liver inflammation. Together, all these components of multimodal therapy showed a sustained functional and cognitive benefit. Multimodal therapies may have systemwide benefits on all dementias, particularly in the context of multimorbidity. Furthermore, these therapies provide generalized health benefits, as many of the factors - such as inflammation - that impact cognitive function also impact other systems.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: J Alzheimers Dis Parkinsonism Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: J Alzheimers Dis Parkinsonism Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos
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