1. Academic Validation
  2. Comparative Analysis of Aducanumab, Zagotenemab and Pioglitazone as Targeted Treatment Strategies for Alzheimer's Disease

Comparative Analysis of Aducanumab, Zagotenemab and Pioglitazone as Targeted Treatment Strategies for Alzheimer's Disease

  • Aging Dis. 2021 Dec 1;12(8):1964-1976. doi: 10.14336/AD.2021.0719.
Morteza Abyadeh 1 Vivek Gupta 2 Veer Gupta 3 Nitin Chitranshi 2 Yunqi Wu 4 Ardeshir Amirkhani 4 Anna Meyfour 5 Samran Sheriff 2 Ting Shen 2 Kunal Dhiman 3 H Salekdeh Ghasem 6 A Haynes Paul 6 L Graham Stuart 2 Mehdi Mirzaei 2
Affiliations

Affiliations

  • 1 1Cell Science Research Center, Department of Molecular Systems Biology, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
  • 2 2Department of Clinical Medicine, Macquarie University, Macquarie Park, NSW, Australia.
  • 3 3School of Medicine, Deakin University, VIC, Australia.
  • 4 4Australian Proteome Analysis Facility, Macquarie University, Macquarie Park, NSW, Australia.
  • 5 5Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Center, Research institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • 6 6Department of Molecular Sciences, Macquarie University, Macquarie Park, NSW, Australia.
Abstract

Alzheimer's disease (AD) is the leading cause of dementia that has remained a major medical, sociocultural and economical challenge globally. Previously developed treatments like anticholinesterase inhibitors (AChEIs) and N-methyl-D-aspartate receptor (NMDAR) antagonists only provide short-term symptomatic improvement and do not prevent progression. Repeated setbacks and failures over the past 25 years in AD clinical trials have hindered efforts to develop effective AD treatments. Fortunately, Aducanumab, a specific anti-amyloid β antibody, has shown promising clinical results and was recently approved by the Food and Drug Administration (FDA) through an accelerated approval pathway. This has raised hopes for AD patients; however post-approval trials are necessary to estimate the true scope of its clinical benefits. We have reviewed several AD clinical studies and summarized the experience to date with Aducanumab and two other potential AD drugs including Zagotenemab (an anti-tau antibody) and Pioglitazone (nuclear Peroxisome-Proliferator Activated Receptor γ (PPARγ) agonist). These have shown mixed results so far and the next few years will be critical to elucidate and interpret their broad long-term protective effects. A concerted effort is required to understand and strengthen the translation of pre-clinical findings from these drugs to routine clinical practice.

Keywords

Aducanumab; Alzheimer’s disease; Pioglitazone; Zagotenemab.

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