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Serum TDP-43 levels can help to identify common neuropathological changes associated with frontotemporal dementia

Date:
October 20, 2022
Source:
University of Eastern Finland
Summary:
A recent study sought to identify FTD patients with TDP-43 accumulation from a large patient cohort, which included all of the most common subtypes of the disease. TDP-43 levels were measured from patients' blood samples using a sensitive single-molecule array (Simoa) technology.
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额颞叶痴呆(FTD)是一种最common causes of progressive dementia in working-age people. However, making a diagnosis and a prognosis is often challenging because the frontotemporal dementia spectrum includes several subtypes that differ in terms of symptoms, genetics and neuropathology, i.e., changes in the brain associated with the disease. Typically, proteins accumulating in the brain of patients with FTD and harming their neurons are either TDP-43 or tau proteins. Understanding the neuropathological changes in patients already at the diagnostic stage would be particularly helpful in terms of assessing their prognosis and possible future treatments.

A recent study from the University of Eastern Finland, the University of Oulu and the University of Brescia in Italy sought to identify FTD patients with TDP-43 accumulation from a large patient cohort, which included all of the most common subtypes of the disease. TDP-43 levels were measured from patients' blood samples using a sensitive single-molecule array (Simoa) technology.

The researchers found that serum TDP-43 levels were considerably lower in patients carrying theC9orf72repeat expansion or with motoneuron disease. Previous studies have shown that these patients typically accumulate the TDP-43 protein in their brain. Lower levels of TDP-43 were not observed in carriers ofMAPTmutations, who typically have tau accumulation in their brain.

"Our current diagnostic methods are not sensitive or accurate enough to differentiate patients with TDP-43 neuropathology from other frontotemporal dementia patients. However, this study shows that TDP-43 is a potentially useful biomarker for this purpose, if more specific and sensitive analysis methods can be developed," says Postdoctoral Researcher and Co-lead Author Kasper Katisko, MD, PhD, of the University of Eastern Finland.

In the future, it is likely that a simple blood sample can be used to differentiate between the actual neuropathological subtypes of frontotemporal dementia and other forms of dementia, too. This will make differential diagnostics increasingly rapid and accurate, enabling the development of patient-specific interventions affecting disease progression.

The findings were published inAlzheimer's Research & Therapy。这个项目是由研究总监Annakaisa Haapasalo at A.I. Virtanen Institute for Molecular Sciences and by Research Director Eino Solje at the Institute of Clinical Medicine at the University of Eastern Finland.

The project was funded by the Finnish Medical Foundation, the Finnish-Norwegian Medical Foundation, the Olvi Foundation, the Maire Taponen Foundation, the Päivikki and Sakari Sohlberg Foundation, the Yrjö Jahnsson Foundation, the Finnish Cultural Foundation, the Maud Kuistila Memorial Foundation, the Finnish Brain Foundation, the Orion Research Foundation, the Instrumentarium Science Foundation, the Sigrid Jusélius Foundation, the Academy of Finland, and the Finnish Association for Supporting ALS Research. The project is part of the FinFTD consortium's research on frontotemporal dementia.


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Materialsprovided byUniversity of Eastern Finland注意:内容可能被编辑风格d length.


Journal Reference:

  1. Kasper Katisko, Nadine Huber, Tarja Kokkola, Päivi Hartikainen, Johanna Krüger, Anna-Leena Heikkinen, Veera Paananen, Ville Leinonen, Ville E. Korhonen, Seppo Helisalmi, Sanna-Kaisa Herukka, Valentina Cantoni, Yasmine Gadola, Silvana Archetti, Anne M. Remes, Annakaisa Haapasalo, Barbara Borroni, Eino Solje.Serum total TDP-43 levels are decreased in frontotemporal dementia patients with C9orf72 repeat expansion or concomitant motoneuron disease phenotypeAlzheimer's Research & Therapy, 2022; 14 (1) DOI:10.1186/s13195-022-01091-8

Cite This Page:

University of Eastern Finland. "Serum TDP-43 levels can help to identify common neuropathological changes associated with frontotemporal dementia." ScienceDaily. ScienceDaily, 20 October 2022. /releases/2022/10/221020112843.htm>.
University of Eastern Finland. (2022, October 20). Serum TDP-43 levels can help to identify common neuropathological changes associated with frontotemporal dementia.ScienceDaily。Retrieved December 13, 2023 from www.koonmotors.com/releases/2022/10/221020112843.htm
University of Eastern Finland. "Serum TDP-43 levels can help to identify common neuropathological changes associated with frontotemporal dementia." ScienceDaily. www.koonmotors.com/releases/2022/10/221020112843.htm (accessed December 13, 2023).

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