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University College London/University of Gothenburg PhD course “Biomarkers in neurodegenerative diseases” 2019—course organisation


Biomarkers are increasingly employed for effective research into neurodegenerative diseases. They have become essential for reaching an accurate clinical diagnosis, monitoring disease, and refining entry criteria for participation in clinical treatment trials, and will be key in measuring target engagement and treatment outcome in disease-modifying therapies. Emerging techniques and research combining different biomarker modalities continue to strengthen our understanding of the underlying pathology and the sequence of pathogenic events. Given recent advances, we are now at a pivotal stage in biomarker research. PhD students working in the field of neurodegenerative disease require a working knowledge of a range of biomarkers available and their limitations, to correctly interpret scientific literature and to design and conduct successful research studies themselves. Here, we outline the University College London/University of Gothenburg “Biomarkers in neurodegenerative diseases course”, the first initiative of its kind aimed to bring together both experts and PhD students from all areas within the field of neurodegeneration, to provide comprehensive knowledge of biomarker research for the next generation of scientists.


This paper is an introduction to a series of reviews based on the course as below:

  • Paper 1: University College London/University of Gothenburg course “Biomarkers in neurodegenerative diseases 2019”—course organisation (Ayesha Khatun et al.)

  • Paper 2: The utility of biomarkers for neurodegenerative diseases: clinical and research perspectives (Alexander J Ehrenberg et al.)

  • Paper 3: Fluid biomarkers in neurodegenerative diseases: perspectives from the University College London/University of Gothenburg course (Pawel Obrocki et al.)

  • Paper 4: Imaging biomarkers in neurodegeneration: Current and future perspectives (Peter NE Young et al.)

The field of biomarker research in neurodegenerative diseases continues to rapidly grow to include an increasing number of modalities and techniques. These provide complementary strengths in identifying neurodegenerative diseases early, reaching consensus diagnosis in both research and clinical settings, and will be key in refining clinical trial inclusion criteria, disease monitoring, measuring target engagement in disease-modifying therapies as well as in assessing associations between biomarker-defined pathology with clinical endpoints.

The first “Biomarker in neurodegenerative diseases” course was held at the University of Gothenburg (UGOT) in 2018 after local researchers Michael Schöll and Henrik Zetterberg who work in highly complementary fields within neurodegeneration identified a lack of international doctoral-level education in multimodal biomarker research. They considered this an opportunity to bring together their wider network of colleagues into a course expressing the breadth of biomarker practice in neurodegeneration, with an emphasis on Alzheimer’s disease (AD).

The outline of the course is published to serve as an example for other course organisations in the field as well as an introduction to a series of biomarker reviews written by the course delegates.

The second edition of the course was organised as a collaborative initiative between University College London (UCL) and UGOT in April 2019, and we intend to continue offering the course alternating between both sites.

The overall course aim is to provide PhD students from different fields with basic and practical knowledge about both bodily fluid- and brain imaging-derived biomarkers for neurodegenerative diseases. Students are expected to achieve a broad understanding of disciplines, including advanced brain imaging, and neurochemistry technologies used as research and clinical tools including:

  • Neurochemistry

  • Biomarkers in cerebrospinal fluid (CSF)

  • Biomarkers in blood

  • Structural and functional magnetic resonance imaging (MRI)

  • Positron emission tomography (PET)

UGOT and UCL are leading international centres with complementary expertise in fluid and imaging biomarkers. We anticipated that this collaboration would strengthen the quality of biomarker training across both institutions and beyond, as well as foster new research collaborations and provide delegates with outstanding networking opportunities internationally.

Following completion of the course, delegates were expected to be able to:

  • Explain basic concepts in fluid- and image-based biomarker research

  • Describe how different biomarkers relate to each other in a temporal, pathogenic, and regional (anatomical) context of different neurodegenerative diseases

  • Conduct the planning of a project within their own area of research where the use of the discussed biomarkers is explained

  • Use basic tools to evaluate biomarker data

  • Interpret biomarker profiles in different neurodegenerative diseases

  • Understand when biomarkers/methods can and cannot be applied

  • Analyse the predictive value of the respective biomarkers in different conditions

Methods: overview of the biomarker course

This year’s course at UCL ran over 4 days (Fig. 1) in April 2019. A total of 52 students including international delegates took part, with a further 23 on the waiting list.

Delegates included a mixture of students from clinical medical research background (50%), natural sciences/medicine (41%), and health care sciences (2.9%). The course was aimed at international PhD students working broadly in the field of biomarkers in neurodegeneration. Students who were unable to register for the 2019 course were given priority to register for the 2020 course in April. In addition to the lectures, a self-directed group exercise was assigned with groups of four to six delegates. Based on knowledge acquired during the course, delegates were asked to develop a research project proposal and subsequently delivered a 15-min study proposal presentation in front of an expert panel. We collected prospective information from delegates on their area of research and split groups according to expertise to try and achieve a degree of balance. We also aimed to mix delegates from the same institutions and to balance gender.

Fig. 1

UGOT/UCL Biomarkers in Neurodegeneration 2019 course timetable

We also focussed on mechanisms for enhancing the student experience through a buddy scheme and the organisation of evening social events (Fig. 1). The buddy scheme identified delegates within the UK and allocated them up to three colleagues from outside the UK who could contact them for advice on travel/accommodation and life in London.

At the end, students were asked to fill in a feedback questionnaire to help us improve future courses (Table 1). Overall, students were satisfied with the course (97%) and felt that the aim of the course was clear and fulfilled, with administration of the course well carried through (94%).

Table 1 Course feedback

Students felt that the lecturers in general had good teaching skills and showed interest in student learning (99%) and that lectures themselves were excellent (97%).

Students were provided with course literature and pre-reading materials which they felt were relevant in the relation to the aims (88%), and 68% of students felt that the examination was relevant in relation to the aims and purpose of the course; however, no alternative examinations were suggested.

Ninety-five percent of students agreed that the balance between lectures and the practical elements was good. Eighty-three percent felt that the course content was relevant to their individual research, and 91% agreed that they would recommend the course to other doctoral students.

We will aim to revise the examination component of the course as it had received the lowest score at 68%.

The following topics were covered (in order of delivery):

  • Introduction to neurodegenerative diseases pathology—Dr Tammaryn Lashley

A definitive diagnosis for a neurodegenerative disease can only be given, at present, by post-mortem examination of the brain. This lecture focussed on the work at the Queen Square Brain Bank where underlying pathological features are observed macroscopically and microscopically. Alzheimer’s disease (AD) is diagnosed using standard criteria based on the presence and spread of extracellular amyloid-β (Aβ) and intracellular tau. Frontotemporal dementia is a heterogeneous group of diseases that clinically overlap, and the underlying pathological hallmarks could be one of three major proteins: tau in FTLD-Tau, TDP-43 in FTLD-TDP, and FUS in FTLD-FUS. Here, we go through the major pathological hallmarks used to identify and diagnose the different diseases. We also highlight that these neurodegenerative diseases can co-exist [1,2,3,4,5,6].

  • Introduction to PET imaging—Dr Kerstin Heurling

This lecture discussed PET as a molecular imaging method, based on the detection of disintegration of short-lived radioactive isotopes incorporated in pharmacological molecules (known as PET tracers or ligands) with affinity to a physiological target, such as beta-amyloid [7]. Medical images are created, showing the distribution of the radioactivity, corresponding to the amount of target in the tissue imaged. Absolute quantification of the tracer binding requires long scanning times and plasma sampling, but semi-quantitative measures such as the ratio of radioactivity concentration in a region of interest (ROI) relative to one without target (a measure known as standardised uptake value ratio (SUVR)) is often sufficient [8].

  • Genetics—Professor John Hardy

This talk discussed the genetic analysis of Alzheimer’s disease, Parkinson’s disease, and tauopathies. It pointed out that in all genetic cases overexpression of the primary protein deposited gives rise to disease: APP duplication causes AD, SNCA duplication causes PD, and MAPT duplications cause tauopathies. Other Mendelian causes also often lead to overproduction of the deposited protein. This talk discussed how many of the risk genes for “sporadic” late onset disease are involved in the clearance of these same proteins. In the case of amyloid, this clearance is largely microglial; in the case of synuclein, the clearance is largely lysosomal; and in the case of tau, the clearance is at least partly through the ubiquitin proteasome. Thus, there is a consistency in the pathogenesis of these diseases. Overproduction of these proteins and a problem in clearance are the general causes of these diseases [9].

  • Introduction to MRI—Professor Nick Fox

This talk focussed on structural MRI (sMRI) in both clinical and research settings. It provided an overview of the principles of image formation and how what can be “seen” is determined by image resolution and contrast. The basic physics of MRI was introduced, and elements of a modern MR scanner were briefly reviewed. It also discussed how sMRI remains the mainstay of clinical imaging in dementia. The lecture also looked at the evolving roles of clinical imaging: which had moved from a purely exclusionary approach to one where one gains positive support for a particular diagnosis [10,11,12].

  • Amyloid and tau PET imaging—Professor William Jagust

Measurement of aggregated proteins in the brain in ageing and dementia has become a standard approach to characterising research participants in clinical, translational, and therapeutic studies. This lecture reviewed the approaches to biomarker characterisation using PET scanning with ligands that bind to the key pathological hallmarks, aggregated amyloid-β (Aβ) and tau proteins. This approach has helped to establish a new framework for research classification [13] and contributed to our understanding of the pathophysiology of AD [14]. The lecture further discussed the dynamics between these measures, age and cognition.

  • PET imaging of synaptic and neurodegeneration—Dr Stephen Carter

The AD biomarker model [15] indicates neurodegeneration occurs late in the disease process. The PET biomarkers [18F] FDG and [11C]UCB-J measure neurodegeneration and changes in synaptic integrity in vivo. The well-established and most used PET ligand [18F] FDG measures reductions in brain glucose metabolism whereas novel ligand [11C]UCB-J assesses reduced synaptic density. This lecture summarised studies for each biomarker, including how imaging data is typically processed, analysed, and interpreted [15,16,17].

  • Introduction to lumbar puncture—Professor Jonathan Schott

Ultimately, any CSF biomarkers for dementia need to be applied in clinical practice, and the results interpreted on individual patient basis. In this lecture, the case for the use of molecular diagnostics in the differential diagnosis of dementia—and in particular a positive diagnosis of AD—were made, alongside a review of the core CSF biomarkers currently in use, proposed “good use” criteria, the practicalities of CSF sampling and storage, and interpretation of results including the advantages and limitations of using cut-points. Finally, the diagnostic role of CSF biomarkers for individual patients was illustrated using a number of patient case studies [18,19,20].

  • Immunochemical methods—Dr Ulf Andreasson

Immunochemical methods are widely used both for established biomarkers and in the search for new ones. The lecture covered the principles of different methods and platforms, including ultra-sensitive ones [21], as well as multiplex methods. Some possible sources of interference were discussed, and the importance of assessing the performance by technical validation of an assay was stressed [22].

  • Mass spectrometry and proteomics—Dr Johan Gobom

This lecture focussed on mass spectrometry, an analytical technique used to measure the molecular mass of a broad range of analytes, ranging from small volatile molecules to large biomolecules. The ability to identify and quantify large numbers of proteins and peptides in biological samples by mass spectrometry has given rise to the research field proteomics, which is applied in many research areas, such as neuroscience [23]. Performing proteomic analysis of clinical samples—clinical proteomics—can be used to identify new biomarkers [24]. Clinical proteomics is still a young field; while clinical proteomic studies have resulted in the identification of hundreds of new candidate CSF markers of Alzheimer’s disease [25], the majority remains to be validated [24].

  • Core CSF biomarkers—Professor Henrik Zetterberg

This lecture revisited the evidence on what the standard CSF biomarkers for AD may represent. It concluded that the CSF concentration of the 42 amino acid-long isoform of Aβ (Aβ42) correlates inversely with plaque pathology in the brain and that the ratio of Aβ42 to Aβ40 (CSF Aβ42/Aβ40 ratio) corrects for inter-individual differences in amyloidogenic processing of the amyloid precursor protein (APP), resulting in an even more accurate plaque pathology test with 90–95% concordance with amyloid PET. CSF total and phosphorylated tau (T-tau and P-tau, respectively) are not direct but rather predictive markers of AD-type neurodegeneration and tangle pathology. Recent stable isotope kinetics studies in humans and human-derived cell models [26], as well as earlier studies in mouse models of AD [27], suggest that neurons affected by Aβ pathology phosphorylate and secrete more tau into the CSF in an active process. Such neurons may eventually degenerate and develop tangle pathology, explaining why CSF tau and tau PET correlations appear in late-stage disease but are difficult to discern in pre-dementia disease stages.

  • Fluid-derived biomarkers for inflammation—Professor Henrik Zetterberg

The lecture discussed the small but significant changes in CSF that are suggestive of microglial and astrocytic activation (CSF sTREM2 and YKL-40, respectively) in AD. CSF interleukin and cytokine concentrations are most often relatively normal. Classical neuroinflammation changes in CSF (e.g. increased CSF cell counts and CSF/serum albumin ratio) should raise suspicion on a primary neuroinfectious or inflammatory disease. For example, neuroborreliosis should be excluded [28].

  • Use of biomarkers in clinical trials—Professor Henrik Zetterberg/Professor Kaj Blennow

The lecture looked at several potential uses of biomarkers in clinical trials, mainly for AD. Biomarkers may be used to diagnose and exclude patients with neuroinflammatory and neuroinfectious conditions. Specific imaging or fluid biomarkers for AD pathology may be used as supporting diagnostic markers in the clinic and as additional inclusion criteria in studies of anti-AD drugs. Depending on the mechanism of action of the drug, specific imaging or fluid markers may be used for drug effect monitoring. There are also a number of downstream markers that a disease-modifying drug is expected to have an effect on, irrespective of the mechanism of action. If a drug is effective at slowing neurodegeneration, CSF neurofilament light and/or T-tau concentrations should decrease and MRI changes should progress slower. Finally, it was discussed that biomarkers could be used as safety markers in clinical trials (e.g. MRI for ARIA and CSF cell count and CSF/serum albumin ratio for treatment-induced neuroinflammation) [29].

  • Neurogranin in CSF relation to cognition and neurodegeneration in AD—Dr Eric Portelius

The lecture covered what we have learned so far about the post-synaptic protein neurogranin. Neurogranin is highly expressed in the brain, especially in the cortex, hippocampus, and amygdala, and several studies have shown that the cerebrospinal fluid levels of the protein are increased in AD patients compared to healthy controls. In addition, increased levels of neurogranin seem to be specific for AD since the levels seem not to be increased in other diseases affecting the central nervous system [30].

  • Blood-based biomarkers—Dr Nicholas Ashton

The rapid advancement of ultra-sensitive platforms for protein analysis has enabled the investigation of neuropathological proteins to be measured readily in blood samples. This has tremendous implications for the clinical management and patient monitoring in therapeutic trials of neurodegenerative diseases. This lecture began with an overview of the previous two decades of efforts in the search for a blood-based biomarker for AD, focusing on the challenges and limitations that have been encountered. Building on lectures covering the advancements in immunological assays and mass spectrometry, it discussed the latest research in how amyloid and neurofilament light proteins measured in blood predict cognitive decline and related imaging measures [30,31,32,33].

  • Lipidomics and metabolomics—Dr Jörg Hanrieder

Imaging mass spectrometry is an emerging chemical imaging modality allowing comprehensive delineation of spatial distribution pattern of biochemical species in situ, including metabolites, neurotransmitters, lipids, neuropeptides, and small proteins [34]. The lecture covered basic principles of imaging MS modalities along with the more established “omics” method paradigms based on tissue and body fluid extraction and liquid chromatography and mass spectrometry. A particular focus lies here on using these novel tools for probing neurodegenerative disease pathology both in human brain as well as in animal model systems [35].

  • Tau species as biomarkers in tauopathies—Dr Kina Höglund

The role of CSF total tau was discussed across both AD and other tauopathies. The value of tau assays to measure tau and p-tau was examined, looking at their diagnostic significance in primary and secondary tauopathies. The lecture also highlighted the complexity and heterogeneity of tau in CSF, where several tau fragments coming from proteolytic cleavage are present, which are not measured by traditional assays [36, 37]. Results from novel assay directed to N-terminal and C-terminal protein fragments were also presented, suggesting that their implementation in research settings could improve both the diagnostic profiling of tauopathies and the understanding of the disease aetiology.

  • Other MRI biomarkers—Dr Joana Pereira

This lecture introduced the students to the growing field of brain connectomics and the methods that can be used to assess functional and structural brain connectivity on functional magnetic resonance imaging and diffusion tensor imaging. It also provided a detailed description of the properties of the human brain connectome using concepts from graph theory [38]. For instance, the small-worldness is a property that can be used to characterise the balance between long-distance and short-distance brain connectivity whereas the modularity defines how well the whole brain network can be subdivided into subnetworks which generally overlap with well-known brain systems. These network properties and many others can be used to reveal fundamental aspects of normal brain organisation and highlight important aspects of underlying brain pathology in neurodegenerative disorders such as Alzheimer’s disease. For example, there is increasing evidence that brain regions with a higher number of connections show a greater disease-related vulnerability and may constitute important pathways for the spread of brain pathology such as amyloid-β and tau. Thus, network models could be used to monitor disease progression along connectional pathways and improve the early diagnosis of neurodegenerative diseases.

  • Biomarker panels for protein profiling—Ms Hanna Mann

There are many different approaches to identify potential biomarkers, and genomic technologies have historically led the way, but this does not provide us with the whole story. This presentation focussed on protein biomarker discovery using the Proximity Extension Assay (PEA) technology from Olink Proteomics, making it possible to analyse over 1100 protein biomarkers using very small volumes of plasma, serum, or CSF and how multi-omics approaches can advance precision medicine [39].

There was a specific focus on the two Neurology protein panels and examples from scientific publications in the neurology field. Multi-omics strategies and large data sets present new opportunities but also challenges when designing and implementing biomarker studies, and this lecture included an introduction to different study design scenarios.

  • Molecular imaging in Parkinson’s disease—Dr Andrea Varrone

This lecture provided an overview of the neuropathological features of movement disorders and Parkinson’s disease and its relevance to imaging. Three major topics were discussed: protein misfolding, neurodegeneration, and microglia activation. Emphasis was given to the description of how PET can be applied to image those pathological features in vivo.

The first part of the lecture discussed the status of PET imaging of alpha-synuclein, tau and amyloid-β. At present, the development of a PET tracer for imaging alpha-synuclein is still a major challenge, mainly due to the fact that high affinity and selectivity are required to be able to image Lewy pathology in vivo. More data are available on tau and amyloid imaging in Parkinson’s disease and related movement disorders. A systematic review has shown that the prevalence of amyloid-positive cases is approximately 70% in case of dementia with Lewy bodies (DLB) and approximately 1/3 in cases of PD with dementia [40]. Tau accumulation increases in the spectrum of Lewy body disease and the load of tau increases together with burden of amyloid [41]. In DLB, amyloid burden tends to be lower than in AD. In the DLB cases that are amyloid positive, there is a greater involvement of primary cortices and less prominent involvement of the temporal cortex [41].

Specific areas of tau accumulation have been reported in patients with progressive supranuclear palsy, with more prominent involvement of the globus pallidus, substantia nigra, and dentate nucleus of the cerebellum [42]. Extended involvement of the white matter has been associated with increase of severity of motor symptoms [43]. In corticobasal syndrome, tau accumulation has been observed in the white matter with prevalent involvement of the precentral gyrus [44]. First-generation tau tracers used so far do present some limitations, related to the presence of off-target binding in some areas, such as the basal ganglia, that are primarily affected by the pathology. The introduction of second-generation tau radioligands might be useful to evaluate more specifically the patterns of tau observed in PSP and CBS.

The second part of the lecture has focussed on the review of the tracers available to study nigrostriatal dopaminergic degeneration in PD. The current view is that alpha-synuclein accumulation is associated with synaptopathy leading to early degeneration in the synaptic terminals, followed by later degeneration in the axons and cell bodies of the substantia nigra. The development of 18F-FE-PE2I as DAT tracer has provided for the first time the possibility to study in vivo the entire nigrostriatal system [45]. In early PD patients, the DAT along the axons and in the substantia nigra is relatively preserved compared with the striatum, suggesting that most of the cell bodies and projections are still preserved in the early stages of the disease and their function might be restored with proper treatment.

The third part of the lecture has reviewed the status of imaging of microglia activation in PD and related disorders. Initial studies with the first-generation TSPO radioligand [11C]PK11195 have reported increased binding to TSPO in PD, as well as in MSA, PSP, and CBD. Subsequent studies in PD patients with second-generation TSPO radioligands have not replicated the initial findings [46, 47]. Therefore, it is still controversial whether it is possible to image microglia activation in PD, considering the complexity of the process and the different expression in relation to the stage of the disease.

  • Concordance of fluid- and imaging-based biomarkers—Dr Niklas Mattsson

CSF biomarkers and PET have similar and high accuracy to detect Aβ pathology in vivo, especially at the dementia stage of AD [48]. However, some studies suggest that reductions in CSF Aβ1–42 may precede increased uptake of Aβ PET [49, 50]. This discrepancy has been used to study the earliest regions affected by Aβ accumulation in AD [51] and to construct an in vivo amyloid PET staging system to monitor the spatiotemporal spread of Aβ [52]. For tau, most CSF and PET measures are only moderately correlated which each other [53, 54]. One possible explanation for this is that CSF tau measures change early and reflect the presence of a disease state of AD, while tau PET changes progressively over the course of the disease and is more related to the disease stage. Available data suggest that CSF tau may represent changes in the soluble metabolism of tau in response to beta-amyloid pathology, which precede the deposition of tau aggregates that is visualised by tau PET [55, 56].

Course organisation

Dr Michael Schöll (University of Gothenburg and University College London) is an Associate Professor in Molecular Medicine (UGOT) and a Principal Research Fellow (UCL) with a focus on neuroimaging. He started the course in Gothenburg in 2018 in collaboration with Professor Henrik Zetterberg. His research aims to use neuroimaging and neuropathological changes to assess neurodegeneration in comparison to healthy ageing.

Dr Ross W Paterson (University College London) is a Senior Research Fellow and Honorary Consultant Neurologist at the Dementia Research Centre at UCL with interests in CSF biomarkers in neurodegenerative diseases and young onset and rapidly progressive dementias.

Ayesha Khatun (University College London) is a Study Coordinator for the local Familial AD study at The Dementia Research Centre, with an MSc in Neuroscience and an interest in fluid biomarkers in dementia.

Future directions

The course will be offered again at the University of Gothenburg in April 2020. Interested PhD students are invited to contact or and visit the following website for more information:

Future revisions of the courses aim to include biomarkers encompassing an even wider reach of neurodegenerative diseases. We further aim to include a biomarker statistics workshop and a scientific paper writing class, as well as focus on emerging novel tools and techniques that probe alternative neurophysiological data and novel biomarkers.


Given the developments in disease-modifying drugs for neurodegenerative diseases, especially AD, there is a clear need for educational efforts delivering the latest research from both the fields of imaging- and fluid-derived biomarkers for neurodegenerative diseases. The UGOT/UCL course organised in 2018 and 2019, with plans to offer the course on an annual basis, aims to provide a comprehensive learning and networking platform for international doctoral-level (and above) biomarker researchers. We believe that bringing together prominent lecturers and the next generation of researchers in the biomarker field will result in informed and orchestrated scientific endeavours as well as in creating an open international scientific community.

Availability of data and materials

This review does not contain any analysable data. All sources cited in this paper are publicly available.





Alzheimer’s disease


Amyloid precursor protein


Amyloid-related imaging abnormalities


Cerebrospinal fluid


Frontotemporal lobar degeneration


Fused in sarcoma


Microtubule-associated protein tau


Magnetic resonance imaging


Parkinson’s disease


Positron emission tomography


Region of interest


Standardised uptake value ratio


TAR DNA-binding protein 43


  1. 1.

    Thal DR, Del Tredici K, Braak H. Neurodegeneration in normal brain aging and disease. Sci Aging Knowledge Environ. 2004;23:pe26.

    Google Scholar 

  2. 2.

    Braak H, Braak E. Staging of Alzheimer’s disease-related neurofibrillary changes. Neurobiol Aging. 1995;16(3):271–8 discussion 278–84.

    CAS  PubMed  Google Scholar 

  3. 3.

    Mirra SS, Heyman A, Mckeel D, Sumi SM, Crain BJ, Brownlee LM, Vogel FS, Hughes JP, van Belle G, Berg L. The Consortium to Establish a Registry for Alzheimer’s Disease (CERAD). Part II. Standardisation of the neuropathologic assessment of Alzheimer’s disease. Neurology. 1991;41(4):479–86.

    CAS  PubMed  Google Scholar 

  4. 4.

    Montine TJ, Phelps CH, Beach TG, Bigio EH, Cairns NJ, Dickson DW, Duyckaerts C, Frosch MP, Masliah E, Mirra SS, Nelson PT, Schneider JA, Thal DR, Trojanowski JQ, Vinters HV, Hyman BT. National Institute of Aging; Alzheimer’s Association. National Institute on Aging-Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach. Acta Neuropathol. 2012;123(1):1–11.

    CAS  PubMed  Google Scholar 

  5. 5.

    Lashley T, Rohrer J, Bandopadhyay R, et al. A comparative clinical, pathological, and biochemical study of FUS proteinopathies. Brain. 2011;134(Pt 9):2548–64.

    PubMed  PubMed Central  Google Scholar 

  6. 6.

    Lashley T, Rohrer JD, Mead S, Revesz T. Review: an update on clinical, genetic, and pathological aspects of frontotemporal lobar degenerations. Neuropathol Appl Neurobiol. 2015;41(7):858–81.

    PubMed  Google Scholar 

  7. 7.

    Mathis CA, Lopresti BJ, Ikonomovic MD, Klunk WE. Small molecule PET tracers for imaging proteinopathies. Semin Nucl Med. 2017;47:553–75.

    PubMed  PubMed Central  Google Scholar 

  8. 8.

    Heurling K, et al. Quantitative positron emission tomography in brain research. Brain Res. 2017;1670:220–34.

    CAS  PubMed  Google Scholar 

  9. 9.

    Selkoe DJ, Hardy J. The amyloid hypothesis of Alzheimer’s disease at 25 years. EMBO Mol Med. 2016;8(6):595–608.

    CAS  PubMed  PubMed Central  Google Scholar 

  10. 10.

    Dementia: assessment, management and support for people living with dementia and their carers. NICE guideline (NG97). Published date: June 2018.

  11. 11.

    Frisoni GB, Fox NC, Jack CR Jr, Scheltens P, Thompson PM. The clinical use of structural MRI in Alzheimer’s disease. Nat Rev Neurol. 2010;6(2):67–77.

    PubMed  PubMed Central  Google Scholar 

  12. 12.

    Harper L, Fumagalli GG, Barkhof F, Scheltens P, O’Brien JT, Bouwman F, Burton EJ, Rohrer JD, Fox NC, Ridgway GR, Schott JM. MRI visual rating scales in the diagnosis of dementia: evaluation in 184 post-mortem confirmed cases. Brain. 2016;139(Pt 4):1211–25.

    PubMed  PubMed Central  Google Scholar 

  13. 13.

    Jack CR, Bennett DA, Blennow K, Carillo MC, Dunn B, Haeberlein SB, Holtzman DM, Jagust W, Jessen F, Karlawish J, Liu E, Molineuvo JL, Montine T, Phelps C, Rankin KP, Rowe CC, Scheltens P, Siemers E, Snyder HM, Sperling R. NIA-AA research framework: toward a biological definition of Alzheimer’s disease. Alzheimers Dement. 2018;14:535–62.

    PubMed  PubMed Central  Google Scholar 

  14. 14.

    Jagust WJ. Imaging the evolution of pathophysiology of Alzheimer’s disease. Nat Rev Neurosci. 2018;19:687–700.

    CAS  PubMed  PubMed Central  Google Scholar 

  15. 15.

    Jack CR Jr, Knopman DS, Jagust WJ, Peterson RC, Weiner MW, Aisen PS, Shaw LM, Vemuri P, Wiste HJ, Weigand SD, Lesnick TG, Panktratz VS, Donohue MC, Trojanowski JQ. Tracking pathophysiological processes in Alzheimer’s disease: an updated hypothetical model of dynamic biomarkers. Lancet Neurol. 2013;12(2):207–16.

    CAS  PubMed  PubMed Central  Google Scholar 

  16. 16.

    Kato T, Inui Y, Nakamura A, Ito K. Brain fluorodeoxyglucose (FDG) PET in dementia. Ageing Res Rev. 2016;30:73–84.

    PubMed  Google Scholar 

  17. 17.

    Chen MK, Mecca AP, Naganawa M, Finnema SJ, Toyonaga T, Lin SF, Najafzadeh S, Ropchan J, Lu Y, McDonald JW, Michalak HR, Nabulsi NB, Arnsten AFT, Huang Y, Carson RE, van Dyck CH. Assessing synaptic density in Alzheimer’s disease with synaptic vesicle glycoprotein 2A positron emission tomographic imaging. JAMA Neurol. 2018;75(10):1215–24.

    PubMed  PubMed Central  Google Scholar 

  18. 18.

    Olsson B, Lautner R, Andreasson U, Öhrfelt A, Portelius E, Bjerke M, Hölttä M, Rosèn C, Olsson C, Strobel G, Wu E, Dakin E, Petzold M, Blennow K, Zetterberg H. CSF and blood biomarkers for the diagnosis of Alzheimer’s disease: a systematic review and meta-analysis. Lancet Neurol. 2016;15(7):673–84.

    CAS  PubMed  Google Scholar 

  19. 19.

    Duits FH, Martinez-Lage P, Paquet C, Engelborghs S, Lleó A, Hausner L, Molinuevo JL, Stomrud E, Farotti L, IHGB R, Tsolaki M, Skarsgárd C, Åstrand R, Wallin A, Vyhnalek M, Holmber-Clausen M, Forlenza OV, Ghezzi L, Ingelsson M, Hoff EI, Roks G, de Mendoca A, Papma JM, Izagirre A, Taga M, Struyfs H, Alcolea DA, Frölich L, Balasa M, Minthon L, JWR T, Persso S, Zetterberg H, van der Flier WM, Teunissen CE, Scheltens P, Blennow K. Performance and complications of lumbar puncture in memory clinics: results of the multicenter lumbar puncture feasibility study. Alzheimers Dement. 2016;12(2):154–63.

    PubMed  Google Scholar 

  20. 20.

    Shaw LM, Arias J, Blennow K, Galasko D, Molinuevo JL, Salloway S, Schindler S, Carrillo MC, Hendrix JA, Ross A, Illes J, Ramus C, Fifer S. Appropriate criteria for lumbar puncture and cerebrospinal fluid testing in the diagnosis of Alzheimer’s disease. Alzheimers Dement. 2018;14(11):1505–21.

    PubMed  Google Scholar 

  21. 21.

    Andreasson U, et al. Update on ultrasensitive technologies to facilities research on blood biomarkers for central nervous system disorders. Alzheimers Dement (Amst). 2016;3:98–102.

    Google Scholar 

  22. 22.

    Andreasson U, et al. A practical guide to immunoassay method validation. Front Neurol. 2015;6:179. eCollection 2015.

  23. 23.

    Hosp F, Mann M. A primer on concepts and applications of proteomics in neuroscience. Neuron. 2017;96(3):558–71.

    CAS  PubMed  Google Scholar 

  24. 24.

    Gobom J. Advancing cerebrospinal fluid biomarker discovery by mass spectrometry. Neurodegenerative Dis Manag. 2015;5(5):371–3.

    Google Scholar 

  25. 25.

    Brinkmalm A, et al. Fluid-based proteomics targeted on pathophysiological processes and pathologies in neurodegenerative diseases. J Neurochem. 2018.

  26. 26.

    Sato C, Barthémely NR, Mawuenyega KG, Patterson BW, Gordon BA, Jockel-Balsarotti J, Sullivan M, Crisp MJ, Kasten T, Kirmess KM, Kanaan NM, Yarasheski KE, Baker-Nigh A, Benziger TLS, Miller TM, Karch CM, Bateman RJ. Tau kinetics in neurons and the human central nervous system. Neuron. 2018;98(4):861–4.

    CAS  PubMed  PubMed Central  Google Scholar 

  27. 27.

    Maia LF, Kaeser SA, Reichwald J, Hruscha M, Martus P, Staufenbiel M, Jucker M. Changes in amyloid-β and Tau in cerebrospinal fluid of transgenic mice overexpressing amyloid precursor protein. Sci Transl Med. 2013;5(194):194re2.

    PubMed  Google Scholar 

  28. 28.

    Andreasen N, Blennow K, Zetterberg H. Neuroinflammation screening in immunotherapy trials against Alzheimer’s disease. Int J Alzheimers Dis. 2010;2010:638379.

    PubMed  PubMed Central  Google Scholar 

  29. 29.

    Hampel H, Frank R, Broich K, Teipel SJ, Katz RG, Hardy J, Herholz K, Bokde AL, Jessen F, Hoessler YC, Sanhai WR, Zetterberg H, Woodcock J, Blennow K. Biomarkers for Alzheimer’s disease: academic, industry and regulatory perspectives. Nat Rev Drug Discov. 2010;9(7):560–74.

    CAS  PubMed  Google Scholar 

  30. 30.

    Portelius E, Olsson B, Höglund K, Cullen NC, Kvartsberg H, Andreasson U, Zetterberg H, Sandelius Å, Shaw LM, Lee VMY, Irwin DJ, Grossman M, Weintraub D, Chen-Plotkin A, Wolk DA, McCluskey L, Elman L, McBride J, Toledo JB, Trojanowski JQ, Blennow K. Cerebrospinal fluid neurogranin concentration in neurodegeneration: relation to clinical phenotypes and neuropathology. Acta Neuropathol. 2018;136(3):363–76.

    CAS  PubMed  PubMed Central  Google Scholar 

  31. 31.

    Khalil M, Teunisse CE, Otto M, Piehl F, Sormani MP, Gattringer T, Barro C, Kappos L, Comabella M, Fazekas F, Petzold A, Blennow K, Zetterberg H, Kuhle J. Neurofilaments as biomarkers in neurological disorders. Nat Rev Neurol. 2018;14(10):577–89.

    CAS  PubMed  Google Scholar 

  32. 32.

    Ashton NJ, Schöll M, Heurling K, Gkanatsiou E, Portelius E, Höglund K, Brinkmalm G, Hye A, Blennow K, Zetterberg H. Update on biomarkers for amyloid pathology in Alzheimer’s disease. Biomark Med. 2018;12(7):799–812.

    CAS  PubMed  Google Scholar 

  33. 33.

    Zetterberg H, Blennow K. From cerebrospinal fluid to blood; the third wave of fluid biomarkers for Alzheimer’s disease. J Alzheimers Dis. 2018;64(s1):S271–9.

    PubMed  Google Scholar 

  34. 34.

    Michno W, Wehrli PM, Blennow K, Zetterberg H, Hanrieder J. Molecular imaging mass spectrometry for probing protein dynamics in neurodegenerative diseases pathology. J Neurochem. 2018.

  35. 35.

    Michno W, Nyström S, Wehrli P, Lashley T, Brinkmalm G, Guerard L, Syvänen S, Sehlin D, Kaya I, Brinet D, Nilsson KPR, Hammarström P, Blennow K, Zetterberg H, Hanrieder J. Pyroglutamation of amyloid-βx-42 (Aβx-42) followed by Aβ1-40 deposition underlies plaque polymorphism in progressing Alzheimer’s disease pathology. J Biol Chem. 2019;294(17):6719–32.

    CAS  PubMed  PubMed Central  Google Scholar 

  36. 36.

    Quinn JP, Corbett NJ, Kellett KAB, Hooper NM. Tau proteolysis in the pathogenesis of tauopathies: neurotoxic fragments and novel biomarkers. J Alzheimers Dis. 2018;63(1):13–33.

    CAS  PubMed  PubMed Central  Google Scholar 

  37. 37.

    Meredith JE, Sankaranaravanan S, Guss V, Lanzetti AJ, Berisha F, Neely RJ, Slemmon JR, Portelius E, Zetterberg H, Blennow K, Soares H, Ahlijanian M, Albright CF. Characterization of novel CSF tau and ptau biomarkers for Alzheimer’s disease. PLoS One. 2013;8(10):e76523.

    CAS  PubMed  Google Scholar 

  38. 38.

    Sporns Olaf. The human connectome: a complex network. Ann New York Acad Sci. 2011;1:109–25.

    Google Scholar 

  39. 39.

    Assarsson E, Lundberg M, Holmquist G, Björkesten J, Thorsen SB, Ekman D, Eriksson A, Rennel Dickens E, Ohlsson S, Edfeldt G, Andersson A-C, Lindstedt P, Stenvang J, Gullberg M, Fredriksson S. Homogenous 96-plex PEA immunoassay exhibiting high sensitivity, specificity, and excellent scalability. PLoS One. 2014;9(4):e95192. eCollection 2014.

    PubMed  PubMed Central  Google Scholar 

  40. 40.

    Petrou M, Dwamena BA, Foerster BR, MacEachern MP, Bohnen NI, Müller ML, Albin RL, Frey KA. Amyloid deposition in Parkinson’s disease and cognitive impairment: a systematic review. Mov Disord. 2015;30(7):928–35.

    CAS  PubMed  PubMed Central  Google Scholar 

  41. 41.

    Lee SH, Cho H, Choi JY, Lee JH, Ryu YH, Lee MS, Lyoo CH. Distinct patterns of amyloid-dependent tau accumulation in Lewy body diseases. Mov Disord. 2018;33(2):262–72.

    CAS  PubMed  Google Scholar 

  42. 42.

    Cho H, Choi JY, Hwang MS, Lee SH, Ryu YH, Lee MS, Lyoo CH. Subcortical (18)F-AV-1451 binding patterns in progressive supranuclear palsy. Mov Disord. 2017;32(1):134–40.

    CAS  PubMed  Google Scholar 

  43. 43.

    Endo H, Shimada H, Sahara N, Ono M, Koga S, Kitamura S, Niwa F, Hirano S, Kimura Y, Ichise M, Shinotoh H, Zhang MR, Kuwabara S, Dickson DW, Toda T, Suhara T, Higuchi M. In vivo binding of a tau imaging probe, [(11) C]PBB3, in patients with progressive supranuclear palsy. Mov Disord. 2019;34(5):744–54.

    CAS  PubMed  PubMed Central  Google Scholar 

  44. 44.

    Kikuchi A, Okamura N, Hasegawa T, Harada R, Watanuki S, Funaki Y, Hiraoka K, Baba T, Sugeno N, Oshima R, Yoshida S, Kobayashi J, Ezura M, Kobayashi M, Tano O, Mugikura S, Iwata R, Ishiki A, Furukawa K, Arai H, Furumoto S, Tashiro M, Yanai K, Kudo Y, Takeda A, Aoki M. In vivo visualization of tau deposits in corticobasal syndrome by 18F-THK5351 PET. Neurology. 2016;87(22):2309–16.

    CAS  PubMed  PubMed Central  Google Scholar 

  45. 45.

    Fazio P, Svenningsson P, Cselényi Z, Halldin C, Farde L, Varrone A. Nigrostriatal dopamine transporter availability in early Parkinson’s disease. Mov Disord. 2018;33(4):592–9.

    CAS  PubMed  Google Scholar 

  46. 46.

    Koshimori Y, Ko JH, Mizrahi R, Rusjan P, Mabrouk R, Jacobs MF, Christopher L, Hamani C, Lang AE, Wilson AA, Houle S, Strafella AP. Imaging striatal microglial activation in patients with Parkinson’s disease. PLoS One. 2015;10(9):e0138721.

    PubMed  PubMed Central  Google Scholar 

  47. 47.

    Varnäs K, Cselényi Z, Jucaite A, Halldin C, Svenningsson P, Farde L, Varrone A. PET imaging of [(11)C]PBR28 in Parkinson’s disease patients does not indicate increased binding to TSPO despite reduced dopamine transporter binding. Eur J Nucl Med Mol Imaging. 2019;46(2):367–75.

    PubMed  Google Scholar 

  48. 48.

    Blennow K, Mattsson N, Schöll M, Hansson O, Zetterberg H. Amyloid biomarkers in Alzheimer’s disease. Trends Pharmacol Sci. 2015;36:297–309.

    CAS  PubMed  Google Scholar 

  49. 49.

    Mattson N, Insel PS, Donohue M, Landau S, Jagust W, Shaw LM, Trojanowski JQ, Zetterberg H, Blennow K, Weiner M. Independent information from cerebrospinal fluid β-amyloid and florbetapir imaging in Alzheimer’s disease. Brain. 2015;138:772–83.

    Google Scholar 

  50. 50.

    Palmqvist S, Mattsson N, Hansson O. Cerebrospinal fluid analysis detects cerebral β-amyloid accumulation earlier than positron emission tomography. Brain. 2016;139:1226–36.

    PubMed  PubMed Central  Google Scholar 

  51. 51.

    Palmqvist S, Schöll M, Mattsson N, Stomrud E, Zetterberg H, Blennow K, Landau S, Jagust W, Hansson O. ADNI, BioFINDER study. The first stage of amyloid-β accumulation: where it starts and how it affects brain connectivity and neurodegeneration. Nat Commun. 2018;8:1214.

    Google Scholar 

  52. 52.

    Mattsson N, Palmqvist S, Stomrud E, Vogel JW, Hansson O. Staging β-amyloid pathology with amyloid PET imaging. JAMA Neurol. 2019.

    Google Scholar 

  53. 53.

    Gordon BA, Friedrichsen K, Brier M, Blazey T, Su Y, Christensen J, Aldea P, McConathy J, Holtzman DM, Cairns NJ, Morris JC, Fagan AM, Ances BM, Benziger TL. The relationship between cerebrospinal fluid markers of Alzheimer pathology and positron emission tomography tau imaging. Brain. 2016;139(Pt 8):2249–60.

    PubMed  PubMed Central  Google Scholar 

  54. 54.

    Chhatwal JO, Schultz AP, Marshall GA, Boot B, Gomez-Isla T, Dumurgier J, LaPoint M, Scherzer C, Roe AD, Hyman BT, Sperling RA, Johnson KA. Temporal T807 binding correlates with CSF tau and phospho-tau in normal elderly. Neurology. 2016;87(9):920–6.

    CAS  PubMed  PubMed Central  Google Scholar 

  55. 55.

    Mattson N, Schöll M, Strandberg O, Smith R, Palmqvist S, Insel PS, Hägerström D, Ohlsson T, Zetterberg H, Jögi J, Blennow K, Hansson O. 18F-AV-1451 and CSF T-tau and P-tau as biomarkers in Alzheimer’s disease. EMBO Mol Med. 2017;9:1212–23.

    Google Scholar 

  56. 56.

    Mattsson N, Smith R, Strandberg O, Palmqvist S, Schöll M, Insel PS, Hägerström D, Ohlsson T, Zetterberg H, Blennow K, Jögi J, Hansson O. Comparing 18F-AV-1451 with CSF T-tau and P-tau for diagnosis of Alzheimer’s disease. Neurology. 2018;90:388–95.

    Google Scholar 

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The UCL Biomedical Research Centre (BRC) provided funding for the “Biomarkers in neurodegeneration” course that this review is based on. Olink Proteomics provided funding for social activities. RWP is funded as an NIHR Academic Clinical Lecturer. MS is funded by the Knut and Alice Wallenberg Foundation (WCMTM), the Swedish Research Council, the Swedish Alzheimer Foundation, and the Swedish ALF agreement. Open access funding provided by University of Gothenburg.

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AK, MS, and RWP wrote the manuscript and MS critically reviewed the manuscript. All authors read and approved the final manuscript.

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This review article is part of a series of articles that has stemmed from the “Biomarkers in Neurodegeneration” 2019 course run collaboratively between UCL and the University of Gothenburg. The attendees of this course have authored the other articles in this series with the presenters of this course critically reviewing their work.

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Correspondence to Michael Schöll.

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Khatun, A., Paterson, R.W. & Schöll, M. University College London/University of Gothenburg PhD course “Biomarkers in neurodegenerative diseases” 2019—course organisation. Alz Res Therapy 12, 18 (2020).

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  • Neurodegenerative diseases
  • Biomarkers
  • Tau
  • Amyloid
  • Positron emission tomography
  • Magnetic resonance imaging
  • Cerebrospinal fluid
  • Blood biomarkers