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Visual Assessment of Brain Perfusion MRI Scans in Dementia: a Pilot Study
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för kirurgiska vetenskaper, Radiologi.
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för kirurgiska vetenskaper, Radiologi.
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för kirurgiska vetenskaper, Radiologi.
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för kirurgiska vetenskaper.
Vise andre og tillknytning
2016 (engelsk)Inngår i: Journal of Neuroimaging, ISSN 1051-2284, E-ISSN 1552-6569, Vol. 26, nr 3, s. 324-330Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

PURPOSE: Functional imaging is becoming increasingly important for the detection of neurodegenerative disorders. Perfusion MRI with arterial spin labeling (ASL) has been reported to provide promising diagnostic possibilities but is not yet widely used in routine clinical work. The aim of this study was to compare, in a clinical setting, the visual assessment of subtracted ASL CBF maps with and without additional smoothing, to FDG-PET data.

METHODS: Ten patients with a clinical diagnosis of dementia and 11 age-matched cognitively healthy controls were examined with pseudo-continuous ASL (pCASL) and 18F-Fluorodeoxyglucose positron emission tomography (FDG-PET). Three diagnostic physicians visually assessed the pCASL maps after subtraction only, and after postprocessing using Gaussian smoothing and GLM-based beta estimate functions. The assessment scores were compared to FDG PET values. Furthermore, the ability to discriminate patients from healthy elderly controls was assessed.

RESULTS: Smoothing improved the correlation between visually assessed regional ASL perfusion scores and the FDG PET SUV-r values from the corresponding regions. However, subtracted pCASL maps discriminated patients from healthy controls better than smoothed maps. Smoothing increased the number of false-positive patient identifications. Application of beta estimate functions had only a marginal effect.

CONCLUSION: Spatial smoothing of ASL images increased false positive results in the discrimination of hypoperfusion conditions from healthy elderly. It also decreased interreader agreement. However, regional characterization and subjective perception of image quality was improved.

sted, utgiver, år, opplag, sider
2016. Vol. 26, nr 3, s. 324-330
Emneord [en]
Arterial spin labeling; smoothing; visual assessment; brain perfusion; clinical setting
HSV kategori
Identifikatorer
URN: urn:nbn:se:uu:diva-266305DOI: 10.1111/jon.12296ISI: 000382869200012PubMedID: 26376736OAI: oai:DiVA.org:uu-266305DiVA, id: diva2:867700
Tilgjengelig fra: 2015-11-06 Laget: 2015-11-06 Sist oppdatert: 2017-12-01bibliografisk kontrollert
Inngår i avhandling
1. ­­­Visual assessment of perfusion and metabolism in neurodegenerative dementia
Åpne denne publikasjonen i ny fane eller vindu >>­­­Visual assessment of perfusion and metabolism in neurodegenerative dementia
2016 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

A worldwide demographic shift is currently occurring, with rapidly increasing numbers of elderly individuals. Since the incidence of neurodegenerative disease generally increases with age, this entails an increase in dementia prevalence. There are several strong incentives for establishing robust and widely available imaging methods for the early diagnosis of these diseases. Atrophy patterns are evident only late in the disease process, and the distinction from healthy ageing can often be elusive. For early diagnosis, physiologic parameters such as perfusion or metabolism must be assessed. The available modalities all have restricted clinical usefulness. The main aim of this thesis was to advance the clinical usefulness of perfusion and metabolism imaging in patients with neurodegenerative dementia, with a focus on visual assessment.

A cohort of patients with neurodegenerative dementia was included, along with an age-matched control group. All subjects underwent MRI, including a pseudocontinuous ASL sequence and FDG-PET. In papers II and III, a subgroup containing both patients and controls underwent a second FDG-PET with reduced dose. In paper IV, the material was combined with a similar cohort from Amsterdam.

Paper I showed that spatial smoothing increased the correlation between visually assessed perfusion and metabolism levels as displayed with FDG-PET. However, the distinction between patients and healthy controls was less satisfactory due to false positives.

Paper II showed that differences in regional standard uptake value ratios between normal- and low-dose FDG-PET were small and without clinically significant bias.

Paper III showed that the diagnostic performance of Z-score maps showing regions of significant deficits in metabolism was highly similar in normal- and low-dose FDG-PET images. 

Paper IV showed that ASL perfusion-based Z-score maps can be used for diagnostic purposes with high specificity, but inferior sensitivity, compared to FDG-PET.

In conclusion, the included studies address aspects of the visual assessment of perfusion and metabolism neuroimaging, with a focus on clinical usefulness in diagnosing neurodegenerative dementia.

sted, utgiver, år, opplag, sider
Uppsala: Acta Universitatis Upsaliensis, 2016. s. 65
Serie
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, ISSN 1651-6206 ; 1266
Emneord
Dementia, Neurodegenerative, Brain imaging, Diagnostics, Neuroradiology, Neuroimaging, Demens, Neurodegenerativ, Hjärnavbildning, diagnostik, Neuroradiologi, Neuroimaging
HSV kategori
Forskningsprogram
Radiologi
Identifikatorer
urn:nbn:se:uu:diva-304731 (URN)978-91-554-9714-9 (ISBN)
Disputas
2016-12-07, Gunnesalen, Akademiska Sjukhuset, ing 10, 751 85, Uppsala, 09:00 (engelsk)
Opponent
Veileder
Tilgjengelig fra: 2016-11-14 Laget: 2016-10-08 Sist oppdatert: 2016-11-30

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