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Interaction of developmental venous anomalies with resting-state functional MRI measures

Abstract:

BACKGROUND AND PURPOSE: Functional MR imaging of the brain, used for both clinical and neuroscientific applications, relies on measuring fluctuations in blood oxygenation. Such measurements are susceptible to noise of vascular origin. The purpose of this study was to assess whether developmental venous anomalies, which are frequently observed normal variants, can bias fMRI measures by appearing as true neural signal.

MATERIALS AND METHODS: Large developmental venous anomalies (1 in each of 14 participants) were identified from a large neuroimaging cohort (n = 814). Resting-state fMRI data were decomposed using independent component analysis, a data-driven technique that creates distinct component maps representing aspects of either structured noise or true neural activity. We searched all independent components for maps that exhibited a spatial distribution of their signals following the topography of developmental venous anomalies.

RESULTS: Of the 14 developmental venous anomalies identified, 10 were clearly present in 17 fMRI independent components in total. While 9 (52.9%) of these 17 independent components were dominated by venous contributions and 2 (11.8%) by motion artifacts, 2 independent components (11.8%) showed partial neural signal contributions and 5 independent components (29.4%) unambiguously exhibited typical neural signal patterns.

CONCLUSIONS: Developmental venous anomalies can strongly resemble neural signal as measured by fMRI. They are thus a potential source of bias in fMRI analyses, especially when present in the cortex. This could impede interpretation of local activity in patients, such as in presurgical mapping. In scientific studies with large samples, developmental venous anomaly confounds could be mainly addressed using independent component analysis-based denoising.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.3174/ajnr.a5847

Authors


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Role:
Author
ORCID:
0000-0003-4390-3464
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Role:
Author
ORCID:
0000-0002-1238-6225
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Role:
Author
ORCID:
0000-0002-9706-7599
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Role:
Author
ORCID:
0000-0001-8966-3684
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Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author
ORCID:
0000-0003-1981-391X


Publisher:
American Society of Neuroradiology
Journal:
American Journal of Neuroradiology More from this journal
Volume:
39
Issue:
12
Pages:
2326-2331
Publication date:
2018-12-14
Acceptance date:
2018-08-25
DOI:
EISSN:
1936-959X
ISSN:
0195-6108
Pmid:
30385467


Language:
English
Keywords:
Pubs id:
pubs:943727
UUID:
uuid:87f1d916-fe79-474b-9aee-07da914cac6b
Local pid:
pubs:943727
Source identifiers:
943727
Deposit date:
2019-04-30

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