Staging Hemodynamic Failure With Blood Oxygen-Level–Dependent Functional Magnetic Resonance Imaging Cerebrovascular Reactivity
Author(s) -
Jorn Fierstra,
Christiaan Hendrik Bas van Niftrik,
Geoffrey Warnock,
Susanne Wegener,
Marco Piccirelli,
Athina Pangalu,
Giuseppe Esposito,
Antonios Valavanis,
Alfred Buck,
Andreas R. Luft,
Oliver Bozinov,
Luca Regli
Publication year - 2018
Publication title -
stroke
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.397
H-Index - 319
eISSN - 1524-4628
pISSN - 0039-2499
DOI - 10.1161/strokeaha.117.020010
Subject(s) - medicine , cerebral blood flow , magnetic resonance imaging , hemodynamics , perfusion , cardiology , blood oxygen level dependent , positron emission tomography , functional magnetic resonance imaging , perfusion scanning , stroke (engine) , stage (stratigraphy) , neuroimaging , blood flow , nuclear medicine , radiology , mechanical engineering , paleontology , biology , engineering , psychiatry
Background and Purpose— Increased stroke risk correlates with hemodynamic failure, which can be assessed with (15 O-)H2 O positron emission tomography (PET) cerebral blood flow (CBF) measurements. This gold standard technique, however, is not established for routine clinical imaging. Standardized blood oxygen-level–dependent (BOLD) functional magnetic resonance imaging+CO2 is a noninvasive and potentially widely applicable tool to assess whole-brain quantitative cerebrovascular reactivity (CVR). We examined the agreement between the 2 imaging modalities and hypothesized that quantitative CVR can be a surrogate imaging marker to assess hemodynamic failure.Methods— Nineteen data sets of subjects with chronic cerebrovascular steno-occlusive disease (age, 60±11 years; 4 women) and unilaterally impaired perfusion reserve on Diamox-challenged (15 O-)H2 O PET were studied and compared with a standardized BOLD functional magnetic resonance imaging+CO2 examination within 6 weeks (8±19 days). Agreement between quantitative CBF- and CVR-based perfusion reserve was assessed. Hemodynamic failure was staged according to PET findings: stage 0: normal CBF, normal perfusion reserve; stage I: normal CBF, decreased perfusion reserve; and stage II: decreased CBF, decreased perfusion reserve. The BOLD CVR data set of the same subjects was then matched to the corresponding stage of hemodynamic failure.Results— PET-based stage I versus stage II could also be clearly separated with BOLD CVR measurements (CVR for stage I 0.11 versus CVR for stage II −0.03;P <0.01). Hemispheric and middle cerebral artery territory difference analyses (ie, affected versus unaffected side) showed a significant correlation for CVR impairment in the affected hemisphere and middle cerebral artery territory (P <0.01,R 2 =0.47 andP =0.02,R 2 = 0.25, respectively).Conclusions— BOLD CVR corresponded well to CBF perfusion reserve measurements obtained with (15 O-)H2 O-PET, especially for detecting hemodynamic failure in the affected hemisphere and middle cerebral artery territory and for identifying hemodynamic failure stage II. BOLD CVR may, therefore, be considered for prospective studies assessing stroke risk in patients with chronic cerebrovascular steno-occlusive disease, in particular because it can potentially be implemented in routine clinical imaging.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom