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A mathematical model for temporal cerebral blood flow response to acetazolamide evaluated in patients with Moyamoya disease
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för kirurgiska vetenskaper, Molekylär avbildning och medicinsk fysik. Uppsala Univ Hosp, Med Phys, Uppsala, Sweden.ORCID-id: 0000-0002-2502-6026
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för kirurgiska vetenskaper, Molekylär avbildning och medicinsk fysik. Uppsala Univ Hosp, Med Phys, Uppsala, Sweden.ORCID-id: 0000-0002-1498-1327
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för medicinska vetenskaper, Neurokirurgi.ORCID-id: 0000-0002-4556-5721
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för kirurgiska vetenskaper, Molekylär avbildning och medicinsk fysik. Uppsala Univ Hosp, Med Phys, Uppsala, Sweden.ORCID-id: 0000-0002-0853-9305
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2024 (engelsk)Inngår i: Magnetic Resonance Imaging, ISSN 0730-725X, E-ISSN 1873-5894, Vol. 110, s. 35-42Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Background: Paired cerebral blood flow (CBF) measurement is usually acquired before and after vasoactive stimulus to estimate cerebrovascular reserve (CVR). However, CVR may be confounded because of variations in time-to-maximum CBF response (tmax) following acetazolamide injection. With a mathematical model, CVR can be calculated insensitive to variations in tmax, and a model offers the possibility to calculate additional model-derived parameters. A model that describes the temporal CBF response following a vasodilating acetazolamide injection is proposed and evaluated.

Methods: A bi-exponential model was adopted and fitted to four CBF measurements acquired using arterial spin labelling before and initialised at 5, 15 and 25 min after acetazolamide injection in a total of fifteen patients with Moyamoya disease. Curve fitting was performed using a non-linear least squares method with a priori constraints based on simulations.

Results: Goodness of fit (mean absolute error) varied between 0.30 and 0.62 ml·100 g-1·min-1. Model-derived CVR was significantly higher compared to static CVR measures. Maximum CBF increase occurred earlier in healthy- compared to diseased vascular regions.

Conclusions: The proposed mathematical model offers the possibility to calculate CVR insensitive to variations in time to maximum CBF response which gives a more detailed characterisation of CVR compared to static CVR measures. Although the mathematical model adapts generally well to this dataset of patients with MMD it should be considered as experimental; hence, further studies in healthy populations and other patient cohorts are warranted.

sted, utgiver, år, opplag, sider
Elsevier, 2024. Vol. 110, s. 35-42
Emneord [en]
Acetazolamide, Cerebral blood flow, Cerebrovascular reserve, Modelling, Moyamoya disease
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Identifikatorer
URN: urn:nbn:se:uu:diva-530446DOI: 10.1016/j.mri.2024.03.044ISI: 001229899800001PubMedID: 38574981OAI: oai:DiVA.org:uu-530446DiVA, id: diva2:1865884
Forskningsfinansiär
Erik, Karin och Gösta Selanders FoundationThe Swedish Stroke AssociationThe Swedish Brain FoundationTilgjengelig fra: 2024-06-05 Laget: 2024-06-05 Sist oppdatert: 2024-06-05bibliografisk kontrollert

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Fahlström, MarkusSousa, Joao M.Svedung Wettervik, TeodorBerglund, JohanEnblad, PerLewén, AndersWikström, Johan
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