Evidence map›Paper›PMID 42210666›Full record

ArticleJournal of magnetic resonance imaging : JMRI2026

Cerebral Blood Transit in Sickle Cell Anemia.

Wesley T Richerson, Megan A Aumann, Alexander K Song, Samantha Davis, Lauren Milner, Maria Garza, Dann Martin, L Taylor Davis, Sumit Pruthi, Lori C Jordan and 1 more

Abstract read
In one paragraph

Article in Journal of magnetic resonance imaging : JMRI, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Wesley T RichersonDepartment of Neurology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Megan A AumannDepartment of Neurology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0002-3924-8455
Alexander K SongDepartment of Neurology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Samantha DavisDivision of Pediatric Neurology, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID https://orcid.org/0009-0004-5245-2647
Lauren MilnerDivision of Pediatric Neurology, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Maria GarzaDepartment of Neurology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Dann MartinDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
L Taylor DavisDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Sumit PruthiDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0002-4035-0852
Lori C JordanDepartment of Neurology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Manus J DonahueDepartment of Neurology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Funding

Biomarkers of ischemic brain injury in adults with sickle cell diseaseR01HL155207 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DONAHUE, MANUS J, JORDAN, LORI CHAFFIN · 2022 to 2025
$2.8M
Mechanisms of cerebral infarcts and brain oxygen utilization in anemiaR01NS123281 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Manus J Donahue, Lori Chaffin Jordan · 2022 to 2026
$2.4M
Cerebral blood flow resistance mapping to identify amyloid-related imaging abnormality (ARIA) risk in Alzheimer's diseaseF32AG097081 · NIA · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHERSON, WESLEY T · 2025 to 2025
$76k
NHLBI NIH HHS R01 HL155207NHLBI NIH HHS R01HL155207NIA NIH HHS F32 AG097081NIA NIH HHS F32AG097081NINDS NIH HHS R01 NS123281NINDS NIH HHS R01NS123281
6 · The paper itself

Abstract

backgroundSickle cell anemia (SCA) patients upregulate cerebral blood flow to compensate for decreased arterial oxygen content. Such hyperemic conditions can manifest as venous hyperintense signal on arterial spin labeling (ASL) MRI, which may reflect faster capillary blood transit, altered oxygen extraction fraction (OEF), and infarct risk. PURPOSE: To implement multi-delay ASL to quantify cerebral arterial arrival time (AAT), arterial transit time (ATT) to tissue, and venous arrival time (VAT) and to test whether reductions in these parameters are present in SCA and relate to condition severity. STUDY TYPE: Prospective, cross-sectional. SUBJECTS: Adults with SCA (n = 40; age = 28.1 ± 7.1 years; sex = 47.5% female) and nonanemic controls (n = 24; age = 30.6 ± 6.6 years; sex = 37.5% male). FIELD STRENGTH/SEQUENCE: 3 T 3D T ASSESSMENT: Multi-delay PASL was used to quantify AAT, gray matter ATT, VAT, and labeled venous blood volume. Venous hyperintensities and OEF were quantified from 3D pCASL and TRUST, respectively. Infarcts and vasculopathy were assessed from radiological review. STATISTICAL TESTS: AAT, gray matter ATT, VAT, and labeled venous blood volume were evaluated using a Wilcoxon rank-sum test; ANOVA assessed relationships with venous hyperintense signal. Continuous variable relationships were assessed using Spearman rank-correlation (significance: two-sided p < 0.05).

resultsVenous labeled blood volume was significantly increased in SCA (median = 0.015 mL; IQR = 0.0087-0.023 mL) versus control (median = 0.0047 mL; IQR = 0.0032-0.0092 mL) participants, whereas VAT was significantly reduced in SCA (median = 2.53 s; IQR = 2.23-2.72 s) versus control (median = 2.75 s; IQR = 2.63-2.80 s) participants. AAT, gray matter ATT, and VAT values were not significantly related to OEF (AAT: p = 0.38; gray matter ATT: p = 0.24; VAT: p = 0.48) or prior infarct (AAT: p = 0.99; gray matter ATT: p = 0.88; VAT: p = 0.98). AAT and gray matter ATT, but not VAT (p = 0.153), were directly related to hemoglobin.

conclusionSCA patients had elevated labeled venous blood volume and shorter VAT. Differential relationships between blood transit and hemoglobin across vascular compartments provides support for venous blood kinetics not representing a simple sequela of anemia severity. EVIDENCE LEVEL: 2. TECHNICAL STAGE OF DEVELOPMENT: 2.

Indexed as

Anemia, Sickle CellCerebrovascular CirculationMagnetic Resonance ImagingAdultBlood Flow VelocityBrainCerebral ArteriesCross-Sectional StudiesFemaleHumansMaleOxygenPerfusion Magnetic Resonance ImagingProspective StudiesSpin LabelsYoung AdultOxygenSpin Labelsarterial spin labelingarterial transit timebolus arrival timecapillary shuntingcerebral hemodynamicssickle cell anemia

Identifiers

PMID42210666
PMCPMC13387424

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.