Evidence map›Paper›PMID 41195759›Full record

ArticleHuman brain mapping2025

Investigating Disruptions in Information Flow due to Sickle Cell Disease Using Granger Causality.

Nahom Mossazghi, Helmet T Karim, Nadim Farhat, Tales Santini, Enrico M Novelli, Tamer Ibrahim, Sossena Wood

Abstract read
In one paragraph

Article in Human brain mapping, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

7 authors.

Nahom MossazghiDepartment of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania, USA.
Helmet T KarimDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID 0000-0002-9286-0694
Nadim FarhatDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Tales SantiniDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Enrico M NovelliDepartment of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Tamer IbrahimDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Sossena WoodDepartment of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania, USA.ORCID 0000-0003-3079-1096

Funding

Imaging Advancements in Small Vessel and CSF Flow Pathophysiology of Pre-clinical Alzheimer's DiseaseR01AG063525 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI AIZENSTEIN, HOWARD J, COHEN, ANN D. · 2019 to 2023
$3.7M
Neurovascular Determinants of Cognitive Function in Adults with Sickle Cell DiseaseR01HL127107 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NOVELLI, ENRICO M · 2016 to 2020
$3.6M
High Performance Imaging for Assessment of Small Vessel Disease in Older Adults with DepressionR01MH111265 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI AIZENSTEIN, HOWARD J, IBRAHIM, TAMER S · 2016 to 2020
$3.6M
Bioengineering in Psychiatry Training ProgramT32MH119168 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI AIZENSTEIN, HOWARD J, IBRAHIM, TAMER S · 2019 to 2023
$1.1M
Integrative Training in Neural InterfacingT32EB029365 · NIBIB · CARNEGIE-MELLON UNIVERSITY · PI HE, BIN · 2021 to 2025
$1.0M
Center for Machine Learning and Health, School of Computer Science, Carnegie Mellon UniversityNHLBI NIH HHS R01 HL127107NIA NIH HHS R01 AG063525NIBIB NIH HHS T32 EB029365NIH HHS R01AG063525NIH HHS R01HL127107NIH HHS R01MH111265NIH HHS T32EB029365-04NIH HHS T32MH119168NIMH NIH HHS R01 MH111265NIMH NIH HHS T32 MH119168
6 · The paper itself

Abstract

Sickle cell disease (SCD) is an inherited blood disorder caused by a mutation in the beta-globin gene, resulting in chronic complications, including cognitive decline-particularly in executive functions. Neuroimaging studies have identified structural and functional abnormalities associated with SCD; however, the directionality of information flow between brain networks and how disruptions in these interactions contribute to cognitive deficits remains poorly understood. This study employed Granger causality (GC) analysis to investigate effective connectivity and information flow between brain regions and resting-state networks using ultra-high-field 7T MRI in adult patients with SCD (n = 51) and age-, sex-, and race-matched controls (n = 44). We first performed a whole-brain network analysis, followed by an examination of specific brain regions within the default mode network (DMN), executive control network (ECN), dorsal attention network (DAN), and ventral attention network (VAN). For each analysis, we computed both the magnitude and directionality of information flow to capture the strength and directional influence of connectivity between brain regions. While patients with SCD exhibited a higher magnitude of information flow compared to controls, this difference was only statistically significant when computed at the brain region level, not at the resting-state network level. In terms of directionality, afferent flow from DAN and VAN to ECN was significantly greater in patients with SCD than in controls. Subtype analysis revealed that patients with severe SCD demonstrated significantly higher magnitude of information flow than those with mild SCD and controls. We also observed subtype-specific differences in afferent flow to ECN: mild SCD patients showed significant flow from VAN, while severe SCD patients showed significant flow from DAN. Additionally, multiple regression analyzes assessing correlations between information flow and cognitive performance showed that controls had higher R

Indexed as

Anemia, Sickle CellBrainCognitive DysfunctionConnectomeDefault Mode NetworkNerve NetAdultExecutive FunctionFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedYoung Adult7T MRIeffective connectivityexecutive control networkGranger causalityresting statesickle cell disease

Identifiers

PMID41195759
PMCPMC12590372

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.