Evidence map›Paper›PMID 42065117›Full record

ArticleImaging neuroscience (Cambridge, Mass.)

Brain functional network connectivity interpolation characterizes the neuropsychiatric continuum and heterogeneity.

Xinhui Li, Eloy Geenjaar, Zening Fu, Godfrey D Pearlson, Vince D Calhoun

Abstract read
In one paragraph

Article in Imaging neuroscience (Cambridge, Mass.). 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

5 · Who and what money

Authors and funding

5 authors.

Xinhui LiTri-institutional Center for Translational Research in Neuroimaging and Data Science, Georgia State University, Georgia Institute of Technology, Emory University, Atlanta, GA, United States.ORCID https://orcid.org/0000-0001-5604-9493
Eloy GeenjaarTri-institutional Center for Translational Research in Neuroimaging and Data Science, Georgia State University, Georgia Institute of Technology, Emory University, Atlanta, GA, United States.ORCID https://orcid.org/0000-0001-5448-6358
Zening FuTri-institutional Center for Translational Research in Neuroimaging and Data Science, Georgia State University, Georgia Institute of Technology, Emory University, Atlanta, GA, United States.ORCID https://orcid.org/0000-0002-1591-4900
Godfrey D PearlsonDepartment of Psychiatry, School of Medicine, Yale University, New Haven, CT, United States.ORCID https://orcid.org/0000-0002-7525-5185
Vince D CalhounTri-institutional Center for Translational Research in Neuroimaging and Data Science, Georgia State University, Georgia Institute of Technology, Emory University, Atlanta, GA, United States.ORCID https://orcid.org/0000-0001-9058-0747

Funding

Multivariate methods for identifying multitask/multimodal brain imaging biomarkersR01EB006841 · NIBIB · THE MIND RESEARCH NETWORK · PI VINCE D CALHOUN, Sergey Plis · 2007 to 2026
$9.8M
Male/Female differences in psychosis and mood disorders:Dynamic imaging-genomic models for characterizing and predicting psychosis and mood dR01MH118695 · NIMH · GEORGIA STATE UNIVERSITY · PI ADALI, TULAY, CALHOUN, VINCE D · 2019 to 2023
$3.8M
Training in Computational Neural EngineeringT32EB025816 · NIBIB · GEORGIA INSTITUTE OF TECHNOLOGY · PI Michael Robert Borich, Christopher John Rozell · 2019 to 2026
$1.9M
NIBIB NIH HHS R01 EB006841NIBIB NIH HHS T32 EB025816NIMH NIH HHS R01 MH118695
6 · The paper itself

Abstract

Psychiatric and neurodevelopmental disorders such as schizophrenia (SZ) and autism spectrum disorder (ASD) are challenging to characterize in part due to their heterogeneous presentation in individuals, with symptoms now believed to exist on a continuum. Conventional diagnostic and neuroimaging analytical approaches rely on subjective assessment or group differences, but typically ignore progression between groups or heterogeneity within a group. To estimate the neuropsychiatric continuum and heterogeneity, we proposed a functional network connectivity (FNC) interpolation framework based on a variational autoencoder (VAE) using static FNC (sFNC) and dynamic FNC (dFNC) data from controls and patients with SZ or ASD. We demonstrated that VAEs significantly outperformed a linear baseline and a semi-supervised counterpart. For both sFNC and dFNC interpolation, the generated results effectively captured representative and generalizable properties in the original data. The interpolated continua from controls to patients in both SZ and ASD revealed group-wise gradients characterized by reduced positive correlations within the auditory, sensorimotor, and visual networks, as well as between the subcortical and cerebellar domains. In contrast, anti-correlations weakened between the subcortical domain and the sensory domains, and between the cerebellar domain and the sensory domains. Finally, we showed examples of how to generate continuous FNC data following group- or state-based trajectories in the VAE latent space. The proposed framework offers added advantages over traditional methods, including data-driven discovery of hidden relationships, visualization of individual differences, imputation of missing values along a continuous spectrum, and estimation of the stage where an individual falls within the continuum.

Indexed as

autism spectrum disorderfunctional network connectivitypsychosis continuumpsychosis heterogeneityschizophreniavariational autoencoder

Identifiers

PMID42065117
PMCPMC13125074

What OpenQuestion holds

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Registered trials

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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.