Evidence map›Paper›PMID 29259537›Full record

ArticleFrontiers in neuroscience2017

A Hierarchical Bayesian Model for the Identification of PET Markers Associated to the Prediction of Surgical Outcome after Anterior Temporal Lobe Resection.

Sharon Chiang, Michele Guindani, Hsiang J Yeh, Sandra Dewar, Zulfi Haneef, John M Stern, Marina Vannucci

Abstract read
In one paragraph

Article in Frontiers in neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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.

Sharon ChiangDepartment of Statistics, Rice University, Houston, TX, United States.
Michele GuindaniDepartment of Statistics, University of California, Irvine, Irvine, CA, United States.
Hsiang J YehDepartment of Neurology, University of California, Los Angeles, Los Angeles, CA, United States.
Sandra DewarDepartment of Neurology, University of California, Los Angeles, Los Angeles, CA, United States.
Zulfi HaneefDepartment of Neurology, Baylor College of Medicine, Houston, TX, United States.
John M SternDepartment of Neurology, University of California, Los Angeles, Los Angeles, CA, United States.
Marina VannucciDepartment of Statistics, Rice University, Houston, TX, United States.

Funding

TRAINING PROGRAM IN COMPUTATIONAL BIOLOGY AND MEDICINET15LM007093 · NLM · RICE UNIVERSITY · PI Lydia E. Kavraki · 1992 to 2026
$20.8M
Training Program in Biostatistics for Cancer ResearchT32CA096520 · NCI · RICE UNIVERSITY · PI KIMMEL, MAREK, YUAN, YING · 2003 to 2023
$4.5M
Simutaneous fMRI and EEG of Epileptogenic Brain RegionsK23NS044936 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI STERN, JOHN M · 2004 to 2008
$807k
NCI NIH HHS T32 CA096520NINDS NIH HHS K23 NS044936NLM NIH HHS T15 LM007093
6 · The paper itself

Abstract

We develop an integrative Bayesian predictive modeling framework that identifies individual pathological brain states based on the selection of fluoro-deoxyglucose positron emission tomography (PET) imaging biomarkers and evaluates the association of those states with a clinical outcome. We consider data from a study on temporal lobe epilepsy (TLE) patients who subsequently underwent anterior temporal lobe resection. Our modeling framework looks at the observed profiles of regional glucose metabolism in PET as the phenotypic manifestation of a latent individual pathologic state, which is assumed to vary across the population. The modeling strategy we adopt allows the identification of patient subgroups characterized by latent pathologies differentially associated to the clinical outcome of interest. It also identifies imaging biomarkers characterizing the pathological states of the subjects. In the data application, we identify a subgroup of TLE patients at high risk for post-surgical seizure recurrence after anterior temporal lobe resection, together with a set of discriminatory brain regions that can be used to distinguish the latent subgroups. We show that the proposed method achieves high cross-validated accuracy in predicting post-surgical seizure recurrence.

Indexed as

Bayesian hierarchical modelmixture modelPólya-Gamma distributionpositron emission tomography (PET)spatially-informed priorvariable selection

Identifiers

PMID29259537
PMCPMC5723403

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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.