Evidence map›Paper›PMID 38546872›Full record

ArticleBrain structure & function2024

Robust thalamic nuclei segmentation from T1-weighted MRI using polynomial intensity transformation.

Julie P Vidal, Lola Danet, Patrice Péran, Jérémie Pariente, Meritxell Bach Cuadra, Natalie M Zahr, Emmanuel J Barbeau, Manojkumar Saranathan

Abstract read
In one paragraph

Article in Brain structure & function, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

  1. Trial
  2. Thalamic Nuclei Atrophy in Type 1 Diabetes Mellitus Across Disease Duration.Journal of magnetic resonance imaging : JMRI · 2026
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  7. Diencephalic integrity explains aspects of hippocampal amnesia.Cerebral cortex (New York, N.Y. : 1991) · 2026
    Article
  8. Thalamic nuclei insights into Alzheimer's disease.bioRxiv : the preprint server for biology · 2026
    Article
  9. Article
  10. Article
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  13. A deep learning framework for comprehensive segmentation of deep grey nuclei.medRxiv : the preprint server for health sciences · 2025
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Julie P VidalCNRS, CerCo (Brain and Cognition Research Center), Paul Sabatier University, Toulouse, France.
Lola DanetINSERM, ToNiC (Toulouse NeuroImaging Center), Paul Sabatier University, Toulouse, France.
Patrice PéranINSERM, ToNiC (Toulouse NeuroImaging Center), Paul Sabatier University, Toulouse, France.
Jérémie ParienteINSERM, ToNiC (Toulouse NeuroImaging Center), Paul Sabatier University, Toulouse, France.
Meritxell Bach CuadraCIBM Center for Biomedical Imaging, Radiology Department, Lausanne University and University Hospital, Lausanne, Switzerland.
Natalie M ZahrDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA.
Emmanuel J BarbeauCNRS, CerCo (Brain and Cognition Research Center), Paul Sabatier University, Toulouse, France.
Manojkumar SaranathanDepartment of Radiology, University of Massachusetts Chan Medical School, Worcester, MA, USA. manojkumar.saranathan@umassmed.edu.

Funding

Next-Generation Thalamic Nuclei Visualization and Segmentation MethodsR01EB032674 · NIBIB · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Manojkumar Saranathan · 2022 to 2026
$1.8M
NIBIB NIH HHS 7R01EB032674NIBIB NIH HHS R01 EB032674
6 · The paper itself

Abstract

Accurate segmentation of thalamic nuclei, crucial for understanding their role in healthy cognition and in pathologies, is challenging to achieve on standard T1-weighted (T1w) magnetic resonance imaging (MRI) due to poor image contrast. White-matter-nulled (WMn) MRI sequences improve intrathalamic contrast but are not part of clinical protocols or extant databases. In this study, we introduce histogram-based polynomial synthesis (HIPS), a fast preprocessing transform step that synthesizes WMn-like image contrast from standard T1w MRI using a polynomial approximation for intensity transformation. HIPS was incorporated into THalamus Optimized Multi-Atlas Segmentation (THOMAS) pipeline, a method developed and optimized for WMn MRI. HIPS-THOMAS was compared to a convolutional neural network (CNN)-based segmentation method and THOMAS modified for the use of T1w images (T1w-THOMAS). The robustness and accuracy of the three methods were tested across different image contrasts (MPRAGE, SPGR, and MP2RAGE), scanner manufacturers (PHILIPS, GE, and Siemens), and field strengths (3 T and 7 T). HIPS-transformed images improved intra-thalamic contrast and thalamic boundaries, and HIPS-THOMAS yielded significantly higher mean Dice coefficients and reduced volume errors compared to both the CNN method and T1w-THOMAS. Finally, all three methods were compared using the frequently travelling human phantom MRI dataset for inter- and intra-scanner variability, with HIPS displaying the least inter-scanner variability and performing comparably with T1w-THOMAS for intra-scanner variability. In conclusion, our findings highlight the efficacy and robustness of HIPS in enhancing thalamic nuclei segmentation from standard T1w MRI.

Indexed as

Image Processing, Computer-AssistedMagnetic Resonance ImagingThalamic NucleiAdultFemaleHumansMaleNeural Networks, ComputerWhite MatterStructural imagingThalamic nuclei segmentationThalamusTHOMAS

Identifiers

PMID38546872
PMCPMC11147736

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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.