Evidence map›Paper›PMID 28739120›Full record

ArticleNeuroImage2018

Detecting stable individual differences in the functional organization of the human basal ganglia.

Manuel Garcia-Garcia, Aki Nikolaidis, Pierre Bellec, R Cameron Craddock, Brian Cheung, Francisco X Castellanos, Michael P Milham

Abstract read
In one paragraph

Article in NeuroImage, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

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

  1. Pooled it
  2. Review
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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.

Manuel Garcia-GarciaPhyllis Green and Randolph Cowen Institute for Pediatric Neuroscience, Department of Child and Adolescent Psychiatry, NYU Langone Medical Center, New York, NY, USA.
Aki NikolaidisCenter for the Developing Brain, Child Mind Institute, New York, NY, USA.
Pierre BellecMcConnell Brain Imaging Center, Montreal Neurological Institute, McGill University, Montreal, Canada.
R Cameron CraddockCenter for the Developing Brain, Child Mind Institute, New York, NY, USA; Nathan Kline Institute for Psychiatric Research, Orangeburg, NY, USA.
Brian CheungCenter for the Developing Brain, Child Mind Institute, New York, NY, USA.
Francisco X CastellanosPhyllis Green and Randolph Cowen Institute for Pediatric Neuroscience, Department of Child and Adolescent Psychiatry, NYU Langone Medical Center, New York, NY, USA; Nathan Kline Institute for Psychiatric Research, Orangeburg, NY, USA.
Michael P MilhamCenter for the Developing Brain, Child Mind Institute, New York, NY, USA; Nathan Kline Institute for Psychiatric Research, Orangeburg, NY, USA. Electronic address: Michael.Milham@childmind.org.

Funding

Longitudinal Discovery of Brain Developmental TrajectoriesU01MH099059 · NIMH · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI MILHAM, MICHAEL PETER · 2013 to 2017
$3.7M
Developmental Variations in Corticostriatal Thalamocortical Circuits and their Relationship to PsychopathologyR21MH118556 · NIMH · CHILD MIND INSTITUTE, INC. · PI NIKOLAIDIS, AKI · 2019 to 2020
$419k
NIMH NIH HHS R21 MH118556NIMH NIH HHS U01 MH099059
6 · The paper itself

Abstract

Moving from group level to individual level functional parcellation maps is a critical step for developing a rich understanding of the links between individual variation in functional network architecture and cognitive and clinical phenotypes. Still, the identification of functional units in the brain based on intrinsic functional connectivity and its dynamic variations between and within subjects remains challenging. Recently, the bootstrap analysis of stable clusters (BASC) framework was developed to quantify the stability of functional brain networks both across and within subjects. This multi-level approach utilizes bootstrap resampling for both individual and group-level clustering to delineate functional units based on their consistency across and within subjects, while providing a measure of their stability. Here, we optimized the BASC framework for functional parcellation of the basal ganglia by investigating a variety of clustering algorithms and similarity measures. Reproducibility and test-retest reliability were computed to validate this analytic framework as a tool to describe inter-individual differences in the stability of functional networks. The functional parcellation revealed by stable clusters replicated previous divisions found in the basal ganglia based on intrinsic functional connectivity. While we found moderate to high reproducibility, test-retest reliability was high at the boundaries of the functional units as well as within their cores. This is interesting because the boundaries between functional networks have been shown to explain most individual phenotypic variability. The current study provides evidence for the consistency of the parcellation of the basal ganglia, and provides the first group level parcellation built from individual-level cluster solutions. These novel results demonstrate the utility of BASC for quantifying inter-individual differences in the functional organization of brain regions, and encourage usage in future studies.

Indexed as

IndividualityAdultBasal GangliaBrain MappingFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedYoung Adult

Identifiers

PMID28739120
PMCPMC7025720

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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.