Literature DB >> 28795120

Cognitive and anatomical data in a healthy cohort of adults.

P D Watson1, E J Paul1, G E Cooke1, N Ward1, J M Monti1, K M Horecka1,2, C M Allen1, C H Hillman1,3, N J Cohen1,2, A F Kramer1,2, A K Barbey1,2,4,5,6,7,8.   

Abstract

We present data from a sample of 190 healthy adults including assessments of 4 cognitive factor scores, 12 cognitive tests, and 115 MRI-assessed neuroanatomical variables (cortical thicknesses, cortical and sub-cortical volumes, fractional anisotropy, and radial diffusivity). These data were used in estimating underlying sources of individual variation via independent component analysis (Watson et al., In press) [25].

Entities:  

Keywords:  Fluid intelligence; Independent component analysis; Individual differences; Neuroanatomy; Tractography

Year:  2016        PMID: 28795120      PMCID: PMC5540669          DOI: 10.1016/j.dib.2016.03.100

Source DB:  PubMed          Journal:  Data Brief        ISSN: 2352-3409


Specifications Table Value of the data These data characterize individual variation across demographic, neuroanatomical, and cognitive factors. These provide a useful model of individual variation that can be used to control for individual differences. The relationship between these data and other neuroimaging (such as resting state) and cognitive data remains unexplored and would be a fruitful area of collaboration. These data can be used to estimate patterns of joint variance across and within different neuroimaging and behavioral methods. These patterns can be used to test specific cognitive–anatomical linkages.

Data

The data (Supplementary Table 1) includes cognitive and anatomical variables collected prior to a large, multi-modal cognitive training study [25]. They include: Demographic measures (i.e., age, sex, and education). Cardiovascular fitness measures. 4 cognitive factors estimated via structural equation modeling [15]. Scores from the battery of 12 cognitive tests used to estimate these factors. 35 cortical thickness estimates and volume estimates for these same regions. 11 sub-cortical volumetric estimates. Total brain and total intracranial volume estimates. 7 estimates of ventricular size. 5 estimates of corpus callosum. 12 estimates of fractional anisotropy and in matter tracts. 12 estimates of radial diffusivity in white matter tracts.

Experimental design, materials and methods

Demographics

The 190 participants consisted of 85 females, and 105 males. The age range in our sample was 18–44 years, with a median of 22 years, and a mean of 24.3 years. The mean educational level of the participants was “some college” (i.e., median score 3, mean score 3.6) as reported on a scale from 1 to 5, where 1 denoted “less than a high school diploma”, 2 denoted “high school diploma or equivalent”, 3 denoted “some college”, 4 denoted “college degree”, and 5 denoted “post-graduate education.”

Aerobic fitness assessment

Maximal oxygen consumption (VO2max) was measured using a computerized indirect calorimetry system (ParvoMedics True Max 2400) and a modified Balke protocol [1] with averages for oxygen uptake (VO2) and respiratory exchange ratio (RER) assessed every 20 s. Participants ran on a motor-driven treadmill at a constant speed, with 2.0% increases in grade every two minutes until volitional exhaustion. The raw value was adjusted for body size, age, and gender to produce a VO2max percentile score.

Cognitive tests and factor scores

Participants received a battery of 12 cognitive tests designed to estimate underlying latent variables corresponding to cognitive constructs (see Table 1). The four latent variables of interest were fluid intelligence (gf), working memory (wm), executive function (ef), and episodic memory (em). Each of these latent variables was measured with three cognitive tests as follows. Fluid intelligence (gf) was measured by the BOMAT, number series, and letter sets tests [3,4,7]. Working memory (wm) was measured by the reading, rotation, and symmetry span tests [8,23]. Executive function (ef) was measured by the Garavan, Keep Track, and Stroop tests [14], [22], [26]. Episodic memory (em) was measured by immediate free recall, words, pictures and paired associates tests [23], [24], [9]. Using a structural equation modeling approach [15], across the larger sample of 518 participants, we extracted estimates of the four cognitive construct latent variables (i.e., gf, wm, ef, em). Because Garavan and Stroop produce error scores, while all others are measures of accuracy, we inverted these two values (i.e., multiplied by −1) in order to ensure all cognitive variables had the same sign.
Table 1

Included measures.

Data categoriesSpecific measures
Demographics & cardiovascular fitnessAge
Years of education
Sex
VO2max percentile
CognitionFluid intelligence (fluid g)
Working memory (wm)
Executive function (ef)
Episodic memory (em)
BOMAT (correct trials)
Number series (correct trials)
Letter Sets (correct trials)
Reading span
Rotation span
Symmetry span
Garavan (inverse total errors)
Keep Track Words Recalled
Stroop (inverse cost)
Immediate free recall Words
Immediate free recall Pictures
Immediate free recall Paired
Associates
Cortical thicknessesSuperior parietal
Postcentral
Precuneus
Lateral occipital
Mean cortical thickness
Superior temporal
Inferior parietal
Paracentral
Precentral
Middle temporal
Banks of superior temporal sulcus
Insula
Superior frontal
Supramarginal
Transverse temporal
Rostral middle frontal
Caudal middle frontal
Pars triangularis
Pars opercularis
Lateral orbitofrontal
Pars orbitalis
Frontal pole
Posterior cingulate
Inferior temporal
Cuneus
Peri calcarine
Rostral anterior cingulate
Medial orbitofrontal
Caudal anterior cingulate
Isthmus cingulate
Fusiform
Temporal pole
Lingual
Entorhinal
Parahippocampal
Cortical volumesMiddle temporal
Inferior parietal
Inferior temporal
Rostral anterior cingulate
Posterior cingulate
Rostral middle frontal
Superior frontal
Precentral
Supra marginal
Lateral orbitofrontal
Fusiform
Precuneus
Insula
Medial orbitofrontal
Postcentral
Superior temporal
Caudal middle frontal
Paracentral
Superior parietal
Isthmus cingulate
Lateral occipital
Transverse temporal
Pars orbitalis
Pars opercularis
Caudal anterior cingulate
Pars triangularis
Entorhinal
Temporal pole
Parahippocampal
Frontal pole
Peri calcarine
Cuneus
Lingual
Sub-cortical volumesTotal Brain volume
Total Intracranial Volume
Hippocampus
Ventral Diencephalon
Cerebellum Cortex
Cerebellum White Matter
Thalamus
Brain Stem
Amygdala
Putamen
Accumbens area
Pallidum
Caudate
VentriclesSurface Holes
Lateral Ventricle
Choroid plexus
Third Ventricle
Cerebrospinal fluid
Inferior Lateral Ventricle
Fourth Ventricle
Corpus callosumCC Posterior
CC Mid Posterior
CC Central
CC Mid Anterior
CC Anterior
White matter tractography (Fractional Anisotropy)Inferior fronto-occipital fasciculus
Superior longitudinal fasciculus
Temporal superior longitudinal fasciculus
Inferior longitudinal fasciculus
Anterior thalamic radiation
Forceps minor
Uncinate fasciculus
Cingulum bundle
Corticospinal tract
Forceps major
Hippocampal cingulum bundle
White matter tractography (Radial Diffusivity)Inferior fronto-occipital fasciculus
Superior longitudinal fasciculus
Temporal superior longitudinal fasciculus
Inferior longitudinal fasciculus
Anterior thalamic radiation
Forceps minor
Uncinate fasciculus
Cingulum bundle
Corticospinal tract
Forceps major
Hippocampal cingulum bundle
Included measures.

Structural MRI protocol

High resolution T1-weighted brain images were acquired using a 3D MPRAGE (Magnetization Prepared Rapid Gradient Echo Imaging) protocol with 192 contiguous axial slices, collected in ascending fashion parallel to the anterior and posterior commissures, echo time (TE)=2.32 ms, repetition time (TR)=1900 ms, field of view (FOV)=230 mm, acquisition matrix 256 mm×256 mm, slice thickness=0.90 mm, and flip angle=9°. All images were collected on a Siemens Magnetom Trio 3T whole-body MRI scanner.

Automated volumetrics, cortical thickness estimates, and white-matter tractography

Automated brain tissue segmentation and reconstruction of the T1-weighted structural MRI images were performed using the standard recon-all processing pipeline in FreeSurfer, version 5.2.0 (Released May, 2013; http://surfer-nmr.mgh.harvard.edu/). This produced estimates of 1) cortical thickness, 2) cortical volumes, 3) sub-cortical volumes, 4) ventricles, and 5) corpus callosum [5], [6], [10], [11], [12], [13]. Segmentations and tractography were manually checked for errors. Estimates in the left and right hemispheres were summed to produce bilateral estimates, and all values were converted to z-scores to control for differences in scale. A complete list of estimated structures appears in Table 1. FreeSurfer produced automated segmentation that closely approximates hand tracing, but like all segmentation procedures may introduce systematic bias. The diffusion tensor imaging estimates for fractional anisotropy (FA) and radial diffusivity (RD) data was analyzed using tract-based spatial statistics in FSL [19], [20], [21]. This pipeline involves fitting a tensor model to the raw diffusion data using fMRIDB׳s diffusion toolbox, and non-brain tissues were removed using FSL׳s brain extraction tool. All subjects׳ FA data were then aligned into a common space using the nonlinear registration tool FNIRT [18], [2]. Next, the mean FA image was created and thinned to create a mean FA skeleton that represents the centers of all tracts common to the group. Each subject׳s aligned FA data was then projected onto this skeleton to create an estimate of the subject-level value associated with each tract.
Subject areaNeuroscience
More specific subject areaAnatomical Neuroimaging
Type of dataTable of cognitive testing data and MRI assessed structural data.
How data was acquiredCognitive testing, Freesurfer automated segmentation of T1 weighted 3D MPRAGE images on a Siemens Magnetom Trio 3T whole-body MRI
Data formatAnalyzed
Experimental factorsBrief description of any pretreatment of samples
Experimental featuresMulti-modal MRI collection prior to a large cognitive training intervention.
Data source locationUrbana, Illinois
Data accessibilityPublic repository: Open Science framework INSIGHT project: https://osf.io/9ezwc/
  17 in total

1.  Working memory, short-term memory, and general fluid intelligence: a latent-variable approach.

Authors:  Randall W Engle; Stephen W Tuholski; James E Laughlin; Andrew R A Conway
Journal:  J Exp Psychol Gen       Date:  1999-09

2.  Nonrigid registration using free-form deformations: application to breast MR images.

Authors:  D Rueckert; L I Sonoda; C Hayes; D L Hill; M O Leach; D J Hawkes
Journal:  IEEE Trans Med Imaging       Date:  1999-08       Impact factor: 10.048

3.  Whole brain segmentation: automated labeling of neuroanatomical structures in the human brain.

Authors:  Bruce Fischl; David H Salat; Evelina Busa; Marilyn Albert; Megan Dieterich; Christian Haselgrove; Andre van der Kouwe; Ron Killiany; David Kennedy; Shuna Klaveness; Albert Montillo; Nikos Makris; Bruce Rosen; Anders M Dale
Journal:  Neuron       Date:  2002-01-31       Impact factor: 17.173

4.  Verbal Paired Associates tests limits on validity and reliability.

Authors:  Bob Uttl; Peter Graf; Laura K Richter
Journal:  Arch Clin Neuropsychol       Date:  2002-08       Impact factor: 2.813

5.  The generality of working memory capacity: a latent-variable approach to verbal and visuospatial memory span and reasoning.

Authors:  Michael J Kane; David Z Hambrick; Stephen W Tuholski; Oliver Wilhelm; Tabitha W Payne; Randall W Engle
Journal:  J Exp Psychol Gen       Date:  2004-06

6.  Underlying sources of cognitive-anatomical variation in multi-modal neuroimaging and cognitive testing.

Authors:  P D Watson; E J Paul; G E Cooke; N Ward; J M Monti; K M Horecka; C M Allen; C H Hillman; N J Cohen; A F Kramer; A K Barbey
Journal:  Neuroimage       Date:  2016-01-22       Impact factor: 6.556

Review 7.  Advances in functional and structural MR image analysis and implementation as FSL.

Authors:  Stephen M Smith; Mark Jenkinson; Mark W Woolrich; Christian F Beckmann; Timothy E J Behrens; Heidi Johansen-Berg; Peter R Bannister; Marilena De Luca; Ivana Drobnjak; David E Flitney; Rami K Niazy; James Saunders; John Vickers; Yongyue Zhang; Nicola De Stefano; J Michael Brady; Paul M Matthews
Journal:  Neuroimage       Date:  2004       Impact factor: 6.556

8.  Sequence-independent segmentation of magnetic resonance images.

Authors:  Bruce Fischl; David H Salat; André J W van der Kouwe; Nikos Makris; Florent Ségonne; Brian T Quinn; Anders M Dale
Journal:  Neuroimage       Date:  2004       Impact factor: 6.556

9.  An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest.

Authors:  Rahul S Desikan; Florent Ségonne; Bruce Fischl; Brian T Quinn; Bradford C Dickerson; Deborah Blacker; Randy L Buckner; Anders M Dale; R Paul Maguire; Bradley T Hyman; Marilyn S Albert; Ronald J Killiany
Journal:  Neuroimage       Date:  2006-03-10       Impact factor: 6.556

10.  Tract-based spatial statistics: voxelwise analysis of multi-subject diffusion data.

Authors:  Stephen M Smith; Mark Jenkinson; Heidi Johansen-Berg; Daniel Rueckert; Thomas E Nichols; Clare E Mackay; Kate E Watkins; Olga Ciccarelli; M Zaheer Cader; Paul M Matthews; Timothy E J Behrens
Journal:  Neuroimage       Date:  2006-04-19       Impact factor: 6.556

View more
  1 in total

1.  Data Citation in Neuroimaging: Proposed Best Practices for Data Identification and Attribution.

Authors:  Leah B Honor; Christian Haselgrove; Jean A Frazier; David N Kennedy
Journal:  Front Neuroinform       Date:  2016-08-12       Impact factor: 4.081

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.