Evidence map›Paper›PMID 31176294›Full record

ArticleNeuroImage. Clinical2019

Structural magnetic resonance imaging demonstrates abnormal cortical thickness in Down syndrome: Newborns to young adults.

Jacob Levman, Allissa MacDonald, Nicole Baumer, Patrick MacDonald, Natalie Stewart, Ashley Lim, Liam Cogger, Tadashi Shiohama, Emi Takahashi

Open access · goldAbstract read
In one paragraph

Article in NeuroImage. Clinical, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.7field-weighted citation impact, top 11% of its field
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

19 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Structural abnormalities in paediatric moyamoya disease revealed by clinical magnetic resonance imaging, regionally distributed relative signal intensities and volumes.International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience · 2022
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
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

9 authors at 2 institutions in 2 countries.

Jacob LevmanDivision of Newborn Medicine, Department of Medicine, Boston Children's Hospital, 401 Park Dr., Boston, MA 02215, USA; Department of Pediatrics, Harvard Medical School, Boston, MA, USA; Department of Mathematics, Statistics and Computer Science, St. Francis Xavier University, Antigonish, NS B2G 2W5, Canada. Electronic address: jacob.levman@childrens.harvard.edu.
Allissa MacDonaldDepartment of Biology, St. Francis Xavier University, Antigonish, NS B2G 2W5, Canada.
Nicole BaumerDepartment of Neurology, Boston Children's Hospital, 300 Longwood Ave, Boston, MA 02115, USA.
Patrick MacDonaldDivision of Newborn Medicine, Department of Medicine, Boston Children's Hospital, 401 Park Dr., Boston, MA 02215, USA.
Natalie StewartDivision of Newborn Medicine, Department of Medicine, Boston Children's Hospital, 401 Park Dr., Boston, MA 02215, USA.
Ashley LimDivision of Newborn Medicine, Department of Medicine, Boston Children's Hospital, 401 Park Dr., Boston, MA 02215, USA.
Liam CoggerDepartment of Mathematics, Statistics and Computer Science, St. Francis Xavier University, Antigonish, NS B2G 2W5, Canada.
Tadashi ShiohamaDivision of Newborn Medicine, Department of Medicine, Boston Children's Hospital, 401 Park Dr., Boston, MA 02215, USA.
Emi TakahashiDivision of Newborn Medicine, Department of Medicine, Boston Children's Hospital, 401 Park Dr., Boston, MA 02215, USA; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Boston Children's Hospital · USSt. Francis Xavier University · CA

Funding

Development of Brain Connectivity in Human Fetus, Newborn, and Toddler AgesR01HD078561 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI TAKAHASHI (OKI), EMI · 2014 to 2018
$1.7M
MRI-based biomarkers for regional brain abnormalities in autism spectrum disorder: From newborns to young adultsR21MH118739 · NIMH · BOSTON CHILDREN'S HOSPITAL · PI TAKAHASHI (OKI), EMI · 2018 to 2019
$487k
Brain Development in Down Syndrome during Fetal, Newborn, and Infant StagesR21HD098606 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI TAKAHASHI (OKI), EMI · 2019 to 2020
$484k
Assessment of white matter connectivity in Alexander diseaseR03NS101372 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI TAKAHASHI (OKI), EMI · 2018 to 2019
$177k
Aberrant Patterns of Human Brain Connectivity and Gyral StructuresR03NS091587 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI TAKAHASHI (OKI), EMI · 2015 to 2016
$177k
NICHD NIH HHS R01 HD078561NICHD NIH HHS R21 HD098606NIMH NIH HHS R21 MH118739NINDS NIH HHS R03 NS091587NINDS NIH HHS R03 NS101372
6 · The paper itself

Abstract

Down syndrome (DS) is a genetic disorder caused by an extra copy of all or part of chromosome 21 and is characterized by intellectual disability. We performed a retrospective analysis of 47 magnetic resonance imaging (MRI) examinations of participants with DS (aged 5 to 22 years) and compared them with a large cohort of 854 brain MRIs obtained from neurotypical participants (aged 5 to 32 years) with the objective of assessing the clinical presentation of Down syndrome, towards better understanding the neurological development associated with the condition. An additional cohort of 26 MRI exams from patients with DS and 139 exams from neurotypical participants (aged 0-5 years) are included as part of a supplementary analysis. Regionally distributed cortical thickness measurements, including average measurements as well as standard deviations (intra-regional cortical thickness variability) were extracted from each examination. The largest effect sizes observed were associated with increased average cortical thickness in the postcentral gyrus with specific abnormalities observed in Brodmann's areas 1 and 3b in DS, which was observed across all age ranges. We also observed strong effect sizes associated with decreased cortical thickness variability in the lateral orbitofrontal gyrus, the postcentral gyrus and more in DS participants. Findings suggest regionally irregular gray matter development in DS that can be detected with MRI.

Indexed as

AdolescentAdultCerebral CortexChildChild, PreschoolDown SyndromeFemaleHumansInfantInfant, NewbornMagnetic Resonance ImagingMaleRetrospective StudiesYoung AdultCortical thicknessDevelopmentDown syndromeNeuroanatomyVariability

Identifiers

PMID31176294
PMCPMC6551568
OpenAlexW2947086160

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.