Evidence map›Paper›PMID 37602266›Full record

ArticleFrontiers in neurology2023

C-NODDI: a constrained NODDI model for axonal density and orientation determinations in cerebral white matter.

Maryam H Alsameen, Zhaoyuan Gong, Wenshu Qian, Matthew Kiely, Curtis Triebswetter, Christopher M Bergeron, Luis E Cortina, Mary E Faulkner, John P Laporte, Mustapha Bouhrara

Abstract read
In one paragraph

Article in Frontiers in neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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.

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3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

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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

10 authors.

Maryam H AlsameenLaboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health, Baltimore, MD, United States.
Zhaoyuan GongLaboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health, Baltimore, MD, United States.
Wenshu QianLaboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health, Baltimore, MD, United States.
Matthew KielyLaboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health, Baltimore, MD, United States.
Curtis TriebswetterLaboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health, Baltimore, MD, United States.
Christopher M BergeronLaboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health, Baltimore, MD, United States.
Luis E CortinaLaboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health, Baltimore, MD, United States.
Mary E FaulknerLaboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health, Baltimore, MD, United States.
John P LaporteLaboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health, Baltimore, MD, United States.
Mustapha BouhraraLaboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health, Baltimore, MD, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Neurite orientation dispersion and density imaging (NODDI) provides measures of neurite density and dispersion through computation of the neurite density index (NDI) and the orientation dispersion index (ODI). However, NODDI overestimates the cerebrospinal fluid water fraction in white matter (WM) and provides physiologically unrealistic high NDI values. Furthermore, derived NDI values are echo-time (TE)-dependent. In this work, we propose a modification of NODDI, named constrained NODDI (C-NODDI), for NDI and ODI mapping in WM. Methods: Using NODDI and C-NODDI, we investigated age-related alterations in WM in a cohort of 58 cognitively unimpaired adults. Further, NDI values derived using NODDI or C-NODDI were correlated with the neurofilament light chain (NfL) concentration levels, a plasma biomarker of axonal degeneration. Finally, we investigated the TE dependence of NODDI or C-NODDI derived NDI and ODI. Results: ODI derived values using both approaches were virtually identical, exhibiting constant trends with age. Further, our results indicated a quadratic relationship between NDI and age suggesting that axonal maturation continues until middle age followed by a decrease. This quadratic association was notably significant in several WM regions using C-NODDI, while limited to a few regions using NODDI. Further, C-NODDI-NDI values exhibited a stronger correlation with NfL concentration levels as compared to NODDI-NDI, with lower NDI values corresponding to higher levels of NfL. Finally, we confirmed the previous finding that NDI estimation using NODDI was dependent on TE, while NDI derived values using C-NODDI exhibited lower sensitivity to TE in WM. Conclusion: C-NODDI provides a complementary method to NODDI for determination of NDI in white matter.

Indexed as

agingaxonal densityMRINODDIwhite matter

Identifiers

PMID37602266
PMCPMC10435293

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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.