Evidence map›Paper›PMID 39476715›Full record

ArticleJournal of the neurological sciences2024

The intersection of race and sex on the clinical and cognitive progression of multiple sclerosis.

Shannin N Moody, Morganne Manuel, Auriel Willette, Elizabeth Shirtcliff, Brian Copeland, Jesus Lovera, Deidre Devier

Erratum issuedAbstract read
In one paragraph

Article in Journal of the neurological sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Shannin N MoodyDepartment of Neurology | School of Medicine, Louisiana State University Health Sciences Center, New Orleans, LA, USA. Electronic address: smood1@lsuhsc.edu.
Morganne ManuelDepartment of Cellular Biology and Anatomy, Medical College of Georgia at Augusta University, Augusta, GA, USA.
Auriel WilletteDepartment of Neurology, Rutgers University, New Brunswick, NJ, USA.
Elizabeth ShirtcliffDepartment of Psychology University of Oregon, Eugene, OR, USA.
Brian CopelandDepartment of Neurology | School of Medicine, Louisiana State University Health Sciences Center, New Orleans, LA, USA.
Jesus LoveraDepartment of Neurology | School of Medicine, Louisiana State University Health Sciences Center, New Orleans, LA, USA.
Deidre DevierDepartment of Neurology | School of Medicine, Louisiana State University Health Sciences Center, New Orleans, LA, USA; Department of Cell Biology and Anatomy, Louisiana State University Health Sciences Center, New Orleans, LA, USA.

Funding

Stress Biology and Psychosocial stressors as mechanisms for Racial Health Disparities in Neural and Clinical Impairments of Multiple SclerosisK00NS125815 · NINDS · LSU HEALTH SCIENCES CENTER · PI MOODY, SHANNIN NICOLE · 2023 to 2025
$217k
Stress Biology and Psychosocial stressors as mechanisms for Racial Health Disparities in Neural and Clinical Impairments of Multiple SclerosisF99NS125815 · NINDS · LSU HEALTH SCIENCES CENTER · PI MOODY, SHANNIN NICOLE · 2022 to 2022
$48k
NINDS NIH HHS F99 NS125815NINDS NIH HHS K00 NS125815
6 · The paper itself

Abstract

objectiveBlack populations show increased incidences of diagnosis, worse disease severity, and earlier likelihood of mortality due to MS. Clinical outcomes are also linked to biological sex and as with Black individuals, MS characteristics between sexes have also shifted overtime. This study examined whether clinical disease progression differed by race and sex for patients with MS.

design"Black" (N = 47) and "White" (N = 58) participants with MS (82 % female) were recruited from a longitudinal examination of the impact of race and sex on the cognition and disease duration of patients in the gulf south region of the United States.

resultsBlack participants had shorter disease durations [F (1,103) = 4.70, p = .03], (MDiff = [-3.96]) and were younger [F (1, 103) = 14.25, p < .001], (MDiff = [-9.04]). Despite this, Black individuals had worse SDMT t-scores [F (1, 103) = 5.22, p = .024], (MDiff = [-4.62])]. Women exhibited higher MSSS scores [F (1, 96) = 5.59, p = .02], (MDiff = [-2.15]). Specifically, Black women were younger than White women [F (1, 84) = 14.47, p < .001], (MDiff = [-9.15])] and had shorter disease durations [F (1, 84) = 6.04, p = .016], (MDiff = [-4.57])] yet scored lower on the SDMT T-scores [F (1, 84) = 6.11, p = .015], (MDiff = [-5.51])].

conclusionFindings suggest an interaction between race and sex may influence clinical progression in MS. Despite being younger and having shorter disease durations Black participants with MS, specifically Black women exhibited worse clinical outcomes. SUMMARY: For women and men, MS incidence among Black Americans has become similar to White Americans. However, Black individuals experience greater disease severity and earlier mortality. Clinical impairment often accompanies MS. We examined the influence of race and sex on clinical status using the Symbol Digit Modalities Test t-scores (SDMT T-scores) and Multiple Sclerosis Severity Scores (MSSS) in Black (N = 47) and White (N = 58) patients with MS. Women exhibited higher MSSS scores than men [F (1, 96) = 5.59, p = .02], (MDiff = [-2.15]). Black participants had shorter disease durations [F (1, 103) = 4.70, p = .03], (MDiff = [-3.96]) and were younger [F (1, 103) = 14.25, p < .001], (MDiff = [-9.04]). Despite this, Black individuals had worse SDMT T-scores [F (1, 103) = 5.22, p = .024], (MDiff = [-4.62])]. Specifically, Black women were younger than White women [F (1, 84) = 14.47, p < .001], (MDiff = [-9.15])] and had shorter disease durations [F (1, 84) = 6.04, p = .016], (MDiff = [-4.57])] yet scored lower on the SDMT T-scores [F (1, 84) = 6.11, p = .015], (MDiff = [-5.51])]. These findings suggest that an interaction between race and sex may influence clinical progression in MS.

Indexed as

Disease ProgressionMultiple SclerosisAdultBlack or African AmericanCognition DisordersFemaleHumansLongitudinal StudiesMaleMiddle AgedNeuropsychological TestsSeverity of Illness IndexSex FactorsWhiteBlack or African AmericanIntersectional frameworkMinority healthMultiple sclerosis

Identifiers

PMID39476715
PMCPMC11587816

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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.