Evidence map›Paper›PMID 39715474›Full record

Observational studyNeurology2025

Association of Menopause With Functional Outcomes and Disease Biomarkers in Women With Multiple Sclerosis.

Hannah E Silverman, Alan Bostrom, Alyssa N Nylander, Amit Akula, Ann A Lazar, Refujia Gomez, Adam Santaniello, Adam Renschen, Meagan Michaela Harms, Tiffany P Cooper and 8 more

Abstract readObservational Study
In one paragraph

Observational study in Neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
  2. The Neurology of Menopause.Current neurology and neuroscience reports · 2026
    Review
  3. Menopause is a physiological progression event for women with multiple sclerosis: No.Multiple sclerosis (Houndmills, Basingstoke, England) · 2026
    Article
  4. Menopause is a physiological progression event for women with multiple sclerosis: Yes.Multiple sclerosis (Houndmills, Basingstoke, England) · 2026
    Article
  5. Review
  6. Article
  7. Neurologic Complications of Pregnancy and Menopause.Continuum (Minneapolis, Minn.) · 2026
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Impact of sex on multiple sclerosis therapy.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Review
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

18 authors.

Hannah E SilvermanDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.ORCID 0000-0003-1200-6517
Alan BostromDivision of Oral Epidemiology, Department of Preventive and Restorative Dental Sciences, University of California, San Francisco;and.
Alyssa N NylanderDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.ORCID 0000-0002-1976-3847
Amit AkulaDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.ORCID 0000-0003-2867-7569
Ann A LazarDivision of Oral Epidemiology, Department of Preventive and Restorative Dental Sciences, University of California, San Francisco;and.
Refujia GomezDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.ORCID 0000-0003-0730-8019
Adam SantanielloDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.ORCID 0000-0002-9816-5932
Adam RenschenDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.
Meagan Michaela HarmsDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.
Tiffany P CooperDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.
Robin LincolnDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.ORCID 0000-0002-9603-7566
Shane PooleDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.ORCID 0000-0002-3203-151X
Ahmed AbdelhakDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.ORCID 0000-0001-9731-4169
Roland G HenryDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.
Jorge OksenbergDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.ORCID 0000-0002-3613-9544
Stephen L HauserDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.ORCID 0000-0002-4932-4001
Bruce Anthony Campbell CreeDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.ORCID 0000-0001-7689-2533
Riley BoveDepartment of Neurology, UCSF Weill Institute for Neurosciences, University of California San Francisco.ORCID 0000-0002-2034-8800

Funding

The Role of B cells in the Origin and Progression of Multiple SclerosisR35NS111644 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI STEPHEN L HAUSER · 2019 to 2026
$9.1M
NINDS NIH HHS R35 NS111644
6 · The paper itself

Abstract

BACKGROUND AND

objectiveThe impact of menopause on the brain is not well understood. Hormonal changes, including puberty and pregnancy, influence the onset and course of multiple sclerosis (MS). After menopause, a worsening of MS disease trajectory measured on the clinician-rated Expanded Disability Status Scale (EDSS) was reported in some, but not all, studies. Evaluating the association between menopause and more objective measures of CNS injury is warranted. This study sought to assess the trajectory of objective functional outcomes and disease biomarkers in women with MS before and after menopause in a longitudinal prospective observational cohort.

methodsData were collected prospectively from a longitudinally followed MS cohort, including the performance-based Multiple Sclerosis Functional Composite (MSFC) as the primary functional outcome and the paraclinical marker of neuronal injury serum neurofilament light chain (sNfL) as the primary biomarker outcome. Outcomes were analyzed using segmented linear mixed model regressions adjusted for age, BMI, and tobacco use, with a change in slope at the time of menopause, as the a priori inflection point.

resultsOne hundred and eighty-four postmenopausal women met inclusion criteria. Participants were followed for a median of 13 years (interquartile range [IQR] = 4, range: 1-17). The median MS duration was 24 years (IQR = 13, range: 3-64), and the median EDSS score was 2.5 (IQR = 2, range: 0-8). The median age at natural menopause was 50 years (IQR = 5, range: 33-60); 17% of participants used any systemic menopausal hormone therapy. Menopause reflected an inflection point in MSFC worsening (slope difference 0.08, 95% CI 0.01, 0.14, DISCUSSION: The menopausal transition may represent an inflection in accumulation of neuronal injury and functional decline in MS.

Indexed as

BiomarkersMenopauseMultiple SclerosisNeurofilament ProteinsAdultCohort StudiesDisability EvaluationDisease ProgressionFemaleHumansLongitudinal StudiesMiddle AgedProspective StudiesBiomarkersneurofilament protein LNeurofilament Proteins

Identifiers

PMID39715474
PMCPMC11666275

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.