Evidence map›Paper›PMID 30540774›Full record

ArticlePloS one2018

Increased Alzheimer's risk during the menopause transition: A 3-year longitudinal brain imaging study.

Lisa Mosconi, Aneela Rahman, Ivan Diaz, Xian Wu, Olivia Scheyer, Hollie Webb Hristov, Shankar Vallabhajosula, Richard S Isaacson, Mony J de Leon, Roberta Diaz Brinton

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 140 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed, 9 pooled it
9.3field-weighted citation impact, top 1% 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.

NCT06978218 completednot on this mapstarted 2025, after this paper: background citation

Cognitive Changes in Menopause: A Comparative Analysis of Brain Fog and Quality of Life

TypeobservationalSponsorMerve CoskunRan2025 to 2025Enrolled122ConditionsMenopause, Cognitive Dysfunction, Memory Disorders, Quality of Life
NCT07021664 not yet recruitingnot on this mapstarted 2025, after this paper: background citation

Santé, Imagerie et Cognition à Travers la Transition ménopausique

TypeobservationalSponsorUniversité de SherbrookeRan2025 to 2026Enrolled45ConditionsMenopause
3 · Its place in the literature

Who cites it

140 citing papers in PubMed, 9 syntheses or guidelines pooled it, 219 citations in OpenAlex.

  1. Pooled it
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  5. Systematic review ofFrontiers in aging neuroscience · 2023
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  16. The Neurology of Menopause.Current neurology and neuroscience reports · 2026
    Review
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80 more citing papers are in PubMed but not listed here.

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 at 3 institutions in 1 country.

Lisa MosconiDepartment of Neurology, Weill Cornell Medical College, New York, NY, United States of America.
Aneela RahmanDepartment of Neurology, Weill Cornell Medical College, New York, NY, United States of America.ORCID 0000-0002-3803-9379
Ivan DiazDivision of Biostatistics and Epidemiology, Department of Healthcare Policy and Research, Weill Cornell Medicine, New York, NY, United States of America.
Xian WuDivision of Biostatistics and Epidemiology, Department of Healthcare Policy and Research, Weill Cornell Medicine, New York, NY, United States of America.
Olivia ScheyerDepartment of Neurology, Weill Cornell Medical College, New York, NY, United States of America.
Hollie Webb HristovDepartment of Neurology, Weill Cornell Medical College, New York, NY, United States of America.
Shankar VallabhajosulaDepartment of Radiology, Weill Cornell Medical College, New York NY, United States of America.
Richard S IsaacsonDepartment of Neurology, Weill Cornell Medical College, New York, NY, United States of America.
Mony J de LeonDepartment of Psychiatry, New York University School of Medicine, New York, NY, United States of America.
Roberta Diaz BrintonDepartments of Pharmacology and Neurology, College of Medicine, University of Arizona, Tucson, United States of America.
Cornell University · USNew York University · USUniversity of Arizona · US

Funding

Timing of Menopausal Hormone Therapy across Perimenopause to Menopause Transition: Neuroimmune System in BrainP01AG026572 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ROBERTA EILEEN BRINTON · 2006 to 2026
$53.7M
Sex Differences in the Molecular Determinants of Alzheimer's Disease Risk: Prodromal EndophenotypeR01AG057931 · NIA · UNIVERSITY OF ARIZONA · PI BRINTON, ROBERTA EILEEN, CHANG, RUI · 2018 to 2022
$6.0M
Maternal history of Alzheimer's predisposes children to amyloid beta-related hypoR01AG035137 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MOSCONI, LISA · 2010 to 2014
$2.7M
NIA NIH HHS P01 AG026572NIA NIH HHS R01 AG035137NIA NIH HHS R01 AG057931
6 · The paper itself

Abstract

Two thirds of all persons with late-onset Alzheimer's disease (AD) are women. Identification of sex-based molecular mechanisms underpinning the female-based prevalence of AD would advance development of therapeutic targets during the prodromal AD phase when prevention or delay in progression is most likely to be effective. This 3-year brain imaging study examines the impact of the menopausal transition on Alzheimer's disease (AD) biomarker changes [brain β-amyloid load via 11C-PiB PET, and neurodegeneration via 18F-FDG PET and structural MRI] and cognitive performance in midlife. Fifty-nine 40-60 year-old cognitively normal participants with clinical, neuropsychological, and brain imaging exams at least 2 years apart were examined. These included 41 women [15 premenopausal controls (PRE), 14 perimenopausal (PERI), and 12 postmenopausal women (MENO)] and 18 men. We used targeted minimum loss-based estimation to evaluate AD biomarker and cognitive changes. Older age was associated with baseline Aβ and neurodegeneration markers, but not with rates of change in these biomarkers. APOE4 status influenced change in Aβ load, but not neurodegenerative changes. Longitudinally, MENO and PERI groups showed declines in estrogen-dependent memory tests as compared to men (p < .04). Adjusting for age, APOE4 status, and vascular risk confounds, the MENO and PERI groups exhibited higher rates of CMRglc decline as compared to males (p ≤ .015). The MENO group exhibited the highest rate of hippocampal volume loss (p's ≤ .001), and higher rates of Aβ deposition than males (p < .01). CMRglc decline exceeded Aβ and atrophy changes in all female groups vs. men. These findings indicate emergence and progression of a female-specific hypometabolic AD-endophenotype during the menopausal transition. These findings suggest that the optimal window of opportunity for therapeutic intervention to prevent or delay progression of AD endophenotype in women is early in the endocrine aging process.

Indexed as

AgedAlzheimer DiseaseAmyloid beta-PeptidesApolipoprotein E4BiomarkersBrainCognitive DysfunctionDisease ProgressionFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMemoryMenopauseMiddle AgedNeuroimagingAmyloid beta-PeptidesApolipoprotein E4Biomarkers

Identifiers

PMID30540774
PMCPMC6291073
OpenAlexW2904496251

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.