Evidence map›Paper›PMID 37357294›Full record

ArticleThe journal of prevention of Alzheimer's disease2023

Reproductive Markers in Alzheimer's Disease Progression: The Framingham Heart Study.

H Ding, Y Li, T F A Ang, Y Liu, S Devine, R Au, P M Doraiswamy, C Liu

Open access · diamondAbstract read
In one paragraph

Article in The journal of prevention of Alzheimer's disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

H DingHuitong Ding, Chunyu Liu, Crosstown Building 801, Massachusetts Avenue Boston, MA 02118, USA, dinghfut@bu.edu, liuc@bu.edu.
Y Li
T F A Ang
Y Liu
S Devine
R Au
P M Doraiswamy
C Liu
Framingham Heart Study · USBoston University · USDuke University · US

Funding

TBDU19AG068753 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Lindsay A. Farrer · 2020 to 2026
$42.4M
EPIDEMIOLOGY OF DEMENTIA IN THE FRAMINGHAM STUDYR01AG008122 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI AU, RHODA, SESHADRI, SUDHA · 1989 to 2015
$14.4M
MRI, Genetics &Cognitive Precursors of AD &DementiaR01AG016495 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI AU, RHODA · 1999 to 2016
$12.5M
HEALTH CONDITIONS OF ELDERLY PUERTO RICANSR01AG016209 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI PALLONI, ALBERTO B. · 2000 to 2007
$6.8M
Mitochondrial DNA Copy Number and Sequence Variation in Relation to Age, Alzheimer's Disease Related Phenotypes and Age-related Metabolic TraitsR01AG059727 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI LIU, CHUNYU, SATIZABAL, CLAUDIA L · 2018 to 2021
$2.6M
Life's Essential 8, Digital Cognitive Markers, and Alzheimer's Disease RiskR01AG086303 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Chunyu Liu · 2025 to 2026
$886k
NIA NIH HHS R01 AG008122NIA NIH HHS R01 AG016209NIA NIH HHS R01 AG016495NIA NIH HHS R01 AG059727NIA NIH HHS R01 AG086303NIA NIH HHS U19 AG068753
6 · The paper itself

Abstract

backgroundReproductive status, such as the age of menarche or menopause, may be linked to cognitive abilities and risk for incident Alzheimer's disease (AD) but the evidence is conflicting. It is also not fully known if these factors interact with cortical beta-amyloid deposition.

objectivesTo study the relationship between reproductive risks, sex hormone markers and risk for decline in specific cognitive domains in women. DESIGN, SETTING AND

participantsWe analyzed the association of reproductive markers (age at menarche, number of births, age at menopause, sex hormone-binding globulin, estradiol, estrone, total testosterone, free testosterone) with incident AD and annualized cognitive decline in the community-based longitudinal Framingham Heart Study (FHS) Offspring women 60 years and older (n=772, mean age 68 years, mean follow-up 10.7 ± 3 years). We used the Cox proportional hazards regression model and linear regression model, adjusting for covariates. OUTCOME MEASURES: Incident AD dementia as well as the annualized change in memory, language, attention and executive functions.

resultsOlder age at menopause was associated with a lower risk of incident AD dementia (p = 0.047, 6% lower risk per older year) after adjusting for baseline age, education, hormone therapy status, and MMSE score. Older age at menopause was significantly associated with a slower annualized decline in memory (beta = 0.085, p = 0.00059). The lower level of plasma Aβ42 was also associated with a higher risk of incident AD (HR = 0.97, 95% CI = 0.95, 0.99; p = 0.0039) but there was no significant interaction effect with age at menarche, age at menopause or plasma sex hormone levels.

conclusionYounger age at menopause is a risk factor for late-life memory decline and incident AD. This risk appears to be independent of Aβ42 pathology. Further studies to understand the biological and social mechanisms underlying the differential effects of reproductive risks are warranted.

Indexed as

Alzheimer DiseaseCognitive DysfunctionAgedFemaleGonadal Steroid HormonesHumansLongitudinal StudiesTestosteroneGonadal Steroid HormonesTestosteronecognitive functionincident Alzheimer’s diseaseReproductive risks of women

Identifiers

PMID37357294
PMCPMC13264159
OpenAlexW4327653256

What OpenQuestion holds

Textmetadata
LicenceTDM
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.