Evidence map›Paper›PMID 35114556›Full record

ArticleAtherosclerosis2022

Menopausal hormone therapy and risk of cardiovascular events in women with prediabetes or type 2 diabetes: A pooled analysis of 2917 postmenopausal women.

Yilin Yoshida, Zhipeng Chen, Robin L Baudier, Marie Krousel-Wood, Amanda H Anderson, Vivian A Fonseca, Franck Mauvais-Jarvis

Open access · greenAbstract read
In one paragraph

Article in Atherosclerosis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

7 authors at 1 institution in 2 countries.

Yilin YoshidaSection of Endocrinology and Metabolism, Deming Department of Medicine, Tulane University School of Medicine, United States; Tulane Center of Excellence in Sex-Based Biology & Medicine, Tulane University, United States; Southeast Louisiana VA Medical Center, New Orleans, LA, United States. Electronic address: yyoshida1@tulane.edu.
Zhipeng ChenDepartment of Biostatistics and Data Science, Tulane University School of Public Health and Tropical Medicine, United States.
Robin L BaudierDepartment of Epidemiology, Tulane University School of Public Health and Tropical Medicine, United States.
Marie Krousel-WoodSection of General Internal Medicine, Deming Department of Medicine, Tulane University School of Medicine, United States; Department of Epidemiology, Tulane University School of Public Health and Tropical Medicine, United States; Tulane Center of Excellence in Sex-Based Biology & Medicine, Tulane University, United States.
Amanda H AndersonDepartment of Epidemiology, Tulane University School of Public Health and Tropical Medicine, United States.
Vivian A FonsecaSection of Endocrinology and Metabolism, Deming Department of Medicine, Tulane University School of Medicine, United States; Southeast Louisiana VA Medical Center, New Orleans, LA, United States.
Franck Mauvais-JarvisSection of Endocrinology and Metabolism, Deming Department of Medicine, Tulane University School of Medicine, United States; Tulane Center of Excellence in Sex-Based Biology & Medicine, Tulane University, United States; Southeast Louisiana VA Medical Center, New Orleans, LA, United States.
Tulane University · US

Funding

Tulane COBRE in Cardiometabolic Diseases Clinical Research CoreP20GM109036 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI Katherine Teresa Mills · 2016 to 2026
$25.3M
Tulane Building Interdisciplinary Research Careers in Women's Health (BIRCWH)K12HD043451 · NICHD · TULANE UNIVERSITY OF LOUISIANA · PI KROUSEL-WOOD, MARIE · 2002 to 2023
$9.9M
Targeting the estrogen receptor-α to protect functional β-cell mass in womenR01DK074970 · NIDDK · TULANE UNIVERSITY OF LOUISIANA · PI Franck Mauvais-Jarvis · 2007 to 2026
$6.0M
The Gut Microbiome and The Metabolome in Chronic Kidney DiseaseR01DK107566 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI ANDERSON, AMANDA HYRE, WU, GARY D. · 2016 to 2020
$2.8M
Measures of Fibrosis and Clinical Outcomes in Chronic Kidney DiseaseR01DK104730 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI ANDERSON, AMANDA HYRE · 2015 to 2019
$1.9M
Building Interdisciplinary Research Careers in Women's HealthK12AR084224 · NIAMS · TULANE UNIVERSITY OF LOUISIANA · PI Marie Krousel-Wood · 2024 to 2026
$1.6M
Repurposing estrogens to improve pancreatic islet transplantationR01DK107444 · NIDDK · TULANE UNIVERSITY OF LOUISIANA · PI MAUVAIS-JARVIS, FRANCK · 2016 to 2019
$1.5M
The role of the androgen receptor in insulin secretionI01BX003725 · VA · SOUTHEAST LOUISIANA VETERANS HEALTH CARE · PI MAUVAIS-JARVIS, FRANCK · 2018 to 2022
–
BLRD VA I01 BX003725NIAMS NIH HHS K12 AR084224NICHD NIH HHS K12 HD043451NIDDK NIH HHS R01 DK074970NIDDK NIH HHS R01 DK104730NIDDK NIH HHS R01 DK107444NIDDK NIH HHS R01 DK107566NIGMS NIH HHS P20 GM109036
6 · The paper itself

Abstract

BACKGROUND AND

aimsThe effect of MHT on cardiovascular disease (CVD) risk among women with prediabetes or type 2 diabetes (PreDM or T2DM) is unclear. We examined the association between ever or early use MHT and CVD risk in postmenopausal women with PreDM or T2DM, and the potential modifying effect of race.

methods2,917 postmenopausal women with PreDM or T2DM were pooled from 3 prospective CVD cohorts (the Atherosclerosis Risk in Communities, the Multi-Ethnic Study of Atherosclerosis, and the Jackson Heart Study). Ever (yes vs no) or early use of MHT (MHT initiated ≤5 vs > 5 years since menopause), and their associations with ischemic stroke, coronary heart disease (CHD), and atherosclerotic cardiovascular disease (ASCVD) were assessed using Cox proportional hazards models.

resultsDuring a median follow-up of 15 years, 264 stroke, 484 CHD, and 659 ASCVD events were observed. In fully adjusted models, ever use of MHT was associated with reduced risk of stroke (hazard ratio 0.86, 95% CI 0.76-0.98), CHD (0.85, 0.74-0.98), and ASCVD (0.83, 0.73-0.95) in white women with PreDM or T2DM. Early use of MHT was associated with reduced risk of stroke (0.82, 0.72-0.95), CHD (0.85, 0.74-0.98), and ASCVD (0.82, 0.70-0.96) in the white group. No risk reduction with ever or early use of MHT was found for black women with PreDM or T2DM.

conclusionsMHT is associated with statistically reduced CVD risk among white but not black women with PreDM or DM. Race is an effect modifier in the association between MHT use and CVD.

Indexed as

Cardiovascular DiseasesCoronary DiseaseDiabetes Mellitus, Type 2Prediabetic StateFemaleHumansMenopausePostmenopauseProspective StudiesRisk AssessmentRisk FactorsCVDMenopausal hormone therapyWomen with pre-diabetes or type 2 diabetes

Identifiers

PMID35114556
PMCPMC8905583
OpenAlexW4206956844

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.