Evidence map›Paper›PMID 36760556›Full record

ArticleFrontiers in cardiovascular medicine2023

Sex differences in contributors to coronary microvascular dysfunction.

Alan C Kwan, Janet Wei, David Ouyang, Joseph E Ebinger, C Noel Bairey Merz, Daniel Berman, Susan Cheng

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 16 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

7 authors at 2 institutions in 1 country.

Alan C KwanDepartment of Cardiology, Smidt Heart Institute, Los Angeles, CA, United States.
Janet WeiDepartment of Cardiology, Smidt Heart Institute, Los Angeles, CA, United States.
David OuyangDepartment of Cardiology, Smidt Heart Institute, Los Angeles, CA, United States.
Joseph E EbingerDepartment of Cardiology, Smidt Heart Institute, Los Angeles, CA, United States.
C Noel Bairey MerzDepartment of Cardiology, Smidt Heart Institute, Los Angeles, CA, United States.
Daniel BermanDepartment of Cardiology, Smidt Heart Institute, Los Angeles, CA, United States.
Susan ChengDepartment of Cardiology, Smidt Heart Institute, Los Angeles, CA, United States.
Cedars-Sinai Smidt Heart Institute · USCedars-Sinai Medical Center · US

Funding

The Microvascular Aging and Eicosanoids - Women's Evaluation of Systemic Aging Tenacity (MAE-WEST) ("You are never too old to become younger!") Specialized Center for Research Excellence (SCORE)U54AG065141 · NIA · CEDARS-SINAI MEDICAL CENTER · PI SHYY, JOHN YJ · 2020 to 2024
$8.7M
Cardiac microstructure and the immune-inflammatory response to SARS-CoV-2R01HL131532 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI CHENG, SUSAN, LI, DEBIAO · 2016 to 2025
$6.6M
Women's Ischemia Syndrome Evaluation (WISE) Coronary Vascular DysfunctionR01HL090957 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI BAIREY MERZ, CATHLEEN NOEL, PEPINE, CARL J · 2008 to 2013
$3.5M
Myocardial Steatosis in Women with Coronary Microvascular Dysfunction: Defining the Pathway to Heart Failure with Preserved Ejection Fraction (HFpEF)R01HL153500 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI WEI, JANET · 2021 to 2025
$3.2M
Implementation Science to Improve Cardiovascular Health: Leveraging EHR Systems to Advance Care of Resistant HypertensionK23HL153888 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI EBINGER, JOSEPH · 2020 to 2024
$929k
Deep Learning Assessment of the Right Ventricle: Function, Etiology, and PrognosisK99HL157421 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI OUYANG, DAVID · 2021 to 2022
$313k
NHLBI NIH HHS K23 HL153888NHLBI NIH HHS K99 HL157421NHLBI NIH HHS R01 HL090957NHLBI NIH HHS R01 HL131532NHLBI NIH HHS R01 HL153500NIA NIH HHS U54 AG065141
6 · The paper itself

Abstract

Background: Coronary microvascular dysfunction (CMD) has differences in prevalence and presentation between women and men; however, we have limited understanding about underlying contributors to sex differences in CMD. Myocardial perfusion reserve index (MPRI), as semi-quantitative measure of myocardial perfusion derived from cardiac magnetic resonance (CMR) imaging has been validated as a measure of CMD. We sought to understand the sex differences in the relations between the MPRI and traditional measures of cardiovascular disease by CMR. Methods: A retrospective analysis of a single-center cohort of patients receiving clinical stress CMR from 2015 to 2022 was performed. Patients with calculated MPRI and no visible perfusion defects consistent with obstructive epicardial coronary disease were included. We compared associations between MPRI versus traditional cardiovascular risk factors and markers of cardiac structure/function in sex-stratified populations using univariable and multivariable regression models. Results: A total of 229 patients [193 female, 36 male, median age 57 (47-67) years] were included in the analysis. In the female population, no traditional cardiovascular risk factors were associated with MPRI, whereas in the male population, diabetes (β: -0.80, Conclusion: The findings suggest different underlying pathophysiology of CMD in men versus women, with lower MPRI in male patients fitting a more "traditional" atherosclerotic profile.

Indexed as

cardiac fibrosiscardiac MRI (CMR)cardiac remodelingcoronary microvascular dysfunction (CMD)myocardial perfusion reserve indexsex differences

Identifiers

PMID36760556
PMCPMC9902873
OpenAlexW4317821524

What OpenQuestion holds

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LicenceCC BY
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.