Evidence map›Paper›PMID 40013361›Full record

Observational studyArteriosclerosis, thrombosis, and vascular biology2025

Sex-Divergent Blood Pressure Associations With Multiorgan System Metabolic Stress-Brief Report.

Alan C Kwan, Minhao Wang, Hongwei Ji, Brian Claggett, David Ouyang, Hirsh D Trivedi, Sonia Sharma, John Y-J Shyy, Amanda Velazquez, Joseph E Ebinger and 1 more

Abstract readObservational StudyComparative Study
In one paragraph

Observational study in Arteriosclerosis, thrombosis, and vascular biology, 2025. 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
–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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Alan C KwanDepartment of Cardiology, Smidt Heart Institute (A.C.K., M.W., D.O., J.E.E., S.C.), Cedars-Sinai Medical Center, Los Angeles, CA.ORCID 0000-0002-4393-1011
Minhao WangDepartment of Cardiology, Smidt Heart Institute (A.C.K., M.W., D.O., J.E.E., S.C.), Cedars-Sinai Medical Center, Los Angeles, CA.ORCID 0000-0003-0160-0254
Hongwei JiTsinghua Medicine, Tsinghua University, Beijing, China (H.J.).ORCID 0000-0003-3657-4666
Brian ClaggettCardiovascular Division, Brigham and Women's Hospital, Boston, MA (B.C.).ORCID 0000-0002-4215-9218
David OuyangDepartment of Cardiology, Smidt Heart Institute (A.C.K., M.W., D.O., J.E.E., S.C.), Cedars-Sinai Medical Center, Los Angeles, CA.ORCID 0000-0002-3813-7518
Hirsh D TrivediKarsh Division of Gastroenterology and Hepatology, Department of Medicine (H.T.), Cedars-Sinai Medical Center, Los Angeles, CA.ORCID 0000-0002-8328-9211
Sonia SharmaLa Jolla Institute for Immunology, CA (S.S.).
John Y-J ShyyDivision of Cardiology, Department of Medicine, University of California, San Diego, La Jolla (J.S.).ORCID 0000-0002-5625-753X
Amanda VelazquezDepartment of Surgery (A.V.), Cedars-Sinai Medical Center, Los Angeles, CA.ORCID 0000-0002-7620-4443
Joseph E EbingerDepartment of Cardiology, Smidt Heart Institute (A.C.K., M.W., D.O., J.E.E., S.C.), Cedars-Sinai Medical Center, Los Angeles, CA.ORCID 0000-0002-0587-1572
Susan ChengDepartment of Cardiology, Smidt Heart Institute (A.C.K., M.W., D.O., J.E.E., S.C.), Cedars-Sinai Medical Center, Los Angeles, CA.ORCID 0000-0002-4977-036X

Funding

UCLA Clinical Translational Science InstituteUL1TR001881 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ARLEEN F. BROWN, ARASH NAEIM · 2016 to 2026
$118.1M
The Effect of Nanoparticle Encapsulated Resveratrol on Treatment of PeriodontitisKL2TR001882 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Elizabeta Nemeth · 2016 to 2026
$13.1M
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
Eicosanoids, Chronic Kidney Disease Progression, and Associated Cardiovascular RiskR01DK141162 · NIDDK · CEDARS-SINAI MEDICAL CENTER · PI Susan Cheng · 2024 to 2026
$3.6M
Bioactive Metabolites Modulate Immune-Related Adverse Events in Cancer ImmunotherapyR01CA256133 · NCI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI DENNIS, EDWARD A, SHARMA, SONIA · 2021 to 2025
$3.5M
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
NCATS NIH HHS KL2 TR001882NCATS NIH HHS UL1 TR001881NCI NIH HHS R01 CA256133NHLBI NIH HHS K23 HL153888NIA NIH HHS U54 AG065141NIDDK NIH HHS R01 DK141162
6 · The paper itself

Abstract

backgroundWomen experience excess cardiovascular risk compared with men in the setting of similar metabolic disease burden. We aimed to examine sex differences in the vascular response to various forms of metabolic stress.

methodsWe conducted an observational study of 4299 adult participants (52% women, aged 59±13 years) of the National Health and Nutrition Examination Survey 2017 to 2018 cohort and 110 225 adult outpatients (55% women, aged 64±16 years) from the Cedars-Sinai Medical Center in 2019. We used natural splines to examine the association of systemic and organ-specific measures of metabolic stress including body mass index, hemoglobin A1c, hepatic FIB-4 (Fibrosis-4) score, and CKD-EPI estimated glomerular filtration rate with systolic blood pressure (SBP). Piecewise linear models were generated using normal value thresholds (body mass index <25 kg/m

resultsWomen compared with men demonstrated larger magnitudes and an earlier onset of increase in SBP per increment increase across all metabolic stress measures. The slope of SBP increase per increment of each metabolic measure was greater for women than men particularly for metabolic measures within the normal range, with slope differences of 1.86 mm Hg per kg/m

conclusionsWomen exhibited greater SBP alteration in the setting of multiple types of metabolic stress, particularly in periods representing the transition from metabolic health to disease. These findings suggest potential benefit of early metabolic health interventions as part of efforts to mitigate vascular risks in both women and men.

Indexed as

Blood PressureCardiovascular DiseasesStress, PhysiologicalAdultAgedBody Mass IndexFemaleGlomerular Filtration RateGlycated HemoglobinHumansMaleMiddle AgedNutrition SurveysRisk AssessmentRisk FactorsSex FactorsGlycated Hemoglobinhemoglobin A1c protein, humanheart disease risk factorsmetabolic diseasesoutpatientsrisk factorssex characteristics

Identifiers

PMID40013361
PMCPMC11936467

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Registered trials

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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.