Evidence map›Paper›PMID 39453653›Full record

ArticleJAMA network open2024

Male Gender Expressivity and Diagnosis and Treatment of Cardiovascular Disease Risks in Men.

Nathaniel J Glasser, Jacob C Jameson, Elbert S Huang, Ian M Kronish, Stacy Tessler Lindau, Monica E Peek, Elizabeth L Tung, Harold A Pollack

Abstract read
In one paragraph

Article in JAMA network open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
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.

Nathaniel J GlasserSection of General Internal Medicine, University of Chicago, Chicago, Illinois.
Jacob C JamesonCenter for Health Decision Science, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
Elbert S HuangSection of General Internal Medicine, University of Chicago, Chicago, Illinois.
Ian M KronishCenter for Behavioral Cardiovascular Health, Columbia University Irving Medical Center, New York, New York.
Stacy Tessler LindauDepartment of Obstetrics & Gynecology, University of Chicago, Chicago, Illinois.
Monica E PeekSection of General Internal Medicine, University of Chicago, Chicago, Illinois.
Elizabeth L TungSection of General Internal Medicine, University of Chicago, Chicago, Illinois.
Harold A PollackCenter for Chronic Disease Research and Policy, University of Chicago, Chicago, Illinois.

Funding

Wave IV Data CollectionP01HD031921 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HARRIS, KATHLEEN MULLAN · 1994 to 2020
$86.1M
Voice-Activated Technology to Improve Mobility & Reduce Health Disparities: EngAGEing African American Older Adult-Care Partner DyadsP50MD017349 · NIMHD · UNIVERSITY OF CHICAGO · PI BAIG, ARSHIYA AHMED · 2021 to 2025
$24.3M
Research Design, Data, and Analytics CoreP30DK092949 · NIDDK · UNIVERSITY OF CHICAGO · PI MILDA Renne SAUNDERS · 2011 to 2026
$10.0M
My Diabetes My CommunityR01DK127961 · NIDDK · UNIVERSITY OF CHICAGO · PI HUANG, ELBERT S., LINDAU, STACY TESSLER · 2020 to 2020
$5.4M
Community Intervention to Reduce CardiovascuLar Disease in Chicago (CIRCL-Chicago)UH3HL154297 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Abel N. Kho, JUSTIN D SMITH · 2023 to 2026
$4.4M
CommunityRx-DementiaR01AG064949 · NIA · UNIVERSITY OF CHICAGO · PI HUANG, ELBERT S., LINDAU, STACY TESSLER · 2019 to 2023
$4.0M
Implementation of EMR-Integrated Referrals to Link Clinical and Community Services to Reduce Health InequityR01HL150909 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVE, GAURAV J, LINDAU, STACY TESSLER · 2020 to 2024
$3.9M
Implementing Remote Patient Monitoring to Improve Hypertension Control in a Primary Care NetworkR01HL152699 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI KRONISH, IAN MATTHEW · 2021 to 2025
$3.5M
CommunityRx for Hunger - Resubmission 01R01MD012630 · NIMHD · UNIVERSITY OF CHICAGO · PI LINDAU, STACY TESSLER · 2019 to 2023
$3.3M
Community Intervention to Reduce CardiovascuLar Disease in Chicago (CIRCL-Chicago)UG3HL154297 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI DAVIS, PARIS, KHO, ABEL N. · 2020 to 2022
$3.1M
Social Modulation of Transitions in Diabetes: Synthesizing Data Sets and Biomeasure AssaysR01AG060756 · NIA · UNIVERSITY OF CHICAGO · PI HUANG, ELBERT S., MCCLINTOCK, MARTHA KENT · 2019 to 2023
$3.1M
Training Program in Comparative Effectiveness Research for Suicide PreventionT32MH125815 · NIMH · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI MIGUEL HERNAN, MATTHEW K NOCK · 2022 to 2026
$1.2M
NHLBI NIH HHS K23 HL145090NHLBI NIH HHS R01 HL150909NHLBI NIH HHS R01 HL152699NHLBI NIH HHS UG3 HL154297NHLBI NIH HHS UH3 HL154297NIA NIH HHS K24 AG069080NIA NIH HHS R01 AG060756NIA NIH HHS R01 AG064949NICHD NIH HHS P01 HD031921NIDDK NIH HHS P30 DK092949NIDDK NIH HHS R01 DK127961NIMHD NIH HHS P50 MD017349NIMHD NIH HHS R01 MD012630NIMH NIH HHS T32 MH125815
6 · The paper itself

Abstract

Importance: Male gender expressivity (MGE), which reflects prevalent sociocultural pressures to convey masculinity, has been associated with health. Yet, little is known about associations of MGE with the diagnosis and treatment of modifiable cardiovascular disease (CVD) risks. Objective: To investigate associations of MGE with modifiable CVD risk diagnoses and treatment in men. Design, Setting, and Participants: This population-based cohort study included data from waves I (1994-1995), IV (2008-2009), and V (2016-2018) of the US National Longitudinal Study of Adolescent to Adult Health (Add Health). Participants were male adolescents (age 12-18 years) followed up longitudinally through younger adulthood (age 24-32 years) and adulthood (age 32-42 years). Data were analyzed from January 5, 2023, to August 28, 2024. Exposure: Male gender expressivity was quantified in adolescence and younger adulthood using an empirically-derived and validated measurement technique that incorporates participants' responses to existing Add Health survey items to capture how similarly participants behave to same-gendered peers. Main Outcomes and Measures: Outcomes included self-reported diagnoses of CVD risk conditions (hypertension, diabetes, or hyperlipidemia) in adult men with elevated blood pressure, hemoglobin A1c, or non-high-density lipoprotein cholesterol levels, and self-reported treatment with antihypertensive, hypoglycemic, or lipid-lowering medications in adults reporting hypertension, diabetes, or hyperlipidemia. Multivariable regression was used to examine associations of adolescent and younger adult MGE with adult CVD risk diagnoses and treatment, adjusting for sociodemographic covariates. Results: Among 4230 eligible male participants, most were non-Hispanic White (2711 [64%]) and privately insured (3338 [80%]). Their mean (SD) age was 16.14 (1.81) years in adolescence, 29.02 (1.84) years in younger adulthood, and 38.10 (1.95) years in adulthood. Compared with participants whose younger adult MGE was below average, those with higher younger adult MGE were overall less likely to report hypertension (22% vs 26%; P < .001), diabetes (5% vs 8%; P < .001), and hyperlipidemia (19% vs 24%; P < .001) diagnoses and diabetes treatment (3% vs 5%; P = .02) as adults. In multivariable models, every SD increase in adolescent MGE was associated with lower probabilities of adult hypertension treatment (MGE,-0.11; 95% CI, -0.16 to -0.6) and diabetes diagnoses (MGE, -0.15; 95% CI, -0.27 to -0.03). Higher younger adult MGE was associated with lower probabilities of adult hypertension diagnoses (MGE, -0.04; 95% CI, -0.07 to -0.01), hypertension treatment (MGE, -0.07; 95% CI, -0.13 to -0.01), and diabetes treatment (MGE, -0.10; 95% CI, -0.20 to -0.01). Adolescent and younger adult MGE outcomes were not associated with other adult CVD outcomes. Conclusions and Relevance: In this cohort study of US males, higher adolescent and younger adult MGE was associated with lower adult hypertension and diabetes diagnoses and treatment. These findings suggest that males with high MGE may bear distinctive risks and correspondingly benefit from tailored public health efforts to prevent downstream CVD.

Indexed as

Cardiovascular DiseasesAdolescentAdultChildCohort StudiesHeart Disease Risk FactorsHumansHypertensionLongitudinal StudiesMaleMasculinityRisk FactorsUnited StatesYoung Adult

Identifiers

PMID39453653
PMCPMC11512345

What OpenQuestion holds

Textmetadata
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.