Published October 25, 2024 | Version v1
Journal article Open

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

Description

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.

Data availability

See Supplement 2.

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Additional details

Identifiers

DOI
10.1001/jamanetworkopen.2024.41281
Other
oai:uchicago.tind.io:13822

Funding

National Institute of Child Health and Human Development
P01 HD31921
Health Resources and Services Administration
National Research Service Institutional Research Training Grant
National Institutes of Health
K24AG069080
National Institutes of Health
R01AG060756
National Institutes of Health
P30DK092949
National Institutes of Health
P50MD017349
National Institutes of Health
R01 HL152699
National Institutes of Health
1K23HL145090-01
National Institutes of Health
R01AG064949
National Institutes of Health
R01MD012630
National Institutes of Health
5R01HL150909
National Institutes of Health
UG3HL154297
National Institutes of Health
1R01DK127961

UChicago Information

Division(s)
Biological Sciences Division, Crown Family School of Social Work, Policy, and Practice
Department(s)
Medicine, Obstetrics and Gynecology, Public Health Sciences
Center(s) or Institute(s)
Center for Chronic Disease Research and Policy, Center for the Study of Race, Politics and Culture, Chicago Center for Diabetes Translation Research, Health Lab, MacLean Center for Clinical Medical Ethics