Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Multicenter Study
. 2022 Sep 28;107(10):e4004-e4014.
doi: 10.1210/clinem/dgac469.

Multicenter Analysis of Cardiometabolic-related Diagnoses in Transgender and Gender-Diverse Youth: A PEDSnet Study

Affiliations
Multicenter Study

Multicenter Analysis of Cardiometabolic-related Diagnoses in Transgender and Gender-Diverse Youth: A PEDSnet Study

Anna Valentine et al. J Clin Endocrinol Metab. .

Abstract

Context: Studies on cardiometabolic health in transgender and gender-diverse youth (TGDY) are limited to small cohorts.

Objective: This work aimed to determine the odds of cardiometabolic-related diagnoses in TGDY compared to matched controls in a cross-sectional analysis, using a large, multisite database (PEDSnet).

Methods: Electronic health record data (2009-2019) were used to determine odds of cardiometabolic-related outcomes based on diagnosis, anthropometric, and laboratory data using logistic regression among TGDY youth vs controls. The association of gender-affirming hormone therapy (GAHT) with these outcomes was examined separately among TGDY. TGDY (n = 4172) were extracted from 6 PEDSnet sites and propensity-score matched on 8 variables to controls (n = 16 648). Main outcomes measures included odds of having cardiometabolic-related diagnoses among TGDY compared to matched controls, and among TGDY prescribed GAHT compared to those not prescribed GAHT.

Results: In adjusted analyses, TGDY had higher odds of overweight/obesity (1.2; 95% CI, 1.1-1.3) than controls. TGDY with a testosterone prescription alone or in combination with a gonadotropin-releasing hormone agonist (GnRHa) had higher odds of dyslipidemia (1.7; 95% CI, 1.3-2.3 and 3.7; 95% CI, 2.1-6.7, respectively) and liver dysfunction (1.5; 95% CI, 1.1-1.9 and 2.5; 95% CI, 1.4-4.3) than TGDY not prescribed GAHT. TGDY with a testosterone prescription alone had higher odds of overweight/obesity (1.8; 95% CI, 1.5-2.1) and hypertension (1.6 95% CI, 1.2-2.2) than those not prescribed testosterone. Estradiol and GnRHa alone were not associated with greater odds of cardiometabolic-related diagnoses.

Conclusion: TGDY have increased odds of overweight/obesity compared to matched controls. Screening and tailored weight management, sensitive to the needs of TGDY, are needed.

Keywords: body mass index; cardiometabolic; cholesterol; gender dysphoria; hormone therapy; pediatric.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Odds of cardiometabolic-related diagnoses among TGDY vs controls. The forest plots show the odds ratios and 95% CIs of cardiometabolic-related diagnoses among TGDY compared to controls. Higher odds ratios (> 1) indicate that TGDY are more likely to have the listed diagnosis. Lower odds ratios (< 1) indicate that TGDY are less likely to have the listed diagnosis. Unadjusted analyses are shown in gray squares; adjusted analyses (for overweight/obesity, depression, and antipsychotic medication use) are shown in black circles. Overweight/obesity and PCOS not adjusted for overweight/obesity. *P < .01. PCOS, polycystic ovary syndrome; TGDY, transgender and gender-diverse youth.
Figure 2.
Figure 2.
Odds of cardiometabolic outcomes by prescription among transgender and gender-diverse youth. The forest plots show the adjusted odds ratios and 95% CIs of cardiometabolic health outcomes among TGDY prescribed these medications compared to those not prescribed these medications. Higher odds ratios (> 1) indicate that TGDY prescribed these medications are more likely to have the listed diagnosis compared to TGDY not prescribed these medications. Lower odds ratios (< 1) indicate that TGDY on these medications are less likely to have the listed diagnosis compared to TGDY not on these medications. *P < .01, **P < .001, ***P < .0001. TGDY, transgender and gender-diverse youth.

Comment in

  • Cardiometabolic Outcomes in Transgender Youth.
    O'Connell MA, Pang KC. O'Connell MA, et al. J Clin Endocrinol Metab. 2022 Nov 25;107(12):e4380-e4381. doi: 10.1210/clinem/dgac592. J Clin Endocrinol Metab. 2022. PMID: 36221797 No abstract available.

References

    1. Johns MM, Lowry R, Andrzejewski J, et al. . Transgender identity and experiences of violence victimization, substance use, suicide risk, and sexual risk behaviors among high school students—19 states and large urban school districts, 2017. Morb Mortal Wkly Rep. 2019;68(3):67-71. doi:10.15585/mmwr.mm6803a3 - DOI - PMC - PubMed
    1. Hembree WC, Cohen-Kettenis PT, Gooren L, et al. . Endocrine treatment of gender-dysphoric/gender-incongruent persons: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2017;102(11):3869-3903. doi:10.1210/jc.2017-01658 - DOI - PubMed
    1. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders: DSM-5. 5th ed.American Psychiatric Association; 2013:xliv, 947.
    1. Nota NM, Wiepjes CM, de Blok CJM, Gooren LJG, Kreukels BPC, den Heijer M. Occurrence of acute cardiovascular events in transgender individuals receiving hormone therapy. Circulation. 2019;139(11):1461-1462. doi:10.1161/CIRCULATIONAHA.118.038584 - DOI - PubMed
    1. Islam N, Nash R, Zhang Q, et al. . Is there a link between hormone use and diabetes incidence in transgender people? Data from the STRONG cohort. J Clin Endocrinol Metab. 2022;107(4):e1549-e1557. doi:10.1210/clinem/dgab832 - DOI - PMC - PubMed

Publication types