Jaime Perez

Dec 31, 2024 | nature.com | Matthew Loria |Tomasz Tabernacki |Shubham Gupta |Kirtishri Mishra |Swagata Banik |Carly Goldblatt | +5 more

The objective of this study is to evaluate the risk of being diagnosed with an eating disorder among transgender and gender-diverse (TGD) individuals, specifically examining how this risk differs following gender-affirming medical therapy (GAMT). The study utilizes electronic medical record (EMR) data from the TriNetX database. A total of 90,955 TGD individuals were identified in the TriNetX database. TGD individuals were divided into cohorts according to gender-affirming interventions they received. To assess the risk of eating disorder diagnoses across groups, we applied a Cox proportional hazards model with gender-affirming care as a time-varying covariate. Here we show that transfeminine individuals receiving hormone therapy (HT) have a significantly higher likelihood of being diagnosed with an eating disorder compared to those without intervention (HR:1.67, 95% CI:1.41, 1.98). Conversely, transmasculine individuals on HT exhibit a reduced risk of being diagnosed with an eating disorder relative to those without intervention (HR: 0.83, 95% CI: 0.76, 0.90). After undergoing gender-affirming medical therapy, the risk of eating disorder diagnosis increases for transfeminine individuals and decreases for transmasculine individuals. The observed differences in risk between transfeminine and transmasculine individuals on GAMT may be attributed to factors such as gendered societal norms, variations in screening practices, and the physiological effects of hormone therapy on eating disorder symptomatology. Further research is needed to clarify these influences and support tailored interventions. Loria, Tabernacki et al. investigate the risk of eating disorder diagnoses among transgender and gender-diverse individuals. Transfeminine individuals on hormone therapy are more likely to be diagnosed with eating disorders, while transmasculine individuals on hormone or surgical therapy are less likely to receive such diagnoses. Transgender and gender-diverse (TGD) individuals are at a higher risk of developing eating disorders, but the effects of gender-affirming interventions on this risk is not well known. Our study used data from nearly 91,000 TGD individuals to explore how hormone therapy and surgical transitioning might influence eating disorder diagnosis risk. We found that transfeminine individuals (those assigned male at birth who identify as female) on hormone therapy were more likely to be diagnosed with an eating disorder, while transmasculine individuals (those assigned female at birth who identify as male) on hormone therapy were less likely to receive such a diagnosis compared to TGD individuals not on hormone therapy. This difference in risk between transfeminine and transmasculine individuals may be explained by gendered societal norms, variations in screening practices, and the physiological effects of hormone therapy on eating disorder symptoms. Our findings highlight the need for supportive care and careful screening for eating disorders in TGD individuals receiving gender-affirming interventions.

Jun 5, 2024 | nature.com | Austin Thompson |Danly O. Omil-Lima |Jaime Perez |Erin Jesse |Mohit Khera |Nannan Thirumavalavan | +1 more

Hypogonadism is understudied in men requiring solid organ transplants, particularly among lung transplant recipients. Improvement in serum testosterone levels has been reported in kidney and liver transplantation. Using the TriNetX Research Network, we performed a retrospective cohort study to evaluate the incidence of peri-transplant hypogonadism and the natural course of serum testosterone following successful lung transplantation. Men aged ≥ 18 with a lung transplant and total testosterone drawn within one year pre- and post-transplant were included. Men with receipt of testosterone therapy were excluded. A low testosterone (<300 ng/dL) and normal testosterone (≥300 ng/dL) cohort was created before employing descriptive and analytic statistics to investigate the incidence of peri-transplant hypogonadism and the change in serum testosterone levels following lung transplantation. In our entire cohort, lung transplantation was not associated with a significant increase in post-transplant serum testosterone (329.86 ± 162.56 ng/dL pre-transplant and 355.13 ± 216.11 ng/dL post-transplant, p = 0.483). The number of men with low testosterone decreased by 9.8% following lung transplantation but was not significant, p = 0.404. In this pilot study, no significant change in the number of hypogonadal men nor serum testosterone levels was observed among men undergoing lung transplantation.