Department of Women's and Children's Health, Uppsala University, 753 09 Uppsala, Sweden.
Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, 171 77 Stockholm, Sweden.
Eur J Prev Cardiol. 2022 Nov 8;29(15):2017-2026. doi: 10.1093/eurjpc/zwac133.
We compared the incidence of cardiovascular disease (CVD) in transgender participants with a diagnosis of gender dysphoria (GD) with and without gender-affirming hormone therapy (GAHT) to the incidence observed in the general population.
The population-based cohort included all individuals >10 years in Sweden linked to Swedish nationwide healthcare Registers (2006-16). Two comparator groups without GD/GAHT were matched (1:10) on age, county of residence, and on male and female birth-assigned sex, respectively. Cox proportional models provided hazard ratios (HRs) and 95% confidence intervals (CI) for CVD outcomes. Among 1779 transgender individuals [48% birth-assigned males (AMAB), 52% birth-assigned females (AFAB)], 18 developed CVD, most of which were conduction disorders. The incidence of CVD for AFAB individuals with GD was 3.7 per 1000 person-years (95% CI: 1.4-10.0). Assigned male at birth individuals with GD had an incidence of CVD event of 7.1 per 1000 person-years (95% CI: 4.2-12.0). The risk of CVD event was 2.4 times higher in AMAB individuals (HR: 2.4, 95% CI: 1.3-4.2) compared with cisgender women, and 1.7 higher compared with cisgender men (HR: 1.7, 95% CI: 1.0-2.9). Analysis limited to transgender individuals without GAHT yielded similar results to those with GAHT treatment.
The incidence of CVD among GD/GAHT individuals was low, although increased compared with matched individuals without GD and similar to the incidence among GD/no GAHT individuals, thus not lending support for a causal relationship between treatment and CVD outcomes. Larger studies with longer follow-up are needed to verify these findings, as well as possible effect modification by comorbidity.
我们比较了患有性别认同障碍(GD)和未接受性别肯定激素治疗(GAHT)的跨性别参与者与普通人群中心血管疾病(CVD)的发生率。
该基于人群的队列包括瑞典全国性医疗登记处(2006-16 年)中所有年龄在 10 岁以上的个体。两个没有 GD/GAHT 的对照组分别根据年龄、居住地和男性和女性出生时分配的性别进行 1:10 匹配。Cox 比例风险模型提供了 CVD 结局的风险比(HR)和 95%置信区间(CI)。在 1779 名跨性别者中[48%为出生时分配为男性(AMAB),52%为出生时分配为女性(AFAB)],18 人发生了 CVD,其中大多数为传导障碍。患有 GD 的 AFAB 个体的 CVD 发生率为每 1000 人年 3.7 例(95%CI:1.4-10.0)。患有 GD 的出生时分配为男性的个体 CVD 事件的发生率为每 1000 人年 7.1 例(95%CI:4.2-12.0)。与顺性别女性相比,AMAB 个体发生 CVD 事件的风险高 2.4 倍(HR:2.4,95%CI:1.3-4.2),与顺性别男性相比高 1.7 倍(HR:1.7,95%CI:1.0-2.9)。对未接受 GAHT 的跨性别者进行分析,结果与接受 GAHT 治疗者相似。
GD/GAHT 个体的 CVD 发生率较低,尽管与没有 GD 的匹配个体相比有所增加,但与 GD/无 GAHT 个体的发生率相似,因此不支持治疗与 CVD 结局之间存在因果关系。需要更大规模、随访时间更长的研究来验证这些发现,以及可能的合并症对结果的影响。