Logel Santhi N, Maru Johsias, Whitehead Jax, Brady Cassandra, Walch Abby, Lasarev Michael, Rehm Jennifer L, Millington Kate
Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics, University of Wisconsin-Madison School of Medicine and Public Health, Madison, Wisconsin, USA.
Division of Pediatric Endocrinology, Department of Pediatrics, Benioff Children's Hospitals, University of California San Francisco, San Francisco, California, USA.
Transgend Health. 2024 Jun 17;9(3):197-204. doi: 10.1089/trgh.2022.0079. eCollection 2024 Jun.
The objective of this study is to determine the prevalence of certain autoimmune diseases in transgender and gender diverse (TGD) youth.
A multicenter, retrospective analysis was conducted from January 2013 to January 2019 of youth ≤26 years of age with concurrent diagnoses of gender dysphoria (GD) and at least one of the studied autoimmune diseases. Prevalence rates were calculated and compared to previously reported rates. Statistical significance was determined using second generation -values as pooled estimates of prevalence rates across study sites compared to a range of rates reported in the literature.
During the study period, 128 of 3812 (3.4%) youth evaluated for GD had a concurrent diagnosis of at least one of the studied autoimmune diseases. Three autoimmune diseases had prevalence rates significantly higher than those previously documented in the literature (second generation -value=0.000): type 1 diabetes mellitus (112.8/10,000, 95% confidence interval [CI]: 83.8-151.8), systemic lupus erythematosus (13.1/10,000, 95% CI: 5.5-31.5), and Graves' disease (12.3/10,000, 95% CI: 4.0-38.4).
There is an increased prevalence of certain autoimmune diseases in youth who identify as TGD presenting for subspecialty care. Limitations such as retrospective study design, selection bias, and reliance on electronic medical records make it difficult to draw wide-reaching conclusions about these findings. This study highlights the need for more research to delineate the impacts of unrecognized or untreated GD on autoimmune disease development and control.
本研究的目的是确定跨性别和性别多样化(TGD)青少年中某些自身免疫性疾病的患病率。
对2013年1月至2019年1月期间年龄≤26岁、同时诊断为性别焦虑症(GD)和至少一种所研究的自身免疫性疾病的青少年进行了多中心回顾性分析。计算患病率并与先前报告的患病率进行比较。使用第二代P值作为各研究地点患病率的汇总估计值,与文献中报告的一系列患病率进行比较,以确定统计学意义。
在研究期间,接受GD评估的3812名青少年中有128名(3.4%)同时诊断出至少一种所研究的自身免疫性疾病。三种自身免疫性疾病的患病率显著高于先前文献记载的患病率(第二代P值=0.000):1型糖尿病(112.8/10000,95%置信区间[CI]:83.8-151.8)、系统性红斑狼疮(13.1/10000,95%CI:5.5-31.5)和格雷夫斯病(12.3/10000,95%CI:4.0-38.4)。
在寻求专科护理的TGD青少年中,某些自身免疫性疾病的患病率有所增加。回顾性研究设计、选择偏倚和对电子病历的依赖等局限性使得难以就这些发现得出广泛的结论。本研究强调需要更多研究来阐明未识别或未治疗的GD对自身免疫性疾病发展和控制的影响。