Reisner Sari L, Deutsch Madeline B, Mayer Kenneth H, Potter Jennifer, Gonzalez Alex, Keuroghlian Alex S, Hughto Jaclyn Mw, Campbell Juwan, Asquith Andrew, Pardee Dana J, Pletta David R, Radix Asa
Division of Endocrinology, Diabetes and Hypertension, Brigham and Women's Hospital, Boston, MA, United States.
Harvard Medical School, Boston, MA, United States.
JMIR Res Protoc. 2021 Mar 1;10(3):e24198. doi: 10.2196/24198.
Transgender and gender diverse (TGD) adults in the United States experience health disparities, especially in HIV infection. Medical gender affirmation (eg, hormone therapy and gender-affirming surgeries) is known to be medically necessary and to improve some health conditions. To our knowledge, however, no studies have assessed the effects of gender-affirming medical care on HIV-related outcomes.
This study aims to evaluate the effects of medical gender affirmation on HIV-related outcomes among TGD primary care patients. Secondary objectives include characterizing mental health, quality of life, and unmet medical gender affirmation needs.
LEGACY is a longitudinal, multisite, clinic-based cohort of adult TGD primary care patients from two federally qualified community health centers in the United States: Fenway Health in Boston, and Callen-Lorde Community Health Center in New York. Eligible adult TGD patients contribute electronic health record data to the LEGACY research data warehouse (RDW). Patients are also offered the option to participate in patient-reported surveys for 1 year of follow-up (baseline, 6-month, and 12-month assessments) with optional HIV and sexually transmitted infection (STI) testing. Biobehavioral data from the RDW, surveys, and biospecimen collection are linked. HIV-related clinical outcomes include pre-exposure prophylaxis uptake (patients without HIV), viral suppression (patients with HIV), and anogenital STI diagnoses (all patients). Medical gender affirmation includes hormones, surgeries, and nonhormonal and nonsurgical interventions (eg, voice therapy).
The contract began in April 2018. The cohort design was informed by focus groups with TGD patients (n=28) conducted between August-October 2018 and in collaboration with a community advisory board, scientific advisory board, and site-specific research support coalitions. Prospective cohort enrollment began in February 2019, with enrollment expected to continue through August 2020. As of April 2020, 7821 patients are enrolled in the LEGACY RDW and 1756 have completed a baseline survey. Participants have a median age of 29 years (IQR 11; range 18-82). More than one-third (39.7%) are racial or ethnic minorities (1070/7821, 13.68% Black; 475/7821, 6.07% multiracial; 439/7821, 5.61% Asian or Pacific Islander; 1120/7821, 14.32% other or missing) and 14.73% (1152/7821) are Hispanic or Latinx. By gender identity, participants identify as 33.79% (2643/7821) male, 37.07% (2900/7821) female, 21.74% (1700/7821) nonbinary, and 7.39% (578/7821) are unsure or have missing data. Approximately half (52.0%) of the cohort was assigned female sex at birth, and 5.4% (421/7821) are living with HIV infection.
LEGACY is an unprecedented opportunity to evaluate the impact of medical gender affirmation on HIV-related health. The study uses a comprehensive research methodology linking TGD patient biobehavioral longitudinal data from multiple sources. Patient-centeredness and scientific rigor are assured through the ongoing engagement of TGD communities, clinicians, scientists, and site clinical staff undergirded by epidemiological methodology. Findings will inform evidence-based clinical care for TGD patients, including optimal interventions to improve HIV-related outcomes.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/24198.
美国的跨性别和性别多样化(TGD)成年人面临健康差异,尤其是在艾滋病毒感染方面。医学性别肯定(如激素疗法和性别肯定手术)已知在医学上是必要的,并且能改善一些健康状况。然而,据我们所知,尚无研究评估性别肯定医疗对艾滋病毒相关结局的影响。
本研究旨在评估医学性别肯定对TGD初级保健患者艾滋病毒相关结局的影响。次要目标包括描述心理健康、生活质量以及未满足的医学性别肯定需求。
LEGACY是一项纵向、多地点、基于诊所的队列研究,研究对象为来自美国两个联邦合格社区健康中心的成年TGD初级保健患者:波士顿的芬威健康中心和纽约的卡伦 - 洛德社区健康中心。符合条件的成年TGD患者将电子健康记录数据贡献给LEGACY研究数据仓库(RDW)。患者还可选择参与患者报告的调查,进行为期1年的随访(基线、6个月和12个月评估),并可选择进行艾滋病毒和性传播感染(STI)检测。来自RDW、调查和生物样本采集的生物行为数据相互关联。艾滋病毒相关临床结局包括暴露前预防措施的采用情况(未感染艾滋病毒的患者)、病毒抑制情况(感染艾滋病毒的患者)以及肛门生殖器性传播感染诊断情况(所有患者)。医学性别肯定包括激素、手术以及非激素和非手术干预措施(如嗓音治疗)。
该合同于2018年4月开始。队列设计参考了2018年8月至10月期间与28名TGD患者进行的焦点小组讨论结果,并与社区咨询委员会、科学咨询委员会以及特定地点的研究支持联盟合作开展。前瞻性队列招募于2019年2月开始,预计招募将持续至2020年8月。截至2020年4月,7821名患者已纳入LEGACY RDW,1756名患者已完成基线调查。参与者的年龄中位数为29岁(四分位间距11;范围18 - 82岁)。超过三分之一(39.7%)为种族或族裔少数群体(1070/7821,13.68%为黑人;475/7821,6.07%为多种族;439/7821,5.61%为亚洲或太平洋岛民;1120/7821,14.32%为其他或缺失),14.73%(1152/7821)为西班牙裔或拉丁裔。按性别认同划分,参与者中33.79%(2643/7821)为男性,37.07%(2900/7821)为女性,21.74%(1700/7821)为非二元性别,7.39%(578/7821)不确定或数据缺失。该队列中约一半(52.0%)在出生时被指定为女性,5.4%(421/7821)感染了艾滋病毒。
LEGACY是评估医学性别肯定对艾滋病毒相关健康影响的前所未有的机会。该研究采用了一种综合研究方法,将来自多个来源的TGD患者生物行为纵向数据相联系。通过TGD社区、临床医生、科学家和地点临床工作人员在流行病学方法支持下的持续参与,确保了以患者为中心和科学严谨性。研究结果将为TGD患者的循证临床护理提供信息,包括改善艾滋病毒相关结局的最佳干预措施。
国际注册报告识别码(IRRID):DERR1 - 10.2196/24198