Gender-affirming interventions and prognosis in multiple sclerosis.

IF 5
Nur Neyal, Nabeela Nathoo, Elizabeth J Cathcart-Rake, Orhun H Kantarci, Burcu Zeydan
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Abstract

Background: Gender-affirming hormone therapy (GAHT) may increase multiple sclerosis (MS) risk, yet MS disease course among transgender and gender-diverse (TGD) individuals remains understudied. We aimed to evaluate the disease course in TGD individuals with MS (TGD-MS).

Methods: Seventeen TGD-MS were identified. Ten TGD-MS on GAHT (five transgender women with MS (TW-MS) and five transgender men with MS (TM-MS)) were investigated further for MS outcomes of symptomatic (clinical)/asymptomatic (radiological) disease activity and progressive MS (PMS) onset.

Results: TW-MS (mean = 54.5 years, range = 35.1-66.3) were older than TM-MS (39.2 years, range = 29.6-47.2) at last follow-up. MS onset was later in TW-MS (31.5 years, range = 25.1-39.1) than in TM-MS (21.0 years, range = 15.0-29.8). Three patients (one TW-MS, two TM-MS) experienced symptomatic activity after GAHT initiation (8-10 months); in two patients (one TW-MS, one TM-MS), this marked symptomatic MS onset. Seven patients (four TW-MS, three TM-MS) had ⩾1 clinical/radiological disease activity. Four had PMS; all were TW-MS. In three, GAHT initiation preceded PMS onset (1-5 years). Disability was higher in TW-MS than in TM-MS.

Conclusion: MS disease course may be modified by GAHT and may differ between TW-MS and TM-MS, highlighting the need for larger long-term studies to overcome disparities in MS care. Comprehensive GAHT history, timely management, and closer follow-up are warranted in TGD-MS.

性别肯定干预和多发性硬化症的预后。
背景:性别确认激素治疗(GAHT)可能增加多发性硬化症(MS)的风险,但变性人和性别多样化(TGD)个体的MS病程仍未得到充分研究。我们的目的是评估TGD患者合并MS (TGD-MS)的病程。方法:鉴定17个TGD-MS。对10例TGD-MS(5名变性MS女性(TW-MS)和5名变性MS男性(TM-MS))进行了进一步的MS结局调查,包括症状(临床)/无症状(放射学)疾病活动性和进展性MS (PMS)发病。结果:TW-MS(平均54.5岁,范围35.1 ~ 66.3岁)比TM-MS(39.2岁,范围29.6 ~ 47.2岁)年龄大。TW-MS的发病时间(31.5年,范围= 25.1-39.1)晚于TM-MS(21.0年,范围= 15.0-29.8)。3例患者(1例TW-MS, 2例TM-MS)在GAHT启动后(8-10个月)出现症状活动;在2例患者(1例TW-MS, 1例TM-MS)中,这标志着症状性MS发作。7名患者(4名TW-MS, 3名TM-MS)的临床/放射学疾病活动大于或等于1。4人有经前综合症;均为TW-MS。在3例中,经前症候群发病前(1-5年)就开始了GAHT治疗。TW-MS组致残率高于TM-MS组。结论:GAHT可能改变多发性硬化症病程,并且在TW-MS和TM-MS之间可能存在差异,强调需要更大规模的长期研究来克服多发性硬化症治疗的差异。在TGD-MS中,需要全面的gat病史,及时的管理和更密切的随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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