Ramasamy Indra
Conquest Hospital, Hastings TN37 7RD, UK.
J Clin Med. 2024 Aug 29;13(17):5134. doi: 10.3390/jcm13175134.
Transgender people experience distress due to gender incongruence (i.e., a discrepancy between their gender identity and sex assigned at birth). Gender-affirming hormone treatment (GAHT) is a part of gender reassignment treatment. The therapeutic goals of the treatment are to develop the physical characteristics of the affirmed gender as far as possible. Guidelines have been developed for GAHT, which recommend dosage as well as different formulations of oestrogen and testosterone for treatment. Questions arise about the metabolic side effects of hormone treatment. Establishing reference ranges for common analytes in transgender individuals remains a task for laboratory medicine. It has been suggested once GAHT is commenced, the reference ranges for affirmed gender are reported for red blood cells, haemoglobin and haematocrit. For transgender assigned-female-at-birth (AFAB) people, testosterone concentrations are recommended to be within the reference interval established for cisgender men and for transgender assigned-male-at-birth (AMAB) people, estradiol concentrations are within the reference range for cisgender women. Sex-specific reference ranges are available for certain laboratory tests, and these may be organ (e.g., heart)-specific. Transgender-specific reference ranges may be a requirement for such tests. Laboratories may need to make decisions on how to report other tests in the transgender population, e.g., eGFR. Interpretation of further tests (e.g., reproductive hormones) can be individualized depending on clinical information. Electronic medical record systems require fields for gender identity/biological sex at birth so that laboratory results can be flagged appropriately. In this review, we aim to summarise the current position of the role of the laboratory in the clinical care of the transgender individual. Prior to the review, we will summarise the genetics of sex determination, the aetiology of gender incongruence, and the recommendations for GAHT and monitoring for the transgender population.
跨性别者因性别不一致(即其性别认同与出生时被指定的性别之间存在差异)而感到痛苦。性别肯定激素治疗(GAHT)是性别重置治疗的一部分。该治疗的目标是尽可能发展出被认同性别的身体特征。已经制定了GAHT指南,其中推荐了治疗的剂量以及雌激素和睾酮的不同配方。激素治疗的代谢副作用引发了一些问题。确定跨性别个体常见分析物的参考范围仍是检验医学的一项任务。有人建议,一旦开始GAHT治疗,就应报告被认同性别的红细胞、血红蛋白和血细胞比容的参考范围。对于出生时被指定为女性(AFAB)的跨性别者,建议睾酮浓度在为顺性别男性确定的参考区间内;对于出生时被指定为男性(AMAB)的跨性别者,雌二醇浓度在顺性别女性的参考范围内。某些实验室检查有性别特异性参考范围,这些范围可能是器官(如心脏)特异性的。跨性别特异性参考范围可能是此类检查的要求。实验室可能需要决定如何报告跨性别群体的其他检查结果,例如估算肾小球滤过率(eGFR)。进一步检查(如生殖激素)的解读可根据临床信息进行个体化。电子病历系统需要有出生时性别认同/生物学性别的字段,以便能适当地标记实验室结果。在本综述中,我们旨在总结实验室在跨性别个体临床护理中的当前作用。在进行综述之前,我们将总结性别决定的遗传学、性别不一致的病因,以及针对跨性别群体的GAHT建议和监测方法。