Vlot Mariska C, Klink Daniel T, den Heijer Martin, Blankenstein Marinus A, Rotteveel Joost, Heijboer Annemieke C
Department of Clinical Chemistry, Endocrine Laboratory, VU University Medical Center, de Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands; Department of Internal Medicine, section Endocrinology, VU University Medical Center, de Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands.
Center of Expertise on Gender Dysphoria, VU University Medical Center, de Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands; Department of Pediatric Endocrinology, VU University Medical Center, de Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands.
Bone. 2017 Feb;95:11-19. doi: 10.1016/j.bone.2016.11.008. Epub 2016 Nov 11.
Puberty is highly important for the accumulation of bone mass. Bone turnover and bone mineral density (BMD) can be affected in transgender adolescents when puberty is suppressed by gonadotropin-releasing hormone analogues (GnRHa), followed by treatment with cross-sex hormone therapy (CSHT). We aimed to investigate the effect of GnRHa and CSHT on bone turnover markers (BTMs) and bone mineral apparent density (BMAD) in transgender adolescents. Gender dysphoria was diagnosed based on diagnostic criteria according to the DSM-IV (TR). Thirty four female-to-male persons (transmen) and 22 male-to-female persons (transwomen)were included. Patients were allocated to a young (bone age of <15years in transwomen or <14 in transmen) or old group (bone age of ≥15years in transwomen or ≥14years in transmen). All were treated with GnRHa triptorelin and CSHT was added in incremental doses from the age of 16years. Transmen received testosterone esters (Sustanon, MSD) and transwomen received 17-β estradiol. P1NP, osteocalcin, ICTP and BMD of lumbar spine (LS) and femoral neck (FN) were measured at three time points. In addition, BMAD and Z-scores were calculated. We found a decrease of P1NP and 1CTP during GnRHa treatment, indicating decreased bone turnover (young transmen 95% CI -74 to -50%, p=0.02, young transwomen 95% CI -73 to -43, p=0.008). The decrease in bone turnover upon GnRHa treatment was accompanied by an unchanged BMAD of FN and LS, whereas BMAD Z-scores of predominantly the LS decreased especially in the young transwomen. Twenty-four months after CSHT the BTMs P1NP and ICTP were even more decreased in all groups except for the old transmen. During CSHT BMAD increased and Z-scores returned towards normal, especially of the LS (young transwomen CI 95% 0.1 to 0.6, p=0.01, old transwomen 95% CI 0.3 to 0.8, p=0.04). To conclude, suppressing puberty by GnRHa leads to a decrease of BTMs in both transwomen and transmen transgender adolescents. The increase of BMAD and BMAD Z-scores predominantly in the LS as a result of treatment with CSHT is accompanied by decreasing BTM concentrations after 24months of CSHT. Therefore, the added value of evaluating BTMs seems to be limited and DXA-scans remain important in follow-up of bone health of transgender adolescents.
青春期对于骨量积累极为重要。当促性腺激素释放激素类似物(GnRHa)抑制青春期,随后进行跨性别激素治疗(CSHT)时,跨性别青少年的骨转换和骨矿物质密度(BMD)可能会受到影响。我们旨在研究GnRHa和CSHT对跨性别青少年骨转换标志物(BTMs)和骨矿物质表观密度(BMAD)的影响。根据《精神疾病诊断与统计手册》第四版(修订版)(DSM-IV[TR])的诊断标准诊断性别焦虑症。纳入了34名女性变男性者(男跨女)和22名男性变女性者(女跨男)。患者被分为年轻组(女跨男骨龄<14岁或男跨女骨龄<15岁)或老年组(女跨男骨龄≥14岁或男跨女骨龄≥15岁)。所有患者均接受GnRHa曲普瑞林治疗,并从16岁起递增剂量添加CSHT。男跨女接受睾酮酯(长效睾酮,默克雪兰诺),女跨男接受17-β雌二醇。在三个时间点测量腰椎(LS)和股骨颈(FN)的I型前胶原氨基端前肽(P1NP)、骨钙素、I型胶原交联羧基末端肽(ICTP)和BMD。此外,计算BMAD和Z评分。我们发现GnRHa治疗期间P1NP和ICTP降低,表明骨转换减少(年轻男跨女95%可信区间-74至-50%,p=0.02;年轻女跨男95%可信区间-73至-43,p=0.008)。GnRHa治疗后骨转换降低伴随着FN和LS的BMAD无变化,而主要是LS的BMAD Z评分降低,尤其是年轻女跨男。CSHT治疗24个月后,除老年男跨女外,所有组的BTMs P1NP和ICTP进一步降低。CSHT治疗期间BMAD增加,Z评分恢复正常,尤其是LS(年轻女跨男95%可信区间0.1至0.6,p=0.01;老年女跨男95%可信区间0.3至0.8,p=0.04)。总之,GnRHa抑制青春期导致女跨男和男跨女跨性别青少年的BTMs降低。CSHT治疗导致主要是LS的BMAD和BMAD Z评分增加,同时CSHT治疗24个月后BTM浓度降低。因此,评估BTMs的附加价值似乎有限,双能X线吸收法扫描在跨性别青少年骨骼健康随访中仍然很重要。