Use of Teriparatide, Denosumab, and Romosozumab in a Postpartum Monogenic Osteoporosis With a WNT1 Pathogenic Variation.

JCEM case reports Pub Date : 2025-03-26 eCollection Date: 2025-04-01 DOI:10.1210/jcemcr/luaf053
Thiago Cavalcanti Matos, Mariana Kistemann Gonçalves Dias, Andre Silva Franco
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Abstract

Early-onset osteoporosis (EOOP) is a form of osteoporosis (OP) that affects young people, and its etiologies include subclinical diseases, nutritional deficiencies, medications, or even genetic variants. We present a case of a 28-year-old woman with a history of vertebral and rib fractures immediately post partum. Although negative evaluation for secondary causes of OP, her bone densitometry showed a Z score of -4.7 in the lumbar spine (LS) and -3.3 both in the total hip (TH) and femoral neck (FN). Classified as very high-risk OP, anabolic treatment with teriparatide was initiated, with the addition of denosumab. At the end of this initial treatment, the patient showed partial improvement in her bone densitometry, leading to further investigation with a genetic panel. A pathogenic variant of the WNT1 gene (Chr12:48 981 551 AC > A) was identified. Consequently, romosozumab was considered, despite its absence in the official indication for such or similar cases, due to biological plausibility since it inhibits sclerostin, an inhibitor of the WNT pathway. Finally, the patient showed significant improvement in bone densitometry, with a total increase of +42.1% in lumbar spine bone mineral density (BMD) and +16.6% in total hip BMD.

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特立帕肽、地诺单抗和罗莫索单抗在产后单基因骨质疏松症WNT1致病变异中的应用
早发性骨质疏松症(EOOP)是一种影响年轻人的骨质疏松症(OP),其病因包括亚临床疾病、营养缺乏、药物治疗,甚至遗传变异。我们提出一个28岁的妇女与椎骨和肋骨骨折的历史,产后立即。虽然对OP的继发性原因的评估为阴性,但她的骨密度测量显示腰椎(LS)的Z评分为-4.7,全髋关节(TH)和股骨颈(FN)的Z评分为-3.3。归类为高危OP,开始使用特立帕肽进行合成代谢治疗,并添加地诺单抗。在初始治疗结束时,患者的骨密度测量出现部分改善,因此需要进行进一步的遗传小组调查。鉴定出WNT1基因的致病性变异(Chr12:48 981 551 AC > A)。因此,尽管romosozumab在此类或类似病例的官方适应症中没有,但由于其抑制WNT通路抑制剂硬化蛋白的生物学合理性,因此考虑了romosozumab。最后,患者骨密度测量有明显改善,腰椎骨密度(BMD)总增加+42.1%,髋部骨密度总增加+16.6%。
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