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盐耗型先天性肾上腺皮质增生症的盐皮质激素替代治疗。

Mineralocorticoid replacement therapy in salt-wasting congenital adrenal hyperplasia.

机构信息

Endocrinology in Charlottenburg, Berlin, Germany.

Department of Endocrinology and Metabolism, Charite-Universitätsmedizin, Campus Mitte, Berlin, Germany.

出版信息

Clin Endocrinol (Oxf). 2024 Oct;101(4):346-358. doi: 10.1111/cen.14959. Epub 2023 Aug 11.

Abstract

Patients with salt-wasting congenital adrenal hyperplasia (SW-CAH) usually show pronounced impairment of aldosterone secretion and, therefore, also require mineralocorticoid replacement. While a lot of research and discussion focusses on the glucocorticoid therapy in SW-CAH to replace the missing cortisol and to control adrenal androgen excess, very little research is dealing with mineralocorticoid replacement. However, recent data demonstrated an increased cardiovascular risk in adult CAH patients urging to reflect also on the current mineralocorticoid replacement therapy. In this review, we explain the role and function of the mineralocorticoid receptor, its ligands and inhibitors and its relevance for the therapy of patients with SW-CAH. We performed an extensive literature search and present data on mineralocorticoid therapy in SW-CAH patients as well as clinical advice how to monitor and optimise mineralocorticoid replacement therapy.

摘要

患有失盐型先天性肾上腺皮质增生症(SW-CAH)的患者通常表现出明显的醛固酮分泌受损,因此也需要进行盐皮质激素替代治疗。尽管有大量的研究和讨论集中在 SW-CAH 的糖皮质激素治疗上,以替代缺失的皮质醇并控制肾上腺雄激素过多,但很少有研究涉及盐皮质激素替代治疗。然而,最近的数据表明,成年 CAH 患者的心血管风险增加,这促使我们也对当前的盐皮质激素替代治疗进行反思。在这篇综述中,我们解释了盐皮质激素受体、其配体和抑制剂的作用和功能,以及它们对治疗 SW-CAH 患者的重要性。我们进行了广泛的文献检索,并介绍了 SW-CAH 患者盐皮质激素治疗的数据,以及如何监测和优化盐皮质激素替代治疗的临床建议。

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