Hypoparathyroidism: diagnosis, management and emerging therapies

IF 40 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Nature Reviews Endocrinology Pub Date : 2025-02-04 DOI:10.1038/s41574-024-01075-8
Sarah Khan, Aliya A. Khan
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Abstract

Hypoparathyroidism is characterized by inadequate parathyroid hormone (PTH) secretion or action and results in hypocalcaemia, and can lead to hyperphosphataemia and hypercalciuria. Most cases of hypoparathyroidism occur as a complication of surgery, with the remainder due to causes including autoimmune disease, genetic causes, infiltrative diseases, mineral deposition or due to abnormalities in serum levels of magnesium. Hypoparathyroidism can cause multisystem disease, with long-term complications resulting from ectopic calcification as well as renal complications with nephrocalcinosis, nephrolithiasis and renal impairment in addition to respiratory, cardiac or neurological manifestations. Conventional therapy consists of oral calcium salts and active vitamin D but it has limitations, including fluctuations in serum levels of calcium and a high pill burden, and can increase the risk of long-term complications. By contrast, PTH replacement therapy can effectively achieve normal serum levels of calcium, and lower serum levels of phosphate. The long-acting PTH analogue, palopegteriparatide, has been shown to normalize urine levels of calcium. In addition, PTH replacement therapy reduces the pill burden. Palopegteriparatide is also associated with improved quality of life in comparison to conventional therapy. This Review summarizes current recommendations regarding the pathophysiology, evaluation and management of hypoparathyroidism and also references the 2022 international hypoparathyroidism guidelines. Palopegteriparatide has now been approved as PTH replacement therapy for hypoparathyroidism. Emerging therapies will also be presented in this Review. Hypoparathyroidism is a rare condition characterized by inadequate levels of parathyroid hormone (PTH) or resistance to PTH, leading to a wide range of health complications and reduced quality of life. This Review provides an update on the current understanding of hypoparathyroidism, its clinical management, and novel and emerging therapies.

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甲状旁腺功能减退:诊断、管理和新兴疗法
甲状旁腺功能减退症的特征是甲状旁腺激素(PTH)分泌或作用不足,导致低钙血症,并可导致高磷血症和高钙尿症。大多数甲状旁腺功能减退是手术的并发症,其余原因包括自身免疫性疾病、遗传原因、浸润性疾病、矿物质沉积或血清镁水平异常。甲状旁腺功能减退症可引起多系统疾病,除呼吸、心脏或神经系统表现外,还可引起异位钙化、肾钙化症、肾结石和肾损害等肾脏并发症的长期并发症。传统疗法包括口服钙盐和活性维生素D,但它有局限性,包括血清钙水平的波动和较高的药丸负担,并可能增加长期并发症的风险。相比之下,甲状旁腺激素替代疗法可以有效地达到正常的血清钙水平,降低血清磷酸盐水平。长效甲状旁腺激素类似物palopegteriparatide已被证明能使尿钙水平正常化。此外,甲状旁腺激素替代疗法减少了药物负担。与常规治疗相比,Palopegteriparatide也与改善生活质量有关。本综述总结了目前关于甲状旁腺功能减退的病理生理学、评估和管理的建议,并参考了2022年国际甲状旁腺功能减退指南。Palopegteriparatide已被批准作为甲状旁腺功能低下的甲状旁腺激素替代疗法。新兴疗法也将在本综述中介绍。
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来源期刊
Nature Reviews Endocrinology
Nature Reviews Endocrinology 医学-内分泌学与代谢
CiteScore
42.00
自引率
0.70%
发文量
158
审稿时长
6-12 weeks
期刊介绍: Nature Reviews Endocrinology aspires to be the foremost platform for reviews and commentaries catering to the scientific communities it serves. The journal aims to publish articles characterized by authority, accessibility, and clarity, enhanced with easily understandable figures, tables, and other visual aids. The goal is to offer an unparalleled service to authors, referees, and readers, striving to maximize the usefulness and impact of each article. Nature Reviews Endocrinology publishes Research Highlights, Comments, News & Views, Reviews, Consensus Statements, and Perspectives relevant to researchers and clinicians in the fields of endocrinology and metabolism. Its broad scope ensures that the work it publishes reaches the widest possible audience.
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