Individualized management of primary hyperparathyroidism.

IF 9.2 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Journal of Internal Medicine Pub Date : 2026-06-01 Epub Date: 2026-04-06 DOI:10.1111/joim.70089
Jens Bollerslev, Filomena Cetani, Neil Gittoes, Lars Rolighed
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引用次数: 0

Abstract

Primary hyperparathyroidism (PHPT) is a common endocrine disease that typically presents in peri- and postmenopausal women. PHPT is due to a single parathyroid adenoma in most cases, which leads to stable hypercalcemia over years. Nowadays, the diagnosis is often coincidental, reached by chance in subjects without specific symptoms-asymptomatic PHPT. However, the patients might have subtle disease-related manifestations. Management standards have been reviewed through international workshops over more than three decades, leading to absolute and relative indications for parathyroidectomy (PTX), the only curative treatment. The alternative to PTX is observation without intervention in asymptomatic patients without organ manifestations and only mildly elevated calcium levels (mild PHPT). On the basis of recent literature, our aim is to challenge current recommendations for managing PHPT with focus on mild asymptomatic disease, integrating informed patient preferences. Considering the changing patient demography with increasing life expectancy, more sensitive visualization procedures, improved surgical techniques, and new data on PHPT-related morbidity, we test some of the established indications for PTX, particularly age as an isolated criterion, and the validity of a circulating calcium "threshold" for considering PTX. Additionally, bone mineral density (BMD) decreases for at least a decade with observation in contrast to PTX, where BMD normalizes after surgery and remains stable in the axial compartments for years. Therefore, skeletal-related thresholds for PTX also deserve review. In conclusion, we suggest integrating more clinical outcomes and wider perspectives in decision-making for the management of mild PHPT, taking patient preferences into consideration, and focusing on informed and shared decision-making.

原发性甲状旁腺功能亢进的个体化治疗。
原发性甲状旁腺功能亢进(PHPT)是一种常见的内分泌疾病,通常出现在围绝经期和绝经后妇女。PHPT是由于一个单一的甲状旁腺瘤在大多数情况下,导致稳定的高钙血症多年。如今,诊断常常是巧合,在没有特定症状的受试者中偶然得出-无症状PHPT。然而,患者可能有细微的疾病相关表现。三十多年来,通过国际研讨会对管理标准进行了审查,导致甲状旁腺切除术(PTX)的绝对和相对适应症,这是唯一的治愈治疗方法。PTX的替代方案是对无器官表现且只有轻度钙水平升高的无症状患者进行无干预的观察。在最近文献的基础上,我们的目标是挑战目前关于PHPT治疗的建议,将重点放在轻度无症状疾病上,整合知情的患者偏好。考虑到患者人口统计学的变化,预期寿命的增加,更敏感的可视化程序,改进的手术技术,以及phpt相关发病率的新数据,我们测试了PTX的一些既定适应症,特别是作为孤立标准的年龄,以及考虑PTX的循环钙“阈值”的有效性。此外,与PTX相比,观察到骨密度(BMD)下降至少十年,PTX的骨密度在手术后恢复正常,并在轴室保持稳定数年。因此,PTX的骨骼相关阈值也值得回顾。综上所述,我们建议在轻度PHPT的治疗决策中考虑更多的临床结果和更广泛的视角,考虑患者的偏好,并注重知情和共同决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Internal Medicine
Journal of Internal Medicine 医学-医学:内科
CiteScore
22.00
自引率
0.90%
发文量
176
审稿时长
4-8 weeks
期刊介绍: JIM – The Journal of Internal Medicine, in continuous publication since 1863, is an international, peer-reviewed scientific journal. It publishes original work in clinical science, spanning from bench to bedside, encompassing a wide range of internal medicine and its subspecialties. JIM showcases original articles, reviews, brief reports, and research letters in the field of internal medicine.
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