Department of Endocrinology, Key Laboratory of Endocrinology, National Health Commission, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Science, Beijing, China.
Department of Clinical Nutrition, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Science, Beijing, China.
Front Endocrinol (Lausanne). 2022 Nov 16;13:1050305. doi: 10.3389/fendo.2022.1050305. eCollection 2022.
Pseudohypoparathyroidism (PHP) is a rare disease, especially when combined with pregnancy. We aimed to explore the changes in serum calcium/parathyroid hormone (PTH) level and medical treatment in a case series of PHP during pregnancy and the postpartum period.
A total of five PHP patients with six pregnancies were enrolled. The classification of PHP was based on (epi)genetic analysis. Clinical characteristics, biochemical indices, and treatment strategies before, during, and after pregnancy were retrospectively collected.
All patients received calcium and vitamin D agents with nearly normal serum calcium before pregnancy except patient 2 who was found hypocalcemic during gestation. All patients chose Cesarean section, and one suffered preterm delivery due to oligoamnios. The neonatal birth weight ranged from 2,250 to 4,300 g, and all neonates were free of hypocalcemia-related symptoms. The change in calcium metabolism was inconsistent including stable, improved, or worsened during pregnancy. Serum PTH level remained low in the first two trimesters in patients with stable and improved conditions while increased in the last two trimesters in patients with a worsened condition. Serum calcium changed inconsistently while PTH increased consistently during lactation. For patients who did not breastfeed, calcium homeostasis improved after delivery.
Calcium homeostasis and medicine dosage changed differently in PHP patients during pregnancy and lactation. However, most patients had good pregnancy outcomes. Serum PTH levels might predict changes in calcium metabolism during pregnancy.
假性甲状旁腺功能减退症(PHP)是一种罕见的疾病,特别是在合并妊娠时。我们旨在探讨 PHP 患者在妊娠及产后期间血清钙/甲状旁腺激素(PTH)水平变化及治疗方法。
共纳入 5 例 PHP 患者,6 次妊娠。PHP 的分类基于(表型)遗传学分析。回顾性收集了妊娠前、妊娠期间和产后的临床特征、生化指标和治疗策略。
除了在妊娠期间发现低钙血症的患者 2 外,所有患者在妊娠前均接受了钙剂和维生素 D 治疗,血清钙接近正常。所有患者均选择剖宫产,1 例因羊水过少而早产。新生儿出生体重为 2250~4300 g,均无低钙血症相关症状。钙代谢变化不一致,包括稳定、改善或恶化。在病情稳定和改善的患者中,血清 PTH 水平在妊娠前 2 个孕期保持较低水平,而在病情恶化的患者中在妊娠后 2 个孕期升高。在哺乳期,血清钙变化不一致,而 PTH 持续升高。对于未母乳喂养的患者,分娩后钙稳态得到改善。
PHP 患者在妊娠和哺乳期钙稳态和药物剂量的变化不同,但大多数患者妊娠结局良好。血清 PTH 水平可能预测妊娠期间钙代谢的变化。