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假性甲状旁腺功能减退症患者的骨化三醇和左甲状腺素剂量

Calcitriol and Levothyroxine Dosing for Patients With Pseudohypoparathyroidism.

作者信息

Antoun Jacqueline, Williamson Dylan, Hubler Merla, Shoemaker Ashley H

机构信息

Vanderbilt University School of Medicine, Nashville, TN 37212, USA.

Division of Pediatric Endocrinology, Vanderbilt University Medical Center, Nashville, TN 37212, USA.

出版信息

J Endocr Soc. 2021 Oct 27;5(12):bvab161. doi: 10.1210/jendso/bvab161. eCollection 2021 Dec 1.

Abstract

Pseudohypoparathyroidism (PHP) is a rare hormone resistance syndrome caused by mutations in . This cross-sectional study investigated whether PHP patients with parathyroid hormone (PTH), thyrotropin (thyroid stimulating hormone; TSH), and free thyroxine (T4) levels at goal required higher doses of levothyroxine and calcitriol than recommended by current guidelines to overcome mineral ion abnormalities due to hormone resistance. Baseline demographic and clinical data of participants enrolled in PHP research studies between 2012-2021 were collected via retrospective chart review. Longitudinally, data were recorded at a maximum frequency of once a year starting at 1 year of age. The PTH at goal (PAG) group was defined as PTH < 150 pg/mL and calcium ≥ 8.4 mg/dL, and the TSH and free T4 at goal (TAG) group was defined as TSH < 5 mIU/L and free T4 ≥ 0.8 ng/dL. The PAG group (n = 74) was prescribed higher calcitriol doses than the PTH not at goal (PNAG) group (n = 50) (0.9 ± 1.1 vs 0.5 ± 0.9 mcg/day,  = 0.04) and 21% of individual patients were prescribed ≥ 1.5 mcg of calcitriol daily. This remained true after normalization for body weight (0.013 ± 0.015 vs 0.0067 ± 0.0095 mcg/kg/day,  = 0.008). There was no statistically significant difference in levothyroxine dosing between the TAG group (n = 122) and TSH and free T4 not at goal (TNAG) group (n = 45) when normalized for weight (2.0 ± 0.7 vs 1.8 ± 0.7 mcg/kg/day,  = 0.2). More than one-third of patients with PHP had PTH levels not at goal and some patients required calcitriol doses ≥ 1.5 mcg/day to meet current treatment goals.

摘要

假性甲状旁腺功能减退症(PHP)是一种由……突变引起的罕见激素抵抗综合征。这项横断面研究调查了甲状旁腺激素(PTH)、促甲状腺激素(甲状腺刺激激素;TSH)和游离甲状腺素(T4)水平达标的PHP患者是否需要比现行指南推荐剂量更高的左甲状腺素和骨化三醇,以克服由于激素抵抗导致的矿物质离子异常。通过回顾性病历审查收集了2012年至2021年期间参加PHP研究的参与者的基线人口统计学和临床数据。纵向来看,从1岁开始,数据记录的最大频率为每年一次。目标PTH(PAG)组定义为PTH<150 pg/mL且钙≥8.4 mg/dL,目标TSH和游离T4(TAG)组定义为TSH<5 mIU/L且游离T4≥0.8 ng/dL。PAG组(n = 74)的骨化三醇剂量高于未达目标PTH(PNAG)组(n = 50)(0.9±1.1 vs 0.5±0.9 mcg/天,P = 0.04),21%的个体患者每天服用≥1.5 mcg的骨化三醇。体重标准化后情况依然如此(0.013±0.015 vs 0.0067±0.0095 mcg/kg/天,P = 0.008)。体重标准化后,TAG组(n = 122)和未达目标TSH及游离T4(TNAG)组(n = 45)的左甲状腺素剂量无统计学显著差异(2.0±0.7 vs 1.8±0.7 mcg/kg/天,P = 0.2)。超过三分之一的PHP患者PTH水平未达目标,一些患者需要≥1.5 mcg/天的骨化三醇剂量才能达到当前治疗目标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95f6/8579912/b5127bd4f854/bvab161f0001.jpg

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