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格雷夫斯病中维生素 D 与骨代谢:一项前瞻性研究。

Vitamin D and bone metabolism in Graves' disease: a prospective study.

机构信息

Department of Endocrinology and Diabetes, Uppsala University Hospital, 751 85, Uppsala, Sweden.

Department of Medical Sciences, Uppsala University, Uppsala, Sweden.

出版信息

J Endocrinol Invest. 2023 Feb;46(2):425-433. doi: 10.1007/s40618-022-01927-y. Epub 2022 Sep 27.

Abstract

PURPOSE

Vitamin D and osteoporosis in Graves' disease (GD) have been examined in cross-sectional studies with divergent results. Here, we prospectively studied vitamin D metabolism and bone health in patients with newly diagnosed GD.

METHODS

Thirty consecutive patients with de novo overt thyrotoxicosis diagnosed with GD were included. At diagnosis, none of the patients were treated with vitamin D or anti-osteoporotic drugs. All patients were initially treated with antithyroid drugs. Blood samplings were taken at baseline and at 6 weeks, 3, 6, 12 and 24 months after treatment start. Serum levels of 25OHD3, 1,25OH2D3, calcium, parathyroid hormone (PTH), and C-terminal telopeptides of Type I collagen (CTX-I) were analysed. Bone mineral density (BMD) was measured at baseline, and 1 and 2 years after treatment initiation.

RESULTS

At diagnosis, patients with GD did not have vitamin D deficiency. There were no significant correlations between levels of 25OHD3 and thyrotoxicosis. Upon treatment of the thyrotoxicosis, serum calcium fell transiently, and PTH and 1,25OH2D3 increased. 25OHD3 fell within the normal range and stabilised at 6 months. CTX-I fell over 12 months, BMD increased significantly up to 2 years, p = 0.002, < 0.001 and 0.005 in the spine, left total hip and left femoral neck, respectively.

CONCLUSIONS

The present data underline that thyrotoxicosis has a negative impact on bone health and demonstrate fine-tuned dynamics in bone and vitamin D metabolism. Upon treatment, bone health improved over a follow-up period of 24 months despite rising PTH. Increased conversion of 25OHD3 to 1,25OH2D3 occurs during treatment of GD.

摘要

目的

维生素 D 和格雷夫斯病(GD)中的骨质疏松症已在具有不同结果的横断面研究中进行了检查。在这里,我们前瞻性研究了新诊断的 GD 患者的维生素 D 代谢和骨骼健康。

方法

连续纳入 30 例新诊断的显性甲状腺毒症 GD 患者。在诊断时,没有患者接受维生素 D 或抗骨质疏松药物治疗。所有患者最初均接受抗甲状腺药物治疗。在治疗开始时、6 周、3 个月、6 个月、12 个月和 24 个月时采集血样。分析血清 25OHD3、1,25OH2D3、钙、甲状旁腺激素(PTH)和 I 型胶原 C 端肽(CTX-I)的水平。在治疗开始后 1 年和 2 年时测量骨密度(BMD)。

结果

在诊断时,GD 患者没有维生素 D 缺乏症。25OHD3 水平与甲状腺毒症之间没有显著相关性。在治疗甲状腺毒症时,血清钙短暂下降,PTH 和 1,25OH2D3 增加。25OHD3 在正常范围内下降并在 6 个月时稳定。CTX-I 在 12 个月内下降,BMD 显著增加,直至 2 年,脊柱、左侧总髋部和左侧股骨颈分别为 p<0.001、<0.001 和 0.005。

结论

目前的数据强调甲状腺毒症对骨骼健康有负面影响,并证明了骨骼和维生素 D 代谢的精细动态。在治疗过程中,尽管 PTH 升高,但骨骼健康在 24 个月的随访期间得到改善。在治疗 GD 期间,25OHD3 向 1,25OH2D3 的转化增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4312/9859854/860709fdaeb9/40618_2022_1927_Fig1_HTML.jpg

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