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尽管存在纯合子维生素D受体突变,但成年期骨量正常且血钙正常。

Normal bone mass and normocalcemia in adulthood despite homozygous vitamin D receptor mutations.

作者信息

Damiani F M, Martin R M, Latronico A C, Ferraz-de-Souza B

机构信息

Division of Endocrinology and Laboratory of Medical Investigation 18 - LIM-18, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, Av Dr Arnaldo, 455 sala 3324 (LIM-18), São Paulo, SP, 01246-903, Brazil.

出版信息

Osteoporos Int. 2015 Jun;26(6):1819-23. doi: 10.1007/s00198-015-3076-3. Epub 2015 Feb 24.

Abstract

UNLABELLED

Adding to the debate around vitamin D's effects on skeletal health, we report the long-term follow-up of two patients with severe vitamin D receptor mutations, who had normal bone mass acquisition and normalization of calcemia around puberty, suggesting that vitamin D might not be essential for skeletal health in adulthood.

INTRODUCTION

Vitamin D plays a pivotal role in calcium homeostasis, and the consequences of vitamin D insufficiency for skeletal health, as well as the importance of its supplementation, are a matter of great interest. Individuals bearing homozygous vitamin D receptor (VDR) defects present with severe hypocalcemic rickets in early infancy due to vitamin D resistance.

METHODS

Here, we report the follow-up of two patients with hereditary vitamin D-resistant rickets (HVDRR), focusing on bone mass acquisition and evolution of calcemia.

RESULTS

Patient 1 is a 30-year-old male bearing a homozygous p.Arg30* nonsense mutation in the VDR DNA-binding domain, who presented at 6 months. From 9 years of age, treatment requirement decreased progressively. Follow-up with DXA showed normal bone mass acquisition. In adulthood, he maintains normocalcemia without calcium supplementation and has no signs of bone fragility. Patient 2 is a 37-year-old female with milder HVDRR and alopecia due to a homozygous p.Gly319Val mutation in the VDR ligand-binding domain. Around puberty, hypercalciuria and kidney stones were detected, resulting in suspension of treatment. Follow-up with DXA revealed normal bone mass, and she maintained normocalcemia without supplementation during gestation and lactation.

CONCLUSIONS

The long-term follow-up of HVDRR provides insights into the role of vitamin D in human calcium homeostasis and bone health. The normalization of calcemia and normal bone mass acquisition despite a permanently dysfunctional VDR suggest that vitamin D might not be essential for skeletal health in adulthood. Extrapolation of these findings may have implications in broader clinical settings, especially considering widespread vitamin D supplementation.

摘要

未标注

在围绕维生素D对骨骼健康影响的争论中,我们报告了两名维生素D受体严重突变患者的长期随访情况,这两名患者在青春期前后骨量获取正常且血钙正常化,提示维生素D对成年期骨骼健康可能并非必不可少。

引言

维生素D在钙稳态中起关键作用,维生素D不足对骨骼健康的影响及其补充的重要性备受关注。纯合子维生素D受体(VDR)缺陷个体因维生素D抵抗在婴儿早期表现为严重的低钙性佝偻病。

方法

在此,我们报告两名遗传性维生素D抵抗性佝偻病(HVDRR)患者的随访情况,重点关注骨量获取和血钙变化。

结果

患者1是一名30岁男性,VDR DNA结合域存在纯合子p.Arg30*无义突变,6个月时发病。从9岁起,治疗需求逐渐减少。双能X线吸收法(DXA)随访显示骨量获取正常。成年后,他不补充钙剂维持血钙正常,且无骨脆性迹象。患者2是一名37岁女性,因VDR配体结合域纯合子p.Gly319Val突变患有较轻的HVDRR和脱发。青春期前后,检测到高钙尿症和肾结石,导致治疗中断。DXA随访显示骨量正常,她在妊娠和哺乳期不补充钙剂维持血钙正常。

结论

HVDRR的长期随访为维生素D在人体钙稳态和骨骼健康中的作用提供了见解。尽管VDR永久功能失调,但血钙正常化和骨量获取正常提示维生素D对成年期骨骼健康可能并非必不可少。这些发现的外推可能在更广泛的临床环境中有意义,特别是考虑到广泛的维生素D补充情况。

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