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一例无毒的维生素D中毒病例。

A nontoxic case of vitamin D toxicity.

作者信息

Chakraborty Sutirtha, Sarkar Ajoy Krishna, Bhattacharya Chandramouli, Krishnan Prasad, Chakraborty Subhosmito

机构信息

Department of Biochemistry, Peerless Hospital and B. K. Roy Research Center, Kolkata, India

Department of Internal Medicine, Peerless Hospital and B. K. Roy Research Center, Kolkata, India.

出版信息

Lab Med. 2015 Spring;46(2):146-9; quiz e31. doi: 10.1309/LM5URN1QIR7QBLXK.

Abstract

Vitamin D toxicity also known as hypervitaminosis D was previously believed to be rare. But with an increase in vitamin D supplementation several cases have been reported in literature. Fat soluble vitamins like Vitamin D, due to their ability to accumulate in the body, have a higher potential for toxicity than water soluble vitamins. The main clinical consequence of vitamin D toxicity is hypercalcemia. In this report we describe an adult female patient who developed very high serum Vitamin D levels (746 ng/mL, RI: 20 to 50) as a result of medication error. Inspite of such high serum concentrations the patient was without any clinical symptoms and had normal serum calcium. We critically discuss the mechanism of toxicity and hypothesize the possible molecular/metabolic factors which might have been responsible for this nontoxic presentation. This case study highlights the fact that physicians need to consider the risk of medication errors while prescribing Vitamin D therapy. Clinical trials to study Vitamin D toxicity in humans is not possible ethically. Thus the evidence base regarding the safety profile of Vitamin D supplementation in humans has been build through case reports. This review of the paradoxical clinico-laboratory manifestation of hypervitaminosis D could possibly contribute to existing literature.

摘要

维生素D中毒,也称为维生素D过多症,以前被认为很罕见。但随着维生素D补充剂使用的增加,文献中已报道了多起病例。像维生素D这样的脂溶性维生素,由于其在体内蓄积的能力,比水溶性维生素具有更高的中毒风险。维生素D中毒的主要临床后果是高钙血症。在本报告中,我们描述了一名成年女性患者,由于用药错误,其血清维生素D水平极高(746 ng/mL,参考区间:20至50)。尽管血清浓度如此之高,但患者没有任何临床症状,血清钙水平正常。我们批判性地讨论了中毒机制,并推测了可能导致这种无中毒表现的分子/代谢因素。本病例研究强调了医生在开具维生素D治疗处方时需要考虑用药错误风险这一事实。从伦理角度来看,进行人体维生素D中毒的临床试验是不可能的。因此,关于人体补充维生素D安全性的证据基础是通过病例报告建立起来的。对维生素D过多症矛盾的临床实验室表现的这一综述可能会对现有文献有所贡献。

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