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本文引用的文献

1
Vitamin D Metabolism Revised: Fall of Dogmas.维生素D代谢的修正:教条的陨落。
J Bone Miner Res. 2019 Nov;34(11):1985-1992. doi: 10.1002/jbmr.3884. Epub 2019 Oct 29.
2
A chromatin-based mechanism controls differential regulation of the cytochrome P450 gene in renal and non-renal tissues.基于染色质的机制控制细胞色素 P450 基因在肾组织和非肾组织中的差异调节。
J Biol Chem. 2019 Sep 27;294(39):14467-14481. doi: 10.1074/jbc.RA119.010173. Epub 2019 Aug 22.
3
Vitamin D Supplementation and Prevention of Type 2 Diabetes.维生素 D 补充与 2 型糖尿病预防。
N Engl J Med. 2019 Aug 8;381(6):520-530. doi: 10.1056/NEJMoa1900906. Epub 2019 Jun 7.
4
Marine n-3 Fatty Acids and Vitamin D Supplementation and Primary Prevention. Reply.海洋n-3脂肪酸与维生素D补充剂及一级预防。回复。
N Engl J Med. 2019 May 9;380(19):1879-1880. doi: 10.1056/NEJMc1902636.
5
Targeted genomic deletions identify diverse enhancer functions and generate a kidney-specific, endocrine-deficient pseudo-null mouse.靶向基因组缺失鉴定出多种增强子功能,并生成一种具有肾脏特异性和内分泌缺陷的假纯合子小鼠。
J Biol Chem. 2019 Jun 14;294(24):9518-9535. doi: 10.1074/jbc.RA119.008760. Epub 2019 May 3.
6
Vitamin D and Its Synthetic Analogs.维生素 D 及其合成类似物。
J Med Chem. 2019 Aug 8;62(15):6854-6875. doi: 10.1021/acs.jmedchem.9b00208. Epub 2019 Apr 2.
7
Fasting-Induced Transcription Factors Repress Vitamin D Bioactivation, a Mechanism for Vitamin D Deficiency in Diabetes.禁食诱导转录因子抑制维生素 D 的生物活化,这是糖尿病中维生素 D 缺乏的一种机制。
Diabetes. 2019 May;68(5):918-931. doi: 10.2337/db18-1050. Epub 2019 Mar 4.
8
Obesity Decreases Hepatic 25-Hydroxylase Activity Causing Low Serum 25-Hydroxyvitamin D.肥胖症降低肝脏 25-羟化酶活性,导致血清 25-羟维生素 D 水平降低。
J Bone Miner Res. 2019 Jun;34(6):1068-1073. doi: 10.1002/jbmr.3686. Epub 2019 Feb 21.
9
The good, the bad, and the ugly of calcium supplementation: a review of calcium intake on human health.钙补充的好坏与不足:钙摄入对人类健康影响的综述。
Clin Interv Aging. 2018 Nov 28;13:2443-2452. doi: 10.2147/CIA.S157523. eCollection 2018.
10
The Free Hormone Hypothesis: Is Free Serum 25-Hydroxyvitamin D a Better Marker for Bone Mineral Density in Older Women?游离激素假说:游离血清25-羟维生素D是否是老年女性骨密度的更好标志物?
JBMR Plus. 2018 Jun 12;2(6):367-374. doi: 10.1002/jbm4.10059. eCollection 2018 Nov.

维生素D:基础与临床层面其代谢及功能的新观念

Vitamin D: Newer Concepts of Its Metabolism and Function at the Basic and Clinical Level.

作者信息

Bikle Daniel D

机构信息

Department of Medicine and Endocrine Research Unit, Veterans Affairs Medical Center and University of California, San Francisco, California.

出版信息

J Endocr Soc. 2020 Feb 8;4(2):bvz038. doi: 10.1210/jendso/bvz038. eCollection 2020 Feb 1.

DOI:10.1210/jendso/bvz038
PMID:32051922
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7007804/
Abstract

The interest in vitamin D continues unabated with thousands of publications contributing to a vast and growing literature each year. It is widely recognized that the vitamin D receptor (VDR) and the enzymes that metabolize vitamin D are found in many cells, not just those involved with calcium and phosphate homeostasis. In this mini review I have focused primarily on recent studies that provide new insights into vitamin D metabolism, mechanisms of action, and clinical applications. In particular, I examine how mutations in vitamin D metabolizing enzymes-and new information on their regulation-links vitamin D metabolism into areas such as metabolism and diseases outside that of the musculoskeletal system. New information regarding the mechanisms governing the function of the VDR elucidates how this molecule can be so multifunctional in a cell-specific fashion. Clinically, the difficulty in determining vitamin D sufficiency for all groups is addressed, including a discussion of whether the standard measure of vitamin D sufficiency, total 25OHD (25 hydroxyvitamin) levels, may not be the best measure-at least by itself. Finally, several recent large clinical trials exploring the role of vitamin D supplementation in nonskeletal diseases are briefly reviewed, with an eye toward what questions they answered and what new questions they raised.

摘要

人们对维生素D的兴趣持续不减,每年都有成千上万的出版物为浩如烟海且不断增长的文献做出贡献。人们普遍认识到,维生素D受体(VDR)以及代谢维生素D的酶存在于许多细胞中,而不仅仅是参与钙和磷稳态的细胞。在这篇小型综述中,我主要关注了近期的研究,这些研究为维生素D的代谢、作用机制及临床应用提供了新的见解。特别是,我研究了维生素D代谢酶的突变以及它们调控的新信息如何将维生素D代谢与肌肉骨骼系统之外的代谢和疾病等领域联系起来。关于VDR功能调控机制的新信息阐明了该分子如何以细胞特异性方式具有如此多的功能。在临床上,讨论了确定所有人群维生素D充足性的困难,包括探讨维生素D充足性的标准衡量指标——总25OHD(25羟维生素)水平是否并非最佳衡量指标——至少单独使用时并非如此。最后,简要回顾了近期几项探索维生素D补充剂在非骨骼疾病中作用的大型临床试验,关注它们回答了哪些问题以及提出了哪些新问题。