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自身免疫性原发性肾上腺功能不全——当前的诊断方法和未来展望。

Autoimmune primary adrenal insufficiency -current diagnostic approaches and future perspectives.

机构信息

Department of Clinical Science, University of Bergen, Bergen, Norway.

Department of Medicine, Haukeland University Hospital, Bergen, Norway.

出版信息

Front Endocrinol (Lausanne). 2023 Nov 10;14:1285901. doi: 10.3389/fendo.2023.1285901. eCollection 2023.

Abstract

The adrenal glands are small endocrine glands located on top of each kidney, producing hormones regulating important functions in our body like metabolism and stress. There are several underlying causes for adrenal insufficiency, where an autoimmune attack by the immune system is the most common cause. A number of genes are known to confer early onset adrenal disease in monogenic inheritance patterns, usually genetic encoding enzymes of adrenal steroidogenesis. Autoimmune primary adrenal insufficiency is usually a polygenic disease where our information recently has increased due to genome association studies. In this review, we go through the physiology of the adrenals before explaining the different reasons for adrenal insufficiency with a particular focus on autoimmune primary adrenal insufficiency. We will give a clinical overview including diagnosis and current treatment, before giving an overview of the genetic causes including monogenetic reasons for adrenal insufficiency and the polygenic background and inheritance pattern in autoimmune adrenal insufficiency. We will then look at the autoimmune mechanisms underlying autoimmune adrenal insufficiency and how autoantibodies are important for diagnosis. We end with a discussion on how to move the field forward emphasizing on the clinical workup, early identification, and potential targeted treatment of autoimmune PAI.

摘要

肾上腺是位于每个肾脏顶部的小内分泌腺,产生调节身体重要功能的激素,如新陈代谢和应激。肾上腺功能不全有几种潜在的原因,其中免疫系统的自身免疫攻击是最常见的原因。有许多基因已知在单基因遗传模式下导致早发性肾上腺疾病,通常是遗传编码肾上腺类固醇生成酶。自身免疫性原发性肾上腺功能不全通常是一种多基因疾病,由于基因组关联研究,我们最近的信息有所增加。在这篇综述中,我们首先解释了肾上腺的生理学,然后解释了导致肾上腺功能不全的不同原因,特别关注自身免疫性原发性肾上腺功能不全。我们将介绍包括诊断在内的临床概况,以及当前的治疗方法,然后概述遗传原因,包括导致肾上腺功能不全的单基因原因,以及自身免疫性肾上腺功能不全的多基因背景和遗传模式。然后,我们将研究自身免疫性原发性肾上腺功能不全的自身免疫机制,以及自身抗体对诊断的重要性。最后,我们将讨论如何推动该领域的发展,强调自身免疫性 PAI 的临床评估、早期识别和潜在靶向治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf7c/10667925/20f03f48b187/fendo-14-1285901-g001.jpg

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