Suppr超能文献

赖氨酸尿蛋白不耐受症的症状和治疗概述。

Overview of symptoms and treatment for lysinuric protein intolerance.

机构信息

Akita University Graduate School of Medicine, Pediatrics, Akita, Akita, Japan.

出版信息

J Hum Genet. 2019 Sep;64(9):849-858. doi: 10.1038/s10038-019-0620-6. Epub 2019 Jun 18.

Abstract

Lysinuric protein intolerance (LPI) is caused by dysfunction of the dibasic amino acid membrane transport owing to the functional abnormality of yL amino acid transporter-1 (y LAT-1). LPI is associated with autosomal recessive inheritance and pathological variants in the responsible gene SLC7A7 are also observed. The pathophysiology of this disease had earlier been understood as a transport defect in polarized cells (e.g., intestinal or renal tubular epithelium); however, in recent years, transport defects in non-polarized cells such as lymphocytes and macrophages have also been recognized as important. Although the former can cause death, malnutrition, and urea cycle dysfunction (hyperammonemia), the latter can induce renal, pulmonary, and immune disorders. Furthermore, although therapeutic interventions can prevent hyperammonemic episodes to some extent, progression of pulmonary and renal complications cannot be prevented, thereby influencing prognosis. Such pathological conditions are currently being explored and further investigation would prove beneficial. In this study, we have summarized the basic pathology as revealed in recent years, along with the clinical aspects and genetic features.

摘要

赖氨酸尿蛋白不耐受症(LPI)是由于二碱基氨基酸膜转运功能障碍引起的,这是由于 yL 氨基酸转运蛋白-1(y LAT-1)的功能异常所致。LPI 与常染色体隐性遗传有关,也观察到负责基因 SLC7A7 的病理性变异。该疾病的病理生理学以前被理解为极化细胞(例如,肠或肾小管上皮)中的转运缺陷;然而,近年来,非极化细胞(如淋巴细胞和巨噬细胞)中的转运缺陷也被认为是重要的。尽管前者可导致死亡、营养不良和尿素循环功能障碍(高氨血症),但后者可引起肾脏、肺部和免疫紊乱。此外,尽管治疗干预可以在一定程度上预防高氨血症发作,但不能预防肺部和肾脏并发症的进展,从而影响预后。目前正在探索这些病理状况,并进一步研究将证明是有益的。在本研究中,我们总结了近年来揭示的基本病理学,以及临床方面和遗传特征。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验