Suppr超能文献

载脂蛋白 L1、心血管疾病和高血压:问题多于答案。

Apolipoprotein L1, Cardiovascular Disease and Hypertension: More Questions than Answers.

机构信息

Division of Nephrology, Icahn School of Medicine at Mount Sinai, 1 Gustave L. Levy Pl, New York, NY 10029, USA.

Division of Nephrology, Icahn School of Medicine at Mount Sinai, 1 Gustave L. Levy Pl, New York, NY 10029, USA.

出版信息

Cardiol Clin. 2019 Aug;37(3):327-334. doi: 10.1016/j.ccl.2019.04.009. Epub 2019 May 14.

Abstract

Ethnic disparities in health outcomes exist among multiple complex diseases especially cardiovascular disease, hypertension, and kidney disease. Recent discoveries in genetics have taught us that these disparities go beyond environmental and socioeconomic factors. The discovery of ethnic-specific risk variants in the Apolipoprotein L1 (APOL1) gene on chromosome 22 seen only in individuals of recent African ancestry explains a large proportion of kidney disease disparities. In addition, recent large-scale genotype-phenotype association studies have identified associations with cardiovascular disease and hypertension. This review aims to review the recent literature in this field and point toward future directions for research.

摘要

在多种复杂疾病中,尤其是心血管疾病、高血压和肾脏疾病,健康结果存在种族差异。遗传学的最新发现告诉我们,这些差异不仅仅是环境和社会经济因素造成的。最近在只有最近有非洲血统的个体中才发现的 22 号染色体载脂蛋白 L1(APOL1)基因中的种族特异性风险变异体的发现,解释了很大一部分肾脏疾病差异的原因。此外,最近的大规模基因-表型关联研究已经确定了与心血管疾病和高血压的关联。本综述旨在回顾该领域的最新文献,并为未来的研究指明方向。

相似文献

1
Apolipoprotein L1, Cardiovascular Disease and Hypertension: More Questions than Answers.
Cardiol Clin. 2019 Aug;37(3):327-334. doi: 10.1016/j.ccl.2019.04.009. Epub 2019 May 14.
3
APOL1-Associated Nephropathy: A Key Contributor to Racial Disparities in CKD.
Am J Kidney Dis. 2018 Nov;72(5 Suppl 1):S8-S16. doi: 10.1053/j.ajkd.2018.06.020.
4
Apolipoprotein L1 nephropathies: 2017 in review.
Curr Opin Nephrol Hypertens. 2018 May;27(3):153-158. doi: 10.1097/MNH.0000000000000399.
5
The Expanding Role of APOL1 Risk in Chronic Kidney Disease and Cardiovascular Disease.
Semin Nephrol. 2017 Nov;37(6):520-529. doi: 10.1016/j.semnephrol.2017.07.005.
6
The Apolipoprotein L1 Gene and Cardiovascular Disease.
Methodist Debakey Cardiovasc J. 2016 Oct-Dec;12(4 Suppl):2-5. doi: 10.14797/mdcj-12-4s1-2.
8
Joint Associations of Maternal-Fetal APOL1 Genotypes and Maternal Country of Origin With Preeclampsia Risk.
Am J Kidney Dis. 2021 Jun;77(6):879-888.e1. doi: 10.1053/j.ajkd.2020.10.020. Epub 2020 Dec 22.
10
APOL1 polymorphisms and kidney disease: loss-of-function or gain-of-function?
Am J Physiol Renal Physiol. 2019 Jan 1;316(1):F1-F8. doi: 10.1152/ajprenal.00426.2018. Epub 2018 Oct 17.

引用本文的文献

1
Clinical implications of apolipoprotein L1 testing in patients with focal segmental glomerulosclerosis: a review of diagnostic and prognostic implications.
Ann Med Surg (Lond). 2025 Mar 3;87(3):1543-1551. doi: 10.1097/MS9.0000000000003051. eCollection 2025 Mar.

本文引用的文献

2
One Actor, Many Roles: Histopathologies Associated With APOL1 Genetic Variants.
Adv Anat Pathol. 2019 May;26(3):215-219. doi: 10.1097/PAP.0000000000000221.
3
Worldwide Frequencies of APOL1 Renal Risk Variants.
N Engl J Med. 2018 Dec 27;379(26):2571-2572. doi: 10.1056/NEJMc1800748.
4
Nephropathy Risk Variants and Incident Cardiovascular Disease Events in Community-Dwelling Black Adults.
Circ Genom Precis Med. 2018 Jun;11(6):e002098. doi: 10.1161/CIRCGEN.117.002098.
5
The Long-Term Kidney Transplantation Outcomes Network-APOLLO.
Clin J Am Soc Nephrol. 2018 Jun 7;13(6):940-942. doi: 10.2215/CJN.01510218. Epub 2018 Apr 27.
6
Heart Disease and Stroke Statistics-2018 Update: A Report From the American Heart Association.
Circulation. 2018 Mar 20;137(12):e67-e492. doi: 10.1161/CIR.0000000000000558. Epub 2018 Jan 31.
7
Risk Variants Independently Associated With Early Cardiovascular Disease Death.
Kidney Int Rep. 2017 Aug 24;3(1):89-98. doi: 10.1016/j.ekir.2017.08.007. eCollection 2018 Jan.
8
The Expanding Role of APOL1 Risk in Chronic Kidney Disease and Cardiovascular Disease.
Semin Nephrol. 2017 Nov;37(6):520-529. doi: 10.1016/j.semnephrol.2017.07.005.
9
APOL1 Nephropathy: A Population Genetics and Evolutionary Medicine Detective Story.
Semin Nephrol. 2017 Nov;37(6):490-507. doi: 10.1016/j.semnephrol.2017.07.002.

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