血清AKR1A1水平预测非裔2型糖尿病患者eGFR下降率

IF 3 Q1 UROLOGY & NEPHROLOGY
Kidney360 Pub Date : 2025-10-06 DOI:10.34067/KID.0000000966
Lijun Ma, Young A Choi, DengFeng Li, Moin A Saleem, Barry I Freedman
{"title":"血清AKR1A1水平预测非裔2型糖尿病患者eGFR下降率","authors":"Lijun Ma, Young A Choi, DengFeng Li, Moin A Saleem, Barry I Freedman","doi":"10.34067/KID.0000000966","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>African Americans have disproportionately high rates of diabetic kidney disease (DKD). Identification of biomarkers predicting early DKD progression is essential to prescribe protective treatments prior to the development of irreversible histologic lesions and markedly reduced kidney function.</p><p><strong>Methods: </strong>We tested whether AKR1A1 was a marker of early DKD progression via knock-out of AKR1A1 in a human kidney proximal tubule cell line, and by measuring serum AKR1A1 concentrations in African Americans with type 2 diabetes (T2D).</p><p><strong>Results: </strong>AKR1A1 knockout cells had reduced cell viability, and the effect was aggravated by administering high dose palmitate. In addition, higher serum AKR1A1 concentrations in African Americans with T2D and preserved kidney function predicted slower decline rate in estimated glomerular filtration rate over time.</p><p><strong>Conclusions: </strong>AKR1A1 appears to play a critical role in countering toxic effects of fatty acid metabolism and may prevent rapid decline of kidney function in African Americans with T2D.</p>","PeriodicalId":17882,"journal":{"name":"Kidney360","volume":" ","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Serum AKR1A1 Levels Predict eGFR Decline Rate in African Americans with Type 2 Diabetes.\",\"authors\":\"Lijun Ma, Young A Choi, DengFeng Li, Moin A Saleem, Barry I Freedman\",\"doi\":\"10.34067/KID.0000000966\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>African Americans have disproportionately high rates of diabetic kidney disease (DKD). Identification of biomarkers predicting early DKD progression is essential to prescribe protective treatments prior to the development of irreversible histologic lesions and markedly reduced kidney function.</p><p><strong>Methods: </strong>We tested whether AKR1A1 was a marker of early DKD progression via knock-out of AKR1A1 in a human kidney proximal tubule cell line, and by measuring serum AKR1A1 concentrations in African Americans with type 2 diabetes (T2D).</p><p><strong>Results: </strong>AKR1A1 knockout cells had reduced cell viability, and the effect was aggravated by administering high dose palmitate. In addition, higher serum AKR1A1 concentrations in African Americans with T2D and preserved kidney function predicted slower decline rate in estimated glomerular filtration rate over time.</p><p><strong>Conclusions: </strong>AKR1A1 appears to play a critical role in countering toxic effects of fatty acid metabolism and may prevent rapid decline of kidney function in African Americans with T2D.</p>\",\"PeriodicalId\":17882,\"journal\":{\"name\":\"Kidney360\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2025-10-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Kidney360\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.34067/KID.0000000966\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"UROLOGY & NEPHROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Kidney360","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.34067/KID.0000000966","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:非裔美国人糖尿病肾病(DKD)的发病率高得不成比例。识别预测早期DKD进展的生物标志物对于在发生不可逆的组织学病变和显著降低肾功能之前提供保护性治疗至关重要。方法:我们通过敲除人肾近端小管细胞系中的AKR1A1,并通过测量2型糖尿病(T2D)非洲裔美国人血清AKR1A1浓度,来检测AKR1A1是否为早期DKD进展的标志。结果:AKR1A1基因敲除细胞可降低细胞活力,且高剂量棕榈酸盐可加重该作用。此外,患有T2D和保留肾功能的非裔美国人血清AKR1A1浓度较高,预测肾小球滤过率随时间的下降速度较慢。结论:AKR1A1似乎在对抗脂肪酸代谢的毒性作用中起关键作用,并可能阻止非裔美国人T2D患者肾功能的快速下降。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum AKR1A1 Levels Predict eGFR Decline Rate in African Americans with Type 2 Diabetes.

Background: African Americans have disproportionately high rates of diabetic kidney disease (DKD). Identification of biomarkers predicting early DKD progression is essential to prescribe protective treatments prior to the development of irreversible histologic lesions and markedly reduced kidney function.

Methods: We tested whether AKR1A1 was a marker of early DKD progression via knock-out of AKR1A1 in a human kidney proximal tubule cell line, and by measuring serum AKR1A1 concentrations in African Americans with type 2 diabetes (T2D).

Results: AKR1A1 knockout cells had reduced cell viability, and the effect was aggravated by administering high dose palmitate. In addition, higher serum AKR1A1 concentrations in African Americans with T2D and preserved kidney function predicted slower decline rate in estimated glomerular filtration rate over time.

Conclusions: AKR1A1 appears to play a critical role in countering toxic effects of fatty acid metabolism and may prevent rapid decline of kidney function in African Americans with T2D.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Kidney360
Kidney360 UROLOGY & NEPHROLOGY-
CiteScore
3.90
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信