高血压增加多囊肾病患者PKD1和PKD2变异携带者的PPV。

IF 3.3 Q2 GENETICS & HEREDITY
Natalie Telis, Lisa McEwen, Alexandre Bolze, Joshua H Lipschutz, Leon W Sweer, Daniel P Judge, Pamala A Pawloski, Joseph J Grzymski, Catherine Hajek, Kelly M Schiabor Barrett, Nicole L Washington, Elizabeth T Cirulli
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引用次数: 0

摘要

常染色体显性多囊肾病(ADPKD)是KD的主要遗传形式。虽然已经鉴定出PKD1和PKD2基因中罕见的因果变异,但已知它们的外显率、疾病进展和结果各不相同,并且与其他形式的慢性KD (CKD)患者相比,这些携带者的治疗效果滞后。为了开发一种对可能发生疾病的个体具有高敏感性的人群筛查策略,我们描述了在多中心所有患者队列以及UK Biobank中确定的变异携带者ADPKD的表现和进展。我们发现高血压对未来KD诊断的阳性预测值非常高:PKD1和PKD2分别为74%和66%。它也是高度预防性的,高血压在KD诊断前平均发生11年。通过在ADPKD诊断前的疾病前时间点肾功能测量,我们发现PKD1和PKD2变异携带者在临床诊断前平均5年的肾脏功能(EGFR)显著下降。与其他CKD患者不同,54%的高血压变异携带者在疾病诊断前几年达到CKD的诊断阈值,并且他们的egfr与已经诊断的变异携带者在统计学上无法区分。这些发现表明,结合靶向测序和常规监测的人群筛查策略可以高灵敏度地识别ADPKD病例,并支持在当前标准护理前几年开始治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hypertension increases PPV for polycystic kidney disease in PKD1 and PKD2 variant carriers.

Autosomal dominant polycystic kidney disease (ADPKD) is the leading genetic form of KD. Although rare causal variants in the PKD1 and PKD2 genes have been identified, their penetrance and the disease progression and outcome are known to vary, and treatment efficacy in these carriers lags compared to patients with other forms of chronic KD (CKD). To develop a population screening strategy with high sensitivity to individuals likely to develop disease, we characterize the presentation and progression of ADPKD in variant carriers, identified in a multi-center all-comers cohort, as well as the UK Biobank. We show that the positive predictive value of hypertension for future diagnosis of KD is extremely high: 74% and 66% for PKD1 and PKD2, respectively. It is also highly preemptive, with hypertension occurring an average of 11 years before a KD diagnosis. Using pre-disease time point measurements of kidney function prior to their ADPKD diagnosis, we find that PKD1 and PKD2 variant carriers show significantly decreased kidney function (EGFR) an average of 5 years before their clinical diagnosis. Unlike other CKD patients, 54% of variant carriers with hypertension meet the diagnostic threshold for CKD years prior to their disease diagnosis, and their EGFRs are statistically indistinguishable from variant carriers who have already been diagnosed. These findings suggest that a population screening strategy using a combination of targeted sequencing and routine monitoring could identify cases of ADPKD with high sensitivity and support initiating treatment years prior to the current standard of care.

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来源期刊
HGG Advances
HGG Advances Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
4.30
自引率
4.50%
发文量
69
审稿时长
14 weeks
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