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基因检测在慢性肾脏病成人诊断和管理中的临床应用。

The Clinical Utility of Genetic Testing in the Diagnosis and Management of Adults with Chronic Kidney Disease.

机构信息

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota.

Natera, Inc., Austin, Texas.

出版信息

J Am Soc Nephrol. 2023 Dec 1;34(12):2039-2050. doi: 10.1681/ASN.0000000000000249. Epub 2023 Oct 5.

Abstract

SIGNIFICANCE STATEMENT

Accurate diagnosis of a patient's underlying cause of CKD can influence management and ultimately overall health. The single-arm, interventional, prospective Renasight Clinical Application, Review, and Evaluation study assessed the utility of genetic testing with a 385 gene kidney disease panel on the diagnosis and management of 1623 patients with CKD. Among 20.8% of patients who had positive genetic findings, half resulted in a new or reclassified diagnosis. In addition, a change in management because of genetic testing was reported for 90.7% of patients with positive findings, including treatment changes in 32.9%. These findings demonstrate that genetic testing has a significant effect on both CKD diagnosis and management.

BACKGROUND

Genetic testing in CKD has recently been shown to have diagnostic utility with many predicted implications for clinical management, but its effect on management has not been prospectively evaluated.

METHODS

Renasight Clinical Application, Review, and Evaluation RenaCARE (ClinicalTrials.gov NCT05846113 ) is a single-arm, interventional, prospective, multicenter study that evaluated the utility of genetic testing with a broad, 385 gene panel (the Renasight TM test) on the diagnosis and management of adult patients with CKD recruited from 31 US-based community and academic medical centers. Patient medical history and clinical CKD diagnosis were collected at enrollment. Physician responses to questionnaires regarding patient disease categorization and management were collected before genetic testing and 1 month after the return of test results. Changes in CKD diagnosis and management after genetic testing were assessed.

RESULTS

Of 1623 patients with CKD in 13 predefined clinical disease categories (ages, 18-96; median, 55 years), 20.8% ( n =338) had positive genetic findings spanning 54 genes. Positive genetic findings provided a new diagnosis or reclassified a prior diagnosis in 48.8% of those patients. Physicians reported that genetic results altered the management of 90.7% of patients with a positive genetic finding, including changes in treatment plan, which were reported in 32.9% of these patients.

CONCLUSIONS

Genetic testing with a CKD-focused 385 gene panel substantially refined clinical diagnoses and had widespread implications for clinical management, including appropriate treatment strategies. These data support the utility of broader integration of panels of genetic tests into the clinical care paradigm for patients with CKD.

CLINICAL TRIAL REGISTRY NAME AND REGISTRATION NUMBER

ClinicalTrials.gov, NCT05846113 .

摘要

意义陈述

准确诊断患者慢性肾脏病的根本病因可以影响治疗方案,并最终影响整体健康。这项单臂、干预性、前瞻性的 Renasight 临床应用、回顾和评估研究评估了对 1623 名慢性肾脏病患者进行 385 个基因肾脏疾病基因检测对诊断和治疗的作用。在 20.8%的基因检测阳性患者中,有一半导致了新的或重新分类的诊断。此外,90.7%的基因检测阳性患者因基因检测而改变了治疗方案,其中 32.9%的患者改变了治疗方案。这些发现表明,基因检测对慢性肾脏病的诊断和治疗都有显著影响。

背景

最近的研究表明,基因检测在慢性肾脏病中有诊断作用,对临床管理有许多预测意义,但尚未对其对管理的影响进行前瞻性评估。

方法

Renasight 临床应用、回顾和评估 RenaCARE(ClinicalTrials.gov NCT05846113)是一项单臂、干预性、前瞻性、多中心研究,评估了对 31 家美国社区和学术医疗中心招募的慢性肾脏病成年患者进行广泛的 385 个基因(Renasight TM 测试)基因检测对诊断和管理的作用。患者在入组时收集了病史和临床慢性肾脏病诊断。在基因检测前和检测结果返回后 1 个月,医生通过问卷收集了关于患者疾病分类和管理的回复。评估基因检测后慢性肾脏病诊断和管理的变化。

结果

在 13 个预先定义的临床疾病类别(年龄 18-96 岁;中位年龄 55 岁)的 1623 名慢性肾脏病患者中,20.8%(n=338)的基因检测结果呈阳性,涉及 54 个基因。这些患者中有 48.8%的人有新的诊断或重新分类了以前的诊断。有阳性基因检测结果的患者中有 90.7%的人的治疗方案发生了变化,其中 32.9%的患者报告了治疗方案的变化。

结论

对慢性肾脏病患者进行 385 个基因的基因检测大大改善了临床诊断,并对临床管理产生了广泛的影响,包括适当的治疗策略。这些数据支持更广泛地将基因检测纳入慢性肾脏病患者的临床治疗模式。

临床试验注册名称和注册号

ClinicalTrials.gov,NCT05846113。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74cd/10703084/95ac4086e45d/jasn-34-2039-g001.jpg

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