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常染色体显性遗传性多囊肾病的胚胎植入前遗传学诊断咨询。

Preimplantation Genetic Diagnosis Counseling in Autosomal Dominant Polycystic Kidney Disease.

机构信息

Section of Nephrology, Yale University School of Medicine, North Haven, CT.

Department of Medical Sciences, Frank H. Netter, MD School of Medicine, Quinnipiac University, North Haven, CT.

出版信息

Am J Kidney Dis. 2018 Dec;72(6):866-872. doi: 10.1053/j.ajkd.2018.01.048. Epub 2018 Mar 30.

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common hereditary forms of chronic kidney disease. Mutations within PKD1 or PKD2 lead to innumerable fluid-filled cysts in the kidneys and in some instances, end-stage renal disease (ESRD). Affected individuals have a 50% chance of passing the mutation to each of their offspring. Assisted reproductive technology using preimplantation genetic diagnosis (PGD) allows these individuals to reduce this risk to 1% to 2%. We assess the disease burden of 8 individuals with ADPKD who have undergone genetic testing in preparation for PGD. Clinical features that predict high risk for progression to ESRD in patients with ADPKD include genotype, early onset of hypertension, a urologic event before age 35 years, and a large height-adjusted total kidney volume. Patients may have a family history of intracranial aneurysms or complications involving hepatic cysts, which may further influence the decision to pursue PGD. We also explore the cost, risks, and benefits of using PGD. All patients with ADPKD of childbearing potential, regardless of risk for progression to ESRD or risk for a significant disease burden, will likely benefit from genetic counseling.

摘要

常染色体显性多囊肾病(ADPKD)是最常见的慢性肾脏病遗传性形式之一。PKD1 或 PKD2 内的突变导致肾脏中无数充满液体的囊肿,在某些情况下会导致终末期肾病(ESRD)。受影响的个体将突变遗传给每个后代的几率为 50%。使用胚胎植入前遗传学诊断(PGD)的辅助生殖技术可将这种风险降低到 1%至 2%。我们评估了 8 名接受遗传测试以准备 PGD 的 ADPKD 患者的疾病负担。预测 ADPKD 患者进展为 ESRD 的高风险的临床特征包括基因型、高血压的早期发病、35 岁前的泌尿系统事件以及经过身高调整的总肾脏体积较大。患者可能有颅内动脉瘤或涉及肝囊肿的并发症家族史,这可能进一步影响进行 PGD 的决策。我们还探讨了使用 PGD 的成本、风险和益处。所有有生育潜力的 ADPKD 患者,无论是否有进展为 ESRD 的风险或是否存在重大疾病负担,都可能受益于遗传咨询。

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