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在常染色体显性多囊肾病中,囊肿数量而非囊肿生长速率与突变基因相关。

Cyst number but not the rate of cystic growth is associated with the mutated gene in autosomal dominant polycystic kidney disease.

作者信息

Harris Peter C, Bae Kyongtae T, Rossetti Sandro, Torres Vicente E, Grantham Jared J, Chapman Arlene B, Guay-Woodford Lisa M, King Bernard F, Wetzel Louis H, Baumgarten Deborah A, Kenney Philip J, Consugar Mark, Klahr Saulo, Bennett William M, Meyers Catherine M, Zhang Qin Jean, Thompson Paul A, Zhu Fang, Miller J Philip

机构信息

Division of Nephrology and Hypertension, Mayo Clinic College of Medicine, Rochester, MN 55905, USA.

出版信息

J Am Soc Nephrol. 2006 Nov;17(11):3013-9. doi: 10.1681/ASN.2006080835. Epub 2006 Oct 11.

Abstract

Data from serial renal magnetic resonance imaging of the Consortium of Radiologic Imaging Study of PKD (CRISP) autosomal dominant polycystic kidney disease (PKD) population showed that cystic expansion occurs at a consistent rate per individual, although it is heterogeneous in the population, and that larger kidneys are associated with more rapid disease progression. The significance of gene type to disease progression is analyzed in this study of the CRISP cohort. Gene type was determined in 183 families (219 cases); 156 (85.2%) had PKD1, and 27 (14.8%) had PKD2. PKD1 kidneys were significantly larger, but the rate of cystic growth (PKD1 5.68%/yr; PKD2 4.82%/yr) was not different (P = 0.24). Cyst number increased with age, and more cysts were detected in PKD1 kidneys (P < 0.0001). PKD1 is more severe because more cysts develop earlier, not because they grow faster, implicating the disease gene in cyst initiation but not expansion. These insights will inform the development of targeted therapies in autosomal dominant PKD.

摘要

多囊肾病(PKD)放射影像学研究联盟(CRISP)中常染色体显性多囊肾病患者的系列肾脏磁共振成像数据显示,尽管人群中囊肿扩张情况存在异质性,但每个个体的囊肿扩张速率是一致的,而且肾脏越大,疾病进展越快。本研究在CRISP队列中分析了基因类型对疾病进展的意义。确定了183个家庭(219例患者)的基因类型;其中156例(85.2%)为PKD1型,27例(14.8%)为PKD2型。PKD1型患者的肾脏明显更大,但囊肿生长速率(PKD1型为5.68%/年;PKD2型为4.82%/年)并无差异(P = 0.24)。囊肿数量随年龄增加,PKD1型肾脏中检测到的囊肿更多(P < 0.0001)。PKD1型病情更严重是因为更多囊肿更早出现,而非生长更快,这表明疾病基因与囊肿起始有关,而非与囊肿扩张有关。这些见解将为常染色体显性多囊肾病的靶向治疗发展提供依据。

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