A radiomics method based on MR FS-T2WI sequence for diagnosing of autosomal dominant polycystic kidney disease progression
A radiomics method based on MR FS-T2WI sequence for diagnosing of autosomal dominant polycystic kidney disease progression
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DOI：
10.26355/eurrev_202109_26795
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发表时间：
2021-01-01
影响因子：
3.3
通讯作者：
Ma, T.
中科院分区：
文献类型：
--
作者：
Cong, L.;Hua, Q-Q;Ma, T.
目的：目的：建立一种基于FS-T2 WI序列的常染色体显性遗传性多囊肾病（ADPKD）患者肾功能评价的放射组学方法。以肾小球滤过率60 mL/min/1.73 m2为界值，将患者分为两组，其中GFR> 60 mL/min/1.73 m2（包括CKD 1和CKD 2期）的患者59例，GFR> 60 mL/min/1.73 m2（包括CKD 1和CKD 2期）的患者55例。
OBJECTIVE: We aimed to construct/validate a radiomics method based on MR FS-T2WI sequence for the evaluation of kidney function in patients with autosomal dominant polycystic kidney disease (ADPKD).PATIENTS AND METHODS: The clinical data and MRI images of 114 patients with ADPKD were retrospectively analyzed. With a glomerular filtration rate of 60 mL/min per 1.73 m2 as the cutoff value, patients were divided into two groups, where there were 59 patients with GFR X60 mL/min per 1.73 m(2) (including CKD1 and CKD2 phase) and 55 patients with GFR