Validation of a new multiple osteochondromas classification through Switching Neural Networks

被引:33
作者
Mordenti, Marina [1 ]
Ferrari, Enrico [2 ]
Pedrini, Elena [1 ]
Fabbri, Nicola [3 ]
Campanacci, Laura [4 ]
Muselli, Marco [5 ]
Sangiorgi, Luca [1 ]
机构
[1] Rizzoli Orthopaed Inst IOR, Dept Med Genet, I-40136 Bologna, Italy
[2] IMPARA Srl, I-16129 Genoa, Italy
[3] Mem Sloan Kettering Canc Ctr, New York, NY 10065 USA
[4] Rizzoli Orthopaed Inst IOR, Orthopaed Oncol Clin 4, I-40136 Bologna, Italy
[5] Natl Res Council Italy, Inst Elet Comp & Telecommun Engineerin, Genoa, Italy
关键词
multiple osteochondromas; patients classification; EXT1; EXT2; switching neural network; genotypephenotype correlation; GENOTYPE-PHENOTYPE CORRELATION; CHONDROSARCOMA; IDENTIFICATION; EXOSTOSES; RISK;
D O I
10.1002/ajmg.a.35819
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Multiple osteochondromas (MO), previously known as hereditary multiple exostoses (HME), is an autosomal dominant disease characterized by the formation of several benign cartilage-capped bone growth defined osteochondromas or exostoses. Various clinical classifications have been proposed but a consensus has not been reached. The aim of this study was to validate (using a machine learning approach) an easy to use tool to characterize MO patients in three classes according to the number of bone segments affected, the presence of skeletal deformities and/or functional limitations. The proposed classification has been validated (with a highly satisfactory mean accuracy) by analyzing 150 different variables on 289 MO patients through a Switching Neural Network approach (a novel classification technique capable of deriving models described by intelligible rules in if-then form). This approach allowed us to identify ankle valgism, Madelung deformity and limitation of the hip extra-rotation as tags of the three clinical classes. In conclusion, the proposed classification provides an efficient system to characterize this rare disease and is able to define homogeneous cohorts of patients to investigate MO pathogenesis. (c) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:556 / 560
页数:5
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