Abstract

BackgroundThe diagnosis of neuromuscular diseases is strongly based on the histological characterization of muscle biopsies. However, this morphological analysis is mostly a subjective process and difficult to quantify. We have tested if network science can provide a novel framework to extract useful information from muscle biopsies, developing a novel method that analyzes muscle samples in an objective, automated, fast and precise manner.MethodsOur database consisted of 102 muscle biopsy images from 70 individuals (including controls, patients with neurogenic atrophies and patients with muscular dystrophies). We used this to develop a new method, Neuromuscular DIseases Computerized Image Analysis (NDICIA), that uses network science analysis to capture the defining signature of muscle biopsy images. NDICIA characterizes muscle tissues by representing each image as a network, with fibers serving as nodes and fiber contacts as links.ResultsAfter a ‘training’ phase with control and pathological biopsies, NDICIA was able to quantify the degree of pathology of each sample. We validated our method by comparing NDICIA quantification of the severity of muscular dystrophies with a pathologist’s evaluation of the degree of pathology, resulting in a strong correlation (R = 0.900, P <0.00001). Importantly, our approach can be used to quantify new images without the need for prior ‘training’. Therefore, we show that network science analysis captures the useful information contained in muscle biopsies, helping the diagnosis of muscular dystrophies and neurogenic atrophies.ConclusionsOur novel network analysis approach will serve as a valuable tool for assessing the etiology of muscular dystrophies or neurogenic atrophies, and has the potential to quantify treatment outcomes in preclinical and clinical trials.

Highlights

  • The diagnosis of neuromuscular diseases is strongly based on the histological characterization of muscle biopsies

  • Principal component analysis (PCA) [26] allows the degree of pathology of each biopsy image to be visualized graphically based on its position when two or three principal components are represented (Figure 2)

  • We have shown here that Neuromuscular DIseases Computerized Image Analysis (NDICIA) was able to quantify the differences between control and pathological samples that were not used in the feature selection step

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Summary

Introduction

The diagnosis of neuromuscular diseases is strongly based on the histological characterization of muscle biopsies. This morphological analysis is mostly a subjective process and difficult to quantify. Muscular dystrophies (MD) are primary myopathies characterized by a wide variation in fiber size, a rounded shape of atrophic fibers, and fibrosis (an increase of endomysial collagen), which define the dystrophic pattern. Previous attempts to automate the extraction of geometrical characteristics from normal muscle biopsies have been published [11,12,13,14,15,16], but those methods fail to provide an automated analysis or adequate scrutiny of the information derived from the analysis. Our analysis begins at this point, taking into account a large number of samples to study both geometrical and network data to include morphometric and organizational information

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