ArticleBMC medicine2013
Quantifiable diagnosis of muscular dystrophies and neurogenic atrophies through network analysis.
Article in BMC medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed, 25 citations in OpenAlex.
- Entropy as a Geometrical Source of Information in Biological Organizations.Entropy (Basel, Switzerland) · 2022Article
- Individual-specific networks for prediction modelling - A scoping review of methods.BMC medical research methodology · 2022Article
- The topology of vitronectin: A complementary feature for neuroblastoma risk classification based on computer-aided detection.International journal of cancer · 2020Article
- Approach for semi-automated measurement of fiber diameter in murine and canine skeletal muscle.PloS one · 2020Article
- Smoke-induced neuromuscular junction degeneration precedes the fibre type shift and atrophy in chronic obstructive pulmonary disease.The Journal of physiology · 2018Article
- MyoVision: software for automated high-content analysis of skeletal muscle immunohistochemistry.Journal of applied physiology (Bethesda, Md. : 1985) · 2018Article
- Rules of tissue packing involving different cell types: human muscle organization.Scientific reports · 2017Article
- Fundamental physical cellular constraints drive self-organization of tissues.The EMBO journal · 2016Article
- Fhl1 W122S causes loss of protein function and late-onset mild myopathy.Human molecular genetics · 2015Article
- Biotensegrity of the extracellular matrix: physiology, dynamic mechanical balance, and implications in oncology and mechanotherapy.Frontiers in oncology · 2014Review
- Topological progression in proliferating epithelia is driven by a unique variation in polygon distribution.PloS one · 2013Article
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Authors and funding
8 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
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.
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