دورية أكاديمية
The genetic framework of primary ciliary dyskinesia assessed by soft computing analysis.
| العنوان: | The genetic framework of primary ciliary dyskinesia assessed by soft computing analysis. |
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| المؤلفون: | Pifferi M; Department of Pediatrics, University Hospital of Pisa, Pisa, Italy., Boner AL; Pediatric Unit, Department of Surgical Science, Dentistry, Gynecology and Pediatrics, Verona University Medical School, Verona, Italy., Cangiotti A; Electron Microscopy Unit, Department of Experimental and Clinical Medicine, University Hospital of Ancona, Ancona, Italy., Cudazzo A; Department of Computer Science, University of Pisa, Pisa, Italy., Maj D; Department of Pediatrics, University Hospital of Pisa, Pisa, Italy., Gracci S; Department of Pediatrics, University Hospital of Pisa, Pisa, Italy., Michelucci A; Unit of Molecular Genetics, Department of Laboratory Medicine, University Hospital of Pisa, Pisa, Italy., Bertini V; Section of Cytogenetics, Department of Laboratory Medicine, University Hospital of Pisa, Pisa, Italy., Piazza M; Pediatric Unit, Department of Surgical Science, Dentistry, Gynecology and Pediatrics, Verona University Medical School, Verona, Italy., Valetto A; Section of Cytogenetics, Department of Laboratory Medicine, University Hospital of Pisa, Pisa, Italy., Caligo MA; Unit of Molecular Genetics, Department of Laboratory Medicine, University Hospital of Pisa, Pisa, Italy., Peroni D; Department of Pediatrics, University Hospital of Pisa, Pisa, Italy., Bush A; Department of Paediatric Respiratory Medicine, Imperial College and Royal Brompton Hospital, London, UK. |
| المصدر: | Pediatric pulmonology [Pediatr Pulmonol] 2024 Apr; Vol. 59 (4), pp. 891-898. Date of Electronic Publication: 2024 Jan 03. |
| نوع المنشور: | Journal Article |
| اللغة: | English |
| بيانات الدورية: | Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8510590 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1099-0496 (Electronic) Linking ISSN: 10990496 NLM ISO Abbreviation: Pediatr Pulmonol Subsets: MEDLINE |
| أسماء مطبوعة: | Publication: <2005-> : Hoboken, NJ : Wiley-Liss Original Publication: [Philadelphia, PA] : W.B. Saunders, [c1985- |
| مواضيع طبية MeSH: | Kartagener Syndrome*/diagnosis , Kartagener Syndrome*/genetics , Ciliary Motility Disorders*/diagnosis , Ciliary Motility Disorders*/genetics, Humans ; Soft Computing ; Cilia/genetics ; Cilia/ultrastructure ; Microscopy, Video ; Microscopy, Electron, Transmission |
| مستخلص: | Background: International guidelines disagree on how best to diagnose primary ciliary dyskinesia (PCD), not least because many tests rely on pattern recognition. We hypothesized that quantitative distribution of ciliary ultrastructural and motion abnormalities would detect most frequent PCD-causing groups of genes by soft computing analysis. Methods: Archived data on transmission electron microscopy and high-speed video analysis from 212 PCD patients were re-examined to quantitate distribution of ultrastructural (10 parameters) and functional ciliary features (4 beat pattern and 2 frequency parameters). The correlation between ultrastructural and motion features was evaluated by blinded clustering analysis of the first two principal components, obtained from ultrastructural variables for each patient. Soft computing was applied to ultrastructure to predict ciliary beat frequency (CBF) and motion patterns by a regression model. Another model classified the patients into the five most frequent PCD-causing gene groups, from their ultrastructure, CBF and beat patterns. Results: The patients were subdivided into six clusters with similar values to homologous ultrastructural phenotype, motion patterns, and CBF, except for clusters 1 and 4, attributable to normal ultrastructure. The regression model confirmed the ability to predict functional ciliary features from ultrastructural parameters. The genetic classification model identified most of the different groups of genes, starting from all quantitative parameters. Conclusions: Applying soft computing methodologies to PCD diagnostic tests optimizes their value by moving from pattern recognition to quantification. The approach may also be useful to evaluate atypical PCD, and novel genetic abnormalities of unclear disease-producing potential in the future. (© 2024 Wiley Periodicals LLC.) |
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| معلومات مُعتمدة: | None |
| فهرسة مساهمة: | Keywords: artificial intelligence; ciliary motion analysis; ciliary ultrastructure; genetic abnormalities; primary ciliary dyskinesia |
| تواريخ الأحداث: | Date Created: 20240103 Date Completed: 20240329 Latest Revision: 20240329 |
| رمز التحديث: | 20240329 |
| DOI: | 10.1002/ppul.26842 |
| PMID: | 38169302 |
| قاعدة البيانات: | MEDLINE |
Full Text Finder | تدمد: | 1099-0496 |
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| DOI: | 10.1002/ppul.26842 |