دورية أكاديمية
Autophagy-related molecular clusters identified as indicators for distinguishing active and latent TB infection in pediatric patients.
العنوان: | Autophagy-related molecular clusters identified as indicators for distinguishing active and latent TB infection in pediatric patients. |
---|---|
المؤلفون: | Yu Y; Department of Pediatric, Nanjing Lishui People's Hospital, Zhongda Hospital Lishui Branch, Southeast University, Nanjing, China., Hua J; Department of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China., Chen L; Department of Infectious Diseases, Taikang Xianlin Drum Tower Hospital, Affiliated Hospital of Medical College of Nanjing University, Qixia District, NO 188, Lingshan North Road, Qixia District, Nanjing, 210046, China. Chenliang1995@sina.com. |
المصدر: | BMC pediatrics [BMC Pediatr] 2024 Jun 19; Vol. 24 (1), pp. 398. Date of Electronic Publication: 2024 Jun 19. |
نوع المنشور: | Journal Article |
اللغة: | English |
بيانات الدورية: | Publisher: BioMed Central Country of Publication: England NLM ID: 100967804 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2431 (Electronic) Linking ISSN: 14712431 NLM ISO Abbreviation: BMC Pediatr Subsets: MEDLINE |
أسماء مطبوعة: | Original Publication: London : BioMed Central, [2001- |
مواضيع طبية MeSH: | Latent Tuberculosis*/diagnosis , Latent Tuberculosis*/genetics , Autophagy*/genetics, Humans ; Child ; Gene Expression Profiling ; Tuberculosis/genetics ; Tuberculosis/diagnosis ; Diagnosis, Differential ; Biomarkers/metabolism ; Male ; Child, Preschool ; Female |
مستخلص: | Background: Autophagy is crucial for controlling the manifestation of tuberculosis. This study intends to discover autophagy-related molecular clusters as biomarkers for discriminating between latent tuberculosis (LTBI) and active tuberculosis (ATB) in children through gene expression profile analysis. Methods: The expression of autophagy modulators was examined in pediatric patients with LTBI and ATB utilizing public datasets from the Gene Expression Omnibus (GEO) collection (GSE39939 and GSE39940). Results: In a training dataset (GSE39939), patients with LTBI and ATB exhibited the expression of autophagy-related genes connected with their active immune responses. Two molecular clusters associated with autophagy were identified. Compared to Cluster 1, Cluster 2 was distinguished through decreased adaptive cellular immune response and enhanced inflammatory activation, according to single-sample gene set enrichment analysis (ssGSEA). Per the study of gene set variation, Cluster 2's differentially expressed genes (DEGs) played a role in synthesizing transfer RNA, DNA repair and recombination, and primary immunodeficiency. The peak variation efficiency, root mean square error, and area under the curve (AUC) (AUC = 0.950) were all lowered in random forest models. Finally, a seven-gene-dependent random forest profile was created utilizing the CD247, MAN1C1, FAM84B, HSZFP36, SLC16A10, DTX3, and SIRT4 genes, which performed well against the validation dataset GSE139940 (AUC = 0.888). The nomogram calibration and decision curves performed well in identifying ATB from LTBI. Conclusions: In summary, according to the present investigation, autophagy and the immunopathology of TB might be correlated. Furthermore, this investigation established a compelling prediction expression profile for measuring autophagy subtype development risks, which might be employed as possible biomarkers in children to differentiate ATB from LTBI. (© 2024. The Author(s).) |
References: | Microbiol Spectr. 2016 Oct;4(5):. (PMID: 27763261) J Biol Chem. 2011 Nov 4;286(44):38738-38747. (PMID: 21911496) Genes Immun. 2012 Sep;13(6):496-502. (PMID: 22695749) Front Immunol. 2018 Mar 09;9:419. (PMID: 29593712) Nature. 2010 Aug 19;466(7309):973-7. (PMID: 20725040) Infect Dis Clin North Am. 2022 Mar;36(1):49-71. (PMID: 35168714) Am J Physiol Cell Physiol. 2022 Nov 1;323(5):C1444-C1474. (PMID: 36189975) Mol Aspects Med. 2013 Apr-Jun;34(2-3):337-49. (PMID: 23506875) Cell Microbiol. 2006 May;8(5):719-27. (PMID: 16611222) Biomedicines. 2022 Aug 11;10(8):. (PMID: 36009490) Cold Spring Harb Perspect Med. 2015 Jul 17;5(12):. (PMID: 26187873) Pulmonology. 2018 Mar - Apr;24(2):106-114. (PMID: 29502937) BMC Infect Dis. 2013 Jan 28;13:45. (PMID: 23356448) Front Aging Neurosci. 2017 Oct 06;9:329. (PMID: 29056906) PLoS One. 2013 Sep 16;8(9):e73230. (PMID: 24066041) Hum Vaccin Immunother. 2018 Jul 3;14(7):1697-1716. (PMID: 29601253) Clin Chest Med. 2019 Dec;40(4):797-810. (PMID: 31731985) PLoS One. 2012;7(8):e41618. (PMID: 22879892) Lancet Respir Med. 2018 Apr;6(4):299-314. (PMID: 29595511) Virulence. 2019 Dec;10(1):448-459. (PMID: 30322337) J Biol Chem. 2007 Nov 16;282(46):33583-33592. (PMID: 17715127) Genes Immun. 2015 Mar;16(2):142-50. (PMID: 25569266) J Exp Med. 2009 Nov 23;206(12):2583-91. (PMID: 19901083) Scand J Immunol. 2022 Jul;96(1):e13170. (PMID: 35388926) Front Endocrinol (Lausanne). 2019 Jan 07;9:783. (PMID: 30666234) Biotechnol Adv. 2021 Jul-Aug;49:107739. (PMID: 33794304) Med Phys. 2018 Nov;45(11):e1073-e1085. (PMID: 30421814) J Immunol. 2016 Jan 1;196(1):156-67. (PMID: 26608909) Cell Metab. 2020 Mar 3;31(3):580-591.e5. (PMID: 32032542) Am J Physiol Lung Cell Mol Physiol. 2017 Aug 1;313(2):L218-L229. (PMID: 28495854) iScience. 2022 Nov 02;25(12):105482. (PMID: 36404925) Future Microbiol. 2022 Sep;17:1171-1198. (PMID: 35924958) |
فهرسة مساهمة: | Keywords: Active tuberculosis; Autophagy; Children; Latent tuberculosis; Model; Molecular cluster |
المشرفين على المادة: | 0 (Biomarkers) |
تواريخ الأحداث: | Date Created: 20240618 Date Completed: 20240619 Latest Revision: 20240621 |
رمز التحديث: | 20240621 |
مُعرف محوري في PubMed: | PMC11186109 |
DOI: | 10.1186/s12887-024-04881-1 |
PMID: | 38890657 |
قاعدة البيانات: | MEDLINE |
تدمد: | 1471-2431 |
---|---|
DOI: | 10.1186/s12887-024-04881-1 |