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Allergy Asthma Immunol Res. 2019;11(1):104-115.

Different Biological Pathways Are Up-regulated in the Elderly With Asthma: Sputum Transcriptomic Analysis.

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제1저자 김병근 · 교신저자 박흥우

소속 (5)
  1. Department of Internal Medicine, Korea University Medical Center Anam Hospital, Seoul, Korea.
  2. Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.
  3. Institute of Allergy and Clinical Immunology, Seoul National University Medical Research Center, Seoul, Korea.
  4. Department of Internal Medicine, KyungHee University Medical center, Seoul, Korea.
  5. Institute of Allergy and Clinical Immunology, Seoul National University Medical Research Center, Seoul, Korea. guinea71@snu.ac.kr.

Abstract

BACKGROUND Elderly asthma (EA) is increasing, but the pathogenesis is unclear. This study aimed to identify EA-related biological pathways by analyzing genome-wide gene expression profiles in sputum cells.

METHODS A total of 3,156 gene probes with significantly differential expressions between EA and healthy elderly controls were used for a hierarchical clustering of genes to identify gene clusters. Gene set enrichment analysis provided biological information, with replication from Gene Expression Omnibus expression profiles.

RESULTS Fifty-five EA patients and 10 elderly control subjects were enrolled. Two distinct gene clusters were found. Cluster 1 (n = 35) showed a lower eosinophil proportion in sputum and less severe airway obstruction compared to cluster 2 (n = 20). The replication data set also identified 2 gene clusters (clusters 1' and 2'). Among 5 gene sets significantly enriched in cluster 1 and 3 gene sets significantly enriched in cluster 2, we confirmed that 2 were significantly enriched in the replication data set (OXIDATIVE_PHOSPHORYLATION gene set in cluster 1 and EPITHELIAL MESENCHYMAL TRANSITION gene set in cluster 2').

CONCLUSIONS The findings of 2 distinct gene clusters in EA and different biological pathways in each gene cluster suggest 2 different pathogenesis mechanisms underlying EA.

Copyright © 2019 The Korean Academy of Asthma, Allergy and Clinical Immunology · The Korean Academy of Pediatric Allergy and Respiratory Disease.

Keywords

AsthmaCluster analysisElderlyGene expression

Figures

Fig. 1
Fig. 1 Two gene clusters identified in the discovery and replication dataset. (A) Discovery dataset. Three outliers (Pt5, Pt21, and Pt28) were excluded from analysis. (B) Replication dataset. Pt, Patient.
Fig. 2
Fig. 2 Gene sets enriched in each cluster identified in the discovery dataset with FDR P values less than 0.001. (A) Cluster 1, (B) Cluster 2. FDR, false discovery rate; OXPHOS, OXIDATIVE_PHOSPHORYLATION; UPR, UNFOLDED_PROTEIN_RESPONSE, EMT, EPITHELIAL_MESENCHYMAL_TRANSITION.
Fig. 3
Fig. 3 Association between clinical variables and PC1 of the leading edge genes from gene sets enriched in both discovery and replication datasets. (A) Cluster 1, (B) Cluster 2. Figures without P values denote statistically insignificant associations. PC, principal component; OXPHOS, OXIDATIVE_PHOSPHORYLATION; EMT, EPITHELIAL_MESENCHYMAL_TRANSITION.
Fig. 4
Fig. 4 Volcano plot displaying differential expressed genes. The 4 genes (MRPS11, HSPA9, NUDF4, and ACTA1) belong to the leading edge genes of the OXPHOS gene set and 2 genes (SNTB1 and FUCA1) belong to the leading edge genes of the EMT gene set. OXPHOS, OXIDATIVE_PHOSPHORYLATION; EMT, EPITHELIAL_MESENCHYMAL_TRANSITION.

그림 출처: PubMed Central 공개 논문 (PMC6267191)

Conflict of interest statement

There are no financial or other issues that might lead to conflict of interest.

그 밖의 정보
출판 형태
Journal Article
저널
Allergy, asthma & immunology research · ISSN 2092-7355
연구비
Korea University Anam Hospital O1700381
참고문헌
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