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pmid:35646907

The Biological Interaction of SARS-CoV-2 Infection and Osteoporosis: A Preliminary Study.

Xin Kang · Xiaodong Wen · Jingqi Liang · Liang Liu · Yan Zhang · Qiong Wang · Hongmou Zhao

Frontiers in cell and developmental biology · 2022 doi:10.3389/fcell.2022.917907

Paper

complete

Experiment

complete

Data

partial

Analysis

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Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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paper object · 10 fields
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title
The Biological Interaction of SARS-CoV-2 Infection and Osteoporosis: A Preliminary Study.
doi
10.3389/fcell.2022.917907
pmid
35646907
authors array · 7 items
[0]
Xin Kang
[1]
Xiaodong Wen
[2]
Jingqi Liang
[3]
Liang Liu
[4]
Yan Zhang
[5]
Qiong Wang
[6]
Hongmou Zhao
journal
Frontiers in cell and developmental biology
year
2022
abstract
The COVID-19 pandemic caused by the severe acute coronavirus disease 2 (SARS-CoV-2) virus represents an ongoing threat to human health and well-being. Notably, many COVID-19 patients suffer from complications consistent with osteoporosis (OP) following disease resolution yet the mechanistic links between SARS-CoV-2 infection and OP remain to be clarified. The present study was thus developed to explore the potential basis for this link by employing transcriptomic analyses to identify signaling pathways and biomarkers associated with OP and SARS-CoV-2. Specifically, a previously published RNA-sequencing dataset (GSE152418) from Gene Expression Omnibus (GEO) was used to identify the differentially expressed genes (DEGs) in OP patients and individuals infected with SARS-CoV-2 as a means of exploring the underlying molecular mechanisms linking these two conditions. In total, 2,885 DEGs were identified by analyzing the COVID-19 patient dataset, with shared DEGs then being identified by comparison of these DEGs with those derived from an OP patient dataset. Hub genes were identified through a series of bioinformatics approaches and protein-protein interaction analyses. Predictive analyses of transcription factor/gene interactions, protein/drug interactions, and DEG/miRNA networks associated with these DEGs were also conducted. Together, these data highlight promising candidate drugs with the potential to treat both COVID-19 and OP.
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Genes differentially expressed between COVID-19 or OP patients and healthy controls were identified with the R limma package and DESeq2 using the following criteria: p < 0.05 and |logFC| > 1.0.
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Genes differentially expressed between COVID-19 or OP patients and healthy controls were identified with the R limma package and DESeq2 using the following criteria: p < 0.05 and |logFC| > 1.0.
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The study identified 73 differentially expressed genes shared between COVID-19 and osteoporosis patient datasets.
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sections[4] "Identification of DEGs Shared Between COVID-19 and OP" paragraph 2
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The JVenn program was next used to identify 73 DEGs shared between these COVID-19 and OP datasets, suggesting that they may be associated with the biological link between these two conditions (Figure 2).
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Microarray profile of osteoporosis related genes of Indian post menopausal females
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