سجل مستودعي · ncbi-prjna908773
Individuals infected with SARS-CoV-2 vary greatly in their symptomatology and disease progression, likely as a result of numerous genetic, biological and environmental factors…
العنوان في المستودع: Individuals infected with SARS-CoV-2 vary greatly in their symptomatology and disease progression, likely as a result of numerous genetic, biological and environmental factors and their complex interactions.
Individuals infected with SARS-CoV-2 vary greatly in their symptomatology and disease progression, likely as a result of numerous genetic, biological and environmental factors and their complex interactions. Meanwhile, the potential roles of microRNAs (miRNAs) in SARS-CoV-2 infection have not been fully described. MiRNAs have emerged as key post-transcriptional regulators of gene expression, and their dysregulation can be indicative of aberrant immune function. In this study, we characterize the potential roles of mIRNAs in early COVID-19 disease progression. We studied a diverse cohort of 259 patients admitted to hospitals in Abu Dhabi, United Arab Emirates to understand the clinical and biological factors associated with ICU admission during COVID-19 treatment, integrating electronic health records (EHR), global miRNA and RNA expression, and genotyping data. Using EHR, we identified 26 factors correlated with ICU admission, including 8 blood phenotypes such as neutrophil-to-lymphocyte ratio, Interleukin-6, and C-reactive protein levels. Using genome-wide miRNA expression data for a subset of 96 individuals from Southeast Asia and the Middle East and North Africa, we identified 27 miRNAs significantly associated with ICU admission (p < 0.01), and 97 miRNAs associated with at least one of the 8 blood phenotypes. [cross-cor] Integrating expression data for 632 miRNAs and genotyping data for ~260,000 SNPs, we identified 168 significant cis-expression quantitative trait loci (cis-eQTLs), of which 59 were associated with either ICU admission or one of the 8 blood phentoypes. Overall, our findings characterize the miRNA architecture of blood phenotypes during the early stages of COVID-19 infection, identify miRNAs associated with ICU admission and therefore COVID-19 disease severity, and suggest a potential genetic control of miRNA expression during early COVID-19 disease progression. Overall design: Blood samples from patients with SARS-CoV2 infection were collected into tempus tubes at time of diagnosis (i.e. 1st timepoint). Total RNA was extracted from whole blood samples of the 96 patients where miRNA-seq was performed, and mRNA sequencing was performed on the same samples.
تم التحقق من رقم الوصول وارتباطه بدولة خليجية. ولا يثبت التسجيل وحده أن البرنامج البحثي الأوسع ما زال نشطًا.
01 / نظرة عامة على المشروع
ما الذي يثبته السجل.
- النطاق الجغرافي
- United Arab Emirates connection indexed in BioProject metadata
- نوع المشروع
- Repository submission series
- مجال البحث
- Pathogen genomics and infectious disease
- السنوات
- 2022–
- حالة المشروع
- repository_recorded
- أساس تحديد الحالة
- Registered in NCBI BioProject on 2022/12/05; operational lifecycle is not asserted.
- تاريخ دليل الحالة
- 2022-12-05
- الحجم
- 2 BioProject accessions grouped by matching submitter, date, data type and narrative.
02 / المؤسسات والمجتمع
من وما الذي يربطه المشروع.
- الجهات القائدة
- Division of Science and Mathematics, Biology, NYUAD
- الجهات الشريكة
- غير مذكور
- الكائن / المجتمع
- Homo sapiens
03 / البيانات والإتاحة
ما الموجود وكيف يمكن الوصول إليه.
أنواع البيانات
- Transcriptome or Gene expression
- Sequencing
- Transcriptome
إتاحة البيانات
Public repository metadata with linked data where supplied by the submitter
المعرّفات
- BioProject
PRJNA908773 - BioProject
PRJNA908778
04 / الدليل والمصدر
لماذا أُدرج هذا السجل.
أساس الإدراج
Exact country-name match in authoritative NCBI BioProject metadata; repeated submissions are grouped into one Atlas series.
ملاحظة تحريرية
Repository verification confirms the accession and regional connection, not whether the broader research programme remains active.
المصادر
- primary record source تم التحقق في 2026-08-15
- additional record source تم التحقق في 2026-08-15
الإصدار v0.2.0
