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10.1152/ajpheart.00489.2020

http://scihub22266oqcxt.onion/10.1152/ajpheart.00489.2020
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32762561!7509271!32762561
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suck abstract from ncbi

pmid32762561      Am+J+Physiol+Heart+Circ+Physiol 2020 ; 319 (3): H604-H609
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  • Diabetes and COVID-19 risk: an miRNA perspective #MMPMID32762561
  • Mishra PK; Tandon R; Byrareddy SN
  • Am J Physiol Heart Circ Physiol 2020[Sep]; 319 (3): H604-H609 PMID32762561show ga
  • Coronavirus disease 2019 (COVID-19) and diabetes outcomes (CORONADO) trial revealed that 10.6% of patients with diabetes mellitus hospitalized for COVID-19 (COVID-19) die within 7 days. Several studies from New York, Italy, and China confirm that patients with diabetes are at a much higher risk for mortality due to COVID-19. Besides respiratory illness, COVID-19 increases cardiac injury and diabetic ketoacidosis. In the absence of specific guidelines for the prevention and treatment of COVID-19 for patients with diabetes, they remain at higher risk and are more susceptible to COVID-19. Furthermore, there is a scarcity of basic knowledge on how diabetes affects pathogenesis of severe acute respiratory coronavirus (SARS-CoV-2) infection. In patients with diabetes, impaired glucose use alters metabolic and consequently biological processes instigating pathological remodeling, which has detrimental effects on cardiovascular systems. A majority of biological processes are regulated by noncoding microRNAs (miRNAs), which have emerged as a promising therapeutic candidate for several diseases. In consideration of the higher risk of mortality in patients with diabetes and COVID-19, novel diagnostic test and treatment strategy are urgently warranted in post-COVID-19 era. Here, we describe potential roles of miRNA as a biomarker and therapeutic candidate, especially for heart failure, in patients with diabetes and COVID-19.
  • |Angiotensin-Converting Enzyme 2[MESH]
  • |Animals[MESH]
  • |Biomarkers/metabolism[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/epidemiology/*metabolism/pathology[MESH]
  • |Diabetes Complications/*epidemiology[MESH]
  • |Humans[MESH]
  • |MicroRNAs/*genetics/metabolism[MESH]
  • |Pandemics[MESH]
  • |Peptidyl-Dipeptidase A/genetics/metabolism[MESH]


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