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10.2217/pgs-2020-0048

http://scihub22266oqcxt.onion/10.2217/pgs-2020-0048
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32501190!7373206!32501190
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suck abstract from ncbi


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pmid32501190      Pharmacogenomics 2020 ; 21 (10): 695-703
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  • ACE2 and COVID-19: using antihypertensive medications and pharmacogenetic considerations #MMPMID32501190
  • Snyder EM; Johnson BD
  • Pharmacogenomics 2020[Jul]; 21 (10): 695-703 PMID32501190show ga
  • COVID-19 utilizes the ACE2 pathway as a means of infection. Early data on COVID-19 suggest heterogeneity in the severity of symptoms during transmission and infection ranging from no symptoms to death. The source of this heterogeneity is likely multifaceted and may have a genetic component. Demographic and clinical comorbidities associated with the severity of infection suggest that possible variants known to influence the renin-angiotensin-aldosterone (RAAS) system pathway (particularly those that influence ACE2) may contribute to the heterogenous infection response. ACE2 and Ang(1-7) (the product of ACE2) seem to have a protective effect on the pulmonary and cardiac systems. Hypertension medication modulation, may alter ACE2 and Ang(1-7), particularly in variants that have been shown to influence RAAS system function, which could be clinically useful in patients with COVID-19.
  • |*Pharmacogenetics[MESH]
  • |Angiotensin II Type 1 Receptor Blockers/*therapeutic use[MESH]
  • |Angiotensin-Converting Enzyme 2[MESH]
  • |Antihypertensive Agents/*therapeutic use[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/*drug therapy/*genetics[MESH]
  • |Humans[MESH]
  • |Pandemics[MESH]
  • |Peptidyl-Dipeptidase A/*drug effects/*genetics[MESH]
  • |Pharmacogenomic Testing[MESH]
  • |Pneumonia, Viral/*drug therapy/*genetics[MESH]


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