2023
DOI: 10.1002/hsr2.1703
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Exploring the relationship between SARS‐CoV‐2 variants, illness severity at presentation, in‐hospital mortality and COVID‐19 vaccination in a low middle‐income country: A retrospective cross‐sectional study

Muhammad Zain Mushtaq,
Nosheen Nasir,
Syed Faisal Mahmood
et al.

Abstract: Background and AimsCOVID‐19 morbidity and mortality varied globally through the pandemic. We studied the relationship of SARS‐CoV‐2 variants of concern (VOC) with COVID‐19 severity and mortality among hospitalized patients in Pakistan.MethodsA retrospective review of clinical, laboratory, and vaccination data of 197 COVID‐19 adult patients at the Aga Khan University Hospital, Karachi between April 2021, and February 2022 was performed. SARS‐CoV‐2 VOC identified in respiratory samples were analyzed. Univariate … Show more

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Cited by 5 publications
(2 citation statements)
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“…Wuhan S, M, and N repertoires were compared against 16 variants (B.1, Alpha, five Delta, and nine Omicron) to identify epitopes that were lost, gained, or altered in estimated HLA binding affinity between variants ( Figure 2 ). In general, a balanced number of epitopes were lost and gained for all variants; however, BA.1.1 M, BA.4 N, B.1.1.7 S, and BQ.1.1 S repertoires sustained greater epitope loss than gain ( Figures 2A–C , 3 , bottom ), which may contribute to explaining the increased transmission and breakthrough cases seen in these subvariants ( 39 , 40 ). Additionally, spike epitopes in the early variants (B.1 and B.1.1.7) and Omicron VOCs experienced a greater number of epitopes predicted to have reduced binding affinity than increased affinity.…”
Section: Resultsmentioning
confidence: 98%
“…Wuhan S, M, and N repertoires were compared against 16 variants (B.1, Alpha, five Delta, and nine Omicron) to identify epitopes that were lost, gained, or altered in estimated HLA binding affinity between variants ( Figure 2 ). In general, a balanced number of epitopes were lost and gained for all variants; however, BA.1.1 M, BA.4 N, B.1.1.7 S, and BQ.1.1 S repertoires sustained greater epitope loss than gain ( Figures 2A–C , 3 , bottom ), which may contribute to explaining the increased transmission and breakthrough cases seen in these subvariants ( 39 , 40 ). Additionally, spike epitopes in the early variants (B.1 and B.1.1.7) and Omicron VOCs experienced a greater number of epitopes predicted to have reduced binding affinity than increased affinity.…”
Section: Resultsmentioning
confidence: 98%
“…It is worth noting that this spread and its repercussions were not uniform and had many geographical, temporal and demographic variations. They were also heavily influenced by the nature of the RNA virus itself, which was characterised by a successive series of prevalent mutations, each having different levels of disease severity and communicability [14,16].…”
Section: Introductionmentioning
confidence: 99%