Early assessment of the clinical severity of the SARS-CoV-2 omicron variant in South Africa: a data linkage study

被引:725
作者
Wolter, Nicole [1 ,6 ]
Jassat, Waasila [2 ]
Walaza, Sibongile [1 ,7 ]
Welch, Richard [2 ]
Moultrie, Harry [3 ,6 ]
Groome, Michelle [2 ]
Amoako, Daniel Gyamfi [1 ,9 ]
Everatt, Josie [1 ]
Bhiman, Jinal N. [4 ,8 ]
Scheepers, Cathrine [4 ,8 ]
Tebeila, Naume [1 ]
Chiwandire, Nicola [1 ]
du Plessis, Mignon [1 ,6 ]
Govender, Nevashan [2 ]
Ismail, Arshad [5 ]
Glass, Allison [12 ]
Mlisana, Koleka [10 ,13 ]
Stevens, Wendy [6 ,13 ]
Treurnicht, Florette K. [6 ,13 ]
Makatini, Zinhle [6 ,13 ]
Hsiao, Nei-Yuan [13 ,14 ]
Parboosing, Raveen [6 ,11 ,13 ]
Wadula, Jeannette [13 ,16 ]
Hussey, Hannah [15 ]
Davies, Mary-Ann [15 ]
Boulle, Andrew [15 ]
von Gottberg, Anne [1 ,6 ]
Cohen, Cheryl [1 ,7 ]
机构
[1] Natl Hlth Lab Serv, Ctr Resp Dis & Meningitis, Natl Inst Communicable Dis, ZA-2131 Johannesburg, South Africa
[2] Natl Inst Communicable Dis Natl Hlth Lab Serv, Div Publ Hlth Surveillance & Response, Johannesburg, South Africa
[3] Natl Inst Communicable Dis Natl Hlth Lab Serv, Ctr TB, Johannesburg, South Africa
[4] Natl Inst Communicable Dis Natl Hlth Lab Serv, Ctr HIV & STIs, Johannesburg, South Africa
[5] Natl Inst Communicable Dis Natl Hlth Lab Serv, Sequencing Core Facil, Johannesburg, South Africa
[6] Univ Witwatersrand, Fac Hlth Sci, Sch Pathol, Johannesburg, South Africa
[7] Univ Witwatersrand, Fac Hlth Sci, Sch Publ Hlth, Johannesburg, South Africa
[8] Univ Witwatersrand, Fac Hlth Sci, Sch Pathol, SA MRC Antibody Immun Res Unit, Johannesburg, South Africa
[9] Univ KwaZulu Natal, Coll Hlth Sci, Sch Hlth Sci, Durban, South Africa
[10] Univ KwaZulu Natal, Sch Lab Med & Med Sci, Durban, South Africa
[11] Univ KwaZulu Natal, Dept Virol, Durban, South Africa
[12] Lancet Labs, Johannesburg, South Africa
[13] Natl Hlth Lab Serv, Johannesburg, South Africa
[14] Univ Cape Town, Div Med Virol, Cape Town, South Africa
[15] Univ Cape Town, Western Cape Govt Hlth, Cape Town, South Africa
[16] CH Baragwanath Acad Hosp, Dept Clin Microbiol & Infect Dis, Johannesburg, South Africa
基金
比尔及梅琳达.盖茨基金会; 英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1016/S0140-6736(22)00017-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The SARS-CoV-2 omicron variant of concern was identified in South Africa in November, 2021, and was associated with an increase in COVID-19 cases. We aimed to assess the clinical severity of infections with the omicron variant using S gene target failure (SGTF) on the Thermo Fisher Scientific TaqPath COVID-19 PCR test as a proxy. Methods We did data linkages for national, South African COVID-19 case data, SARS-CoV-2 laboratory test data, SARS-CoV-2 genome data, and COVID-19 hospital admissions data. For individuals diagnosed with COVID-19 via TaqPath PCR tests, infections were designated as either SGTF or non-SGTF. The delta variant was identified by genome sequencing. Using multivariable logistic regression models, we assessed disease severity and hospitalisations by comparing individuals with SGTF versus non-SGTF infections diagnosed between Oct 1 and Nov 30, 2021, and we further assessed disease severity by comparing SGTF-infected individuals diagnosed between Oct 1 and Nov 30, 2021, with delta variant-infected individuals diagnosed between April 1 and Nov 9, 2021. Findings From Oct 1 (week 39), 2021, to Dec 6 (week 49), 2021, 161 328 cases of COVID-19 were reported in South Africa. 38 282 people were diagnosed via TaqPath PCR tests and 29 721 SGTF infections and 1412 non-SGTF infections were identified. The proportion of SGTF infections increased from two (3.2%) of 63 in week 39 to 21 978 (97.9%) of 22 455 in week 48. After controlling for factors associated with hospitalisation, individuals with SGTF infections had significantly lower odds of admission than did those with non-SGTF infections (256 [2.4%] of 10 547 vs 121 [ 12. 8%] of 948; adjusted odds ratio [aOR] 0.2, 95% CI 0.1-0.3). After controlling for factors associated with disease severity, the odds of severe disease were similar between hospitalised individuals with SGTF versus non-SGTF infections (42 [21%] of 204 vs 45 [40%] of 113; aOR 0.7, 95% CI 0.3-1.4). Compared with individuals with earlier delta variant infections, SGTF-infected individuals had a significantly lower odds of severe disease (496 [62.5%] of 793 vs 57 [23.4%] of 244; aOR 0.3, 95% CI 0.2-0.5), after controlling for factors associated with disease severity. Interpretation Our early analyses suggest a significantly reduced odds of hospitalisation among individuals with SGTF versus non-SGTF infections diagnosed during the same time period. SGTF-infected individuals had a significantly reduced odds of severe disease compared with individuals infected earlier with the delta variant. Some of this reduced severity is probably a result of previous immunity.
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页码:437 / 446
页数:10
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