英格兰、威尔士和美国各州与新冠肺炎相关的SARS-CoV-2变异株年龄分布(2020年至2022年):对所有原因死亡率的影响。

IF 3.4 Q2 INFECTIOUS DISEASES Infectious Disease Reports Pub Date : 2023-10-08 DOI:10.3390/idr15050058
Rodney P Jones, Andrey Ponomarenko
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引用次数: 0

摘要

自2020年以来,新冠肺炎已在世界各地造成严重死亡。鉴于将新冠肺炎确定为直接死亡原因的模糊性,我们首先调查了2020年和2021年英格兰和威尔士年龄和性别对全因死亡率的影响。由于传染源有自己独特的死亡年龄特征,我们使用9年时间序列和几种不同的方法,将2019年(COVID-19之前的基准年)英格兰和威尔士的单岁死亡调整为病原体-中性单岁基线。然后,这个调整后的基准年被用来证实,在2020年和2021年,大多数43岁以上的男性死亡人数普遍较高。2020年期间(+新冠肺炎,但未接种疫苗),35岁以上的男性和女性人口调整后死亡人数均显著增加。2021年,在广泛接种新冠肺炎疫苗期间,75岁以上男性和女性的全因死亡率可能显著降低;然而,75岁以下的死亡人数逐渐增加。这一发现源于不同严重急性呼吸系统综合征冠状病毒2型变异株的疫苗接种覆盖率和死亡年龄分布。此外,还证明了青春期前后年龄的特定影响,其中女性的死亡率高于男性。有证据表明,出生年份队列也可能参与其中,这表明过去对特定病原体爆发的免疫启动可能导致一些出生队列的死亡率降低。为了具体确定2020年至2023年新冠肺炎变异株的年龄分布,我们采用了每个年龄段可能因新冠肺炎或与之“相关”的总死亡比例。最初的武汉毒株和阿尔法变种在年龄分布上表现出有限的差异,阿尔法变种在84岁以下的死亡比例有所上升。德尔塔变异株专门针对65岁以下的人群。奥密克戎变异株在总死亡率中所占的比例明显较低,65岁以上死亡的相对比例明显较高,随着年龄的增长急剧增加,最高可达100岁左右。在美国各州的年龄带死亡病例中可以看到类似的变体年龄分布,尽管使用年龄带而不是单年年龄会稍微模糊一些。然而,美国的数据显示,男性死亡人数的增加在很大程度上取决于年龄和新冠病毒变种。2021年,相对于全因死亡率的变化,英格兰和威尔士被评估为“因”新冠肺炎(而不是“涉及”新冠肺炎)的死亡尤其被高估。这是2020年末新冠肺炎检测能力提高的副产品。讨论了严重急性呼吸系统综合征冠状病毒2型变异株年龄特异性的潜在结构-功能机制,以及小型非编码RNA(miRNA)的潜在作用。使用来自英格兰的数据,可以表明,未接种疫苗的人确实有一个独特的死于每种变体的年龄特征,并且疫苗接种以一种取决于年龄、性别和变体的方式改变了年龄特征的形状。提出的问题是,基于不同变体的疫苗是否具有特定的年龄特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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COVID-19-Related Age Profiles for SARS-CoV-2 Variants in England and Wales and States of the USA (2020 to 2022): Impact on All-Cause Mortality.

Since 2020, COVID-19 has caused serious mortality around the world. Given the ambiguity in establishing COVID-19 as the direct cause of death, we first investigate the effects of age and sex on all-cause mortality during 2020 and 2021 in England and Wales. Since infectious agents have their own unique age profile for death, we use a 9-year time series and several different methods to adjust single-year-of-age deaths in England and Wales during 2019 (the pre-COVID-19 base year) to a pathogen-neutral single-year-of-age baseline. This adjusted base year is then used to confirm the widely reported higher deaths in males for most ages above 43 in both 2020 and 2021. During 2020 (+COVID-19 but no vaccination), both male and female population-adjusted deaths significantly increased above age 35. A significant reduction in all-cause mortality among both males and females aged 75+ could be demonstrated in 2021 during the widespread COVID-19 vaccination period; however, deaths below age 75 progressively increased. This finding arises from a mix of vaccination coverage and year-of-age profiles of deaths for the different SARS-CoV-2 variants. In addition, specific effects of age around puberty were demonstrated, where females had higher deaths than males. There is evidence that year-of-birth cohorts may also be involved, indicating that immune priming to specific pathogen outbreaks in the past may have led to lower deaths for some birth cohorts. To specifically identify the age profile for the COVID-19 variants from 2020 to 2023, we employ the proportion of total deaths at each age that are potentially due to or 'with' COVID-19. The original Wuhan strain and the Alpha variant show somewhat limited divergence in the age profile, with the Alpha variant shifting to a moderately higher proportion of deaths below age 84. The Delta variant specifically targeted individuals below age 65. The Omicron variants showed a significantly lower proportion of overall mortality, with a markedly higher relative proportion of deaths above age 65, steeply increasing with age to a maximum around 100 years of age. A similar age profile for the variants can be seen in the age-banded deaths in US states, although they are slightly obscured by using age bands rather than single years of age. However, the US data shows that higher male deaths are greatly dependent on age and the COVID variant. Deaths assessed to be 'due to' COVID-19 (as opposed to 'involving' COVID-19) in England and Wales were especially overestimated in 2021 relative to the change in all-cause mortality. This arose as a by-product of an increase in COVID-19 testing capacity in late 2020. Potential structure-function mechanisms for the age-specificity of SARS-CoV-2 variants are discussed, along with potential roles for small noncoding RNAs (miRNAs). Using data from England, it is possible to show that the unvaccinated do indeed have a unique age profile for death from each variant and that vaccination alters the shape of the age profile in a manner dependent on age, sex, and the variant. The question is posed as to whether vaccines based on different variants carry a specific age profile.

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来源期刊
Infectious Disease Reports
Infectious Disease Reports INFECTIOUS DISEASES-
CiteScore
5.10
自引率
0.00%
发文量
82
审稿时长
11 weeks
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