Suppr超能文献

评估 0 至 4 岁儿童及其家庭成员中 SARS-CoV-2 感染的临床和病毒学特征。

Assessment of Clinical and Virological Characteristics of SARS-CoV-2 Infection Among Children Aged 0 to 4 Years and Their Household Members.

机构信息

Department of International Health, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland.

Marshfield Clinic Research Institute, Marshfield, Wisconsin.

出版信息

JAMA Netw Open. 2022 Aug 1;5(8):e2227348. doi: 10.1001/jamanetworkopen.2022.27348.

Abstract

IMPORTANCE

Few studies have prospectively assessed SARS-CoV-2 community infection in children aged 0 to 4 years. Information about SARS-CoV-2 incidence and clinical and virological features in young children could help guide prevention and mitigation strategies.

OBJECTIVE

To assess SARS-CoV-2 incidence, clinical and virological features, and symptoms in a prospective household cohort and to compare viral load by age group, symptoms, and SARS-CoV-2 lineage in young children, older children, and adults.

DESIGN, SETTING, AND PARTICIPANTS: This prospective cohort study enrolled 690 participants from 175 Maryland households with 1 or more children aged 0 to 4 years between November 24, 2020, and October 15, 2021. For 8 months after enrollment, participants completed weekly symptom questionnaires and submitted self-collected nasal swabs for SARS-CoV-2 qualitative real-time reverse transcriptase polymerase chain reaction (RT-PCR) testing, quantitative RT-PCR testing, and viral lineage determination. For the analyses, SARS-CoV-2 Alpha and Delta lineages were considered variants of interest or concern. Sera collected at enrollment and at approximately 4 months and 8 months after enrollment were assayed for SARS-CoV-2 spike and nucleocapsid protein antibodies.

MAIN OUTCOMES AND MEASURES

Incidence, clinical and virological characteristics, and symptoms of SARS-CoV-2 infection by age group and correlations between (1) highest detected viral load and symptom frequency and (2) highest detected viral load and SARS-CoV-2 lineage.

RESULTS

Among 690 participants (355 [51.4%] female and 335 [48.6%] male), 256 individuals (37.1%) were children aged 0 to 4 years, 100 (14.5%) were children aged 5 to 17 years, and 334 (48.4%) were adults aged 18 to 74 years. A total of 15 participants (2.2%) were Asian, 24 (3.5%) were Black, 603 (87.4%) were White, 43 (6.2%) were multiracial, and 5 (0.7%) were of other races; 33 participants (4.8%) were Hispanic, and 657 (95.2%) were non-Hispanic. Overall, 54 participants (7.8%) had SARS-CoV-2 infection during the surveillance period, including 22 of 256 children (8.6%) aged 0 to 4 years, 11 of 100 children (11.0%) aged 5 to 17 years, and 21 of 334 adults (6.3%). Incidence rates per 1000 person-weeks were 2.25 (95% CI, 1.28-3.65) infections among children aged 0 to 4 years, 3.48 (95% CI, 1.59-6.61) infections among children aged 5 to 17 years, and 1.08 (95% CI, 0.52-1.98) infections among adults. Children aged 0 to 17 years with SARS-CoV-2 infection were more frequently asymptomatic (11 of 30 individuals [36.7%]) compared with adults (3 of 21 individuals [14.3%]), with children aged 0 to 4 years most frequently asymptomatic (7 of 19 individuals [36.8%]). The highest detected viral load did not differ between asymptomatic vs symptomatic individuals overall (median [IQR], 2.8 [1.5-3.3] log10 copies/mL vs 2.8 [1.8-4.4] log10 copies/mL) or by age group (median [IQR] for ages 0-4 years, 2.7 [2.4-4.4] log10 copies/mL; ages 5-17 years: 2.4 [1.1-4.0] log10 copies/mL; ages 18-74 years: 2.9 [1.9-4.6] log10 copies/mL). The number of symptoms was significantly correlated with viral load among adults (R = 0.69; P < .001) but not children (ages 0-4 years: R = 0.02; P = .91; ages 5-17 years: R = 0.18; P = .58). The highest detected viral load was greater among those with Delta variant infections (median [IQR], 4.4 [3.9-5.1] log10 copies/mL) than those with infections from variants not of interest or concern (median [IQR], 1.9 [1.1-3.6] log10 copies/mL; P = .009) or those with Alpha variant infections (median [IQR], 2.6 [2.3-3.4] log10 copies/mL; P = .006).

CONCLUSIONS AND RELEVANCE

In this study, SARS-CoV-2 infections were frequently asymptomatic among children aged 0 to 4 years; the presence and number of symptoms did not correlate with viral load. These findings suggest that symptom screening may be insufficient to prevent outbreaks involving young children.

摘要

重要性

很少有研究前瞻性评估 0 至 4 岁儿童的社区 SARS-CoV-2 感染情况。关于年幼儿童 SARS-CoV-2 发病率、临床和病毒学特征以及症状的信息,有助于指导预防和缓解策略。

目的

评估前瞻性家庭队列中 SARS-CoV-2 的发病率、临床和病毒学特征和症状,并比较年幼儿童、年龄较大儿童和成年人的病毒载量、症状和 SARS-CoV-2 谱系。

设计、地点和参与者:本前瞻性队列研究纳入了 2020 年 11 月 24 日至 2021 年 10 月 15 日期间来自马里兰州 175 个家庭的 690 名 0 至 4 岁的 1 名或多名儿童。在入组后 8 个月期间,参与者每周完成症状问卷,并提交自我采集的鼻拭子,用于 SARS-CoV-2 定性实时逆转录酶聚合酶链反应(RT-PCR)检测、定量 RT-PCR 检测和病毒谱系确定。在分析中,SARS-CoV-2 Alpha 和 Delta 谱系被认为是关注或关注的变异。在入组时和入组后约 4 个月和 8 个月收集的血清中检测 SARS-CoV-2 刺突和核衣壳蛋白抗体。

主要结果和措施

按年龄组和(1)最高检测病毒载量与症状频率和(2)最高检测病毒载量与 SARS-CoV-2 谱系之间的相关性,评估 SARS-CoV-2 感染的发病率、临床和病毒学特征以及症状。

结果

在 690 名参与者(355 [51.4%] 女性和 335 [48.6%] 男性)中,256 名(37.1%)为 0 至 4 岁儿童,100 名(14.5%)为 5 至 17 岁儿童,334 名(48.4%)为 18 至 74 岁成年人。共有 15 名参与者(2.2%)为亚洲人,24 名(3.5%)为黑人,603 名(87.4%)为白人,43 名(6.2%)为多种族,5 名(0.7%)为其他种族;33 名参与者(4.8%)为西班牙裔,657 名(95.2%)为非西班牙裔。总的来说,54 名参与者(7.8%)在监测期间感染了 SARS-CoV-2,包括 22 名(8.6%)0 至 4 岁儿童、11 名(11.0%)5 至 17 岁儿童和 21 名(6.3%)成年人。0 至 4 岁儿童的发病率为每 1000 人-周 2.25 例(95%CI,1.28-3.65),5 至 17 岁儿童的发病率为每 1000 人-周 3.48 例(95%CI,1.59-6.61),成年人的发病率为每 1000 人-周 1.08 例(95%CI,0.52-1.98)。SARS-CoV-2 感染的 0 至 17 岁儿童更常无症状(30 名中有 11 名[36.7%]),而成年人中无症状者(21 名中有 3 名[14.3%])较少,0 至 4 岁儿童最常无症状(19 名中有 7 名[36.8%])。无症状者与有症状者之间(中位数[IQR],2.8[1.5-3.3]log10 拷贝/mL 比 2.8[1.8-4.4]log10 拷贝/mL)或按年龄组(0-4 岁的中位数[IQR],2.7[2.4-4.4]log10 拷贝/mL;5-17 岁的中位数[IQR],2.4[1.1-4.0]log10 拷贝/mL;18-74 岁的中位数[IQR],2.9[1.9-4.6]log10 拷贝/mL)的最高检测病毒载量无差异。成人中病毒载量与症状数量呈显著相关性(R=0.69;P<0.001),但儿童(0-4 岁:R=0.02;P=0.91;5-17 岁:R=0.18;P=0.58)中无相关性。Delta 变异感染的最高检测病毒载量(中位数[IQR],4.4[3.9-5.1]log10 拷贝/mL)大于非关注或关注变异感染(中位数[IQR],1.9[1.1-3.6]log10 拷贝/mL;P=0.009)或 Alpha 变异感染(中位数[IQR],2.6[2.3-3.4]log10 拷贝/mL;P=0.006)。

结论和相关性

在这项研究中,0 至 4 岁儿童的 SARS-CoV-2 感染常无症状;症状的存在和数量与病毒载量无关。这些发现表明,症状筛查可能不足以预防涉及幼儿的暴发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/943c/9434363/869c1dd70893/jamanetwopen-e2227348-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验